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NMDA 受体和 L-精氨酸/一氧化氮/环鸟苷酸通路参与了越鞠丸在小鼠体内的抗抑郁样作用。

NMDA receptors and L-arginine/nitric oxide/cyclic guanosine monophosphate pathway contribute to the antidepressant-like effect of Yueju pill in mice.

机构信息

Key Laboratory of Integrative Medicine for Brain Diseases, School of Basic Biomedical Science, Nanjing University of Chinese Medicine, Nanjing 210023, China.

School of Psychology, Nanjing University of Chinese Medicine, Nanjing 210023, China.

出版信息

Biosci Rep. 2019 Sep 16;39(9). doi: 10.1042/BSR20190524. Print 2019 Sep 30.

DOI:10.1042/BSR20190524
PMID:31467174
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6746996/
Abstract

The present study aims to evaluate the involvement of N-methyl-d-aspartate receptor and nitric oxide (NO)/cyclic guanosine monophosphate (cGMP) system in antidepressant-like effects of Yueju pill (YJ), a Chinese herbal medicine. The immobility time in tail suspension test (TST) and forced swim test (FST) was used to assess the antidepressant effects. Prior administration of L-arginine (750 mg/kg, intraperitoneal [i.p.]), a NO synthase substrate that enhances NO signaling or sildenafil (5 mg/kg, i.p.), a phosphodiesterase 5 inhibitor that enhances cGMP, blunted the antidepressant-like activity of YJ (2.7 g/kg, i.g.). Co-treatment of ineffective dose of YJ (1.35 g/kg, i.g.) with one of the reagents that suppress the NO/cGMP signaling, including methylene blue (10 mg/kg, i.p.), an inhibitor of NO synthase; 7-NI (7-nitroinidazole, 30 mg/kg, i.p.), an nNOS specific inhibitor; L-NAME (10 mg/kg, i.p.), a non-specific inhibitor of NO synthase; and MK-801 (0.05 mg/kg, i.p.), an NMDA receptor antagonist, reduced the immobility time in TST and FST, compared with those in vehicle or single drug treatment groups. Neither above drugs alone or co-administrated with YJ affected locomotor activity or anxiety behavior in open field test. Thus, our results suggest that the antidepressant-like action of YJ may depend on the inhibition of NMDA/NO/cGMP pathway.

摘要

本研究旨在评估 N-甲基-D-天冬氨酸受体(N-methyl-d-aspartate receptor)和一氧化氮(nitric oxide,NO)/环鸟苷酸(cyclic guanosine monophosphate,cGMP)系统在越鞠丸(Yueju pill,YJ)抗抑郁样作用中的参与情况。YJ 是一种中药,采用悬尾试验(tail suspension test,TST)和强迫游泳试验(forced swim test,FST)中的不动时间来评估其抗抑郁作用。预先腹腔注射(intraperitoneal,i.p.)NO 合酶底物 L-精氨酸(L-arginine,750 mg/kg)或磷酸二酯酶 5 抑制剂西地那非(sildenafil,5 mg/kg)可增强 NO 信号或 cGMP,从而削弱 YJ(2.7 g/kg,i.g.)的抗抑郁样作用。用抑制 NO/cGMP 信号的试剂之一(包括抑制 NO 合酶的亚甲蓝(methylene blue,10 mg/kg,i.p.)、nNOS 特异性抑制剂 7-NI(7-nitroinidazole,30 mg/kg,i.p.)、非特异性 NO 合酶抑制剂 L-NAME(10 mg/kg,i.p.)和 NMDA 受体拮抗剂 MK-801(0.05 mg/kg,i.p.))与无效剂量的 YJ(1.35 g/kg,i.g.)共同处理,与单独用 YJ 或对照药物处理的动物相比,TST 和 FST 中的不动时间减少。以上药物单独或与 YJ 共同给药均不影响旷场试验中的运动活动或焦虑行为。因此,我们的结果表明,YJ 的抗抑郁样作用可能依赖于 NMDA/NO/cGMP 通路的抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/9a66bc6b4558/bsr-39-bsr20190524-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/e9c3e6060c94/bsr-39-bsr20190524-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/c23b2589abaf/bsr-39-bsr20190524-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/9a66bc6b4558/bsr-39-bsr20190524-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/e9c3e6060c94/bsr-39-bsr20190524-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/c23b2589abaf/bsr-39-bsr20190524-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67dc/6746996/9a66bc6b4558/bsr-39-bsr20190524-g3.jpg

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