Suppr超能文献

JCM-16021 是一种中药配方,可通过减少大鼠结肠 EC 细胞增生和 5-羟色胺含量来减轻 TNBS 诱导的炎症性肠易激综合征内脏痛觉过敏。

JCM-16021, a Chinese Herbal Formula, Attenuated Visceral Hyperalgesia in TNBS-Induced Postinflammatory Irritable Bowel Syndrome through Reducing Colonic EC Cell Hyperplasia and Serotonin Availability in Rats.

机构信息

School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tong, Hong Kong.

出版信息

Evid Based Complement Alternat Med. 2012;2012:239638. doi: 10.1155/2012/239638. Epub 2012 Jun 10.

Abstract

The present study aimed to investigate the analgesic effect of JCM-16021, a revised traditional Chinese herbal formula, on postinflammatory irritable bowel syndrome (PI-IBS) in rats. The trinitrobenzene sulfonic (TNBS) acid-induced PI-IBS model rats were orally administrated with different doses of JCM-16021 (1.2, 2.4, and 4.8 g/kg/d) for 14 consecutive days. The results showed that JCM-16021 treatment dose-dependently attenuated visceral hyperalgesia in PI-IBS rats. Further, the colonic enterochromaffin (EC) cell number, serotonin (5-HT) content, tryptophan hydroxylase expression, and mechanical-stimuli-induced 5-HT release were significantly ameliorated. Moreover, the decreased levels of mucosal cytokines in PI-IBS, especially the helper T-cell type 1- (T(h)1-) related cytokine TNF-α, were also elevated after JCM-16021 treatment. These data demonstrate that the analgesic effect of JCM-16021 on TNBS-induced PI-IBS rats may be medicated via reducing colonic EC cell hyperplasia and 5-HT availability.

摘要

本研究旨在探讨 JCM-16021(一种改良的中药方剂)对大鼠炎性肠易激综合征(PI-IBS)的镇痛作用。采用三硝基苯磺酸(TNBS)诱导的 PI-IBS 大鼠模型,连续 14 天给予不同剂量的 JCM-16021(1.2、2.4 和 4.8 g/kg/d)进行口服治疗。结果表明,JCM-16021 治疗可剂量依赖性地减轻 PI-IBS 大鼠的内脏痛觉过敏。此外,JCM-16021 治疗还显著改善了结肠肠嗜铬(EC)细胞数量、5-羟色胺(5-HT)含量、色氨酸羟化酶表达和机械刺激诱导的 5-HT 释放。此外,JCM-16021 治疗还可提高 PI-IBS 中降低的黏膜细胞因子水平,特别是辅助性 T 细胞 1 型(T(h)1-)相关细胞因子 TNF-α。这些数据表明,JCM-16021 对 TNBS 诱导的 PI-IBS 大鼠的镇痛作用可能是通过减少结肠 EC 细胞增生和 5-HT 可利用性来介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4011/3376539/e305edbad1d5/ECAM2012-239638.001.jpg

相似文献

3
Analgesic effects of electroacupuncture at ST25 and CV12 in a rat model of postinflammatory irritable bowel syndrome visceral pain.
Acupunct Med. 2018 Aug;36(4):240-246. doi: 10.1136/acupmed-2016-011320. Epub 2018 May 2.
4
Analgesic activity of cynaropicrinon on post-inflammatory irritable bowel syndrome visceral hypersensitivity in a rat model.
Exp Ther Med. 2017 Nov;14(5):4476-4482. doi: 10.3892/etm.2017.5037. Epub 2017 Aug 25.

本文引用的文献

1
Subtypes of irritable bowel syndrome on Rome III criteria: a multicenter study.
J Gastroenterol Hepatol. 2012 Apr;27(4):760-5. doi: 10.1111/j.1440-1746.2011.06930.x.
2
Irritable bowel syndrome immune hypothesis. Part two: the role of cytokines.
Rev Esp Enferm Dig. 2010 Dec;102(12):711-7. doi: 10.4321/s1130-01082010001200006.
3
Systematic review of animal models of post-infectious/post-inflammatory irritable bowel syndrome.
J Gastroenterol. 2011 Feb;46(2):164-74. doi: 10.1007/s00535-010-0321-6. Epub 2010 Sep 17.
6
Analgesic effects of JCM-16021 on neonatal maternal separation-induced visceral pain in rats.
World J Gastroenterol. 2010 Feb 21;16(7):837-45. doi: 10.3748/wjg.v16.i7.837.
7
Serotonin release and uptake in the gastrointestinal tract.
Auton Neurosci. 2010 Feb 16;153(1-2):47-57. doi: 10.1016/j.autneu.2009.08.002. Epub 2009 Sep 2.
8
5-HT 3 receptors mediate the time-dependent vagal afferent modulation of nociception during chronic food allergen-sensitized visceral hyperalgesia in rats.
Neurogastroenterol Motil. 2009 Nov;21(11):1222-e113. doi: 10.1111/j.1365-2982.2009.01335.x. Epub 2009 May 26.
9
Treatment of irritable bowel syndrome using complementary and alternative medicine.
J Chin Med Assoc. 2009 Jun;72(6):294-300. doi: 10.1016/S1726-4901(09)70375-2.
10
Postinfectious irritable bowel syndrome.
Gastroenterology. 2009 May;136(6):1979-88. doi: 10.1053/j.gastro.2009.02.074. Epub 2009 May 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验