Neuroprotective and Antiapoptotic Potential of Trigonelline in a Striatal 6-Hydroxydopamine Rat Model of Parkinson’s Disease
Considering neuroprotective and antioxidant effects of trigonelline, our study was undertaken to evaluate its protective effect in a 6-hydroxydopamine-induced model of Parkinson’s disease (PD) in rats. Unilateral intrastriatal 6-OHDA-lesioned rats were pretreated with trigonelline at doses of 50...
Збережено в:
Дата: | 2016 |
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Автори: | , , , |
Формат: | Стаття |
Мова: | English |
Опубліковано: |
Інститут фізіології ім. О.О. Богомольця НАН України
2016
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Назва видання: | Нейрофизиология |
Онлайн доступ: | http://dspace.nbuv.gov.ua/handle/123456789/148313 |
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Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
Цитувати: | Neuroprotective and Antiapoptotic Potential of Trigonelline in a Striatal 6-Hydroxydopamine Rat Model of Parkinson’s Disease / M. Mirzaie, M. Khalili, Z. Kiasalari, M. Roghani // Нейрофизиология. — 2016. — Т. 48, № 3. — С. 197-204. — Бібліогр.: 35 назв. — англ. |
Репозитарії
Digital Library of Periodicals of National Academy of Sciences of UkraineРезюме: | Considering neuroprotective and antioxidant effects of trigonelline, our study was undertaken
to evaluate its protective effect in a 6-hydroxydopamine-induced model of Parkinson’s disease
(PD) in rats. Unilateral intrastriatal 6-OHDA-lesioned rats were pretreated with trigonelline
at doses of 50 and 100 mg/kg. Significant rotational behavior, a significant reduction in the
number of Nissl-stained neurons on the left side of substantia nigra pars compacta (SNC),
increased apoptosis, enhanced levels of malondialdehyde (MDA) and nitrite, and a lower
level of glutathione (GSH) were observed in 6-OHDA-lesioned rats. Trigonelline at a dose of
100 mg/kg significantly reduced rotations, prevented reduction of SNC neurons, prevented
apoptosis, and restored the MDA level. These results suggest that pre-lesion trigonelline
treatment exerts dose-dependent neuroprotective and antiapoptotic effects under conditions
of 6-OHDA toxicity and may be, henceforth, advantageous for the management of early PD. |
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