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Erschienen in: The Cerebellum 3/2009

01.09.2009

Increase in Cerebellar Neurotrophin-3 and Oxidative Stress Markers in Autism

verfasst von: Elizabeth M. Sajdel-Sulkowska, Ming Xu, Noriyuki Koibuchi

Erschienen in: The Cerebellum | Ausgabe 3/2009

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Abstract

Autism is a neurodevelopmental disorder characterized by social and language deficits, ritualistic–repetitive behaviors and disturbance in motor functions. Data of imaging, head circumference studies, and Purkinje cell analysis suggest impaired brain growth and development. Both genetic predisposition and environmental triggers have been implicated in the etiology of autism, but the underlying cause remains unknown. Recently, we have reported an increase in 3-nitrotyrosine (3-NT), a marker of oxidative stress damage to proteins in autistic cerebella. In the present study, we further explored oxidative damage in the autistic cerebellum by measuring 8-hydroxydeoxyguanosine (8-OH-dG), a marker of DNA modification, in a subset of cases analyzed for 3-NT. We also explored the hypothesis that oxidative damage in autism is associated with altered expression of brain neurotrophins critical for normal brain growth and differentiation. The content of 8-OH-dG in cerebellar DNA isolated by the proteinase K method was measured using an enzyme-linked immunosorbent assay (ELISA); neurotrophin-3 (NT-3) levels in cerebellar homogenates were measured using NT-3 ELISA. Cerebellar 8-OH-dG showed trend towards higher levels with the increase of 63.4% observed in autism. Analysis of cerebellar NT-3 showed a significant (p = 0.034) increase (40.3%) in autism. Furthermore, there was a significant positive correlation between cerebellar NT-3 and 3-NT (r = 0.83; p = 0.0408). These data provide the first quantitative measure of brain NT-3 and show its increase in the autistic brain. Altered levels of brain NT-3 are likely to contribute to autistic pathology not only by affecting brain axonal targeting and synapse formation but also by further exacerbating oxidative stress and possibly contributing to Purkinje cell abnormalities.
Literatur
1.
Zurück zum Zitat Bokara KK, Brown E, McCormick R, Yallapragada PR, Rajanna S, Bettaiya R (2008) Lead-induced increase in antioxidant enzymes and lipid peroxidation products in developing rat brain. Biometals 21:9–16PubMedCrossRef Bokara KK, Brown E, McCormick R, Yallapragada PR, Rajanna S, Bettaiya R (2008) Lead-induced increase in antioxidant enzymes and lipid peroxidation products in developing rat brain. Biometals 21:9–16PubMedCrossRef
2.
Zurück zum Zitat Winham GC, Zhang L, Gunier R, Croen LA, Grether JK (2006) Autism spectrum disorders in relation to distribution of hazardous air pollutants in the San Francisco bay area. Environ Health Perspect 114:1438–1444CrossRef Winham GC, Zhang L, Gunier R, Croen LA, Grether JK (2006) Autism spectrum disorders in relation to distribution of hazardous air pollutants in the San Francisco bay area. Environ Health Perspect 114:1438–1444CrossRef
3.
Zurück zum Zitat Palmer RF, Blanchard S, Wood R (2008) Proximity to point sources of environmental mercury release as a predictor of autism prevalence. Health Place 15(1):18–24PubMedCrossRef Palmer RF, Blanchard S, Wood R (2008) Proximity to point sources of environmental mercury release as a predictor of autism prevalence. Health Place 15(1):18–24PubMedCrossRef
4.
Zurück zum Zitat D’Amelio M, Ricci I, Sacco R, Liu X, D’Agruma L, Muscarella LA et al (2005) Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions. Mol Psychiatry 10:1006–1016PubMedCrossRef D’Amelio M, Ricci I, Sacco R, Liu X, D’Agruma L, Muscarella LA et al (2005) Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions. Mol Psychiatry 10:1006–1016PubMedCrossRef
5.
Zurück zum Zitat Kimura-Kuroda J, Nagata I, Kuroda Y (2007) Disrupting effect of hydroxyl-polychlorinated biphenyl (PCB) congeners on neuronal development of cerebellar Purkinje cells: a possible causal factor for the developmental brain disorders. Chemosphere 67:S412–S420PubMedCrossRef Kimura-Kuroda J, Nagata I, Kuroda Y (2007) Disrupting effect of hydroxyl-polychlorinated biphenyl (PCB) congeners on neuronal development of cerebellar Purkinje cells: a possible causal factor for the developmental brain disorders. Chemosphere 67:S412–S420PubMedCrossRef
6.
Zurück zum Zitat Brown GE, Jones SD, MacKewn AS, Plank EJ (2008) An exploration of possible pre- and postnatal correlates of autism: a pilot survey. Psychol Rep 102:273–282PubMedCrossRef Brown GE, Jones SD, MacKewn AS, Plank EJ (2008) An exploration of possible pre- and postnatal correlates of autism: a pilot survey. Psychol Rep 102:273–282PubMedCrossRef
7.
Zurück zum Zitat Sultana R, Perluigi M, Butterfield DA (2006) Protein oxidation, lipid peroxidation in brain of subjects with Alzheimer’s disease: insights into mechanism of neurodegeneration from redox proteomics. Antioxid Redox Signal 8:2021–2037PubMedCrossRef Sultana R, Perluigi M, Butterfield DA (2006) Protein oxidation, lipid peroxidation in brain of subjects with Alzheimer’s disease: insights into mechanism of neurodegeneration from redox proteomics. Antioxid Redox Signal 8:2021–2037PubMedCrossRef
8.
Zurück zum Zitat Neumann H, Hazen L, Weinstein J, Mehl RA, Chin JW (2008) Genetically encoding protein oxidative damage. J Am Chem Soc 130:4028–4033PubMedCrossRef Neumann H, Hazen L, Weinstein J, Mehl RA, Chin JW (2008) Genetically encoding protein oxidative damage. J Am Chem Soc 130:4028–4033PubMedCrossRef
9.
Zurück zum Zitat Sajdel-Sulkowska EM, Lipinski B, Windom H, Audhya T, McGinnis W (2008) Oxidative stress in autism: cerebellar 3 nitrotyrosine levels. Am J Biochem Biotechnol 4:73–84CrossRef Sajdel-Sulkowska EM, Lipinski B, Windom H, Audhya T, McGinnis W (2008) Oxidative stress in autism: cerebellar 3 nitrotyrosine levels. Am J Biochem Biotechnol 4:73–84CrossRef
10.
Zurück zum Zitat Lovell MA, Gabbita SP, Markesbery WR (1999) Increased DNA oxidation and decreased levels of repair products in Alzheimer’s disease ventricular CSF. J Neurochem 72:771–776PubMedCrossRef Lovell MA, Gabbita SP, Markesbery WR (1999) Increased DNA oxidation and decreased levels of repair products in Alzheimer’s disease ventricular CSF. J Neurochem 72:771–776PubMedCrossRef
11.
Zurück zum Zitat Lee SH, Kim I, Chung BC (2007) Increased urinary level of oxidized nucleosides in patients with mild-to-moderate Alzheimer’s disease. Clin Biochem 40:936–938PubMedCrossRef Lee SH, Kim I, Chung BC (2007) Increased urinary level of oxidized nucleosides in patients with mild-to-moderate Alzheimer’s disease. Clin Biochem 40:936–938PubMedCrossRef
12.
Zurück zum Zitat Sato S, Mizuno Y, Hattori N (2005) Urinary 8-hydroxydeoxyguanosine levels as a biomarker for progression of Parkinson disease. Neurology 64:1081–1083PubMed Sato S, Mizuno Y, Hattori N (2005) Urinary 8-hydroxydeoxyguanosine levels as a biomarker for progression of Parkinson disease. Neurology 64:1081–1083PubMed
13.
Zurück zum Zitat Fukuda M, Yamaguchi H, Yamamoto H, Aminaka M, Murakami H, Kamiyama N et al (2008) The evaluation of oxidative damage in children with brain damage using 8-hydroxydeoxyguanosine levels. Brain Dev 30:131–136PubMedCrossRef Fukuda M, Yamaguchi H, Yamamoto H, Aminaka M, Murakami H, Kamiyama N et al (2008) The evaluation of oxidative damage in children with brain damage using 8-hydroxydeoxyguanosine levels. Brain Dev 30:131–136PubMedCrossRef
14.
Zurück zum Zitat Nishioka N, Arnold SE (2004) Evidence for oxidative DNA damage in the hippocampus of elderly patients with chronic schizophrenia. Am J Geriatr Psychiatry 12:167–175PubMed Nishioka N, Arnold SE (2004) Evidence for oxidative DNA damage in the hippocampus of elderly patients with chronic schizophrenia. Am J Geriatr Psychiatry 12:167–175PubMed
15.
Zurück zum Zitat Ming X, Stein TP, Brimacombe M, Johnson WG, Lambert GH, Wagner GC (2005) Increased excretion of lipid peroxidation biomarker in autism. Prostaglandins Leukot Essent Fat Acids 73:379–384CrossRef Ming X, Stein TP, Brimacombe M, Johnson WG, Lambert GH, Wagner GC (2005) Increased excretion of lipid peroxidation biomarker in autism. Prostaglandins Leukot Essent Fat Acids 73:379–384CrossRef
16.
Zurück zum Zitat Courchesne E, Karns CM, Davis HR, Ziccardi R, Carper RA, Tigue ZD (2001) Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study. Neurology 57:245–254PubMed Courchesne E, Karns CM, Davis HR, Ziccardi R, Carper RA, Tigue ZD (2001) Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study. Neurology 57:245–254PubMed
17.
Zurück zum Zitat Whitney ER, Kemper TL, Bauman ML, Rosene DL, Blatt GJ (2008) Cerebellar Purkinje cells are reduced in a subpopulation of autistic brains: a stereological experiment using calbindin-D28k. Cerebellum 7(3):406–416PubMedCrossRef Whitney ER, Kemper TL, Bauman ML, Rosene DL, Blatt GJ (2008) Cerebellar Purkinje cells are reduced in a subpopulation of autistic brains: a stereological experiment using calbindin-D28k. Cerebellum 7(3):406–416PubMedCrossRef
18.
Zurück zum Zitat Chao SL, Moss JM, Harry GJ (2007) Lead-induced alterations of apoptosis and neurotrophic factor mRNA in the developing rat cortex, hippocampus, and cerebellum. J Biochem Mol Toxicol 21:265–272PubMedCrossRef Chao SL, Moss JM, Harry GJ (2007) Lead-induced alterations of apoptosis and neurotrophic factor mRNA in the developing rat cortex, hippocampus, and cerebellum. J Biochem Mol Toxicol 21:265–272PubMedCrossRef
19.
Zurück zum Zitat Marx CE, Vance BJ, Jarskog LF, Chescheir NC, Gilmore JH (1999) Nerve growth factor, brain derived neurotrophic factor and neurotrophin-3 levels in human amniotic fluid. Am J Obstet Gynecol 181:1225–1230PubMedCrossRef Marx CE, Vance BJ, Jarskog LF, Chescheir NC, Gilmore JH (1999) Nerve growth factor, brain derived neurotrophic factor and neurotrophin-3 levels in human amniotic fluid. Am J Obstet Gynecol 181:1225–1230PubMedCrossRef
20.
Zurück zum Zitat Courchesne E, Carper R, Akshoomoff N (2003) Evidence of brain overgrowth in the first year life in autism. JAMA 290:393–394CrossRef Courchesne E, Carper R, Akshoomoff N (2003) Evidence of brain overgrowth in the first year life in autism. JAMA 290:393–394CrossRef
21.
Zurück zum Zitat Rivto ER, Freeman BJ, Scheibel AB, Duong T, Robinson H, Guthrie D, Ritvo A (1986) Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSac Autopsy Research Report. Am. J. Psychiatry 143:862–866 Rivto ER, Freeman BJ, Scheibel AB, Duong T, Robinson H, Guthrie D, Ritvo A (1986) Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSac Autopsy Research Report. Am. J. Psychiatry 143:862–866
22.
Zurück zum Zitat Courchesne E (1991) Neuroanatomic imaging in autism. Pediatrics 87:781–790PubMed Courchesne E (1991) Neuroanatomic imaging in autism. Pediatrics 87:781–790PubMed
23.
Zurück zum Zitat Kemper TL, Bauman ML (1993) The contribution of neuropathologic studies to the understanding of autism. Neurol Clin 11:175–187PubMed Kemper TL, Bauman ML (1993) The contribution of neuropathologic studies to the understanding of autism. Neurol Clin 11:175–187PubMed
24.
Zurück zum Zitat Das KP, Chao SL, White LD, Haines WT, Harry GJ, Tilson HA, Barone S Jr (2001) Differential patterns of nerve growth factor, brain-derived neurotrophic factor and neurotrophin-3 mRNA and protein levels in developing regions of rat brain. Neuroscience 103:739–761PubMedCrossRef Das KP, Chao SL, White LD, Haines WT, Harry GJ, Tilson HA, Barone S Jr (2001) Differential patterns of nerve growth factor, brain-derived neurotrophic factor and neurotrophin-3 mRNA and protein levels in developing regions of rat brain. Neuroscience 103:739–761PubMedCrossRef
25.
Zurück zum Zitat Li S, Qiu F, Xu A, Price SM, Xiang M (2004) Barhl1 regulates migration and survival of cerebellar granule cells by controlling expression of neurotrophin-3 gene. J Neuroscience 24:3104–3114CrossRef Li S, Qiu F, Xu A, Price SM, Xiang M (2004) Barhl1 regulates migration and survival of cerebellar granule cells by controlling expression of neurotrophin-3 gene. J Neuroscience 24:3104–3114CrossRef
26.
Zurück zum Zitat Kawakami H, Nitta A, Matsuyama Y, Kamiya M, Satake K, Sato K et al (2000) Increase in neurotrophin-3 expression followed by Purkinje cell degeneration in the adult rat cerebellum after spinal cord transaction. J Neurosci Res 62:668–674PubMedCrossRef Kawakami H, Nitta A, Matsuyama Y, Kamiya M, Satake K, Sato K et al (2000) Increase in neurotrophin-3 expression followed by Purkinje cell degeneration in the adult rat cerebellum after spinal cord transaction. J Neurosci Res 62:668–674PubMedCrossRef
27.
Zurück zum Zitat Helbock HJ, Beckma KB, Ames BN (1999) 8-Hydroxydeoxyguanosine and 8 hydroxyguanine as biomarkers of oxidative stress. Method Enzymol 300:156–166CrossRef Helbock HJ, Beckma KB, Ames BN (1999) 8-Hydroxydeoxyguanosine and 8 hydroxyguanine as biomarkers of oxidative stress. Method Enzymol 300:156–166CrossRef
28.
Zurück zum Zitat Bershtein LM, Poroshina LVV, TE TEV (2005) Content of 8-hydroxy-2-deoxyguanosine in steroid receptor positive and receptor-negative breast cancer cells. Bull Exp Biol Med 140:88–91PubMedCrossRef Bershtein LM, Poroshina LVV, TE TEV (2005) Content of 8-hydroxy-2-deoxyguanosine in steroid receptor positive and receptor-negative breast cancer cells. Bull Exp Biol Med 140:88–91PubMedCrossRef
29.
Zurück zum Zitat Miller MW, Mooney SM (2004) Chronic exposure to ethanol alters neurotrophin content in the basal forebrain–cortex system in the mature rat: effects on autocrine–paracrine mechanisms. J Neurobiol 60:490–498PubMedCrossRef Miller MW, Mooney SM (2004) Chronic exposure to ethanol alters neurotrophin content in the basal forebrain–cortex system in the mature rat: effects on autocrine–paracrine mechanisms. J Neurobiol 60:490–498PubMedCrossRef
30.
Zurück zum Zitat Abdollahi M, Ranjbar A, Shadnia S, Nikfar S, Rezaiee A (2004) Pesticides and oxidative stress: a review. Med Sci Monit 10:141–147 Abdollahi M, Ranjbar A, Shadnia S, Nikfar S, Rezaiee A (2004) Pesticides and oxidative stress: a review. Med Sci Monit 10:141–147
31.
Zurück zum Zitat Mutter J, Naumann J, Schneider R, Wlach H, Haley B (2005) Mercury and autism: accelerating evidence? Neuro Endocrinol Lett 26:439–446PubMed Mutter J, Naumann J, Schneider R, Wlach H, Haley B (2005) Mercury and autism: accelerating evidence? Neuro Endocrinol Lett 26:439–446PubMed
32.
Zurück zum Zitat Mutter J, Naumann J, Walach H, Daschner F (2005) Amalgam risk assessment with coverage of references up to 2005. Gesundheitswesen 67:204–216PubMedCrossRef Mutter J, Naumann J, Walach H, Daschner F (2005) Amalgam risk assessment with coverage of references up to 2005. Gesundheitswesen 67:204–216PubMedCrossRef
33.
Zurück zum Zitat Bradstreet J, Geier DA, Kartzinel JJ, Adams JB, Geier MR (2003) A case–control study of mercury burden in children with autistic disorders. J Am Phys Surg 8:76–80 Bradstreet J, Geier DA, Kartzinel JJ, Adams JB, Geier MR (2003) A case–control study of mercury burden in children with autistic disorders. J Am Phys Surg 8:76–80
34.
Zurück zum Zitat Serajee FJ, Nabi R, Zhong H, Huq M (2004) Polymorhism in xenobiotic metabolism genes and autism. J Child Neurol 19:413–417PubMed Serajee FJ, Nabi R, Zhong H, Huq M (2004) Polymorhism in xenobiotic metabolism genes and autism. J Child Neurol 19:413–417PubMed
35.
Zurück zum Zitat Zoroglu SS, Armutcu F, Ozen S, Gurel A, Sivasli E, Yetkin O et al (2004) Increased oxidative stress and altered activities of erythrocyte free radical scavenging enzymes in autism. Eur Arch Psychiatr Clin Neurosci 254:143–147 Zoroglu SS, Armutcu F, Ozen S, Gurel A, Sivasli E, Yetkin O et al (2004) Increased oxidative stress and altered activities of erythrocyte free radical scavenging enzymes in autism. Eur Arch Psychiatr Clin Neurosci 254:143–147
36.
Zurück zum Zitat Yorbik O, Sayal A, Akay C, Akbiyik DI, Sohmen T (2002) Investigation of antioxidant enzymes in children with autistic disorder. Prostaglandins Leukot Essent Fat Acids 67:341–343CrossRef Yorbik O, Sayal A, Akay C, Akbiyik DI, Sohmen T (2002) Investigation of antioxidant enzymes in children with autistic disorder. Prostaglandins Leukot Essent Fat Acids 67:341–343CrossRef
37.
Zurück zum Zitat James SJ, Cutler P, Melnyk S, Jernigan S, Janak L, Gaylor DW et al (2004) Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism. Am J Clin Nutr 80:1611–1617PubMed James SJ, Cutler P, Melnyk S, Jernigan S, Janak L, Gaylor DW et al (2004) Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism. Am J Clin Nutr 80:1611–1617PubMed
38.
Zurück zum Zitat James SJ, Melny S, Jernigan S, Cleves MA, Halsted CH, Wong DH et al (2006) Metabolic endotype and related genotypes are associated with oxidative stress in children with autism. Am J Med Genet B Neuropsychiatry Genet 141:947–956CrossRef James SJ, Melny S, Jernigan S, Cleves MA, Halsted CH, Wong DH et al (2006) Metabolic endotype and related genotypes are associated with oxidative stress in children with autism. Am J Med Genet B Neuropsychiatry Genet 141:947–956CrossRef
39.
Zurück zum Zitat Yang IA, Fong KM, Zimmerman PV, Holgate ST, Holloway JW (2008) Genetic susceptibility to the respiratory effects of air pollution. Thorax 63:555–563PubMed Yang IA, Fong KM, Zimmerman PV, Holgate ST, Holloway JW (2008) Genetic susceptibility to the respiratory effects of air pollution. Thorax 63:555–563PubMed
40.
Zurück zum Zitat Buyske S, Williams TA, Mars AE, Stenroos ES, Ming SX, Wang R et al (2006) Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism. BMC 7:8 Buyske S, Williams TA, Mars AE, Stenroos ES, Ming SX, Wang R et al (2006) Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism. BMC 7:8
41.
Zurück zum Zitat Nelson PG, Kuddo T, Song EY, Dambrosia JM, Kohler S, Satyanarayana G, Vandunk C et al (2006) Selected neuropeptides, and cytokines: developmental trajectory and concentrations in neonatal blood of children with autism or Down syndrome. Int J Dev Neurosci 241:73–80CrossRef Nelson PG, Kuddo T, Song EY, Dambrosia JM, Kohler S, Satyanarayana G, Vandunk C et al (2006) Selected neuropeptides, and cytokines: developmental trajectory and concentrations in neonatal blood of children with autism or Down syndrome. Int J Dev Neurosci 241:73–80CrossRef
42.
Zurück zum Zitat Perry EK, Lee MW, Martin-Ruiz CM, Court JA, Volsen SG, Merrit J et al (2001) Cholinergic activity in autism: abnormalities in the cerebral cortex and basal forebrain. Am J Psychiatry 158:1058–1066PubMedCrossRef Perry EK, Lee MW, Martin-Ruiz CM, Court JA, Volsen SG, Merrit J et al (2001) Cholinergic activity in autism: abnormalities in the cerebral cortex and basal forebrain. Am J Psychiatry 158:1058–1066PubMedCrossRef
43.
Zurück zum Zitat Ghosh A, Greenberg ME (1995) Distinct roles for bFGF and NT-3 in the regulation of cortical neurogenesis. Neuron 15:89–103PubMedCrossRef Ghosh A, Greenberg ME (1995) Distinct roles for bFGF and NT-3 in the regulation of cortical neurogenesis. Neuron 15:89–103PubMedCrossRef
44.
Zurück zum Zitat Segal RA, Pomeroy SL, Stiles CD (1995) Axonal growth and fasciculation linked to differential expression of BDNF and NT-3 receptors in developing granule cells. J Neurosci 15:4970–4981PubMed Segal RA, Pomeroy SL, Stiles CD (1995) Axonal growth and fasciculation linked to differential expression of BDNF and NT-3 receptors in developing granule cells. J Neurosci 15:4970–4981PubMed
45.
Zurück zum Zitat Bates B, Hirt L, Thomas SS, Akbarian S, Le D, Amin-Hanjani S et al (2002) Neurotrophin-3 promotes cell death induced in cerebellar ischemia, oxygen-glucose deprivation, and oxidative stress: possible involvement of oxygen free radicals. Neurobiol Dis 9:24–37PubMedCrossRef Bates B, Hirt L, Thomas SS, Akbarian S, Le D, Amin-Hanjani S et al (2002) Neurotrophin-3 promotes cell death induced in cerebellar ischemia, oxygen-glucose deprivation, and oxidative stress: possible involvement of oxygen free radicals. Neurobiol Dis 9:24–37PubMedCrossRef
46.
Zurück zum Zitat Pasarica D, Gheorghiu M, Toparceanu F, Bleotu C, Ichim L, Trandafir T (2005) Neurotrophin-3, TNF-alpha and IL-6 relations in serum and cerebrospinal fluid of ischemic stroke patients. Roum Arch Microbiol Immunol 64:27–33PubMed Pasarica D, Gheorghiu M, Toparceanu F, Bleotu C, Ichim L, Trandafir T (2005) Neurotrophin-3, TNF-alpha and IL-6 relations in serum and cerebrospinal fluid of ischemic stroke patients. Roum Arch Microbiol Immunol 64:27–33PubMed
47.
Zurück zum Zitat Morrison ME, Mason CA (1998) Granule neuron regulation of Purkinje cell development: striking a balance between neurotrophin and glutamate signaling. J Neurosci 18:3563–3573PubMed Morrison ME, Mason CA (1998) Granule neuron regulation of Purkinje cell development: striking a balance between neurotrophin and glutamate signaling. J Neurosci 18:3563–3573PubMed
48.
Zurück zum Zitat Cappelletti G, Maggioni MG, Tedeschi G, Maci R (2003) Protein tyrosine nitration is triggered by nerve growth factor during neuronal differentiation of PC12 cells. Exp Cell Res 288:9–20PubMedCrossRef Cappelletti G, Maggioni MG, Tedeschi G, Maci R (2003) Protein tyrosine nitration is triggered by nerve growth factor during neuronal differentiation of PC12 cells. Exp Cell Res 288:9–20PubMedCrossRef
49.
Zurück zum Zitat Vargas MR, Pehar M, Cassina P, Estavez AG, Beckman JS, Barbeito L (2004) Stimulation of nerve growth factor expression in astrocytes by peroxynitrite. In vivo 18:269–274PubMed Vargas MR, Pehar M, Cassina P, Estavez AG, Beckman JS, Barbeito L (2004) Stimulation of nerve growth factor expression in astrocytes by peroxynitrite. In vivo 18:269–274PubMed
50.
Zurück zum Zitat Behrens MM, Strasser U, Lobner D, Dugan LL (1999) Neurotrophin-mediated potentiation of neuronal injury. Microsc Res Tech 45:276–284PubMedCrossRef Behrens MM, Strasser U, Lobner D, Dugan LL (1999) Neurotrophin-mediated potentiation of neuronal injury. Microsc Res Tech 45:276–284PubMedCrossRef
51.
Zurück zum Zitat Yip J, Soghomonian JJ, Blatt GJ (2007) Decreased GAD67 mRNA levels in cerebellar Purkinje cells in autism: pathophysiological implications. Acta Neuropathol 113:559–568PubMedCrossRef Yip J, Soghomonian JJ, Blatt GJ (2007) Decreased GAD67 mRNA levels in cerebellar Purkinje cells in autism: pathophysiological implications. Acta Neuropathol 113:559–568PubMedCrossRef
52.
Zurück zum Zitat Rout UK, Dhossche DM (2008) A pathogenetic model of autism involving Purkinje cell loss through anti GAD antibodies. Med Hypotheses 71:218–221PubMedCrossRef Rout UK, Dhossche DM (2008) A pathogenetic model of autism involving Purkinje cell loss through anti GAD antibodies. Med Hypotheses 71:218–221PubMedCrossRef
Metadaten
Titel
Increase in Cerebellar Neurotrophin-3 and Oxidative Stress Markers in Autism
verfasst von
Elizabeth M. Sajdel-Sulkowska
Ming Xu
Noriyuki Koibuchi
Publikationsdatum
01.09.2009
Verlag
Springer-Verlag
Erschienen in
The Cerebellum / Ausgabe 3/2009
Print ISSN: 1473-4222
Elektronische ISSN: 1473-4230
DOI
https://doi.org/10.1007/s12311-009-0105-9

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