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荨麻叶对链脲佐菌素诱导的糖尿病小鼠海马中的毒蕈碱胆碱能系统有调节作用。

Urtica dioica leaves modulates muscarinic cholinergic system in the hippocampus of streptozotocin-induced diabetic mice.

作者信息

Patel Sita Sharan, Parashar Arun, Udayabanu Malairaman

机构信息

Department of Pharmacy, Jaypee University of Information Technology, Waknaghat, 173234, Himachal Pradesh, India.

出版信息

Metab Brain Dis. 2015 Jun;30(3):803-11. doi: 10.1007/s11011-014-9646-9. Epub 2014 Dec 17.

Abstract

Diabetes mellitus is a chronic metabolic disorder and has been associated with cognitive dysfunction. In our earlier study, chronic Urtica dioica (UD) treatment significantly ameliorated diabetes induced associative and spatial memory deficit in mice. The present study was designed to explore the effect of UD leaves extract on muscarinic cholinergic system, which has long been known to be involved in cognition. Streptozotocin (STZ) (50 mg/kg, i.p., consecutively for 5 days) was used to induce diabetes followed by treatment with UD extract (50 mg/kg, oral) or rosiglitazone (5 mg/kg, oral) for 8 weeks. STZ-induced diabetic mice showed significant reduction in hippocampal muscarinic acetylcholine receptor-1 and choline acetyltransferase expressions. Chronic diabetes significantly up-regulated the protein expression of acetylcholinesterase associated with oxidative stress in hippocampus. Besides, STZ-induced diabetic mice showed hypolocomotion with up-regulation of muscarinic acetylcholine receptor-4 expression in striatum. Chronic UD treatment significantly attenuated the cholinergic dysfunction and oxidative stress in the hippocampus of diabetic mice. UD had no effect on locomotor activity and muscarinic acetylcholine receptor-4 expression in striatum. In conclusion, UD leaves extract has potential to reverse diabetes mediated alteration in muscarinic cholinergic system in hippocampus and thereby improve memory functions.

摘要

糖尿病是一种慢性代谢紊乱疾病,与认知功能障碍有关。在我们早期的研究中,长期使用荨麻(UD)治疗可显著改善糖尿病诱导的小鼠联想和空间记忆缺陷。本研究旨在探讨UD叶提取物对毒蕈碱胆碱能系统的影响,该系统长期以来被认为与认知有关。使用链脲佐菌素(STZ)(50mg/kg,腹腔注射,连续5天)诱导糖尿病,随后用UD提取物(50mg/kg,口服)或罗格列酮(5mg/kg,口服)治疗8周。STZ诱导的糖尿病小鼠海马毒蕈碱乙酰胆碱受体-1和胆碱乙酰转移酶表达显著降低。慢性糖尿病显著上调海马中与氧化应激相关的乙酰胆碱酯酶蛋白表达。此外,STZ诱导的糖尿病小鼠运动减少,纹状体中毒蕈碱乙酰胆碱受体-4表达上调。长期使用UD治疗可显著减轻糖尿病小鼠海马中的胆碱能功能障碍和氧化应激。UD对纹状体的运动活性和毒蕈碱乙酰胆碱受体-4表达无影响。总之,UD叶提取物有潜力逆转糖尿病介导的海马毒蕈碱胆碱能系统改变,从而改善记忆功能。

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