Lamas-Paz Arantza, Mesquita Mariana, Garcia-Lacarte Marcos, Estévez-Vázquez Olga, Benedé-Ubieto Raquel, Gutierrez Alejandro H, Wu Hanghang, Leal Lasalle Hector, Vaquero Javier, Bañares Rafael, Martínez-Naves Eduardo, Roa Sergio, Nevzorova Yulia A, Jorquera Gonzalo, Cubero Francisco Javier
Department of Immunology, Ophthalmology and Eye Nose and Throat (ENT), Complutense University School of Medicine, Madrid, Spain.
12 de Octubre Health Research Institute (imas12), Madrid, Spain.
Front Nutr. 2024 Apr 18;11:1393014. doi: 10.3389/fnut.2024.1393014. eCollection 2024.
Alcohol misuse, binge drinking pattern, and gender-specific effects in the middle-aged population has been clearly underestimated. In the present study, we focused on understanding gender-specific effects of alcohol exposure on the gut-liver axis and the role of gut microbiota in modulating gender-specific responses to alcohol consumption.
Fifty-two-week-old female and male C57BL/6 mice were fasted for 12 h, and then administered a single oral dose of ethanol (EtOH) (6 g/kg). Controls were given a single dose of PBS. Animals were sacrificed 8 h later. Alternatively, fecal microbiota transplantation (FMT) was performed in 52-week-old male mice from female donors of the same age. Permeability of the large intestine (colon), gut microbiota, liver injury, and inflammation was thoroughly evaluated in all groups.
Middle-aged male mice exposed to EtOH showed a significant increase in gut permeability in the large intestine, evaluated by FITC-dextran assay and ZO-1, OCCLUDIN and MUCIN-2 immuno-staining, compared to PBS-treated animals, whilst female mice of the same age also increased their gut permeability, but displayed a partially maintained intestinal barrier integrity. Moreover, there was a significant up-regulation of TLRs and markers of hepatocellular injury, cell death (AST, TUNEL-positive cells) and lipid accumulation (ORO) in male mice after EtOH exposure. Interestingly, FMT from female donors to male mice reduced gut leakiness, modified gut microbiota composition, ameliorated liver injury and inflammation, TLR activation and the senescence phenotype of middle-aged mice.
Our findings highlighted the relevance of gender in middle-aged individuals who are exposed to alcohol in the gut-liver axis. Moreover, our study revealed that gender-specific microbiota transplantation might be a plausible therapy in the management of alcohol-related disorders during aging.
酒精滥用、暴饮模式以及在中年人群中的性别特异性影响一直被明显低估。在本研究中,我们专注于了解酒精暴露对肠-肝轴的性别特异性影响以及肠道微生物群在调节对酒精消费的性别特异性反应中的作用。
将52周龄的雌性和雄性C57BL/6小鼠禁食12小时,然后单次口服给予乙醇(EtOH)(6克/千克)。对照组给予单剂量的磷酸盐缓冲盐水(PBS)。8小时后处死动物。另外,对52周龄的雄性小鼠进行来自同年龄雌性供体的粪便微生物群移植(FMT)。对所有组的大肠(结肠)通透性、肠道微生物群、肝损伤和炎症进行了全面评估。
与接受PBS处理的动物相比,通过异硫氰酸荧光素-葡聚糖测定法以及ZO-1、闭合蛋白和粘蛋白-2免疫染色评估,暴露于EtOH的中年雄性小鼠大肠的肠道通透性显著增加,而相同年龄的雌性小鼠肠道通透性也增加,但显示出部分维持的肠道屏障完整性。此外,EtOH暴露后雄性小鼠的Toll样受体(TLRs)以及肝细胞损伤、细胞死亡(天冬氨酸转氨酶、TUNEL阳性细胞)和脂质积累(油红O)标志物显著上调。有趣的是,从雌性供体到雄性小鼠的FMT降低了肠道渗漏,改变了肠道微生物群组成,改善了肝损伤和炎症、TLR激活以及中年小鼠的衰老表型。
我们的研究结果突出了性别在肠-肝轴中暴露于酒精的中年个体中的相关性。此外,我们的研究表明,性别特异性微生物群移植可能是衰老过程中酒精相关疾病管理的一种可行疗法。