Jiang Jin-Guang, Luo Qian, Li Shuang-Shuang, Tan Tian-Ying, Xiong Kai, Yang Tao, Xiao Tian-Bao
Department of Colorectal and Anal Surgery, Suqian Hospital of Traditional Chinese Medicine, Suqian 223800, Jiangsu Province, China.
College of Clinical Medicine, Guizhou University of Traditional Chinese Medicine, Guiyang 550000, Guizhou Province, China.
World J Gastrointest Pharmacol Ther. 2023 Mar 5;14(2):4-21. doi: 10.4292/wjgpt.v14.i2.4.
Slow transit constipation (STC) is a disorder with delayed colonic transit. Cinnamic acid (CA) is an organic acid in natural plants, such as (Xuan Shen), with low toxicity and biological activities to modulate the intestinal microbiome.
To explore the potential effects of CA on the intestinal microbiome and the primary endogenous metabolites-short-chain fatty acids (SCFAs) and evaluate the therapeutic effects of CA in STC.
Loperamide was applied to induce STC in mice. The treatment effects of CA on STC mice were assessed from the 24 h defecations, fecal moisture and intestinal transit rate. The enteric neurotransmitters: 5-hydroxytryptamine (5-HT) and vasoactive intestinal peptide (VIP) were determined by the enzyme-linked immunosorbent assay. Hematoxylin-eosin and Alcian blue and Periodic acid Schiff staining were used to evaluate intestinal mucosa's histopathological performance and secretory function. 16S rDNA was employed to analyze the composition and abundance of the intestinal microbiome. The SCFAs in stool samples were quantitatively detected by gas chromatography-mass spectrometry.
CA ameliorated the symptoms of STC and treated STC effectively. CA ameliorated the infiltration of neutrophils and lymphocytes, increased the number of goblet cells and acidic mucus secretion of the mucosa. In addition, CA significantly increased the concentration of 5-HT and reduced VIP. CA significantly improved the diversity and abundance of the beneficial microbiome. Furthermore, the production of SCFAs [including acetic acid (AA), butyric acid (BA), propionic acid (PA) and valeric acid (VA)] was significantly promoted by CA. The changed abundance of and were involved in the production of AA, BA, PA and VA.
CA could treat STC effectively by ameliorating the composition and abundance of the intestinal microbiome to regulate the production of SCFAs.
慢传输型便秘(STC)是一种结肠传输延迟的疾病。肉桂酸(CA)是天然植物如玄参中的一种有机酸,毒性低,具有调节肠道微生物群的生物活性。
探讨CA对肠道微生物群及主要内源性代谢产物短链脂肪酸(SCFAs)的潜在影响,并评估CA对STC的治疗效果。
用洛哌丁胺诱导小鼠产生STC。从24小时排便量、粪便含水量和肠道传输率评估CA对STC小鼠的治疗效果。采用酶联免疫吸附测定法测定肠内神经递质:5-羟色胺(5-HT)和血管活性肠肽(VIP)。采用苏木精-伊红染色、阿尔辛蓝和过碘酸希夫染色评估肠黏膜的组织病理学表现和分泌功能。采用16S rDNA分析肠道微生物群的组成和丰度。通过气相色谱-质谱法定量检测粪便样本中的SCFAs。
CA改善了STC的症状并有效治疗了STC。CA减轻了中性粒细胞和淋巴细胞的浸润,增加了杯状细胞数量和黏膜酸性黏液分泌。此外,CA显著增加了5-HT的浓度并降低了VIP。CA显著改善了有益微生物群的多样性和丰度。此外,CA显著促进了SCFAs[包括乙酸(AA)、丁酸(BA)、丙酸(PA)和戊酸(VA)]的产生。 和 的丰度变化参与了AA、BA、PA和VA的产生。
CA可通过改善肠道微生物群的组成和丰度来调节SCFAs的产生,从而有效治疗STC。