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香草类药物对慢性疲劳综合征影响的研究

Investigation of the effects of vanilloids in chronic fatigue syndrome.

作者信息

Sarvaiya Kuldeep, Goswami Sunita

机构信息

Department of Pharmacology, L.M. College of Pharmacy, Ahmedabad, 380009 Gujarat, India.

Department of Pharmacology, L.M. College of Pharmacy, Ahmedabad, 380009 Gujarat, India.

出版信息

Brain Res Bull. 2016 Oct;127:187-194. doi: 10.1016/j.brainresbull.2016.09.015. Epub 2016 Sep 28.

Abstract

AIM OF THE STUDY

To assess the effectiveness of TRPV1 modulators in animal model of Chronic fatigue syndrome (CFS). To assess central and peripheral behavioral activity of TRPV1 modulators.

MATERIAL AND METHODS

CFS was induced by forcing the rats to swim for 10min for 21 consecutive days. The rats were treated with capsaicin (TRPV1 agonist, 2.5mg/kg) and n-tert-butylcyclohexanol (TRPV1 antagonist, 10mg/kg) for 21days 30min before the exposure to stress procedure. The behavioral consequence of CFS was measured in terms of immobility time, grip strength, locomotor activity, and anxiety level using Rota rod, Actophotometer, and Elevated plus maze model respectively. The other parameters include Plasma corticosterone, adrenal gland and spleen weight, complete blood count, blood urea niterogen (BUN), Lactate dehydrogenase (LDH), Lipid peroxidation, catalase and reduced glutathione (GSH).

RESULTS AND DISCUSSION

TRPV1 modulators reversed (p<0.05) the increase in immobility period, anxiety, spleen weight, BUN and LDH levels, and MDA levels along with decrease in grip strength, locomotor activity, plasma corticosterone, adrenal gland weight, catalase, and GSH. There was also significant increase in total WBC count when compared with the disease control group. The reversal was attributed to modulation of HPA axis, oxidative stress, anaerobic respiration product, muscle degradation product.

CONCLUSION

The present study reveals the effectiveness of n-tert-butylcyclohexanol and capsaicin against chronic fatigue syndrome. The mechanism of action can be attributed to inhibition of TRPV1 channel and thereby modulating pain perception, neuroendocrine function, oxidative stress and immune function.

摘要

研究目的

评估瞬时受体电位香草酸亚型1(TRPV1)调节剂在慢性疲劳综合征(CFS)动物模型中的有效性。评估TRPV1调节剂的中枢和外周行为活性。

材料与方法

通过强迫大鼠连续21天每天游泳10分钟来诱导CFS。在暴露于应激程序前30分钟,用辣椒素(TRPV1激动剂,2.5mg/kg)和N-叔丁基环己醇(TRPV1拮抗剂,10mg/kg)对大鼠进行21天的治疗。分别使用转棒试验、光电活动计和高架十字迷宫模型,根据不动时间、握力、运动活性和焦虑水平来测量CFS的行为后果。其他参数包括血浆皮质酮、肾上腺和脾脏重量、全血细胞计数、血尿素氮(BUN)、乳酸脱氢酶(LDH)、脂质过氧化、过氧化氢酶和还原型谷胱甘肽(GSH)。

结果与讨论

TRPV1调节剂使不动期、焦虑、脾脏重量、BUN和LDH水平以及丙二醛(MDA)水平升高得到逆转(p<0.05),同时使握力、运动活性、血浆皮质酮、肾上腺重量、过氧化氢酶和GSH降低。与疾病对照组相比,白细胞总数也有显著增加。这种逆转归因于下丘脑-垂体-肾上腺(HPA)轴、氧化应激、无氧呼吸产物、肌肉降解产物的调节。

结论

本研究揭示了N-叔丁基环己醇和辣椒素对慢性疲劳综合征的有效性。其作用机制可归因于对TRPV1通道的抑制,从而调节痛觉、神经内分泌功能、氧化应激和免疫功能。

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