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葛根素和氨氯地平改善 D-半乳糖诱导的小鼠齿状回行为和神经发生损伤:与糖皮质激素受体表达的相关性。

Puerarin and Amlodipine Improvement of D-Galactose-Induced Impairments of Behaviour and Neurogenesis in Mouse Dentate Gyrus: Correlation with Glucocorticoid Receptor Expression.

机构信息

State Key Laboratory of Medicinal Chemical Biology, The Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Science, Nankai University, Tianjin, 300071, China.

Tianjin Key Laboratory of Tumour Microenvironment and Neurovascular Regulation, Department of Histology and Embryology, School of Medicine, Nankai University, Tianjin, 300071, China.

出版信息

Neurochem Res. 2017 Nov;42(11):3268-3278. doi: 10.1007/s11064-017-2366-x. Epub 2017 Aug 22.

DOI:10.1007/s11064-017-2366-x
PMID:28831640
Abstract

Glucocorticoid receptors (GRs) exert actions on the hippocampus that are important for memory formation. There are correlations between vascular dysfunctions and GR-related gene expression. Both vascular dysfunction and GR gene expression decline occur during the ageing process. Therefore, hypotensors, which have effects on improving vascular dysfunction, may be able to ameliorate GR gene expression decline in ageing mice and improve ageing-mediated memory deficits. In this study, we hypothesized that hypotensors could alleviate the decline of GR gene expression and ameliorate age-induced learning and memory deficits in a D-gal-induced ageing mice model. In line with our hypothesis, we found that chronic D-gal treatment decreased GR and DCX expression in the hippocampus, leading to learning and memory deficits. Amlodipine (AM) and puerarin (PU) treatment improved GR gene expression decline in the hippocampus and ameliorated the learning and memory deficits of D-gal-treated mice. These changes correlated with enhanced DCX expression and brain-derived neurotrophic factor (BDNF) expression in the hippocampus. Furthermore, PU treatment conveyed better effects than AM treatment, but combination therapy did not enhance the effects on improving GR expression. However, we did not find evidence of these changes in non-D-gal-treated mice that lacked GR gene expression decline. These results suggest that AM and PU could improve D-gal-induced behavioural deficits in correlation with GR gene expression.

摘要

糖皮质激素受体 (GRs) 在海马体上发挥作用,对记忆形成很重要。血管功能障碍与 GR 相关基因表达之间存在相关性。在衰老过程中,血管功能障碍和 GR 基因表达下降都会发生。因此,具有改善血管功能障碍作用的降压药可能能够改善衰老小鼠中 GR 基因表达的下降,并改善衰老引起的记忆缺陷。在这项研究中,我们假设降压药可以减轻 GR 基因表达的下降,并改善 D-半乳糖诱导的衰老小鼠模型中的学习和记忆缺陷。与我们的假设一致,我们发现慢性 D-半乳糖处理会降低海马体中的 GR 和 DCX 表达,导致学习和记忆缺陷。氨氯地平 (AM) 和葛根素 (PU) 治疗改善了 D-半乳糖处理小鼠海马体中 GR 基因表达的下降,并改善了学习和记忆缺陷。这些变化与海马体中 DCX 和脑源性神经营养因子 (BDNF) 表达的增强相关。此外,葛根素治疗比氨氯地平治疗效果更好,但联合治疗并没有增强改善 GR 表达的效果。然而,我们在没有 GR 基因表达下降的非 D-半乳糖处理小鼠中没有发现这些变化的证据。这些结果表明,AM 和 PU 可以改善 D-半乳糖诱导的行为缺陷,与 GR 基因表达相关。

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