肉桂酸调节肠道微生物群和短链脂肪酸,治疗慢传输型便秘。

Jin-Guang Jiang, Qian Luo, Shuang-Shuang Li, Tian-Ying Tan, Kai Xiong, Tao Yang, Tian-Bao Xiao
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引用次数: 1

摘要

背景:慢传输型便秘(STC)是一种结肠运输延迟的疾病。肉桂酸(Cinnamic acid, CA)是天然植物如玄参中的一种有机酸,具有低毒性和调节肠道微生物群的生物活性。目的:探讨CA对肠道微生物组和主要内源性代谢物短链脂肪酸(SCFAs)的潜在影响,评价CA对STC的治疗效果。方法:应用洛哌丁胺诱导小鼠STC。从24 h排便量、粪便水分和肠道转运率评价CA对STC小鼠的治疗效果。采用酶联免疫吸附法测定肠道神经递质:5-羟色胺(5-HT)和血管活性肠肽(VIP)。采用苏木精-伊红染色、阿利新蓝染色和周期性酸希夫染色评价肠黏膜的组织病理学表现和分泌功能。采用16S rDNA分析肠道菌群的组成和丰度。采用气相色谱-质谱联用技术对粪便样品中的SCFAs进行定量检测。结果:CA能改善STC的症状,有效治疗STC。CA改善了中性粒细胞和淋巴细胞的浸润,增加了杯状细胞的数量和粘膜酸性粘液的分泌。此外,CA显著提高了5-HT浓度,降低了VIP。CA显著提高了有益菌群的多样性和丰度。此外,CA显著促进了短链脂肪酸(包括乙酸(AA)、丁酸(BA)、丙酸(PA)和戊酸(VA))的生成。厚壁菌门、Akkermansia、Lachnoclostridium、Monoglobus、UCG.005、Paenalcaligenes、Psychrobacter和不动杆菌(Acinetobacter)的丰度变化参与了AA、BA、PA和VA的生成。CA可以通过改善肠道菌群的组成和丰度来调节scfa的产生,从而有效治疗STC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cinnamic acid regulates the intestinal microbiome and short-chain fatty acids to treat slow transit constipation.

Cinnamic acid regulates the intestinal microbiome and short-chain fatty acids to treat slow transit constipation.

Cinnamic acid regulates the intestinal microbiome and short-chain fatty acids to treat slow transit constipation.

Cinnamic acid regulates the intestinal microbiome and short-chain fatty acids to treat slow transit constipation.

Background: Slow transit constipation (STC) is a disorder with delayed colonic transit. Cinnamic acid (CA) is an organic acid in natural plants, such as Radix Scrophulariae (Xuan Shen), with low toxicity and biological activities to modulate the intestinal microbiome.

Aim: 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.

Methods: 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.

Results: 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 Firmicutes, Akkermansia, Lachnoclostridium, Monoglobus, UCG.005, Paenalcaligenes, Psychrobacter and Acinetobacter were involved in the production of AA, BA, PA and VA.

Conclusion: CA could treat STC effectively by ameliorating the composition and abundance of the intestinal microbiome to regulate the production of SCFAs.

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