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降钙素基因相关肽增强局灶性脑缺血/再灌注大鼠脑中 CREB 磷酸化并减轻 tau 蛋白磷酸化。

Calcitonin gene-related peptide enhances CREB phosphorylation and attenuates tau protein phosphorylation in rat brain during focal cerebral ischemia/reperfusion.

机构信息

Department of Neurology, Affiliated Renmin Hospital, Yunyang Medical College, South Renmin Road 30, Shiyan 442000, Hubei Province, China.

出版信息

Biomed Pharmacother. 2010 Jul;64(6):430-6. doi: 10.1016/j.biopha.2009.06.009. Epub 2009 Oct 23.

DOI:10.1016/j.biopha.2009.06.009
PMID:20537498
Abstract

Calcitonin gene-related peptide (CGRP) is a potent vasodilator and immune cell modulator. Exogenous CGRP could increase the cerebral blood flow significantly and protect the ischemic neurons, but its mechanism is not entirely clear. The effect of CGRP on the expressions of CREB and tau in the ipsilateral parietal cortex were detected in focal cerebral ischemia/reperfusion model. The expression of CREB mRNA decreased in ischemia/reperfusion group (I/R group) compared with that of the sham operation group, and it got highest in CGRP group. CREB expression was lesser in I/R group than sham group, but it became more in CGRP group than I/R group. Phospho-CREB became more in I/R group, and it got most in CGRP group in the cortex. No significant difference was observed on Tau mRNA expression in all the groups. The level of tau hyperphosphorylation at Ser199/202 site and total tau in rat parietal cortex were significantly higher in I/R group than sham group. CGRP significantly inhibited tau hyperphosphorylation and the level of total tau also significantly reduced in CGRP group than that in I/R group. CGRP can upregulate the expression of CREB and phospho-CREB and attenuate the level of tau hyperphosphorylation in the ischemic neurons of the parietal cortex during focal cerebral ischemia/reperfusion. Phosphorylating CREB and inhibiting tau phosphorylation are probably involved in the mechanism of protective effect of CGRP to ischemic neurons.

摘要

降钙素基因相关肽(CGRP)是一种有效的血管舒张剂和免疫细胞调节剂。外源性 CGRP 可显著增加脑血流量并保护缺血神经元,但具体机制尚不完全清楚。本研究在局灶性脑缺血再灌注模型中检测了 CGRP 对同侧顶叶皮质中 CREB 和 tau 表达的影响。与假手术组相比,缺血再灌注组(I/R 组)CREB mRNA 的表达降低,CGRP 组表达最高。I/R 组的 CREB 表达低于 sham 组,而 CGRP 组的 CREB 表达高于 I/R 组。磷酸化 CREB 在 I/R 组中增加最多,在皮质中在 CGRP 组中最多。各组 Tau mRNA 表达无明显差异。I/R 组大鼠顶叶皮质丝氨酸 199/202 位 tau 过度磷酸化和总 tau 水平明显高于 sham 组。CGRP 可显著抑制 tau 过度磷酸化,CGRP 组的总 tau 水平也明显低于 I/R 组。CGRP 可上调 CREB 和磷酸化 CREB 的表达,减轻局灶性脑缺血再灌注顶叶皮质缺血神经元中 tau 的过度磷酸化。磷酸化 CREB 和抑制 tau 磷酸化可能参与了 CGRP 对缺血神经元的保护作用机制。

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