Effects of Atorvastatin on E-Selectin and Myeloperoxidase Expressions After Cerebral Ischemia-Reperfusion Injury in Rats

We examined expressions of E-selectin and myeloperoxidase (MPO) in cerebral tissues after cerebral ischemia-reperfusion (CIR) in rats and evaluated neuroprotective effects of atorvastatin under these conditions. Immunohistochemical methods were used to detect E-selectin and MPO expressioning tiss...

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Бібліографічні деталі
Дата:2014
Автори: Zhong, W., Wu, W., Cao, H., Tu, Q., Tang, X.
Формат: Стаття
Мова:English
Опубліковано: Інститут фізіології ім. О.О. Богомольця НАН України 2014
Назва видання:Нейрофизиология
Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/148306
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Effects of Atorvastatin on E-Selectin and Myeloperoxidase Expressions After Cerebral Ischemia-Reperfusion Injury in Rats / H. Cao, W. Zhong, W. Wu, Q. Tu, X. Tang // Нейрофизиология. — 2014. — Т. 46, № 4. — С. 368-374. — Бібліогр.: 29 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Резюме:We examined expressions of E-selectin and myeloperoxidase (MPO) in cerebral tissues after cerebral ischemia-reperfusion (CIR) in rats and evaluated neuroprotective effects of atorvastatin under these conditions. Immunohistochemical methods were used to detect E-selectin and MPO expressioning tissue. Small numbers of E-selectin- and MPO-positive cells were observed in the sham group within 4 to 24 h time intervals. In the operation group, numerous positive cells were found in the cortex and hippocampus after CIR. E-selectin expression occurred at 4 h, peaked at 12 h, and returned to nearly normal levels at 24 h. However, E-selectin expression in the intervention (CIR + atorvastatin) group was significantly lower than that in the operation group at each time (P < 0.05). Myeloperoxidase had nearly similar timing of changes in E-selectin expression, and MPO expressions at different time points in the intervention group were significantly lower than those in the operation group (P < 0.05). Therefore, expressions of E-selectin and MPO change dynamically after CIR. Atorvastatin, an agent having anti-inflammatory properties, demonstrates an obvious protective effect with respect to acute CIR-related damage.