Mukhtar Imran, Anwar Haseeb, Mirza Osman Asghar, Ali Qasim, Ijaz Muhammad Umar, Hume Michael, Prabhala Bala Krishna, Iftikhar Arslan, Hussain Ghulam, Sohail Muhammad Umar, Khan Kashif Ur Rehman
Department of Physiology, Faculty of Life Sciences, Government College University, Faisalabad, Pakistan.
Department of Drug Design and Pharmacology, University of Copenhagen, Denmark.
Dose Response. 2021 Feb 11;19(1):1559325820987943. doi: 10.1177/1559325820987943. eCollection 2021 Jan-Mar.
In the contemporary research world, the intestinal microbiome is now envisioned as a new body organ. Recently, the gut microbiome represents a new drug target in the gut, since various orthologues of intestinal drug transporters are also found present in the microbiome that lines the small intestine of the host. Owing to this, absorbance of sulpiride by the gut microbiome in an albino rats model was assessed after the oral administration with a single dose of 20mg/kg b.w. The rats were subsequently sacrificed at 2, 3, 4, 5 and 6 hours post oral administration to collect the gut microbial mass pellet. The drug absorbance by the gut microbiome was determined by pursuing the microbial lysate through RP-HPLC-UV. Total absorbance of sulpiride by the whole gut microbiome and drug absorbance per milligram of microbial pellet were found significantly higher at 4 hours post-administration as compared to all other groups. These results affirm the hypothesis that the structural homology between membrane transporters of the gut microbiome and intestinal epithelium of the host might play an important role in drug absorbance by gut microbes in an condition.
在当代研究领域,肠道微生物群现在被视为一个新的身体器官。最近,肠道微生物群成为肠道中的一个新的药物靶点,因为在宿主小肠的微生物群中也发现了各种肠道药物转运蛋白的直系同源物。基于此,在白化大鼠模型中,口服单剂量20mg/kg体重的舒必利后,评估肠道微生物群对其的吸收情况。随后在口服给药后2、3、4、5和6小时处死大鼠,以收集肠道微生物团块。通过RP-HPLC-UV追踪微生物裂解物来测定肠道微生物群对药物的吸收。与所有其他组相比,给药后4小时全肠道微生物群对舒必利的总吸收以及每毫克微生物团块的药物吸收均显著更高。这些结果证实了这样一个假设,即在某种情况下,肠道微生物群的膜转运蛋白与宿主肠道上皮之间的结构同源性可能在肠道微生物对药物的吸收中起重要作用。