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蟾酥及含蟾酥中药的镇痛作用:蟾酥的镇痛作用。

Analgesic Effects of Toad Cake and Toad-cake-containing Herbal Drugs: Analgesic effects of toad cake.

作者信息

Inoue Eiji, Shimizu Yasuharu, Masui Ryo, Usui Tomomi, Sudoh Keiichi

机构信息

Tokyo Research Center, Kyushin Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

J Pharmacopuncture. 2014 Mar;17(1):74-9. doi: 10.3831/KPI.2014.17.010.

Abstract

OBJECTIVES

This study was conducted to clarify the analgesic effect of toad cake and toad-cake-containing herbal drugs.

METHODS

We counted the writhing response of mice after the intraperitoneal administration of acetic acid as a nociceptive pain model and the withdrawal response after the plantar surface stimulation of the hind paw induced by partial sciatic nerve ligation of the mice as a neuropathic pain model to investigate the analgesic effect of toad cake and toad-cake-containing herbal drugs. A co-treatment study with serotonin biosynthesis inhibitory drug 4-chloro- DL-phenylalanine methyl ester hydrochloride (PCPA), the catecholamine biosynthesis inhibitory drug α-methyl- DL-tyrosine methyl ester hydrochloride (AMPT) or the opioid receptor antagonist naloxone hydrochloride was also conducted.

RESULTS

Analgesic effects in a mouse model of nociceptive pain and neuropathic pain were shown by oral administration of toad cake and toad-cake-containing herbal drugs. The effects of toad cake and toad-cake-containing herbal drugs disappeared upon co-treatment with PCPA, but not with AMPT or naloxone in the nociceptive pain model; the analgesic effect of toad-cake-containing herbal drugs also disappeared upon co-treatment with PCPA in the neuropathic pain model.

CONCLUSION

Toad cake and toad-cake-containing herbal drugs have potential for the treatments of nociceptive pain and of neuropathic pain, such as post-herpetic neuralgia, trigeminal neuralgia, diabetic neuralgia, and postoperative or posttraumatic pain, by activation of the central serotonin nervous system.

摘要

目的

本研究旨在阐明蟾酥及含蟾酥的草药的镇痛作用。

方法

我们以腹腔注射醋酸的小鼠扭体反应作为伤害性疼痛模型,以及以小鼠坐骨神经部分结扎后后爪足底表面刺激引起的缩足反应作为神经病理性疼痛模型,来研究蟾酥及含蟾酥的草药的镇痛作用。还进行了与5-羟色胺生物合成抑制药物4-氯-DL-苯丙氨酸甲酯盐酸盐(PCPA)、儿茶酚胺生物合成抑制药物α-甲基-DL-酪氨酸甲酯盐酸盐(AMPT)或阿片受体拮抗剂盐酸纳洛酮的联合治疗研究。

结果

口服蟾酥及含蟾酥的草药在伤害性疼痛和神经病理性疼痛小鼠模型中均显示出镇痛作用。在伤害性疼痛模型中,蟾酥及含蟾酥的草药与PCPA联合治疗后作用消失,但与AMPT或纳洛酮联合治疗后作用未消失;在神经病理性疼痛模型中,含蟾酥的草药与PCPA联合治疗后镇痛作用也消失。

结论

蟾酥及含蟾酥的草药通过激活中枢5-羟色胺神经系统,对治疗伤害性疼痛和神经病理性疼痛,如带状疱疹后神经痛、三叉神经痛、糖尿病性神经痛以及术后或创伤后疼痛具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31e5/4331986/a2a0e1329ee6/2093-6966-v17-n01-074-g001.jpg

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