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Erschienen in: Journal of Natural Medicines 4/2018

09.07.2018 | Original Paper

Hydroxyobtustyrene protects neuronal cells from chemical hypoxia-induced cell death

verfasst von: Takashi Iwai, Kengo Obara, Chihiro Ito, Hiroshi Furukawa, Jun-Ichiro Oka

Erschienen in: Journal of Natural Medicines | Ausgabe 4/2018

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Abstract

Hydroxyobtustyrene is a derivative of cinnamyl phenol isolated from Dalbergia odorifera T. Chen. The heartwood, known as ‘JiangXiang’, is a traditional Chinese medicine. Previous studies showed that hydroxyobtustyrene inhibited the biosynthesis of prostaglandins, which are mediators of neuronal cell death in ischemia. However, it currently remains unclear whether hydroxyobtustyrene protects neurons against ischemic stress. In the present study, we investigated the protective effects of hydroxyobtustyrene against sodium cyanide (NaCN)-induced chemical ischemia. Hippocampal neurons were cultured from the cerebral cortices of E18 Wistar rats. The effects of hydroxyobtustyrene on neuronal survival and trophic effects were estimated under lower and higher cell density conditions. After the treatment of 1 mM NaCN with or without hydroxyobtustyrene, an MTT assay, Hoechst staining, and immunocytochemistry for cyclooxygenase (COX)-2 were performed. Hydroxyobtustyrene increased cell viability under lower, but not normal density conditions. Neither the neurite number nor the length was influenced by hydroxyobtustyrene. NaCN significantly decreased viability and increased fragmentation in cell nuclei, and these changes were prevented by hydroxyobtustyrene. Moreover, NaCN increased the number of COX-2-positive neurons, and this was significantly prevented by the co-treatment with hydroxyobtustyrene. Therefore, hydroxyobtustyrene protected cultured hippocampal neurons against NaCN-induced chemical ischemia, which may be mediated by the inhibition of COX-2 production.
Literatur
1.
Zurück zum Zitat Hotez PJ, Alvarado M, Basanez MG, Bolliger I, Bourne R, Boussinesq M, Brooker SJ, Brown AS, Buckle G, Budke CM, Carabin H, Coffeng LE, Fevre EM, Furst T, Halasa YA, Jasrasaria R, Johns NE, Keiser J, King CH, Lozano R, Murdoch ME, O’Hanlon S, Pion SD, Pullan RL, Ramaiah KD, Roberts T, Shepard DS, Smith JL, Stolk WA, Undurraga EA, Utzinger J, Wang M, Murray CJ, Naghavi M (2014) The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases. PLoS Negl Trop Dis 8:e2865CrossRefPubMedPubMedCentral Hotez PJ, Alvarado M, Basanez MG, Bolliger I, Bourne R, Boussinesq M, Brooker SJ, Brown AS, Buckle G, Budke CM, Carabin H, Coffeng LE, Fevre EM, Furst T, Halasa YA, Jasrasaria R, Johns NE, Keiser J, King CH, Lozano R, Murdoch ME, O’Hanlon S, Pion SD, Pullan RL, Ramaiah KD, Roberts T, Shepard DS, Smith JL, Stolk WA, Undurraga EA, Utzinger J, Wang M, Murray CJ, Naghavi M (2014) The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases. PLoS Negl Trop Dis 8:e2865CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Minnerup J, Sutherland BA, Buchan AM, Kleinschnitz C (2012) Neuroprotection for stroke: current status and future perspectives. Int J Mol Sci 13:11753–11772CrossRefPubMedPubMedCentral Minnerup J, Sutherland BA, Buchan AM, Kleinschnitz C (2012) Neuroprotection for stroke: current status and future perspectives. Int J Mol Sci 13:11753–11772CrossRefPubMedPubMedCentral
3.
Zurück zum Zitat Way JL (1984) Cyanide intoxication and its mechanism of antagonism. Annu Rev Pharmacol Toxicol 24:451–481CrossRefPubMed Way JL (1984) Cyanide intoxication and its mechanism of antagonism. Annu Rev Pharmacol Toxicol 24:451–481CrossRefPubMed
4.
Zurück zum Zitat Carella F, Grassi MP, Savoiardo M, Contri P, Rapuzzi B, Mangoni A (1988) Dystonic-Parkinsonian syndrome after cyanide poisoning: clinical and MRI findings. J Neurol Neurosurg Psychiatry 51:1345–1348CrossRefPubMedPubMedCentral Carella F, Grassi MP, Savoiardo M, Contri P, Rapuzzi B, Mangoni A (1988) Dystonic-Parkinsonian syndrome after cyanide poisoning: clinical and MRI findings. J Neurol Neurosurg Psychiatry 51:1345–1348CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Rosenow F, Herholz K, Lanfermann H, Weuthen G, Ebner R, Kessler J, Ghaemi M, Heiss WD (1995) Neurological sequelae of cyanide intoxication—the patterns of clinical, magnetic resonance imaging, and positron emission tomography findings. Ann Neurol 38:825–828CrossRefPubMed Rosenow F, Herholz K, Lanfermann H, Weuthen G, Ebner R, Kessler J, Ghaemi M, Heiss WD (1995) Neurological sequelae of cyanide intoxication—the patterns of clinical, magnetic resonance imaging, and positron emission tomography findings. Ann Neurol 38:825–828CrossRefPubMed
7.
Zurück zum Zitat Rosenberg NL, Myers JA, Martin WR (1989) Cyanide-induced parkinsonism: clinical, MRI, and 6-fluorodopa PET studies. Neurology 39:142–144CrossRefPubMed Rosenberg NL, Myers JA, Martin WR (1989) Cyanide-induced parkinsonism: clinical, MRI, and 6-fluorodopa PET studies. Neurology 39:142–144CrossRefPubMed
8.
Zurück zum Zitat Gunasekar PG, Sun PW, Kanthasamy AG, Borowitz JL, Isom GE (1996) Cyanide-induced neurotoxicity involves nitric oxide and reactive oxygen species generation after N-methyl-d-aspartate receptor activation. J Pharmacol Exp Ther 277:150–155PubMed Gunasekar PG, Sun PW, Kanthasamy AG, Borowitz JL, Isom GE (1996) Cyanide-induced neurotoxicity involves nitric oxide and reactive oxygen species generation after N-methyl-d-aspartate receptor activation. J Pharmacol Exp Ther 277:150–155PubMed
9.
Zurück zum Zitat Bhattacharya R, Lakshmana Rao PV (2001) Pharmacological interventions of cyanide-induced cytotoxicity and DNA damage in isolated rat thymocytes and their protective efficacy in vivo. Toxicol Lett 119:59–70CrossRefPubMed Bhattacharya R, Lakshmana Rao PV (2001) Pharmacological interventions of cyanide-induced cytotoxicity and DNA damage in isolated rat thymocytes and their protective efficacy in vivo. Toxicol Lett 119:59–70CrossRefPubMed
10.
Zurück zum Zitat Mills EM, Gunasekar PG, Li L, Borowitz JL, Isom GE (1999) Differential susceptibility of brain areas to cyanide involves different modes of cell death. Toxicol Appl Pharmacol 156:6–16CrossRefPubMed Mills EM, Gunasekar PG, Li L, Borowitz JL, Isom GE (1999) Differential susceptibility of brain areas to cyanide involves different modes of cell death. Toxicol Appl Pharmacol 156:6–16CrossRefPubMed
11.
Zurück zum Zitat Prabhakaran K, Li L, Borowitz JL, Isom GE (2002) Cyanide induces different modes of death in cortical and mesencephalon cells. J Pharmacol Exp Ther 303:510–519CrossRefPubMed Prabhakaran K, Li L, Borowitz JL, Isom GE (2002) Cyanide induces different modes of death in cortical and mesencephalon cells. J Pharmacol Exp Ther 303:510–519CrossRefPubMed
12.
Zurück zum Zitat Vane JR, Bakhle YS, Botting RM (1998) Cyclooxygenases 1 and 2. Annu Rev Pharmacol Toxicol 38:97–120CrossRefPubMed Vane JR, Bakhle YS, Botting RM (1998) Cyclooxygenases 1 and 2. Annu Rev Pharmacol Toxicol 38:97–120CrossRefPubMed
13.
Zurück zum Zitat Smith WL, DeWitt DL, Garavito RM (2000) Cyclooxygenases: structural, cellular, and molecular biology. Annu Rev Biochem 69:145–182CrossRefPubMed Smith WL, DeWitt DL, Garavito RM (2000) Cyclooxygenases: structural, cellular, and molecular biology. Annu Rev Biochem 69:145–182CrossRefPubMed
14.
Zurück zum Zitat Gunasekar PG, Borowitz JL, Isom GE (1998) Cyanide-induced generation of oxidative species: involvement of nitric oxide synthase and cyclooxygenase-2. J Pharmacol Exp Ther 285:236–241PubMed Gunasekar PG, Borowitz JL, Isom GE (1998) Cyanide-induced generation of oxidative species: involvement of nitric oxide synthase and cyclooxygenase-2. J Pharmacol Exp Ther 285:236–241PubMed
15.
Zurück zum Zitat Ohanian SH, Borsos T (1975) Lysis of tumor cells by antibody and complement. II. Lack of correlation between amount of C4 and C3 fixed and cell lysis. J Immunol 114:1292–1295PubMed Ohanian SH, Borsos T (1975) Lysis of tumor cells by antibody and complement. II. Lack of correlation between amount of C4 and C3 fixed and cell lysis. J Immunol 114:1292–1295PubMed
16.
Zurück zum Zitat Kawano T, Anrather J, Zhou P, Park L, Wang G, Frys KA, Kunz A, Cho S, Orio M, Iadecola C (2006) Prostaglandin E2 EP1 receptors: downstream effectors of COX-2 neurotoxicity. Nat Med 12:225–229CrossRefPubMed Kawano T, Anrather J, Zhou P, Park L, Wang G, Frys KA, Kunz A, Cho S, Orio M, Iadecola C (2006) Prostaglandin E2 EP1 receptors: downstream effectors of COX-2 neurotoxicity. Nat Med 12:225–229CrossRefPubMed
17.
Zurück zum Zitat Candelario-Jalil E, Fiebich BL (2008) Cyclooxygenase inhibition in ischemic brain injury. Curr Pharm Des 14:1401–1418CrossRefPubMed Candelario-Jalil E, Fiebich BL (2008) Cyclooxygenase inhibition in ischemic brain injury. Curr Pharm Des 14:1401–1418CrossRefPubMed
18.
Zurück zum Zitat Ikeda-Matsuo Y, Tanji H, Narumiya S, Sasaki Y (2011) Inhibition of prostaglandin E2 EP3 receptors improves stroke injury via anti-inflammatory and anti-apoptotic mechanisms. J Neuroimmunol 238:34–43CrossRefPubMed Ikeda-Matsuo Y, Tanji H, Narumiya S, Sasaki Y (2011) Inhibition of prostaglandin E2 EP3 receptors improves stroke injury via anti-inflammatory and anti-apoptotic mechanisms. J Neuroimmunol 238:34–43CrossRefPubMed
19.
20.
Zurück zum Zitat Goda Y, Kiuchi F, Shibuya M, Sankawa U (1992) Inhibitors of prostaglandin biosynthesis from Dalbergia odorifera. Chem Pharm Bull (Tokyo) 40:2452–2457CrossRef Goda Y, Kiuchi F, Shibuya M, Sankawa U (1992) Inhibitors of prostaglandin biosynthesis from Dalbergia odorifera. Chem Pharm Bull (Tokyo) 40:2452–2457CrossRef
21.
Zurück zum Zitat Iwai T, Ito S, Tanimitsu K, Udagawa S, Oka J (2006) Glucagon-like peptide-1 inhibits LPS-induced IL-1β production in cultured rat astrocytes. Neurosci Res 55:352–360CrossRefPubMed Iwai T, Ito S, Tanimitsu K, Udagawa S, Oka J (2006) Glucagon-like peptide-1 inhibits LPS-induced IL-1β production in cultured rat astrocytes. Neurosci Res 55:352–360CrossRefPubMed
22.
Zurück zum Zitat Iwai T, Iinuma Y, Kodani R, Oka J (2008) Neuromedin U inhibits inflammation-mediated memory impairment and neuronal cell-death in rodents. Neurosci Res 61:113–119CrossRefPubMed Iwai T, Iinuma Y, Kodani R, Oka J (2008) Neuromedin U inhibits inflammation-mediated memory impairment and neuronal cell-death in rodents. Neurosci Res 61:113–119CrossRefPubMed
23.
Zurück zum Zitat Yu X, An L (2002) A serum- and antioxidant-free primary culture model of mouse cortical neurons for pharmacological screen and studies of neurotrophic and neuroprotective agents. Cell Mol Neurobiol 22:197–206CrossRefPubMed Yu X, An L (2002) A serum- and antioxidant-free primary culture model of mouse cortical neurons for pharmacological screen and studies of neurotrophic and neuroprotective agents. Cell Mol Neurobiol 22:197–206CrossRefPubMed
25.
Zurück zum Zitat Kaneko A, Sankai Y (2014) Long-term culture of rat hippocampal neurons at low density in serum-free medium: combination of the sandwich culture technique with the three-dimensional nanofibrous hydrogel PuraMatrix. PLoS One 9:e102703CrossRefPubMedPubMedCentral Kaneko A, Sankai Y (2014) Long-term culture of rat hippocampal neurons at low density in serum-free medium: combination of the sandwich culture technique with the three-dimensional nanofibrous hydrogel PuraMatrix. PLoS One 9:e102703CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Fujita R, Yoshida A, Mizuno K, Ueda H (2001) Cell density-dependent death mode switch of cultured cortical neurons under serum-free starvation stress. Cell Mol Neurobiol 21:317–324CrossRefPubMed Fujita R, Yoshida A, Mizuno K, Ueda H (2001) Cell density-dependent death mode switch of cultured cortical neurons under serum-free starvation stress. Cell Mol Neurobiol 21:317–324CrossRefPubMed
27.
Zurück zum Zitat Zhou J, Tang XC (2002) Huperzine A attenuates apoptosis and mitochondria-dependent caspase-3 in rat cortical neurons. FEBS Lett 526:21–25CrossRefPubMed Zhou J, Tang XC (2002) Huperzine A attenuates apoptosis and mitochondria-dependent caspase-3 in rat cortical neurons. FEBS Lett 526:21–25CrossRefPubMed
28.
Zurück zum Zitat Collino M, Aragno M, Mastrocola R, Gallicchio M, Rosa AC, Dianzani C, Danni O, Thiemermann C, Fantozzi R (2006) Modulation of the oxidative stress and inflammatory response by PPAR-γ agonists in the hippocampus of rats exposed to cerebral ischemia/reperfusion. Eur J Pharmacol 530:70–80CrossRefPubMed Collino M, Aragno M, Mastrocola R, Gallicchio M, Rosa AC, Dianzani C, Danni O, Thiemermann C, Fantozzi R (2006) Modulation of the oxidative stress and inflammatory response by PPAR-γ agonists in the hippocampus of rats exposed to cerebral ischemia/reperfusion. Eur J Pharmacol 530:70–80CrossRefPubMed
29.
Zurück zum Zitat Topol EJ (2004) Failing the public health—rofecoxib, Merck, and the FDA. N Engl J Med 351:1707–1709CrossRefPubMed Topol EJ (2004) Failing the public health—rofecoxib, Merck, and the FDA. N Engl J Med 351:1707–1709CrossRefPubMed
30.
Zurück zum Zitat Solomon SD, McMurray JJ, Pfeffer MA, Wittes J, Fowler R, Finn P, Anderson WF, Zauber A, Hawk E, Bertagnolli M, Adenoma Prevention with Celecoxib Study I (2005) Cardiovascular risk associated with celecoxib in a clinical trial for colorectal adenoma prevention. N Engl J Med 352:1071–1080CrossRefPubMed Solomon SD, McMurray JJ, Pfeffer MA, Wittes J, Fowler R, Finn P, Anderson WF, Zauber A, Hawk E, Bertagnolli M, Adenoma Prevention with Celecoxib Study I (2005) Cardiovascular risk associated with celecoxib in a clinical trial for colorectal adenoma prevention. N Engl J Med 352:1071–1080CrossRefPubMed
31.
Zurück zum Zitat FitzGerald GA (2003) COX-2 and beyond: approaches to prostaglandin inhibition in human disease. Nat Rev Drug Discov 2:879–890CrossRefPubMed FitzGerald GA (2003) COX-2 and beyond: approaches to prostaglandin inhibition in human disease. Nat Rev Drug Discov 2:879–890CrossRefPubMed
32.
Zurück zum Zitat Hewett SJ, Bell SC, Hewett JA (2006) Contributions of cyclooxygenase-2 to neuroplasticity and neuropathology of the central nervous system. Pharmacol Ther 112:335–357CrossRefPubMed Hewett SJ, Bell SC, Hewett JA (2006) Contributions of cyclooxygenase-2 to neuroplasticity and neuropathology of the central nervous system. Pharmacol Ther 112:335–357CrossRefPubMed
33.
Zurück zum Zitat Rodrigo R, Fernández-Gajardo R, Gutiérrez R, Matamala JM, Carrasco R, Miranda-Merchak A, Feuerhake W (2013) Oxidative stress and pathophysiology of ischemic stroke: novel therapeutic opportunities. CNS Neurol Disord Drug Targets 12:698–714CrossRefPubMed Rodrigo R, Fernández-Gajardo R, Gutiérrez R, Matamala JM, Carrasco R, Miranda-Merchak A, Feuerhake W (2013) Oxidative stress and pathophysiology of ischemic stroke: novel therapeutic opportunities. CNS Neurol Disord Drug Targets 12:698–714CrossRefPubMed
Metadaten
Titel
Hydroxyobtustyrene protects neuronal cells from chemical hypoxia-induced cell death
verfasst von
Takashi Iwai
Kengo Obara
Chihiro Ito
Hiroshi Furukawa
Jun-Ichiro Oka
Publikationsdatum
09.07.2018
Verlag
Springer Japan
Erschienen in
Journal of Natural Medicines / Ausgabe 4/2018
Print ISSN: 1340-3443
Elektronische ISSN: 1861-0293
DOI
https://doi.org/10.1007/s11418-018-1224-8

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