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口服二十二碳六烯酸可激活自然衰老大鼠海马中的 GDNF-MAPK-CERB 通路。

Oral administration of docosahexaenoic acid activates the GDNF-MAPK-CERB pathway in hippocampus of natural aged rat.

机构信息

Division of Development and Planning, Guangxi University, Nanning, P.R. China.

出版信息

Pharm Biol. 2013 Sep;51(9):1188-95. doi: 10.3109/13880209.2013.784341. Epub 2013 Jun 14.

DOI:10.3109/13880209.2013.784341
PMID:23767459
Abstract

CONTEXT

Docosahexaenoic acid (DHA) is one of the critical fatty acids for optimal health, which affect the expression of nerve growth factor and brain-derived neurotrophic factor in brain.

OBJECTIVE

This study investigates whether DHA supplementation affects lipid peroxidation and activates the glial-derived neurotrophic factor (GDNF)-mitogen-activated protein kinase pathway (MAPK pathway) in hippocampus of natural aged rat.

MATERIALS AND METHODS

Rats were randomly divided into four groups; DHA was orally administered at 80 and 160 mg/kg/day to 24-month female rats for 50 days. The antioxidant parameters and GDNF-GDNF family receptor α-1 (GFRα1)-tyrosine-protein kinase receptor (RET)-MAPK-cyclic AMP response element-binding protein (CERB) pathway were assayed in natural aged rat's hippocampus.

RESULTS AND DISCUSSION

The results demonstrated that DHA supplementation significantly increased the activities of superoxide dismutase (SOD) by 37.39 and 57.69%, glutathione peroxidase (GSH-Px) by 27.62 and 32.57% decreased TBARS level by 28.49 and 49.05%, respectively, but did not significantly affect catalase (CAT), in hippocampus, when compared with the aged group. DHA supplementation in diet resulted in an increase of DHA level in hippocampus. Furthermore, we found that DHA supplementation markedly increased the levels of GDNF and GFRα1 and the phosphorylation of RET, and led to the activation of the MAPK pathway in hippocampus tissue.

CONCLUSION

DHA supplementation can change fatty acids composition, improve antioxidant parameters and activate the GDNF-MAPK pathway in natural aged rat's hippocampus.

摘要

背景

二十二碳六烯酸(DHA)是最佳健康所必需的关键脂肪酸之一,它影响神经生长因子和脑源性神经营养因子在大脑中的表达。

目的

本研究旨在探讨 DHA 补充是否会影响自然衰老大鼠海马中的脂质过氧化作用,并激活胶质细胞衍生的神经营养因子(GDNF)-丝裂原活化蛋白激酶途径(MAPK 途径)。

材料和方法

将大鼠随机分为四组;80 和 160mg/kg/天的 DHA 分别经口给予 24 月龄雌性大鼠 50 天。测定自然衰老大鼠海马中的抗氧化参数和 GDNF-GDNF 家族受体α-1(GFRα1)-酪氨酸蛋白激酶受体(RET)-MAPK-cAMP 反应元件结合蛋白(CERB)途径。

结果与讨论

结果表明,DHA 补充可使超氧化物歧化酶(SOD)的活性分别增加 37.39%和 57.69%,谷胱甘肽过氧化物酶(GSH-Px)的活性分别增加 27.62%和 32.57%,TBARS 水平分别降低 28.49%和 49.05%,但对海马中的过氧化氢酶(CAT)没有显著影响。与衰老组相比,DHA 补充饮食可增加海马中的 DHA 水平。此外,我们发现 DHA 补充可显著增加 GDNF 和 GFRα1 的水平以及 RET 的磷酸化,并导致海马组织中 MAPK 途径的激活。

结论

DHA 补充可改变脂肪酸组成,改善抗氧化参数,并激活自然衰老大鼠海马中的 GDNF-MAPK 途径。

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