D-methionine alleviates cisplatin-induced mucositis by restoring the gut microbiota structure and improving intestinal inflammation

التفاصيل البيبلوغرافية
العنوان: D-methionine alleviates cisplatin-induced mucositis by restoring the gut microbiota structure and improving intestinal inflammation
المؤلفون: Chu-Chyn Ou, Jiuan-Miaw Liao, Jiunn-Liang Ko, Ling-Hui Lee, Li-Yu Chang, Shiang-Suo Huang, Meei-Yn Lin, Cheng-Hsi Wu
المصدر: Therapeutic Advances in Medical Oncology
Therapeutic Advances in Medical Oncology, Vol 11 (2019)
بيانات النشر: SAGE Publications, 2019.
سنة النشر: 2019
مصطلحات موضوعية: Cisplatin, biology, business.industry, gastrointestinal mucositis, Gastrointestinal mucositis, cisplatin, Gut flora, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, medicine.disease, biology.organism_classification, lcsh:RC254-282, D methionine, D-methionine, Lactobacillus, Oncology, Intestinal inflammation, Immunology, medicine, Mucositis, next-generation sequencing, business, Dysbiosis, Original Research, medicine.drug
الوصف: Background: There are close links between chemotherapy-induced intestinal mucositis and microbiota dysbiosis. Previous studies indicated that D-methionine was an excellent candidate for a chemopreventive agent. Here, we investigated the effects of D-methionine on cisplatin-induced mucositis. Materials and methods: Male Wistar rats (176–200 g, 6 weeks old) were given cisplatin (5 mg/kg) and treated with D-methionine (300 mg/kg). Histopathological, digestive enzymes activity, oxidative/antioxidant status, proinflammatory/anti-inflammatory cytokines in intestinal tissues were measured. Next-generation sequencing technologies were also performed to investigate the gut microbial ecology. Results: D-methionine administration increased villus length and crypt depth and improved digestive enzyme (leucine aminopeptidase, sucrose and alkaline phosphatase) activities in the brush-border membrane of cisplatin-treated rats ( p < 0.05). Furthermore, D-methionine significantly attenuated oxidative stress and inflammatory reaction and increased interleukin-10 levels in cisplatin-induced intestinal mucositis ( p < 0.05). Cisplatin administration resulted in high relative abundances of Deferribacteres and Proteobacteria and a low diversity of the microbiota when compared with control groups, D-methionine only and cisplatin plus D-methionine. Cisplatin markedly increased comparative abundances of Bacteroides caccae, Escherichia coli, Mucispirillum schaedleri, Bacteroides uniformis and Desulfovibrio C21-c20, while Lactobacillus was almost completely depleted, compared with the control group. There were higher abundances of Lactobacillus, Lachnospiraceae, and Clostridium butyrium in cisplatin plus D-methionine rats than in cisplatin rats. D-methionine treatment alone significantly increased the number of Lactobacillus reuteri. Conclusion: D-methionine protects against cisplatin-induced intestinal damage through antioxidative and anti-inflammatory effects. By enhancing growth of beneficial bacteria (Lachnospiraceae and Lactobacillus), D-methionine attenuates gut microbiome imbalance caused by cisplatin and maintains gut homeostasis.
تدمد: 1758-8359
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8774f725085389dc2d3a5a6b5a362e17Test
https://doi.org/10.1177/1758835918821021Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....8774f725085389dc2d3a5a6b5a362e17
قاعدة البيانات: OpenAIRE