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他克林和一种中药方剂“肝肠循环”可减轻糖尿病引起的中枢胆碱能神经元丢失和认知功能障碍:在 2 型糖尿病 db/db 小鼠中的阐明。

Diabetes-induced central cholinergic neuronal loss and cognitive deficit are attenuated by tacrine and a Chinese herbal prescription, kangen-karyu: elucidation in type 2 diabetes db/db mice.

机构信息

Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.

出版信息

J Pharmacol Sci. 2011;117(4):230-42. doi: 10.1254/jphs.11115fp. Epub 2011 Nov 12.

DOI:10.1254/jphs.11115fp
PMID:22083044
Abstract

We investigated the effect of kangen-karyu (KK), a Chinese herbal prescription, on cognitive deficits and central cholinergic systems of type 2 diabetic db/db mice. Seven-week-old db/db (Y-db/db) mice received daily administration of test drugs during an experimental period of 12 weeks. At 18 weeks of age (O-db/db), the animals underwent the water maze test. Compared with age-matched control strain mice (O-m/m), vehicle-treated O-db/db mice showed impaired learning and memory performance. KK (100 - 200 mg/kg per day) and the reference drug tacrine (THA: 2.5 mg/kg per day) ameliorated the performance of O-db/db mice without affecting their serum glucose level. O-db/db mice had lower levels of brain-derived neurotrophic factor (BDNF) mRNA and its protein in the brain than O-m/m mice. Expression levels of central cholinergic marker proteins in the hippocampus and the number of cholinergic cells in the medial septum and basal forebrain were also significantly lower in O-db/db than in O-m/m mice, whereas no significant differences in the expression levels of these factors and the cell number were found between Y-m/m and Y-db/db mice. KK and THA treatment significantly reversed the down-regulated levels of cholinergic markers, choline acetyltransferase-positive cell number, and BDNF expression in db/db mice. These findings suggest that KK as well as THA prevents diabetes-induced cognitive deficits by attenuating dysfunction of central cholinergic systems.

摘要

我们研究了一种中药方剂“还原精”(KK)对 2 型糖尿病 db/db 小鼠认知功能障碍和中枢胆碱能系统的影响。7 周龄 db/db(Y-db/db)小鼠在 12 周的实验期间接受每日测试药物治疗。在 18 周龄(O-db/db)时,动物进行水迷宫测试。与同龄对照品系小鼠(O-m/m)相比,载体处理的 O-db/db 小鼠表现出学习和记忆能力受损。KK(每天 100-200mg/kg)和参比药物他克林(THA:每天 2.5mg/kg)改善了 O-db/db 小鼠的表现,而不影响其血清葡萄糖水平。O-db/db 小鼠的脑源性神经营养因子(BDNF)mRNA 及其蛋白水平低于 O-m/m 小鼠。海马中的中枢胆碱能标志物蛋白的表达水平以及中隔和基底前脑中的胆碱能细胞数量在 O-db/db 中也明显低于 O-m/m 小鼠,而 Y-m/m 和 Y-db/db 小鼠之间这些因素的表达水平和细胞数量没有显著差异。KK 和 THA 治疗显著逆转了 db/db 小鼠中胆碱能标志物、胆碱乙酰转移酶阳性细胞数量和 BDNF 表达的下调水平。这些发现表明,KK 以及 THA 通过减轻中枢胆碱能系统的功能障碍来预防糖尿病引起的认知障碍。

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