Yu Ziqing, Zhang Zhaopeng, Hu Chunjie, Xie Lulu, Zhang Ru, Gao Rui, Zhang Zhirun, Wei Xuyang, Li Ting, Guo Junpeng
School of Clinical Medicine, Changchun University of Chinese Medicine Changchun 130117, Jilin, China.
School of Pharmacy, Changchun University of Chinese Medicine Changchun 130117, Jilin, China.
Am J Transl Res. 2024 Nov 15;16(11):7036-7053. doi: 10.62347/RQBJ2018. eCollection 2024.
Constipation is a clinical condition characterized by reduced intestinal motility, dry and hardened stool, and prolonged retention. Common constipation medicines are less stable, and prolonged use can lead to dependency and side effects. , a well-known Traditional Chinese Medicine, is frequently used to alleviate constipation. In this study, we established a loperamide-induced constipation model in mice to investigate the effects of (CDPS) and to explore its underlying pharmacological mechanism. The serum levels of inflammatory factors, gastrointestinal hormones and neurotransmitters of mice were measured by enzyme-linked immunosorbent assay (ELISA). Intestinal tight junction integrity was evaluated using immunohistochemistry, and Western blot was used to detect tight junction protein levels. Gut microbial community structure and metabolite content were determined using 16S rRNA sequencing and metabolomics analysis. Oral CDPS enhanced the intestinal tight junction integrity, improved barrier function of intestinal mucosa, reduced inflammation, restored intestinal microbiota balance, and regulated metabolite levels. Notably, CDPS increased the abundance of beneficial bacteria, including , , group, , , and , while decreasing the abundance of harmful bacteria such as and Proteobacteria. In summary, CDPS may prevent and treat constipation by modulating intestinal flora composition, influencing metabolite profiles, and reinforcing mucosal barrier function.
便秘是一种以肠道蠕动减慢、大便干结和潴留时间延长为特征的临床病症。常见的便秘药物稳定性较差,长期使用会导致依赖性和副作用。著名的中药[具体中药名称未给出]常用于缓解便秘。在本研究中,我们在小鼠中建立了洛哌丁胺诱导的便秘模型,以研究[具体中药名称未给出](CDPS)的作用,并探索其潜在的药理机制。通过酶联免疫吸附测定(ELISA)检测小鼠血清中的炎症因子、胃肠激素和神经递质水平。使用免疫组织化学评估肠道紧密连接的完整性,并使用蛋白质印迹法检测紧密连接蛋白水平。使用16S rRNA测序和代谢组学分析确定肠道微生物群落结构和代谢物含量。口服CDPS可增强肠道紧密连接的完整性,改善肠黏膜屏障功能,减轻炎症,恢复肠道微生物群平衡,并调节代谢物水平。值得注意的是,CDPS增加了有益菌的丰度,包括[具体有益菌名称未给出]、[具体有益菌名称未给出]、[具体有益菌名称未给出]群、[具体有益菌名称未给出]、[具体有益菌名称未给出]和[具体有益菌名称未给出],同时降低了有害菌如[具体有害菌名称未给出]和变形菌门的丰度。总之,CDPS可能通过调节肠道菌群组成、影响代谢物谱和增强黏膜屏障功能来预防和治疗便秘。