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39 肽促肾上腺皮质激素对糖皮质激素受体介导的谷氨酸/γ-氨基丁酸失衡及脑异常致认知缺陷模型的分子机制。

Molecular mechanism of tuberoinfundibular peptide of 39 on glucocorticoid receptor mediated glutamate/GABA imbalance and cerebral abnormalities against cognitive deficit model.

机构信息

Department of Pharmacology, PSG College of Pharmacy, Coimbatore, Tamil Nadu, India.

Department of Pharmaceutics, PSG College of Pharmacy, Coimbatore, Tamil Nadu, India.

出版信息

J Pharm Pharmacol. 2019 Jun;71(6):996-1006. doi: 10.1111/jphp.13085. Epub 2019 Mar 5.

DOI:10.1111/jphp.13085
PMID:30838650
Abstract

OBJECTIVES

This study is designed to evaluate the role of tuberoinfundibular peptide of 39 (TIP39) in connection with glucocorticoid receptor-mediated glutamate/GABA abnormalities in chronic unpredictable mild stress (CUMS) model.

METHODS

Male Sprague-Dawley rats were treated with TIP39 (1 and 10 nmol, i.c.v) and diazepam 2 mg/kg throughout the stress period (28 days) in alternate days. Then, rats were subjected for different behavioural activity followed by biochemical, gene expression and histological examinations.

KEY FINDINGS

Chronic unpredictable mild stress rats showed significant cognitive impairment in Morris water maze, Novel object recognition and Y maze test. This was reversed after TIP39 administration. Moreover, TIP39 significantly decreased the brain glutamate and acetyl cholinesterase levels in CUMS rats, whereas it increases the level of GABA after TIP39 treatment. These changes were evident with increased glutamic acid decarboxylase enzyme activity by TIP39. TIP39 significantly decreased the brain glucocorticoid and mineralocorticoid receptor expression ratio in comparison with CUMS rats. Moreover, histological abnormalities in prefrontal cortex and hippocampus were markedly improved after TIP39 administration in CUMS rats.

CONCLUSIONS

Tuberoinfundibular peptide of 39 can be a potent neuroendocrine modulator in treating cognitive impairment induced by CUMS rats by controlling glucocorticoid receptor-mediated glutamate/GABA abnormalities in brain.

摘要

目的

本研究旨在评估 TIP39 在连接慢性不可预测轻度应激(CUMS)模型中糖皮质激素受体介导的谷氨酸/GABA 异常中的作用。

方法

雄性 Sprague-Dawley 大鼠在应激期(28 天)内每天接受 TIP39(1 和 10 nmol,脑室内)和地西泮 2 mg/kg 的治疗。然后,对大鼠进行不同的行为活动,随后进行生化、基因表达和组织学检查。

主要发现

慢性不可预测轻度应激大鼠在 Morris 水迷宫、新物体识别和 Y 迷宫测试中表现出明显的认知障碍。TIP39 给药后这种情况得到逆转。此外,TIP39 显著降低了 CUMS 大鼠大脑中的谷氨酸和乙酰胆碱酯酶水平,而 TIP39 处理后增加了 GABA 水平。TIP39 通过增加谷氨酸脱羧酶酶活性来实现这些变化。TIP39 显著降低了大脑中糖皮质激素和盐皮质激素受体表达的比值与 CUMS 大鼠相比。此外,TIP39 可显著改善 CUMS 大鼠前额叶皮层和海马体的组织学异常。

结论

TIP39 可作为一种有效的神经内分泌调节剂,通过控制大脑中糖皮质激素受体介导的谷氨酸/GABA 异常,治疗由 CUMS 大鼠引起的认知障碍。

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