Szymczak-Pajor Izabela, Drzewoski Józef, Kozłowska Małgorzata, Krekora Jan, Śliwińska Agnieszka
Department of Nucleic Acid Biochemistry, Medical University of Lodz, 251 Pomorska Str., 92-213 Lodz, Poland.
Central Teaching Hospital of the Medical University of Lodz, 251 Pomorska Str., 92-213 Lodz, Poland.
Pharmaceuticals (Basel). 2025 Jan 6;18(1):55. doi: 10.3390/ph18010055.
It is critical to sustain the diversity of the microbiota to maintain host homeostasis and health. Growing evidence indicates that changes in gut microbial biodiversity may be associated with the development of several pathologies, including type 2 diabetes mellitus (T2DM). Metformin is still the first-line drug for treatment of T2DM unless there are contra-indications. The drug primarily inhibits hepatic gluconeogenesis and increases the sensitivity of target cells (hepatocytes, adipocytes and myocytes) to insulin; however, increasing evidence suggests that it may also influence the gut. As T2DM patients exhibit gut dysbiosis, the intestinal microbiome has gained interest as a key target for metabolic diseases. Interestingly, changes in the gut microbiome were also observed in T2DM patients treated with metformin compared to those who were not. Therefore, the aim of this review is to present the current state of knowledge regarding the association of the gut microbiome with the antihyperglycemic effect of metformin. Numerous studies indicate that the reduction in glucose concentration observed in T2DM patients treated with metformin is due in part to changes in the biodiversity of the gut microbiota. These changes contribute to improved intestinal barrier integrity, increased production of short-chain fatty acids (SCFAs), regulation of bile acid metabolism, and enhanced glucose absorption. Therefore, in addition to the well-recognized reduction of gluconeogenesis, metformin also appears to exert its glucose-lowering effect by influencing gut microbiome biodiversity. However, we are only beginning to understand how metformin acts on specific microorganisms in the intestine, and further research is needed to understand its role in regulating glucose metabolism, including the impact of this remarkable drug on specific microorganisms in the gut.
维持微生物群的多样性对于维持宿主内环境稳定和健康至关重要。越来越多的证据表明,肠道微生物多样性的变化可能与包括2型糖尿病(T2DM)在内的多种疾病的发生发展有关。二甲双胍仍然是治疗T2DM的一线药物,除非有禁忌证。该药物主要抑制肝糖异生,并增加靶细胞(肝细胞、脂肪细胞和肌细胞)对胰岛素的敏感性;然而,越来越多的证据表明它也可能影响肠道。由于T2DM患者存在肠道菌群失调,肠道微生物群作为代谢性疾病的关键靶点受到了关注。有趣的是,与未接受二甲双胍治疗的T2DM患者相比,接受二甲双胍治疗的患者肠道微生物群也发生了变化。因此,本综述的目的是介绍关于肠道微生物群与二甲双胍降糖作用之间关联的当前知识状态。大量研究表明,接受二甲双胍治疗的T2DM患者血糖浓度的降低部分归因于肠道微生物群生物多样性的变化。这些变化有助于改善肠道屏障完整性、增加短链脂肪酸(SCFAs)的产生、调节胆汁酸代谢以及增强葡萄糖吸收。因此,除了众所周知的糖异生减少外,二甲双胍似乎还通过影响肠道微生物群生物多样性发挥其降糖作用。然而,我们才刚刚开始了解二甲双胍如何作用于肠道中的特定微生物,还需要进一步研究以了解其在调节葡萄糖代谢中的作用,包括这种显著药物对肠道中特定微生物的影响。