Stimulation of CB1 Cannabinoid and NMDA Receptors Increases Neuroprotective Effect Against Diazinon-Induced Neurotoxicity
Cannabinoids have been shown to exert a neuroprotective influence in organophosphorusinduced toxicity. In our study, we examined the effects of the cannabinoid receptor agonist WIN55,212-2 and NMDA receptor agonist NMDA on cell death in the pheochromocytoma cell line PC12 subjected to the action o...
Збережено в:
Дата: | 2013 |
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Автори: | , , , , |
Формат: | Стаття |
Мова: | English |
Опубліковано: |
Інститут фізіології ім. О.О. Богомольця НАН України
2013
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Назва видання: | Нейрофизиология |
Онлайн доступ: | http://dspace.nbuv.gov.ua/handle/123456789/148243 |
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Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
Цитувати: | Stimulation of CB1 Cannabinoid and NMDA Receptors Increases Neuroprotective Effect Against Diazinon-Induced Neurotoxicity / F. Bahrami, M. Hashemi, F. Khalili, J. Hashemi, A. Asgari // Нейрофизиология. — 2013. — Т. 45, № 6. — С. 529-536. — Бібліогр.: 31 назв. — англ. |
Репозитарії
Digital Library of Periodicals of National Academy of Sciences of UkraineРезюме: | Cannabinoids have been shown to exert a neuroprotective influence in organophosphorusinduced toxicity. In our study, we examined the effects of the cannabinoid receptor agonist
WIN55,212-2 and NMDA receptor agonist NMDA on cell death in the pheochromocytoma
cell line PC12 subjected to the action of an organophosphorus compound, diazinon. Diazinon
decreased cell viability in a concentration-dependent manner. Following the exposure of
PC12 cells to 200 µM diazinon for 48 h, reductions in cell survival and protein level of
CB1 receptors were observed. Treatment of the cells with 0.1 µM WIN55,212-2 and 100
µM NMDA prior to diazinon exposure significantly elevated the cell survival level and
protein level of CB1 receptors. The cannabinoid antagonist AM251 (1 µM) did not inhibit the
neuroprotection effect induced by WIN55,212-2, indicating that the neuroprotective effect of
this agonist was cannabinoid receptor-independent. The NMDA receptor antagonist MK-801
(1 µM) enhanced diazinon-mediated neurotoxicity suggesting that precisely NMDA receptors
may play a protective role. |
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