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QC08在小鼠抗生素相关性腹泻中的作用。

The role of QC08 in antibiotic-associated diarrhea in mice.

作者信息

Ren Lixuan, Tan Fang, Kim Hyo-Eun, Ma Xin, Kong Chang-Suk

机构信息

Department of Bioscience, Silla University, Busan, 46958 Republic of Korea.

Nutritional Education, Graduate School of Education, Silla University, Busan, 46958 Korea.

出版信息

Food Sci Biotechnol. 2025 May 15;34(11):2625-2634. doi: 10.1007/s10068-025-01881-4. eCollection 2025 Jul.

Abstract

Excessive antibiotic use can lead to gut microbiota dysbiosis, resulting in diarrhea. This study aimed to investigate the effects of QC08 (QC08) on the antibiotic-induced diarrhea mouse model using lincomycin hydrochloride. Mice were divided into five groups: normal, diarrhea, a drug group, high-dose QC08 (QC08-H), low-dose QC08 (QC08-L). Compared with the diarrhea group, the QC08-H and QC08-L groups showed a decrease in serum serotonin, interleukin (IL)-17A, IL-6, and malondialdehyde levels, whereas total antioxidant capacity levels increased. In the colon and small intestine tissues of QC08-H and QC08-L treated mice, mRNA expression of cystic fibrosis transmembrane conductance regulator (CFTR), epidermal growth factor receptor (EGFR), and transforming growth factor β1 (TGFβ1) was significantly downregulated, whereas expression of sodium-hydrogen exchanger 1 (NHE1) and NHE4 was upregulated compared to the AAD model group. Altogether, this in vivo study demonstrates the potential of QC08 in alleviating AAD in mice, providing valuable insights for understanding and potentially treating antibiotic-related gut issues.

摘要

过度使用抗生素会导致肠道微生物群失调,进而引发腹泻。本研究旨在探讨QC08对使用盐酸林可霉素建立的抗生素诱导腹泻小鼠模型的影响。将小鼠分为五组:正常组、腹泻组、药物组、高剂量QC08组(QC08-H)、低剂量QC08组(QC08-L)。与腹泻组相比,QC08-H组和QC08-L组的血清5-羟色胺、白细胞介素(IL)-17A、IL-6和丙二醛水平降低,而总抗氧化能力水平升高。在QC08-H组和QC08-L组处理的小鼠的结肠和小肠组织中,囊性纤维化跨膜传导调节因子(CFTR)、表皮生长因子受体(EGFR)和转化生长因子β1(TGFβ1)的mRNA表达显著下调,而与抗生素相关性腹泻(AAD)模型组相比,钠氢交换体1(NHE1)和NHE4的表达上调。总之,这项体内研究证明了QC08在减轻小鼠AAD方面的潜力,为理解和潜在治疗抗生素相关的肠道问题提供了有价值的见解。

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