Skip to main content
Erschienen in: Drugs 15/2008

01.10.2008 | Review Article

Pathogenesis and Treatment of Pruritus in Cholestasis

verfasst von: Andreas E. Kremer, MD, Ulrich Beuers, Ronald P. J. Oude-Elferink, Thomas Pusl

Erschienen in: Drugs | Ausgabe 15/2008

Einloggen, um Zugang zu erhalten

Abstract

Pruritus is an enigmatic, seriously disabling symptom accompanying cholestatic liver diseases and a broad range of other disorders. Most recently, novel itchspecificneuronal pathways, itch mediators and their relevant receptors have been identified. In addition, new antipruritic therapeutic strategies have been developed and/or are under evaluation. This review highlights recent experimental and clinical findings focusing on the pathogenesis and actual treatment of pruritus in cholestatic liver disease. Evidence-based therapeutic recommendations, including the use of anion exchange resins cholestyramine, colestipol and colesevelam, the microsomal enzyme inducer rifampicin, the opioid receptor antagonists naltrexone and naloxone, and the serotonin reuptake inhibitor sertraline, are provided.
Literatur
1.
Zurück zum Zitat Haffenreffer S. Nosodochium, in quo cutis, eique adaerentium partium, affectus omnes, singulari methodo, et cognoscendi e curandi fidelisime traduntur. Ulmae: Kuhnen; 1660: 98–102 Haffenreffer S. Nosodochium, in quo cutis, eique adaerentium partium, affectus omnes, singulari methodo, et cognoscendi e curandi fidelisime traduntur. Ulmae: Kuhnen; 1660: 98–102
2.
Zurück zum Zitat Stander S, Weisshaar E, Mettang T, et al. Clinical classification of itch: a position paper of the International Forum for the Study of Itch. Acta Derm Venereol 2007; 87(4): 291–4PubMedCrossRef Stander S, Weisshaar E, Mettang T, et al. Clinical classification of itch: a position paper of the International Forum for the Study of Itch. Acta Derm Venereol 2007; 87(4): 291–4PubMedCrossRef
3.
Zurück zum Zitat Heathcote EJ. Management of primary biliary cirrhosis. The American Association for the Study of Liver Diseases practice guidelines. Hepatology 2000 Apr; 31(4): 1005–13 Heathcote EJ. Management of primary biliary cirrhosis. The American Association for the Study of Liver Diseases practice guidelines. Hepatology 2000 Apr; 31(4): 1005–13
4.
Zurück zum Zitat Swain MG. Pruritus and lethargy in the primary biliary cirrhosis patient. In: Neuberger J, editor. Primary biliary cirrhosis. Eastbourne: West End Studios, 1999: 75–81 Swain MG. Pruritus and lethargy in the primary biliary cirrhosis patient. In: Neuberger J, editor. Primary biliary cirrhosis. Eastbourne: West End Studios, 1999: 75–81
5.
Zurück zum Zitat Bergasa NV, Mehlman JK, Jones EA. Pruritus and fatigue in primary biliary cirrhosis. Baillieres Best Pract Res Clin Gastroenterol 2000; 14(4): 643–55PubMedCrossRef Bergasa NV, Mehlman JK, Jones EA. Pruritus and fatigue in primary biliary cirrhosis. Baillieres Best Pract Res Clin Gastroenterol 2000; 14(4): 643–55PubMedCrossRef
6.
Zurück zum Zitat Pusl T, Beuers U. Ursodeoxycholic acid treatment of vanishing bile duct syndromes. World J Gastroenterol 2006 Jun 14; 12(22): 3487–95PubMed Pusl T, Beuers U. Ursodeoxycholic acid treatment of vanishing bile duct syndromes. World J Gastroenterol 2006 Jun 14; 12(22): 3487–95PubMed
7.
Zurück zum Zitat Lucey MR, Neuberger JM, Williams R. Primary biliary cirrhosis in men. Gut 1986; 27(11): 1373–6PubMedCrossRef Lucey MR, Neuberger JM, Williams R. Primary biliary cirrhosis in men. Gut 1986; 27(11): 1373–6PubMedCrossRef
8.
Zurück zum Zitat Bergasa NV, Jones EA. The pruritus of cholestasis: potential pathogenic and therapeutic implications of opioids. Gastroenterology 1995; 108(5): 1582–8PubMedCrossRef Bergasa NV, Jones EA. The pruritus of cholestasis: potential pathogenic and therapeutic implications of opioids. Gastroenterology 1995; 108(5): 1582–8PubMedCrossRef
11.
Zurück zum Zitat Elias E, Burra P. Primary biliary cirrhosis: symptomatic treatment. J Gastroenterol Hepatol 1991 Nov–Dec; 6(6): 570–3PubMedCrossRef Elias E, Burra P. Primary biliary cirrhosis: symptomatic treatment. J Gastroenterol Hepatol 1991 Nov–Dec; 6(6): 570–3PubMedCrossRef
12.
Zurück zum Zitat Elias E. Liver transplantation. J R Coll Physicians Lond 1993; 27(3): 224–32PubMed Elias E. Liver transplantation. J R Coll Physicians Lond 1993; 27(3): 224–32PubMed
13.
Zurück zum Zitat Neuberger J, Jones EA. Liver transplantation for intractable pruritus is contraindicated before an adequate trial of opiate antagonist therapy. Eur J Gastroenterol Hepatol 2001; 13(11): 1393–4PubMedCrossRef Neuberger J, Jones EA. Liver transplantation for intractable pruritus is contraindicated before an adequate trial of opiate antagonist therapy. Eur J Gastroenterol Hepatol 2001; 13(11): 1393–4PubMedCrossRef
14.
Zurück zum Zitat Savin JA, Paterson WD, Oswald I. Scratching during sleep. Lancet 1973; II(7824): 296–7CrossRef Savin JA, Paterson WD, Oswald I. Scratching during sleep. Lancet 1973; II(7824): 296–7CrossRef
15.
Zurück zum Zitat Stein H, Bijak M, Heerd E, et al. Pruritometer 1: portable measuring system for quantifying scratching as an objective measure of cholestatic pruritus [in German]. Biomed Tech (Berl) 1996; 41(9): 248–52CrossRef Stein H, Bijak M, Heerd E, et al. Pruritometer 1: portable measuring system for quantifying scratching as an objective measure of cholestatic pruritus [in German]. Biomed Tech (Berl) 1996; 41(9): 248–52CrossRef
16.
Zurück zum Zitat Bijak M, Mayr W, Rafolt D, et al. Pruritometer 2: portable recording system for the quantification of scratching as objective criterion for the pruritus. Biomed Tech (Berl) 2001; 46(5): 137–41CrossRef Bijak M, Mayr W, Rafolt D, et al. Pruritometer 2: portable recording system for the quantification of scratching as objective criterion for the pruritus. Biomed Tech (Berl) 2001; 46(5): 137–41CrossRef
17.
Zurück zum Zitat Schworer H, Ramadori G. Improvement of cholestatic pruritus by ondansetron [letter]. Lancet 1993; 341(8855): 1277PubMedCrossRef Schworer H, Ramadori G. Improvement of cholestatic pruritus by ondansetron [letter]. Lancet 1993; 341(8855): 1277PubMedCrossRef
18.
Zurück zum Zitat Schworer H, Hartmann H, Ramadori G. Relief of cholestatic pruritus by a novel class of drugs: 5-hydroxytryptamine type 3 (5-HT3) receptor antagonists: effectiveness of ondansetron. Pain 1995; 61(1): 33–7PubMedCrossRef Schworer H, Hartmann H, Ramadori G. Relief of cholestatic pruritus by a novel class of drugs: 5-hydroxytryptamine type 3 (5-HT3) receptor antagonists: effectiveness of ondansetron. Pain 1995; 61(1): 33–7PubMedCrossRef
19.
Zurück zum Zitat O’Donohue JW, Pereira SP, Ashdown AC, et al. A controlled trial of ondansetron in the pruritus of cholestasis. Aliment Pharmacol Ther 2005; 21(8): 1041–5PubMedCrossRef O’Donohue JW, Pereira SP, Ashdown AC, et al. A controlled trial of ondansetron in the pruritus of cholestasis. Aliment Pharmacol Ther 2005; 21(8): 1041–5PubMedCrossRef
20.
Zurück zum Zitat Jones EA, Molenaar HA, Oosting J. Ondansetron and pruritus in chronic liver disease: a controlled study. Hepatogastroenterology 2007; 54(76): 1196–9PubMed Jones EA, Molenaar HA, Oosting J. Ondansetron and pruritus in chronic liver disease: a controlled study. Hepatogastroenterology 2007; 54(76): 1196–9PubMed
21.
Zurück zum Zitat Wolfhagen FH, Sternieri E, Hop WC, et al. Oral naltrexone treatment for cholestatic pruritus: a double-blind, placebo-controlled study. Gastroenterology 1997; 113(4): 1264–9PubMedCrossRef Wolfhagen FH, Sternieri E, Hop WC, et al. Oral naltrexone treatment for cholestatic pruritus: a double-blind, placebo-controlled study. Gastroenterology 1997; 113(4): 1264–9PubMedCrossRef
22.
Zurück zum Zitat Villamil AG, Bandi JC, Galdame OA, et al. Efficacy of lidocaine in the treatment of pruritus in patients with chronic cholestatic liver diseases. Am J Med 2005; 118(10): 1160–3PubMedCrossRef Villamil AG, Bandi JC, Galdame OA, et al. Efficacy of lidocaine in the treatment of pruritus in patients with chronic cholestatic liver diseases. Am J Med 2005; 118(10): 1160–3PubMedCrossRef
23.
Zurück zum Zitat Bergasa NV, McGee M, Ginsburg IH, et al. Gabapentin in patients with the pruritus of cholestasis: a double-blind, randomized, placebo-controlled trial. Hepatology 2006 Nov; 44(5): 1317–23PubMedCrossRef Bergasa NV, McGee M, Ginsburg IH, et al. Gabapentin in patients with the pruritus of cholestasis: a double-blind, randomized, placebo-controlled trial. Hepatology 2006 Nov; 44(5): 1317–23PubMedCrossRef
24.
Zurück zum Zitat von Frey M. Zur physiologie des juckreizes. Arch Neerl Physiol 1922; 7: 142–5 von Frey M. Zur physiologie des juckreizes. Arch Neerl Physiol 1922; 7: 142–5
25.
26.
Zurück zum Zitat Shelley WB, Arthur RP. The neurohistology and neurophysiology of the itch sensation in man. AMA Arch Derm 1957; 76(3): 296–323PubMedCrossRef Shelley WB, Arthur RP. The neurohistology and neurophysiology of the itch sensation in man. AMA Arch Derm 1957; 76(3): 296–323PubMedCrossRef
27.
Zurück zum Zitat McMahon SB, Koltzenburg M. Itching for an explanation. Trends Neurosci 1992; 15(12): 497–501PubMedCrossRef McMahon SB, Koltzenburg M. Itching for an explanation. Trends Neurosci 1992; 15(12): 497–501PubMedCrossRef
28.
29.
30.
Zurück zum Zitat Schmelz M, Schmidt R, Bickel A, et al. Specific C-receptors for itch in human skin. J Neurosci 1997; 17(20): 8003–8PubMed Schmelz M, Schmidt R, Bickel A, et al. Specific C-receptors for itch in human skin. J Neurosci 1997; 17(20): 8003–8PubMed
31.
Zurück zum Zitat Andrew D, Craig AD. Spinothalamic lamina I neurons selectively sensitive to histamine: a central neural pathway for itch. Nat Neurosci 2001; 4(1): 72–7PubMedCrossRef Andrew D, Craig AD. Spinothalamic lamina I neurons selectively sensitive to histamine: a central neural pathway for itch. Nat Neurosci 2001; 4(1): 72–7PubMedCrossRef
32.
Zurück zum Zitat Green BG, Shaffer GS. The sensory response to capsaicin during repeated topical exposures: differential effects on sensations of itching and pungency. Pain 1993; 53(3): 323–34PubMedCrossRef Green BG, Shaffer GS. The sensory response to capsaicin during repeated topical exposures: differential effects on sensations of itching and pungency. Pain 1993; 53(3): 323–34PubMedCrossRef
33.
Zurück zum Zitat Ikoma A, Steinhoff M, Stander S, et al. The neurobiology of itch. Nat Rev Neurosci 2006; 7(7): 535–47PubMedCrossRef Ikoma A, Steinhoff M, Stander S, et al. The neurobiology of itch. Nat Rev Neurosci 2006; 7(7): 535–47PubMedCrossRef
34.
Zurück zum Zitat Davidson S, Zhang X, Yoon CH, et al. The itch-producing agents histamine and cowhage activate separate populations of primate spinothalamic tract neurons. J Neurosci 2007; 27(37): 10007–14PubMedCrossRef Davidson S, Zhang X, Yoon CH, et al. The itch-producing agents histamine and cowhage activate separate populations of primate spinothalamic tract neurons. J Neurosci 2007; 27(37): 10007–14PubMedCrossRef
35.
Zurück zum Zitat Darsow U, Scharein E, Simon D, et al. New aspects of itch pathophysiology: component analysis of atopic itch using the ‘Eppendorf Itch Questionnaire’. Int Arch Allergy Immunol 2001; 124(1-3): 326–31PubMedCrossRef Darsow U, Scharein E, Simon D, et al. New aspects of itch pathophysiology: component analysis of atopic itch using the ‘Eppendorf Itch Questionnaire’. Int Arch Allergy Immunol 2001; 124(1-3): 326–31PubMedCrossRef
36.
Zurück zum Zitat Atanassoff PG, Brull SJ, Zhang J, et al. Enhancement of experimental pruritus and mechanically evoked dysesthesiae with local anesthesia. Somatosens Mot Res 1999; 16(4): 291–8PubMedCrossRef Atanassoff PG, Brull SJ, Zhang J, et al. Enhancement of experimental pruritus and mechanically evoked dysesthesiae with local anesthesia. Somatosens Mot Res 1999; 16(4): 291–8PubMedCrossRef
38.
Zurück zum Zitat Ikoma A, Rukwied R, Stander S, et al. Neurophysiology of pruritus: interaction of itch and pain. Arch Dermatol 2003; 139(11): 1475–8PubMedCrossRef Ikoma A, Rukwied R, Stander S, et al. Neurophysiology of pruritus: interaction of itch and pain. Arch Dermatol 2003; 139(11): 1475–8PubMedCrossRef
40.
Zurück zum Zitat Darsow U, Drzezga A, Frisch M, et al. Processing of histamine-induced itch in the human cerebral cortex: a correlation analysis with dermal reactions. J Invest Dermatol 2000; 115(6): 1029–33PubMedCrossRef Darsow U, Drzezga A, Frisch M, et al. Processing of histamine-induced itch in the human cerebral cortex: a correlation analysis with dermal reactions. J Invest Dermatol 2000; 115(6): 1029–33PubMedCrossRef
41.
Zurück zum Zitat Mochizuki H, Tashiro M, Kano M, et al. Imaging of central itch modulation in the human brain using positron emission tomography. Pain 2003; 105(1-2): 339–46PubMedCrossRef Mochizuki H, Tashiro M, Kano M, et al. Imaging of central itch modulation in the human brain using positron emission tomography. Pain 2003; 105(1-2): 339–46PubMedCrossRef
42.
Zurück zum Zitat Drzezga A, Darsow U, Treede RD, et al. Central activation by histamine-induced itch: analogies to pain processing: a correlational analysis of O-15 H2O positron emission tomography studies. Pain 2001; 92(1–2): 295–305PubMedCrossRef Drzezga A, Darsow U, Treede RD, et al. Central activation by histamine-induced itch: analogies to pain processing: a correlational analysis of O-15 H2O positron emission tomography studies. Pain 2001; 92(1–2): 295–305PubMedCrossRef
43.
Zurück zum Zitat Mochizuki H, Sadato N, Saito DN, et al. Neural correlates of perceptual difference between itching and pain: a human fMRI study. Neuroimage 2007; 36(3): 706–17PubMedCrossRef Mochizuki H, Sadato N, Saito DN, et al. Neural correlates of perceptual difference between itching and pain: a human fMRI study. Neuroimage 2007; 36(3): 706–17PubMedCrossRef
44.
Zurück zum Zitat Yosipovitch G, Duque MI, Fast K, et al. Scratching and noxious heat stimuli inhibit itch in humans: a psychophysical study. Br J Dermatol 2007; 156(4): 629–34PubMedCrossRef Yosipovitch G, Duque MI, Fast K, et al. Scratching and noxious heat stimuli inhibit itch in humans: a psychophysical study. Br J Dermatol 2007; 156(4): 629–34PubMedCrossRef
45.
Zurück zum Zitat Yosipovitch G, Ishiuji Y, Patel TS, et al. The brain processing of scratching. J Invest Dermatol 2008 Jul; 128(7): 1806–11PubMedCrossRef Yosipovitch G, Ishiuji Y, Patel TS, et al. The brain processing of scratching. J Invest Dermatol 2008 Jul; 128(7): 1806–11PubMedCrossRef
46.
Zurück zum Zitat Paus R, Schmelz M, Biro T, et al. Frontiers in pruritus research: scratching the brain for more effective itch therapy. J Clin Invest 2006; 116(5): 1174–86PubMedCrossRef Paus R, Schmelz M, Biro T, et al. Frontiers in pruritus research: scratching the brain for more effective itch therapy. J Clin Invest 2006; 116(5): 1174–86PubMedCrossRef
47.
Zurück zum Zitat Steinhoff M, Bienenstock J, Schmelz M, et al. Neurophysiological, neuroimmunological, and neuroendocrine basis of pruritus. J Invest Dermatol 2006; 126(8): 1705–18PubMedCrossRef Steinhoff M, Bienenstock J, Schmelz M, et al. Neurophysiological, neuroimmunological, and neuroendocrine basis of pruritus. J Invest Dermatol 2006; 126(8): 1705–18PubMedCrossRef
48.
Zurück zum Zitat Jones EA, Bergasa NV. The pruritus of cholestasis: from bile acids to opiate agonists. Hepatology 1990; 11(5): 884–7PubMedCrossRef Jones EA, Bergasa NV. The pruritus of cholestasis: from bile acids to opiate agonists. Hepatology 1990; 11(5): 884–7PubMedCrossRef
49.
Zurück zum Zitat Bergasa NV. Pruritus in primary biliary cirrhosis: pathogenesis and therapy. Clin Liver Dis 2008; 12(2): 385–406PubMedCrossRef Bergasa NV. Pruritus in primary biliary cirrhosis: pathogenesis and therapy. Clin Liver Dis 2008; 12(2): 385–406PubMedCrossRef
50.
Zurück zum Zitat Bergasa NV. Update on the treatment of the pruritus of cholestasis. Clin Liver Dis 2008; 12(1): 219–34PubMedCrossRef Bergasa NV. Update on the treatment of the pruritus of cholestasis. Clin Liver Dis 2008; 12(1): 219–34PubMedCrossRef
51.
52.
Zurück zum Zitat Datta DV, Sherlock S. Cholestyramine for long term relief of the pruritus complicating intrahepatic cholestasis. Gastroenterology 1966; 50(3): 323–32PubMed Datta DV, Sherlock S. Cholestyramine for long term relief of the pruritus complicating intrahepatic cholestasis. Gastroenterology 1966; 50(3): 323–32PubMed
53.
Zurück zum Zitat Stapelbroek JM, van Erpecum KJ, Klomp LW, et al. Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis. Hepatology 2006; 43(1): 51–3PubMedCrossRef Stapelbroek JM, van Erpecum KJ, Klomp LW, et al. Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis. Hepatology 2006; 43(1): 51–3PubMedCrossRef
54.
Zurück zum Zitat Beuers U, Gerken G, Pusl T. Biliary drainage transiently relieves intractable pruritus in primary biliary cirrhosis. Hepatology 2006 Jul; 44(1): 280–1PubMedCrossRef Beuers U, Gerken G, Pusl T. Biliary drainage transiently relieves intractable pruritus in primary biliary cirrhosis. Hepatology 2006 Jul; 44(1): 280–1PubMedCrossRef
55.
Zurück zum Zitat Huet PM, Rautureau M, Dhumeaux D, et al. The effects of biliary drainage in cholestatic hepatitis [in French]. Rev Med Chir Mal Foie 1970; 45(5): 271–8PubMed Huet PM, Rautureau M, Dhumeaux D, et al. The effects of biliary drainage in cholestatic hepatitis [in French]. Rev Med Chir Mal Foie 1970; 45(5): 271–8PubMed
56.
Zurück zum Zitat Rupp N. Indications and results of percutaneous transhepatic bile-duct drainage [in German]. Chirurg 1979; 50(4): 233–8PubMed Rupp N. Indications and results of percutaneous transhepatic bile-duct drainage [in German]. Chirurg 1979; 50(4): 233–8PubMed
57.
Zurück zum Zitat Hall RI, Denyer ME, Chapman AH. Percutaneous-endoscopic placement of endoprostheses for relief of jaundice caused by inoperable bile duct strictures. Surgery 1990; 107(2): 224–7PubMed Hall RI, Denyer ME, Chapman AH. Percutaneous-endoscopic placement of endoprostheses for relief of jaundice caused by inoperable bile duct strictures. Surgery 1990; 107(2): 224–7PubMed
58.
Zurück zum Zitat Jones EA, Bergasa NV. Evolving concepts of the pathogenesis and treatment of the pruritus of cholestasis. Can J Gastroenterol 2000; 14(1): 33–40PubMed Jones EA, Bergasa NV. Evolving concepts of the pathogenesis and treatment of the pruritus of cholestasis. Can J Gastroenterol 2000; 14(1): 33–40PubMed
59.
Zurück zum Zitat Mamianetti A, Tripodi V, Vescina C, et al. Serum bile acids and pruritus in hemodialysis patients. Clin Nephrol 2000; 53(3): 194–8PubMed Mamianetti A, Tripodi V, Vescina C, et al. Serum bile acids and pruritus in hemodialysis patients. Clin Nephrol 2000; 53(3): 194–8PubMed
60.
Zurück zum Zitat Jimenez F, Monte MJ, El-Mir MY, et al. Chronic renal failure-induced changes in serum and urine bile acid profiles. Dig Dis Sci 2002; 47(11): 2398–406PubMedCrossRef Jimenez F, Monte MJ, El-Mir MY, et al. Chronic renal failure-induced changes in serum and urine bile acid profiles. Dig Dis Sci 2002; 47(11): 2398–406PubMedCrossRef
61.
Zurück zum Zitat Murphy GM, Ross A, Billing BH. Serum bile acids in primary biliary cirrhosis. Gut 1972; 13(3): 201–6PubMedCrossRef Murphy GM, Ross A, Billing BH. Serum bile acids in primary biliary cirrhosis. Gut 1972; 13(3): 201–6PubMedCrossRef
62.
Zurück zum Zitat Ghent CN, Bloomer JR, Klatskin G. Elevations in skin tissue levels of bile acids in human cholestasis: relation to serum levels and topruritus. Gastroenterology 1977; 73(5): 1125–30PubMed Ghent CN, Bloomer JR, Klatskin G. Elevations in skin tissue levels of bile acids in human cholestasis: relation to serum levels and topruritus. Gastroenterology 1977; 73(5): 1125–30PubMed
63.
Zurück zum Zitat Freedman MR, Holzbach RT, Ferguson DR. Pruritus in cholestasis: no direct causative role for bile acid retention. Am J Med 1981; 70(5): 1011–6PubMedCrossRef Freedman MR, Holzbach RT, Ferguson DR. Pruritus in cholestasis: no direct causative role for bile acid retention. Am J Med 1981; 70(5): 1011–6PubMedCrossRef
64.
Zurück zum Zitat Bartholomew TC, Summerfield JA, Billing BH, et al. Bile acid profiles of human serum and skin interstitial fluid and their relationship to pruritus studied by gas chromatography-mass spectrometry. Clin Sci (Lond) 1982; 63(1): 65–73 Bartholomew TC, Summerfield JA, Billing BH, et al. Bile acid profiles of human serum and skin interstitial fluid and their relationship to pruritus studied by gas chromatography-mass spectrometry. Clin Sci (Lond) 1982; 63(1): 65–73
65.
Zurück zum Zitat Silverberg DS, Iaina A, Reisin E, et al. Cholestyramine in uraemic pruritus. Br Med J 1997 Mar 19; 1(6063): 752–3CrossRef Silverberg DS, Iaina A, Reisin E, et al. Cholestyramine in uraemic pruritus. Br Med J 1997 Mar 19; 1(6063): 752–3CrossRef
66.
Zurück zum Zitat Chanarin I, Szur L. Relief of intractable pruritis in polycythaemia rubra vera with cholestyramine [letter]. Br J Hematol 1975 Apr; 29(4): 669–70CrossRef Chanarin I, Szur L. Relief of intractable pruritis in polycythaemia rubra vera with cholestyramine [letter]. Br J Hematol 1975 Apr; 29(4): 669–70CrossRef
67.
Zurück zum Zitat Rupprecht R. Neuroactive steroids: mechanisms of action and neuropsychopharmacological properties. Psychoneuroendocrinology 2003; 28(2): 139–68PubMedCrossRef Rupprecht R. Neuroactive steroids: mechanisms of action and neuropsychopharmacological properties. Psychoneuroendocrinology 2003; 28(2): 139–68PubMedCrossRef
68.
Zurück zum Zitat Melcangi RC, Garcia-Segura LM, Mensah-Nyagan AG. Neuroactive steroids: state of the art and new perspectives. Cell Mol Life Sci 2008; 65(5): 777–97PubMedCrossRef Melcangi RC, Garcia-Segura LM, Mensah-Nyagan AG. Neuroactive steroids: state of the art and new perspectives. Cell Mol Life Sci 2008; 65(5): 777–97PubMedCrossRef
69.
Zurück zum Zitat Park-Chung M, Malayev A, Purdy RH, et al. Sulfated and unsulfated steroids modulate gamma-aminobutyric acid A receptor function through distinct sites. Brain Res 1999; 830(1): 72–87PubMedCrossRef Park-Chung M, Malayev A, Purdy RH, et al. Sulfated and unsulfated steroids modulate gamma-aminobutyric acid A receptor function through distinct sites. Brain Res 1999; 830(1): 72–87PubMedCrossRef
70.
Zurück zum Zitat Wu FS, Gibbs TT, Farb DH. Inverse modulation of gamma-aminobutyric acid- and glycine-induced currents by progesterone. Mol Pharmacol 1990; 37(5): 597–602PubMed Wu FS, Gibbs TT, Farb DH. Inverse modulation of gamma-aminobutyric acid- and glycine-induced currents by progesterone. Mol Pharmacol 1990; 37(5): 597–602PubMed
71.
Zurück zum Zitat Park-Chung M, Wu FS, Purdy RH, et al. Distinct sites for inverse modulation of N-methyl-D-aspartate receptors by sulfated steroids. Mol Pharmacol 1997; 52(6): 1113–23PubMed Park-Chung M, Wu FS, Purdy RH, et al. Distinct sites for inverse modulation of N-methyl-D-aspartate receptors by sulfated steroids. Mol Pharmacol 1997; 52(6): 1113–23PubMed
72.
Zurück zum Zitat Weaver Jr CE, Marek P, Park-Chung M, et al. Neuroprotective activity of a new class of steroidal inhibitors of the N-methyl-D-aspartate receptor. Proc Natl Acad Sci U S A 1997; 94(19): 10450–4PubMedCrossRef Weaver Jr CE, Marek P, Park-Chung M, et al. Neuroprotective activity of a new class of steroidal inhibitors of the N-methyl-D-aspartate receptor. Proc Natl Acad Sci U S A 1997; 94(19): 10450–4PubMedCrossRef
73.
Zurück zum Zitat Weaver Jr CE, Park-Chung M, Gibbs TT, et al. 17β-Estradiol protects against NMDA-induced excitotoxicity by direct inhibition of NMDA receptors. Brain Res 1997; 761(2): 338–41PubMedCrossRef Weaver Jr CE, Park-Chung M, Gibbs TT, et al. 17β-Estradiol protects against NMDA-induced excitotoxicity by direct inhibition of NMDA receptors. Brain Res 1997; 761(2): 338–41PubMedCrossRef
74.
Zurück zum Zitat Rupprecht R, Holsboer F. Neuroactive steroids: mechanisms of action and neuropsychopharmacological perspectives. Trends Neurosci 1999; 22(9): 410–6PubMedCrossRef Rupprecht R, Holsboer F. Neuroactive steroids: mechanisms of action and neuropsychopharmacological perspectives. Trends Neurosci 1999; 22(9): 410–6PubMedCrossRef
75.
Zurück zum Zitat Wetzel CH, Hermann B, Behl C, et al. Functional antagonism of gonadal steroids at the 5-hydroxytryptamine type 3 receptor. Mol Endocrinol 1998; 12(9): 1441–51PubMedCrossRef Wetzel CH, Hermann B, Behl C, et al. Functional antagonism of gonadal steroids at the 5-hydroxytryptamine type 3 receptor. Mol Endocrinol 1998; 12(9): 1441–51PubMedCrossRef
76.
Zurück zum Zitat Bullock AE, Clark AL, Grady SR, et al. Neurosteroids modulate nicotinic receptor function in mouse striatal and thalamic synaptosomes. J Neurochem 1997; 68(6): 2412–23PubMedCrossRef Bullock AE, Clark AL, Grady SR, et al. Neurosteroids modulate nicotinic receptor function in mouse striatal and thalamic synaptosomes. J Neurochem 1997; 68(6): 2412–23PubMedCrossRef
77.
Zurück zum Zitat Chen SC, Wu FS. Mechanism underlying inhibition of the capsaicin receptor-mediated current by pregnenolone sulfate in rat dorsal root ganglion neurons. Brain Res 2004; 1027(1–2): 196–200PubMedCrossRef Chen SC, Wu FS. Mechanism underlying inhibition of the capsaicin receptor-mediated current by pregnenolone sulfate in rat dorsal root ganglion neurons. Brain Res 2004; 1027(1–2): 196–200PubMedCrossRef
78.
Zurück zum Zitat Pathirathna S, Brimelow BC, Jagodic MM, et al. New evidence that both T-type calcium channels and GABAA channels are responsible for the potent peripheral analgesic effects of 5alpha-reduced neuroactive steroids. Pain 2005; 114(3): 429–43PubMedCrossRef Pathirathna S, Brimelow BC, Jagodic MM, et al. New evidence that both T-type calcium channels and GABAA channels are responsible for the potent peripheral analgesic effects of 5alpha-reduced neuroactive steroids. Pain 2005; 114(3): 429–43PubMedCrossRef
79.
Zurück zum Zitat Chen SC, Liu BC, Chen CW, et al. Intradermal pregnenolone sulfate attenuates capsaicin-induced nociception in rats. Biochem Biophys Res Commun 2006; 349(2): 626–33PubMedCrossRef Chen SC, Liu BC, Chen CW, et al. Intradermal pregnenolone sulfate attenuates capsaicin-induced nociception in rats. Biochem Biophys Res Commun 2006; 349(2): 626–33PubMedCrossRef
80.
Zurück zum Zitat Green AD, Young KK, Lehto SG, et al. Influence of genotype, dose and sex on pruritogen-induced scratching behavior in the mouse. Pain 2006; 124(1-2): 50–8PubMedCrossRef Green AD, Young KK, Lehto SG, et al. Influence of genotype, dose and sex on pruritogen-induced scratching behavior in the mouse. Pain 2006; 124(1-2): 50–8PubMedCrossRef
81.
Zurück zum Zitat Kancheva R, Hill M, Cibula D, et al. Relationships of circulating pregnanolone isomers and their polar conjugates to the status of sex, menstrual cycle, and pregnancy. J Endocrinol 2007; 195(1): 67–78PubMedCrossRef Kancheva R, Hill M, Cibula D, et al. Relationships of circulating pregnanolone isomers and their polar conjugates to the status of sex, menstrual cycle, and pregnancy. J Endocrinol 2007; 195(1): 67–78PubMedCrossRef
82.
Zurück zum Zitat Reyes H, Sjovall J. Bile acids and progesterone metabolites in intrahepatic cholestasis of pregnancy. Ann Med 2000 Mar; 32(2): 94–106PubMedCrossRef Reyes H, Sjovall J. Bile acids and progesterone metabolites in intrahepatic cholestasis of pregnancy. Ann Med 2000 Mar; 32(2): 94–106PubMedCrossRef
83.
84.
Zurück zum Zitat Glantz A, Reilly SJ, Benthin L, et al. Intrahepatic cholestasis of pregnancy: amelioration of pruritus by UDCA is associated with decreased progesterone disulphates in urine. Hepatology 2008; 47(2): 544–51PubMedCrossRef Glantz A, Reilly SJ, Benthin L, et al. Intrahepatic cholestasis of pregnancy: amelioration of pruritus by UDCA is associated with decreased progesterone disulphates in urine. Hepatology 2008; 47(2): 544–51PubMedCrossRef
85.
Zurück zum Zitat Ahboucha S, Pomier-Layrargues G, Vincent C, et al. Reduced plasma dehydroepiandrosterone sulfate levels are significantly correlated with fatigue severity in patients with primary biliary cirrhosis. Neurochem Int 2008; 52(4–5): 569–74PubMedCrossRef Ahboucha S, Pomier-Layrargues G, Vincent C, et al. Reduced plasma dehydroepiandrosterone sulfate levels are significantly correlated with fatigue severity in patients with primary biliary cirrhosis. Neurochem Int 2008; 52(4–5): 569–74PubMedCrossRef
86.
Zurück zum Zitat Quist RG, Ton-Nu HT, Lillienau J, et al. Activation of mast cells by bile acids. Gastroenterology 1991; 101(2): 446–56PubMed Quist RG, Ton-Nu HT, Lillienau J, et al. Activation of mast cells by bile acids. Gastroenterology 1991; 101(2): 446–56PubMed
87.
Zurück zum Zitat Clements WD, O’Rourke DM, Rowlands BJ, et al. The role of mast cell activation in cholestatic pruritus. Agents Actions 1994; 41: C30–1PubMedCrossRef Clements WD, O’Rourke DM, Rowlands BJ, et al. The role of mast cell activation in cholestatic pruritus. Agents Actions 1994; 41: C30–1PubMedCrossRef
88.
Zurück zum Zitat Rioux KP, Sharkey KA, Wallace JL, et al. Hepatic mucosal mast cell hyperplasia in rats with secondary biliary cirrhosis. Hepatology 1996; 23(4): 888–95PubMedCrossRef Rioux KP, Sharkey KA, Wallace JL, et al. Hepatic mucosal mast cell hyperplasia in rats with secondary biliary cirrhosis. Hepatology 1996; 23(4): 888–95PubMedCrossRef
89.
Zurück zum Zitat Gittlen SD, Schulman ES, Maddrey WC. Raised histamine concentrations in chronic cholestatic liver disease. Gut 1990; 31(1): 96–9PubMedCrossRef Gittlen SD, Schulman ES, Maddrey WC. Raised histamine concentrations in chronic cholestatic liver disease. Gut 1990; 31(1): 96–9PubMedCrossRef
90.
Zurück zum Zitat Beck PW, Handwerker HO. Bradykinin and serotonin effects on various types of cutaneous nerve fibers. Pflugers Arch 1974; 347(3): 209–22PubMedCrossRef Beck PW, Handwerker HO. Bradykinin and serotonin effects on various types of cutaneous nerve fibers. Pflugers Arch 1974; 347(3): 209–22PubMedCrossRef
92.
Zurück zum Zitat Kiefel JM, Cooper ML, Bodnar RJ. Serotonin receptor subtype antagonists in the medial ventral medulla inhibit mesencephalic opiate analgesia. Brain Res 1992; 597(2): 331–8PubMedCrossRef Kiefel JM, Cooper ML, Bodnar RJ. Serotonin receptor subtype antagonists in the medial ventral medulla inhibit mesencephalic opiate analgesia. Brain Res 1992; 597(2): 331–8PubMedCrossRef
93.
94.
Zurück zum Zitat Weisshaar E, Ziethen B, Gollnick H. Can a serotonin type 3 (5-HT3) receptor antagonist reduce experimentally-induced itch? Inflamm Res 1997; 46(10): 412–6PubMedCrossRef Weisshaar E, Ziethen B, Gollnick H. Can a serotonin type 3 (5-HT3) receptor antagonist reduce experimentally-induced itch? Inflamm Res 1997; 46(10): 412–6PubMedCrossRef
95.
Zurück zum Zitat Inagaki N, Nagao M, Igeta K, et al. Scratching behavior in various strains of mice. Skin Pharmacol Appl Skin Physiol 2001; 14(2): 87–96PubMedCrossRef Inagaki N, Nagao M, Igeta K, et al. Scratching behavior in various strains of mice. Skin Pharmacol Appl Skin Physiol 2001; 14(2): 87–96PubMedCrossRef
96.
Zurück zum Zitat Browning J, Combes B, Mayo MJ. Long-term efficacy of sertraline as a treatment for cholestatic pruritus in patients with primary biliary cirrhosis. Am J Gastroenterol 2003; 98(12): 2736–41PubMedCrossRef Browning J, Combes B, Mayo MJ. Long-term efficacy of sertraline as a treatment for cholestatic pruritus in patients with primary biliary cirrhosis. Am J Gastroenterol 2003; 98(12): 2736–41PubMedCrossRef
97.
Zurück zum Zitat Mayo MJ, Handem I, Saldana S, et al. Sertraline as a first-line treatment for cholestatic pruritus. Hepatology 2007; 45(3): 666–74PubMedCrossRef Mayo MJ, Handem I, Saldana S, et al. Sertraline as a first-line treatment for cholestatic pruritus. Hepatology 2007; 45(3): 666–74PubMedCrossRef
98.
Zurück zum Zitat Bernstein JE, Swift R. Relief of intractable pruritus with naloxone. Arch Dermatol 1979; 115(11): 1366–7PubMedCrossRef Bernstein JE, Swift R. Relief of intractable pruritus with naloxone. Arch Dermatol 1979; 115(11): 1366–7PubMedCrossRef
99.
Zurück zum Zitat Thornton JR, Losowsky MS. Opioid peptides and primary biliary cirrhosis. BMJ 1988; 297(6662): 1501–4PubMedCrossRef Thornton JR, Losowsky MS. Opioid peptides and primary biliary cirrhosis. BMJ 1988; 297(6662): 1501–4PubMedCrossRef
100.
Zurück zum Zitat Spivey JR, Jorgensen RA, Gores GJ, et al. Methionine-enkephalin concentrations correlate with stage of disease but not pruritus in patients with primary biliary cirrhosis. Am J Gastroenterol 1994 Nov; 89(11): 2028–32PubMed Spivey JR, Jorgensen RA, Gores GJ, et al. Methionine-enkephalin concentrations correlate with stage of disease but not pruritus in patients with primary biliary cirrhosis. Am J Gastroenterol 1994 Nov; 89(11): 2028–32PubMed
101.
Zurück zum Zitat Swain MG, Rothman RB, Xu H, et al. Endogenous opioids accumulate in plasma in a rat model of acute cholestasis. Gastroenterology 1992; 103(2): 630–5PubMed Swain MG, Rothman RB, Xu H, et al. Endogenous opioids accumulate in plasma in a rat model of acute cholestasis. Gastroenterology 1992; 103(2): 630–5PubMed
102.
Zurück zum Zitat Bergasa NV, Vergalla J, Swain MG, et al. Hepatic concentrations of proenkephalin-derived opioids are increased in a rat model of cholestasis. Liver 1996; 16(5): 298–302PubMed Bergasa NV, Vergalla J, Swain MG, et al. Hepatic concentrations of proenkephalin-derived opioids are increased in a rat model of cholestasis. Liver 1996; 16(5): 298–302PubMed
103.
Zurück zum Zitat Jones EA, Bergasa NV. The pruritus of cholestasis and the opioid system. JAMA 1992; 268(23): 3359–62PubMedCrossRef Jones EA, Bergasa NV. The pruritus of cholestasis and the opioid system. JAMA 1992; 268(23): 3359–62PubMedCrossRef
104.
Zurück zum Zitat Bergasa NV, Sabol SL, Young 3rd WS, et al. Cholestasis is associated with preproenkephalin mRNA expression in the adult rat liver. Am J Physiol 1995; 268 (2 Pt 1): G346–54PubMed Bergasa NV, Sabol SL, Young 3rd WS, et al. Cholestasis is associated with preproenkephalin mRNA expression in the adult rat liver. Am J Physiol 1995; 268 (2 Pt 1): G346–54PubMed
105.
Zurück zum Zitat Bergasa NV, Liau S, Homel P, et al. Hepatic Met-enkephalin immunoreactivity is enhanced in primary biliary cirrhosis. Liver 2002; 22(2): 107–13PubMedCrossRef Bergasa NV, Liau S, Homel P, et al. Hepatic Met-enkephalin immunoreactivity is enhanced in primary biliary cirrhosis. Liver 2002; 22(2): 107–13PubMedCrossRef
106.
Zurück zum Zitat Marzioni M, Svegliati Baroni G, Alpini G, et al. Endogenous opioid peptides and chronic liver disease: from bedside to bench. J Hepatol 2007; 46(4): 583–6PubMedCrossRef Marzioni M, Svegliati Baroni G, Alpini G, et al. Endogenous opioid peptides and chronic liver disease: from bedside to bench. J Hepatol 2007; 46(4): 583–6PubMedCrossRef
107.
Zurück zum Zitat Ballantyne JC, Loach AB, Carr DB. Itching after epidural and spinal opiates. Pain 1988; 33(2): 149–60PubMedCrossRef Ballantyne JC, Loach AB, Carr DB. Itching after epidural and spinal opiates. Pain 1988; 33(2): 149–60PubMedCrossRef
108.
Zurück zum Zitat Thomas DA, Williams GM, Iwata K, et al. Effects of central administration of opioids on facial scratching in monkeys. Brain Res 1992; 585(1–2): 315–7PubMedCrossRef Thomas DA, Williams GM, Iwata K, et al. Effects of central administration of opioids on facial scratching in monkeys. Brain Res 1992; 585(1–2): 315–7PubMedCrossRef
109.
Zurück zum Zitat Bergasa NV, Thomas DA, Vergalla J, et al. Plasma from patients with the pruritus of cholestasis induces opioid receptormediated scratching in monkeys. Life Sci 1993; 53(16): 1253–7PubMedCrossRef Bergasa NV, Thomas DA, Vergalla J, et al. Plasma from patients with the pruritus of cholestasis induces opioid receptormediated scratching in monkeys. Life Sci 1993; 53(16): 1253–7PubMedCrossRef
110.
Zurück zum Zitat Bergasa NV, Rothman RB, Vergalla J, et al. Central mu-opioid receptors are down-regulated in a rat model of cholestasis. J Hepatol 1992; 15(1–2): 220–4PubMedCrossRef Bergasa NV, Rothman RB, Vergalla J, et al. Central mu-opioid receptors are down-regulated in a rat model of cholestasis. J Hepatol 1992; 15(1–2): 220–4PubMedCrossRef
111.
Zurück zum Zitat Nelson L, Vergnolle N, D’Mello C, et al. Endogenous opioidmediated antinociception in cholestatic mice is peripherally, not centrally, mediated. J Hepatol 2006; 44(6): 1141–9PubMedCrossRef Nelson L, Vergnolle N, D’Mello C, et al. Endogenous opioidmediated antinociception in cholestatic mice is peripherally, not centrally, mediated. J Hepatol 2006; 44(6): 1141–9PubMedCrossRef
112.
Zurück zum Zitat Bergasa NV, Talbot TL, Ailing DW, et al. A controlled trial of naloxone infusions for the pruritus of chronic cholestasis. Gastroenterology 1992; 102(2): 544–9PubMed Bergasa NV, Talbot TL, Ailing DW, et al. A controlled trial of naloxone infusions for the pruritus of chronic cholestasis. Gastroenterology 1992; 102(2): 544–9PubMed
113.
Zurück zum Zitat Bergasa NV, Ailing DW, Talbot TL, et al. Effects of naloxone infusions in patients with the pruritus of cholestasis: a double-blind, randomized, controlled trial. Ann Intern Med 1995; 123(3): 161–7PubMed Bergasa NV, Ailing DW, Talbot TL, et al. Effects of naloxone infusions in patients with the pruritus of cholestasis: a double-blind, randomized, controlled trial. Ann Intern Med 1995; 123(3): 161–7PubMed
114.
Zurück zum Zitat Carson KL, Tran TT, Cotton P, et al. Pilot study of the use of naltrexone to treat the severe pruritus of cholestatic liver disease. Am J Gastroenterol 1996; 91(5): 1022–3PubMed Carson KL, Tran TT, Cotton P, et al. Pilot study of the use of naltrexone to treat the severe pruritus of cholestatic liver disease. Am J Gastroenterol 1996; 91(5): 1022–3PubMed
115.
Zurück zum Zitat Bergasa NV, Schmitt JM, Talbot TL, et al. Open-label trial of oral nalmefene therapy for the pruritus of cholestasis. Hepatology 1998; 27(3): 679–84PubMedCrossRef Bergasa NV, Schmitt JM, Talbot TL, et al. Open-label trial of oral nalmefene therapy for the pruritus of cholestasis. Hepatology 1998; 27(3): 679–84PubMedCrossRef
116.
Zurück zum Zitat Terg R, Coronel E, Sorda J, et al. Efficacy and safety of oral naltrexone treatment for pruritus of cholestasis, a crossover, double blind, placebo-controlled study. J Hepatol 2002; 37(6): 717–22PubMedCrossRef Terg R, Coronel E, Sorda J, et al. Efficacy and safety of oral naltrexone treatment for pruritus of cholestasis, a crossover, double blind, placebo-controlled study. J Hepatol 2002; 37(6): 717–22PubMedCrossRef
117.
Zurück zum Zitat Mansour-Ghanaei F, Taheri A, Froutan H, et al. Effect of oral naltrexone on pruritus in cholestatic patients. World J Gastroenterol 2006; 12(7): 1125–8PubMed Mansour-Ghanaei F, Taheri A, Froutan H, et al. Effect of oral naltrexone on pruritus in cholestatic patients. World J Gastroenterol 2006; 12(7): 1125–8PubMed
118.
Zurück zum Zitat Summerfield JA. Naloxone modulates the perception of itch in man. Br J Clin Pharmacol 1980; 10(2): 180–3PubMedCrossRef Summerfield JA. Naloxone modulates the perception of itch in man. Br J Clin Pharmacol 1980; 10(2): 180–3PubMedCrossRef
119.
Zurück zum Zitat Kamei J, Nagase H. Norbinaltorphimine, a selective kappa-opioid receptor antagonist, induces an itch-associated response in mice. Eur J Pharmacol 2001; 418(1–2): 141–5PubMedCrossRef Kamei J, Nagase H. Norbinaltorphimine, a selective kappa-opioid receptor antagonist, induces an itch-associated response in mice. Eur J Pharmacol 2001; 418(1–2): 141–5PubMedCrossRef
120.
Zurück zum Zitat Togashi Y, Umeuchi H, Okano K, et al. Antipruritic activity of the kappa-opioid receptor agonist, TRK-820. Eur J Pharmacol 2002; 435(2-3): 259–64PubMedCrossRef Togashi Y, Umeuchi H, Okano K, et al. Antipruritic activity of the kappa-opioid receptor agonist, TRK-820. Eur J Pharmacol 2002; 435(2-3): 259–64PubMedCrossRef
121.
Zurück zum Zitat Wikstrom B, Geliert R, Ladefoged SD, et al. Kappa-opioid system in uremic pruritus: multicenter, randomized, double-blind, placebo-controlled clinical studies. J Am Soc Nephrol 2005; 16(12): 3742–7PubMedCrossRef Wikstrom B, Geliert R, Ladefoged SD, et al. Kappa-opioid system in uremic pruritus: multicenter, randomized, double-blind, placebo-controlled clinical studies. J Am Soc Nephrol 2005; 16(12): 3742–7PubMedCrossRef
122.
Zurück zum Zitat Bergasa NV. Medical palliation of the jaundiced patient with pruritus. Gastroenterol Clin North Am 2006; 35(1): 113–23PubMedCrossRef Bergasa NV. Medical palliation of the jaundiced patient with pruritus. Gastroenterol Clin North Am 2006; 35(1): 113–23PubMedCrossRef
123.
Zurück zum Zitat Sun YG, Chen ZF. A gastrin-releasing peptide receptor mediates the itch sensation in the spinal cord. Nature 2007; 448(7154): 700–3PubMedCrossRef Sun YG, Chen ZF. A gastrin-releasing peptide receptor mediates the itch sensation in the spinal cord. Nature 2007; 448(7154): 700–3PubMedCrossRef
124.
Zurück zum Zitat Bodo E, Kovacs I, Telek A, et al. Vanilloid receptor-1 (VR1) is widely expressed on various epithelial and mesenchymal cell types of human skin. J Invest Dermatol 2004; 123(2): 410–3PubMedCrossRef Bodo E, Kovacs I, Telek A, et al. Vanilloid receptor-1 (VR1) is widely expressed on various epithelial and mesenchymal cell types of human skin. J Invest Dermatol 2004; 123(2): 410–3PubMedCrossRef
125.
Zurück zum Zitat Stander S, Moormann C, Schumacher M, et al. Expression of vanilloid receptor subtype 1 in cutaneous sensory nerve fibers, mast cells, and epithelial cells of appendage structures. Exp Dermatol 2004; 13(3): 129–39PubMedCrossRef Stander S, Moormann C, Schumacher M, et al. Expression of vanilloid receptor subtype 1 in cutaneous sensory nerve fibers, mast cells, and epithelial cells of appendage structures. Exp Dermatol 2004; 13(3): 129–39PubMedCrossRef
126.
Zurück zum Zitat Shin J, Cho H, Hwang SW, et al. Bradykinin-12-lipoxygenase-VR1 signaling pathway for inflammatory hyperalgesia. Proc Natl Acad Sci U S A 2002; 99(15): 10150–5PubMedCrossRef Shin J, Cho H, Hwang SW, et al. Bradykinin-12-lipoxygenase-VR1 signaling pathway for inflammatory hyperalgesia. Proc Natl Acad Sci U S A 2002; 99(15): 10150–5PubMedCrossRef
127.
Zurück zum Zitat Kim BM, Lee SH, Shim WS, et al. Histamine-induced Ca(2+) influx via the PLA(2)/lipoxygenase/TRPVl pathway in rat sensory neurons. Neurosci Lett 2004; 361(1–3): 159–62PubMedCrossRef Kim BM, Lee SH, Shim WS, et al. Histamine-induced Ca(2+) influx via the PLA(2)/lipoxygenase/TRPVl pathway in rat sensory neurons. Neurosci Lett 2004; 361(1–3): 159–62PubMedCrossRef
128.
Zurück zum Zitat Shim WS, Tak MH, Lee MH, et al. TRPV1 mediates histamine-induced itching via the activation of phospholipase A2 and 12-lipoxygenase. J Neurosci 2007; 27(9): 2331–7PubMedCrossRef Shim WS, Tak MH, Lee MH, et al. TRPV1 mediates histamine-induced itching via the activation of phospholipase A2 and 12-lipoxygenase. J Neurosci 2007; 27(9): 2331–7PubMedCrossRef
129.
Zurück zum Zitat Dvorak M, Watkinson A, McGlone F, et al. Histamine induced responses are attenuated by a cannabinoid receptor agonist in human skin. Inflamm Res 2003; 52(6): 238–45PubMed Dvorak M, Watkinson A, McGlone F, et al. Histamine induced responses are attenuated by a cannabinoid receptor agonist in human skin. Inflamm Res 2003; 52(6): 238–45PubMed
130.
Zurück zum Zitat Binzen U, Greffrath W, Hennessy S, et al. Co-expression of the voltage-gated potassium channel Kv1.4 with transient receptor potential channels (TRPV1 and TRPV2) and the cannabinoid receptor CB1 in rat dorsal root ganglion neurons. Neuroscience 2006; 142(2): 527–39PubMedCrossRef Binzen U, Greffrath W, Hennessy S, et al. Co-expression of the voltage-gated potassium channel Kv1.4 with transient receptor potential channels (TRPV1 and TRPV2) and the cannabinoid receptor CB1 in rat dorsal root ganglion neurons. Neuroscience 2006; 142(2): 527–39PubMedCrossRef
131.
Zurück zum Zitat Stander S, Schmelz M, Metze D, et al. Distribution of cannabinoid receptor 1 (CB1) and 2 (CB2) on sensory nerve fibers and adnexal structures in human skin. J Dermatol Sci 2005; 38(3): 177–88PubMedCrossRef Stander S, Schmelz M, Metze D, et al. Distribution of cannabinoid receptor 1 (CB1) and 2 (CB2) on sensory nerve fibers and adnexal structures in human skin. J Dermatol Sci 2005; 38(3): 177–88PubMedCrossRef
132.
Zurück zum Zitat Ibrahim MM, Porreca F, Lai J, et al. CB2 cannabinoid receptor activation produces antinociception by stimulating peripheral release of endogenous opioids. Proc Natl Acad Sci U S A 2005; 102(8): 3093–8PubMedCrossRef Ibrahim MM, Porreca F, Lai J, et al. CB2 cannabinoid receptor activation produces antinociception by stimulating peripheral release of endogenous opioids. Proc Natl Acad Sci U S A 2005; 102(8): 3093–8PubMedCrossRef
133.
Zurück zum Zitat Hermann H, Petrocellis L, Bisogno T, et al. Dual effect of cannabinoid CB1 receptor stimulation on a vanilloid VR1 receptor-mediated response. Cell Mol Life Sci 2003; 60(3): 607–16PubMedCrossRef Hermann H, Petrocellis L, Bisogno T, et al. Dual effect of cannabinoid CB1 receptor stimulation on a vanilloid VR1 receptor-mediated response. Cell Mol Life Sci 2003; 60(3): 607–16PubMedCrossRef
134.
Zurück zum Zitat Borgeat A, Wilder-Smith OH, Saiah M, et al. Subhypnotic doses of propofol relieve pruritus induced by epidural and intrathecal morphine. Anesthesiology 1992; 76(4): 510–2PubMedCrossRef Borgeat A, Wilder-Smith OH, Saiah M, et al. Subhypnotic doses of propofol relieve pruritus induced by epidural and intrathecal morphine. Anesthesiology 1992; 76(4): 510–2PubMedCrossRef
135.
Zurück zum Zitat Szarvas S, Harmon D, Murphy D. Neuraxial opioid-induced pruritus: a review. J Clin Anesth 2003; 15(3): 234–9PubMedCrossRef Szarvas S, Harmon D, Murphy D. Neuraxial opioid-induced pruritus: a review. J Clin Anesth 2003; 15(3): 234–9PubMedCrossRef
136.
Zurück zum Zitat Borgeat A, Wilder-Smith OH, Mentha G. Subhypnotic doses of propofol relieve pruritus associated with liver disease. Gastroenterology 1993; 104(1): 244–7PubMed Borgeat A, Wilder-Smith OH, Mentha G. Subhypnotic doses of propofol relieve pruritus associated with liver disease. Gastroenterology 1993; 104(1): 244–7PubMed
137.
Zurück zum Zitat Prieto LN. The use of midazolam to treat itching in a terminally ill patient with biliary obstruction. J Pain Symptom Manage 2004; 28(6): 531–2PubMedCrossRef Prieto LN. The use of midazolam to treat itching in a terminally ill patient with biliary obstruction. J Pain Symptom Manage 2004; 28(6): 531–2PubMedCrossRef
138.
Zurück zum Zitat Bergasa NV, Ailing DW, Vergalla J, et al. Cholestasis in the male rat is associated with naloxone-reversible antinociception. J Hepatol 1994; 20(1): 85–90PubMedCrossRef Bergasa NV, Ailing DW, Vergalla J, et al. Cholestasis in the male rat is associated with naloxone-reversible antinociception. J Hepatol 1994; 20(1): 85–90PubMedCrossRef
139.
Zurück zum Zitat Dehpour AR, Sadeghipour HR, Nowroozi A, et al. The effect of the serotonergic system on opioid withdrawal-like syndrome in a mouse model of cholestasis. Hum Psychopharmacol 2000; 15(6): 423–8PubMedCrossRef Dehpour AR, Sadeghipour HR, Nowroozi A, et al. The effect of the serotonergic system on opioid withdrawal-like syndrome in a mouse model of cholestasis. Hum Psychopharmacol 2000; 15(6): 423–8PubMedCrossRef
140.
Zurück zum Zitat Hasanein P, Parviz M, Keshavarz M, et al. Modulation of cholestasis-induced antinociception in rats by two NMDA receptor antagonists: MK-801 and magnesium sulfate. Eur J Pharmacol 2007; 554(2–3): 123–7PubMedCrossRef Hasanein P, Parviz M, Keshavarz M, et al. Modulation of cholestasis-induced antinociception in rats by two NMDA receptor antagonists: MK-801 and magnesium sulfate. Eur J Pharmacol 2007; 554(2–3): 123–7PubMedCrossRef
141.
Zurück zum Zitat Stander S, Streit M, Darsow U, et al. AWMF-leitlinie: diagnostisches und therapeutisches vorgehen bei chronischem pruritus. JDDG 2006; 4: 350–70PubMedCrossRef Stander S, Streit M, Darsow U, et al. AWMF-leitlinie: diagnostisches und therapeutisches vorgehen bei chronischem pruritus. JDDG 2006; 4: 350–70PubMedCrossRef
142.
Zurück zum Zitat Duncan JS, Kennedy HJ, Triger DR. Treatment of pruritus due to chronic obstructive liver disease [letter]. BMJ (Clin Res Ed) 1984; 289(6436): 22CrossRef Duncan JS, Kennedy HJ, Triger DR. Treatment of pruritus due to chronic obstructive liver disease [letter]. BMJ (Clin Res Ed) 1984; 289(6436): 22CrossRef
143.
Zurück zum Zitat Di Padova C, Tritapepe R, Rovagnati P, et al. Double-blind placebo-controlled clinical trial of microporous cholestyramine in the treatment of intra- and extra-hepatic cholestasis: relationship between itching and serum bile acids. Methods Find Exp Clin Pharmacol 1984; 6(12): 773–6PubMed Di Padova C, Tritapepe R, Rovagnati P, et al. Double-blind placebo-controlled clinical trial of microporous cholestyramine in the treatment of intra- and extra-hepatic cholestasis: relationship between itching and serum bile acids. Methods Find Exp Clin Pharmacol 1984; 6(12): 773–6PubMed
144.
Zurück zum Zitat Kondrackiene J, Beuers U, Kupcinskas L. Efficacy and safety of ursodeoxycholic acid versus cholestyramine in intrahepatic cholestasis of pregnancy. Gastroenterology 2005 Sep; 129(3): 894–901PubMedCrossRef Kondrackiene J, Beuers U, Kupcinskas L. Efficacy and safety of ursodeoxycholic acid versus cholestyramine in intrahepatic cholestasis of pregnancy. Gastroenterology 2005 Sep; 129(3): 894–901PubMedCrossRef
145.
Zurück zum Zitat Ghent CN, Carruthers SG. Treatment of pruritus in primary biliary cirrhosis with rifampin: results of a double-blind, crossover, randomized trial. Gastroenterology 1988; 94(2): 488–93PubMed Ghent CN, Carruthers SG. Treatment of pruritus in primary biliary cirrhosis with rifampin: results of a double-blind, crossover, randomized trial. Gastroenterology 1988; 94(2): 488–93PubMed
146.
Zurück zum Zitat Bachs L, Pares A, Elena M, et al. Comparison of rifampicin with phenobarbitone for treatment of pruritus in biliary cirrhosis. Lancet 1989 Mar 18; I(8638): 574–6CrossRef Bachs L, Pares A, Elena M, et al. Comparison of rifampicin with phenobarbitone for treatment of pruritus in biliary cirrhosis. Lancet 1989 Mar 18; I(8638): 574–6CrossRef
147.
Zurück zum Zitat Woolf GM, Reynolds TB. Failure of rifampin to relieve pruritus in chronic liver disease. J Clin Gastroenterol 1990 Apr 12; (2): 174–7 Woolf GM, Reynolds TB. Failure of rifampin to relieve pruritus in chronic liver disease. J Clin Gastroenterol 1990 Apr 12; (2): 174–7
148.
Zurück zum Zitat Podesta A, Lopez P, Terg R, et al. Treatment of pruritus of primary biliary cirrhosis with rifampin. Dig Dis Sci 1991; 36(2): 216–20PubMedCrossRef Podesta A, Lopez P, Terg R, et al. Treatment of pruritus of primary biliary cirrhosis with rifampin. Dig Dis Sci 1991; 36(2): 216–20PubMedCrossRef
149.
Zurück zum Zitat Muller C, Pongratz S, Pidlich J, et al. Treatment of pruritus in chronic liver disease with the 5-hydroxytryptamine receptor type 3 antagonist ondansetron: a randomized, placebo-controlled, double-blind cross-over trial. Eur J Gastroenterol Hepatol 1998; 10(10): 865–70PubMedCrossRef Muller C, Pongratz S, Pidlich J, et al. Treatment of pruritus in chronic liver disease with the 5-hydroxytryptamine receptor type 3 antagonist ondansetron: a randomized, placebo-controlled, double-blind cross-over trial. Eur J Gastroenterol Hepatol 1998; 10(10): 865–70PubMedCrossRef
150.
Zurück zum Zitat Ribalta J, Reyes H, Gonzalez MC, et al. S-adenosyl-L-methionine in the treatment of patients with intrahepatic cholestasis of pregnancy: a randomized, double-blind, placebo-controlled study with negative results. Hepatology 1991; 13(6): 1084–9PubMed Ribalta J, Reyes H, Gonzalez MC, et al. S-adenosyl-L-methionine in the treatment of patients with intrahepatic cholestasis of pregnancy: a randomized, double-blind, placebo-controlled study with negative results. Hepatology 1991; 13(6): 1084–9PubMed
151.
Zurück zum Zitat Roncaglia N, Locatelli A, Arreghini A, et al. A randomised controlled trial of ursodeoxycholic acid and S-adenosyl-l-methionine in the treatment of gestational cholestasis. BJOG 2004; 111(1): 17–21PubMedCrossRef Roncaglia N, Locatelli A, Arreghini A, et al. A randomised controlled trial of ursodeoxycholic acid and S-adenosyl-l-methionine in the treatment of gestational cholestasis. BJOG 2004; 111(1): 17–21PubMedCrossRef
152.
Zurück zum Zitat Binder T, Salaj P, Zima T, et al. Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy. J Perinat Med 2006; 34(5): 383–91PubMedCrossRef Binder T, Salaj P, Zima T, et al. Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy. J Perinat Med 2006; 34(5): 383–91PubMedCrossRef
153.
Zurück zum Zitat Palma J, Reyes H, Ribalta J, et al. Ursodeoxycholic acid in the treatment of cholestasis of pregnancy: a randomized, double-blind study controlled with placebo. J Hepatol 1997 Dec; 27(6): 1022–8PubMedCrossRef Palma J, Reyes H, Ribalta J, et al. Ursodeoxycholic acid in the treatment of cholestasis of pregnancy: a randomized, double-blind study controlled with placebo. J Hepatol 1997 Dec; 27(6): 1022–8PubMedCrossRef
154.
Zurück zum Zitat Batta AK, Salen G, Mirchandani R, et al. Effect of long-term treatment with ursodiol on clinical and biochemical features and biliary bile acid metabolism in patients with primary biliary cirrhosis. Am J Gastroenterol 1993; 88(5): 691–700PubMed Batta AK, Salen G, Mirchandani R, et al. Effect of long-term treatment with ursodiol on clinical and biochemical features and biliary bile acid metabolism in patients with primary biliary cirrhosis. Am J Gastroenterol 1993; 88(5): 691–700PubMed
155.
Zurück zum Zitat Poupon RE, Chretien Y, Poupon R, et al. Serum bile acids in primary biliary cirrhosis: effect of ursodeoxycholic acid therapy. Hepatology 1993 Apr; 17(4): 599–604PubMedCrossRef Poupon RE, Chretien Y, Poupon R, et al. Serum bile acids in primary biliary cirrhosis: effect of ursodeoxycholic acid therapy. Hepatology 1993 Apr; 17(4): 599–604PubMedCrossRef
156.
Zurück zum Zitat Poupon RE, Lindor KD, Cauch-Dudek K, et al. Combined analysis of randomized controlled trials of ursodeoxycholic acid in primary biliary cirrhosis. Gastroenterology 1997 Sep; 113(3): 884–90PubMedCrossRef Poupon RE, Lindor KD, Cauch-Dudek K, et al. Combined analysis of randomized controlled trials of ursodeoxycholic acid in primary biliary cirrhosis. Gastroenterology 1997 Sep; 113(3): 884–90PubMedCrossRef
157.
Zurück zum Zitat Beuers U. Drug insight: Mechanisms and sites of action of ursodeoxycholic acid in cholestasis. Nat Clin Pract Gastroenterol Hepatol 2006 Jun; 3(6): 318–28PubMedCrossRef Beuers U. Drug insight: Mechanisms and sites of action of ursodeoxycholic acid in cholestasis. Nat Clin Pract Gastroenterol Hepatol 2006 Jun; 3(6): 318–28PubMedCrossRef
158.
Zurück zum Zitat Hempfling W, Dilger K, Beuers U. Systematic review: ursodeoxycholic acid: adverse effects and drug interactions. Aliment Pharmacol Ther 2003 Nov 15; 18(10): 963–72PubMedCrossRef Hempfling W, Dilger K, Beuers U. Systematic review: ursodeoxycholic acid: adverse effects and drug interactions. Aliment Pharmacol Ther 2003 Nov 15; 18(10): 963–72PubMedCrossRef
159.
Zurück zum Zitat Lindor KD. Ursodiol for primary sclerosing cholangitis. Mayo Primary Sclerosing Cholangitis-Ursodeoxycholic Acid Study Group. N Engl J Med 1997; 336(10): 691–5 Lindor KD. Ursodiol for primary sclerosing cholangitis. Mayo Primary Sclerosing Cholangitis-Ursodeoxycholic Acid Study Group. N Engl J Med 1997; 336(10): 691–5
160.
Zurück zum Zitat Talwalkar JA, Souto E, Jorgensen RA, et al. Natural history of pruritus in primary biliary cirrhosis. Clin Gastroenterol Hepatol 2003; 1(4): 297–302PubMedCrossRef Talwalkar JA, Souto E, Jorgensen RA, et al. Natural history of pruritus in primary biliary cirrhosis. Clin Gastroenterol Hepatol 2003; 1(4): 297–302PubMedCrossRef
161.
Zurück zum Zitat Balistreri WF, Heubi JE, Whitington P, et al. Ursodeoxycholic acid (UDCA) therapy in pediatric hepatobiliary disease [abstract]. Hepatology 1989; 10: 602A Balistreri WF, Heubi JE, Whitington P, et al. Ursodeoxycholic acid (UDCA) therapy in pediatric hepatobiliary disease [abstract]. Hepatology 1989; 10: 602A
162.
Zurück zum Zitat Narkewicz MR, Smith D, Gregory C, et al. Effect of ursodeoxycholic acid therapy on hepatic function in children with intrahepatic cholestatic liver disease. J Pediatr Gastroenterol Nutr 1998; 26(1): 49–55PubMedCrossRef Narkewicz MR, Smith D, Gregory C, et al. Effect of ursodeoxycholic acid therapy on hepatic function in children with intrahepatic cholestatic liver disease. J Pediatr Gastroenterol Nutr 1998; 26(1): 49–55PubMedCrossRef
163.
Zurück zum Zitat Dinier G, Kocak N, Yuce A, et al. Ursodeoxycholic acid therapy in children with cholestatic liver disease. Turk J Pediatr 1999; 41(1): 91–8 Dinier G, Kocak N, Yuce A, et al. Ursodeoxycholic acid therapy in children with cholestatic liver disease. Turk J Pediatr 1999; 41(1): 91–8
164.
Zurück zum Zitat Datta DV, Sherlock S. Treatment of pruritus of obstructive jaundice with cholestyramine. BMJ 1963; 1(5325): 216–9PubMedCrossRef Datta DV, Sherlock S. Treatment of pruritus of obstructive jaundice with cholestyramine. BMJ 1963; 1(5325): 216–9PubMedCrossRef
165.
Zurück zum Zitat Pusl T, Beuers U. Extrahepatic manifestations of cholestatic liver diseases: pathogenesis and therapy. Clin Rev Allergy Immunol 2005; 28(2): 147–57PubMedCrossRef Pusl T, Beuers U. Extrahepatic manifestations of cholestatic liver diseases: pathogenesis and therapy. Clin Rev Allergy Immunol 2005; 28(2): 147–57PubMedCrossRef
166.
Zurück zum Zitat Rust C, Sauter GH, Oswald M, et al. Effect of cholestyramine on bile acid pattern and synthesis during administration of ursodeoxycholic acid in man. Eur J Clin Invest 2000; 30(2): 135–9PubMedCrossRef Rust C, Sauter GH, Oswald M, et al. Effect of cholestyramine on bile acid pattern and synthesis during administration of ursodeoxycholic acid in man. Eur J Clin Invest 2000; 30(2): 135–9PubMedCrossRef
167.
Zurück zum Zitat Berg CI. Use of colesevalem hydrochloride as a novel therapeutic agent for the managment of refractory pruritus in chronic liver disease [abstract]. Hepatology 2001; 34: 541A Berg CI. Use of colesevalem hydrochloride as a novel therapeutic agent for the managment of refractory pruritus in chronic liver disease [abstract]. Hepatology 2001; 34: 541A
168.
Zurück zum Zitat Xu C, Li CY, Kong AN. Induction of phase I, II and III drug metabolism/transport by xenobiotics. Arch Pharm Res 2005; 28(3): 249–68PubMedCrossRef Xu C, Li CY, Kong AN. Induction of phase I, II and III drug metabolism/transport by xenobiotics. Arch Pharm Res 2005; 28(3): 249–68PubMedCrossRef
169.
Zurück zum Zitat LeCluyse EL. Pregnane X receptor: molecular basis for species differences in CYP3A induction by xenobiotics. Chem Biol Interact 2001; 134(3): 283–9PubMedCrossRef LeCluyse EL. Pregnane X receptor: molecular basis for species differences in CYP3A induction by xenobiotics. Chem Biol Interact 2001; 134(3): 283–9PubMedCrossRef
170.
Zurück zum Zitat Marschall HU, Wagner M, Zollner G, et al. Complementary stimulation of hepatobiliary transport and detoxification systems by rifampicin and ursodeoxycholic acid in humans. Gastroenterology 2005 Aug; 129(2): 476–85PubMed Marschall HU, Wagner M, Zollner G, et al. Complementary stimulation of hepatobiliary transport and detoxification systems by rifampicin and ursodeoxycholic acid in humans. Gastroenterology 2005 Aug; 129(2): 476–85PubMed
171.
Zurück zum Zitat Bachs L, Pares A, Elena M, et al. Effects of long-term rifampicin administration in primary biliary cirrhosis. Gastroenterology 1992 Jun; 102(6): 2077–80PubMed Bachs L, Pares A, Elena M, et al. Effects of long-term rifampicin administration in primary biliary cirrhosis. Gastroenterology 1992 Jun; 102(6): 2077–80PubMed
172.
Zurück zum Zitat Cynamon HA, Andres JM, Iafrate RP. Rifampin relieves pruritus in children with cholestatic liver disease. Gastroenterology 1990; 98(4): 1013–6PubMedCrossRef Cynamon HA, Andres JM, Iafrate RP. Rifampin relieves pruritus in children with cholestatic liver disease. Gastroenterology 1990; 98(4): 1013–6PubMedCrossRef
173.
Zurück zum Zitat Yerushalmi B, Sokol RJ, Narkewicz MR, et al. Use of rifampin for severe pruritus in children with chronic cholestasis. J Pediatr Gastroenterol Nutr 1999; 29(4): 442–7PubMedCrossRef Yerushalmi B, Sokol RJ, Narkewicz MR, et al. Use of rifampin for severe pruritus in children with chronic cholestasis. J Pediatr Gastroenterol Nutr 1999; 29(4): 442–7PubMedCrossRef
174.
Zurück zum Zitat Khurana S, Singh P. Rifampin is safe for treatment of pruritus due to chronic cholestasis: a meta-analysis of prospective randomized-controlled trials. Liver Int 2006 Oct; 26(8): 943–8PubMedCrossRef Khurana S, Singh P. Rifampin is safe for treatment of pruritus due to chronic cholestasis: a meta-analysis of prospective randomized-controlled trials. Liver Int 2006 Oct; 26(8): 943–8PubMedCrossRef
175.
Zurück zum Zitat Tandon P, Rowe BH, Vandermeer B, et al. The efficacy and safety of bile acid binding agents, opioid antagonists, or rifampin in the treatment of cholestasis-associated pruritus. Am J Gastroenterol 2007; 102(7): 1528–36PubMedCrossRef Tandon P, Rowe BH, Vandermeer B, et al. The efficacy and safety of bile acid binding agents, opioid antagonists, or rifampin in the treatment of cholestasis-associated pruritus. Am J Gastroenterol 2007; 102(7): 1528–36PubMedCrossRef
176.
Zurück zum Zitat Prince MI, Burt AD, Jones DE. Hepatitis and liver dysfunction with rifampicin therapy for pruritus in primary biliary cirrhosis. Gut 2002; 50(3): 436–9PubMedCrossRef Prince MI, Burt AD, Jones DE. Hepatitis and liver dysfunction with rifampicin therapy for pruritus in primary biliary cirrhosis. Gut 2002; 50(3): 436–9PubMedCrossRef
177.
Zurück zum Zitat Jones EA, Neuberger J, Bergasa NV. Opiate antagonist therapy for the pruritus of cholestasis: the avoidance of opioid withdrawal-like reactions. QJM 2002; 95(8): 547–52PubMedCrossRef Jones EA, Neuberger J, Bergasa NV. Opiate antagonist therapy for the pruritus of cholestasis: the avoidance of opioid withdrawal-like reactions. QJM 2002; 95(8): 547–52PubMedCrossRef
178.
Zurück zum Zitat Schumann R, Hudcova J. Cholestasis of pregnancy, pruritus and 5-hydroxytryptamine 3 receptor antagonists. Acta Obstet Gynecol Scand 2004; 83(9): 861–2PubMed Schumann R, Hudcova J. Cholestasis of pregnancy, pruritus and 5-hydroxytryptamine 3 receptor antagonists. Acta Obstet Gynecol Scand 2004; 83(9): 861–2PubMed
179.
Zurück zum Zitat Zylicz Z, Krajnik M, Sorge AA, et al. Paroxetine in the treatment of severe non-dermatological pruritus: a randomized, controlled trial. J Pain Symptom Manage 2003; 26(6): 1105–12PubMedCrossRef Zylicz Z, Krajnik M, Sorge AA, et al. Paroxetine in the treatment of severe non-dermatological pruritus: a randomized, controlled trial. J Pain Symptom Manage 2003; 26(6): 1105–12PubMedCrossRef
180.
Zurück zum Zitat Neff GW, O’Brien CB, Reddy KR, et al. Preliminary observation with dronabinol in patients with intractable pruritus secondary to cholestatic liver disease. Am J Gastroenterol 2002; 97(8): 2117–9PubMedCrossRef Neff GW, O’Brien CB, Reddy KR, et al. Preliminary observation with dronabinol in patients with intractable pruritus secondary to cholestatic liver disease. Am J Gastroenterol 2002; 97(8): 2117–9PubMedCrossRef
181.
Zurück zum Zitat Stander S, Reinhardt HW, Luger TA. Topical cannabinoid agonists: an effective new possibility for treating chronic pruritus [in German]. Hautarzt 2006; 57(9): 801–7PubMedCrossRef Stander S, Reinhardt HW, Luger TA. Topical cannabinoid agonists: an effective new possibility for treating chronic pruritus [in German]. Hautarzt 2006; 57(9): 801–7PubMedCrossRef
182.
Zurück zum Zitat Turner IB, Rawlins MD, Wood P, et al. Flumecinol for the treatment of pruritus associated with primary biliary cirrhosis. Aliment Pharmacol Ther 1994; 8(3): 337–42PubMedCrossRef Turner IB, Rawlins MD, Wood P, et al. Flumecinol for the treatment of pruritus associated with primary biliary cirrhosis. Aliment Pharmacol Ther 1994; 8(3): 337–42PubMedCrossRef
183.
Zurück zum Zitat Walt RP, Daneshmend TK, Fellows IW, et al. Effect of stanozolol on itching in primary biliary cirrhosis [letter]. BMJ (Clin Res Ed) 1988; 296(6622): 607CrossRef Walt RP, Daneshmend TK, Fellows IW, et al. Effect of stanozolol on itching in primary biliary cirrhosis [letter]. BMJ (Clin Res Ed) 1988; 296(6622): 607CrossRef
184.
Zurück zum Zitat Hanid MA, Levi AJ. Phototherapy for pruritus in primary biliary cirrhosis [letter]. Lancet 1980; II(8193): 530CrossRef Hanid MA, Levi AJ. Phototherapy for pruritus in primary biliary cirrhosis [letter]. Lancet 1980; II(8193): 530CrossRef
185.
Zurück zum Zitat Cerio R, Murphy GM, Sladen GE, et al. A combination of phototherapy and cholestyramine for the relief of pruritus in primary biliary cirrhosis. Br J Dermatol 1987; 116(2): 265–7PubMedCrossRef Cerio R, Murphy GM, Sladen GE, et al. A combination of phototherapy and cholestyramine for the relief of pruritus in primary biliary cirrhosis. Br J Dermatol 1987; 116(2): 265–7PubMedCrossRef
186.
Zurück zum Zitat Bergasa NV, Link MJ, Keogh M, et al. Pilot study of bright-light therapy reflected toward the eyes for the pruritus of chronic liver disease. Am J Gastroenterol 2001; 96(5): 1563–70PubMedCrossRef Bergasa NV, Link MJ, Keogh M, et al. Pilot study of bright-light therapy reflected toward the eyes for the pruritus of chronic liver disease. Am J Gastroenterol 2001; 96(5): 1563–70PubMedCrossRef
187.
Zurück zum Zitat Cohen LB, Ambinder EP, Wolke AM, et al. Role of plasmapheresis in primary biliary cirrhosis. Gut 1985; 26(3): 291–4PubMedCrossRef Cohen LB, Ambinder EP, Wolke AM, et al. Role of plasmapheresis in primary biliary cirrhosis. Gut 1985; 26(3): 291–4PubMedCrossRef
188.
Zurück zum Zitat Macia M, Aviles J, Navarro J, et al. Efficacy of molecular adsorbent recirculating system for the treatment of intractable pruritus in cholestasis. Am J Med 2003; 114(1): 62–4PubMedCrossRef Macia M, Aviles J, Navarro J, et al. Efficacy of molecular adsorbent recirculating system for the treatment of intractable pruritus in cholestasis. Am J Med 2003; 114(1): 62–4PubMedCrossRef
189.
Zurück zum Zitat Pares A, Cisneros L, Salmeron JM, et al. Extracorporeal albumin dialysis: a procedure for prolonged relief of intractable pruritus in patients with primary biliary cirrhosis. Am J Gastroenterol 2004; 99(6): 1105–10PubMedCrossRef Pares A, Cisneros L, Salmeron JM, et al. Extracorporeal albumin dialysis: a procedure for prolonged relief of intractable pruritus in patients with primary biliary cirrhosis. Am J Gastroenterol 2004; 99(6): 1105–10PubMedCrossRef
190.
Zurück zum Zitat Pusl T, Denk GU, Parhofer KG, et al. Plasma separation and anion adsorption transiently relieve intractable pruritus in primary biliary cirrhosis. J Hepatol 2006 Dec; 45(6): 887–91PubMedCrossRef Pusl T, Denk GU, Parhofer KG, et al. Plasma separation and anion adsorption transiently relieve intractable pruritus in primary biliary cirrhosis. J Hepatol 2006 Dec; 45(6): 887–91PubMedCrossRef
191.
Zurück zum Zitat Emerick KM, Whitington PF. Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome. Hepatology 2002; 35(6): 1501–6PubMedCrossRef Emerick KM, Whitington PF. Partial external biliary diversion for intractable pruritus and xanthomas in Alagille syndrome. Hepatology 2002; 35(6): 1501–6PubMedCrossRef
192.
Zurück zum Zitat Ng VL, Ryckman FC, Porta G, et al. Long-term outcome after partial external biliary diversion for intractable pruritus in patients with intrahepatic cholestasis. J Pediatr Gastroenterol Nutr 2000; 30(2): 152–6PubMedCrossRef Ng VL, Ryckman FC, Porta G, et al. Long-term outcome after partial external biliary diversion for intractable pruritus in patients with intrahepatic cholestasis. J Pediatr Gastroenterol Nutr 2000; 30(2): 152–6PubMedCrossRef
Metadaten
Titel
Pathogenesis and Treatment of Pruritus in Cholestasis
verfasst von
Andreas E. Kremer, MD
Ulrich Beuers
Ronald P. J. Oude-Elferink
Thomas Pusl
Publikationsdatum
01.10.2008
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 15/2008
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200868150-00006

Weitere Artikel der Ausgabe 15/2008

Drugs 15/2008 Zur Ausgabe

Adis Drug Evaluation

Pregabalin

Adis Drug Profile

Ambrisentan

Adis Drug Evaluation

Micafungin