Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha 410008, PR China; Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, 110 Xiangya Road, Changsha 410078, PR China; Engineering Research Center of Applied Technology of Pharmacogenomics, Ministry of Education, 110 Xiangya Road, Changsha 410078, PR China; National Clinical Research Center for Geriatric Disorders, 87 Xiangya Road, Changsha 410008, Hunan, PR China; Hunan Key Laboratory for Bioanalysis of Complex Matrix Samples, Changsha Duxact Biotech Co., Ltd., Changsha 411000, PR China.
Hunan Key Laboratory for Bioanalysis of Complex Matrix Samples, Changsha Duxact Biotech Co., Ltd., Changsha 411000, PR China.
Toxicol Appl Pharmacol. 2020 Mar 15;391:114900. doi: 10.1016/j.taap.2020.114900. Epub 2020 Feb 19.
Methotrexate (MTX) is a widely used therapeutic agent for the treatment of cancer and autoimmune diseases. However, its efficacy is often limited by adverse effects, such as intestinal toxicity. Although treatment with leucovorin (LV) is the most common method to reduce the toxic effects of MTX, it may also compromise the therapeutic effects of MTX. The gut microbiome has been reported to be associated with the intestinal toxicity of MTX. In this study, the intestinal damage of MTX was ameliorated by treatment with LV. Moreover, the population, diversity, and principal components of the gut microbiota in MTX-treated mice were restored by treatment with LV. The only element of the gut microbiota that was significantly changed after treatment with LV was Bifidobacterium, and supplementation with Bifidobacterium longum ameliorated MTX-induced intestinal damage. In conclusion, our results suggest that the balance and the composition of gut microbiota have an important role in the LV-mediated protection against MTX-induced intestinal toxicity. This work provides foundation of data in support of a new potential mechanism for the prevention of MTX-induced intestinal toxicity.
甲氨蝶呤(MTX)是一种广泛用于治疗癌症和自身免疫性疾病的治疗药物。然而,其疗效常受到不良反应的限制,如肠道毒性。虽然用亚叶酸(LV)治疗是减少 MTX 毒性作用的最常用方法,但它也可能影响 MTX 的治疗效果。肠道微生物群已被报道与 MTX 的肠道毒性有关。在本研究中,LV 治疗改善了 MTX 引起的肠道损伤。此外,LV 治疗还恢复了 MTX 处理小鼠的肠道微生物群的种群、多样性和主成分。LV 治疗后唯一显著改变的肠道微生物群元素是双歧杆菌,补充长双歧杆菌可改善 MTX 引起的肠道损伤。总之,我们的研究结果表明,肠道微生物群的平衡和组成在 LV 介导的对抗 MTX 诱导的肠道毒性的保护中起着重要作用。这项工作为预防 MTX 诱导的肠道毒性的新的潜在机制提供了数据支持。