Microbiology and Biotechnology department, Faculty of pharmacy, Delta University for Science and Technology, Gamasa 11152, Egypt.
Clinical pharmacology department, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt; Clinical Pharmacy department, Faculty of pharmacy, Delta University for Science and Technology, Gamasa 11152, Egypt.
Int Immunopharmacol. 2021 Jul;96:107757. doi: 10.1016/j.intimp.2021.107757. Epub 2021 May 13.
Male reproductive dysfunction is one of the overlooked findings of diabetes mellitus (DM) that deserves greater scientific attention. This study is designed to explore the therapeutic potential of metformin and montelukast, in combination with Lactobacillus, for modulation of intestinal flora and suppression of oxidative stress in testicular and liver damage in diabetic male rats. A DM model was induced by streptozotocin (STZ)which caused functional, biochemical, and inflammatory injuries to the testicular and liver tissues. The experimental panel included nine rat groups: normal control, normal control plus metformin, normal control plus montelukast, DM control, DM plus montelukast, DM plus a combination of metformin and Lactobacillus, DM plus a combination of montelukast and Lactobacillus, and DM plus a combination of metformin and montelukast. In parallel, clinical evaluation of microscopic examination scoring, and hepatic and testicular injuries, were evaluated. Biochemical markers including glucose level, lipid profile, inflammatory markers (tumor necrosis factor- (TNF-α) and interleukin-17 (IL-17), Caspase-3, and Bax proteins expressions were measured. The change in the microbiota abundance was investigated using conventional and real-time PCR. The current study revealed a significant difference in the relative abundance of microbiota, where DM is associated with an enormous increase of Bacteroides spp., Clostridium spp., E. coli, and Fusobacterium spp., and a significant decrease in Bifidobacteria spp., and Lactobacillus spp., in contrast with normal control. Metformin and montelukast, in combination with Lactobacillus, significantly reversed the testicular and liver damage caused by STZ. Moreover, the drugs significantly reduced the oxidative, inflammatory, and apoptotic activities induced by STZ.
男性生殖功能障碍是糖尿病(DM)被忽视的发现之一,值得引起更多的科学关注。本研究旨在探讨二甲双胍和孟鲁司特联合乳杆菌,调节肠道菌群和抑制糖尿病雄性大鼠睾丸和肝脏损伤的氧化应激的治疗潜力。采用链脲佐菌素(STZ)诱导 DM 模型,导致睾丸和肝组织的功能、生化和炎症损伤。实验小组包括 9 个大鼠组:正常对照组、正常对照组加二甲双胍、正常对照组加孟鲁司特、DM 对照组、DM 加孟鲁司特、DM 加二甲双胍和乳杆菌的组合、DM 加孟鲁司特和乳杆菌的组合,以及 DM 加二甲双胍和孟鲁司特的组合。同时,对微观检查评分和肝、睾丸损伤进行临床评估。测量生化标志物,包括血糖水平、血脂谱、炎症标志物(肿瘤坏死因子-α(TNF-α)和白细胞介素-17(IL-17)、半胱天冬酶-3 和 Bax 蛋白表达。使用常规和实时 PCR 研究微生物群落丰度的变化。本研究表明,微生物群落的相对丰度存在显著差异,DM 与拟杆菌属、梭菌属、大肠杆菌和梭杆菌属的大量增加以及双歧杆菌属和乳杆菌属的显著减少有关,与正常对照组相比。二甲双胍和孟鲁司特联合乳杆菌显著逆转了 STZ 引起的睾丸和肝脏损伤。此外,这些药物显著降低了 STZ 诱导的氧化、炎症和细胞凋亡活性。