Cheng Ming, Lu Hua, Wu Yangling, Jia Long, Xiang Tao, Deng L I, Zhao Guanlan, Feng Junwei
School of Sports Medicine and Health, Chengdu Sport University, Sichuan, China.
Department of Rehabilitation, Jinniu District People's Hospital of Chengdu, Sichuan, China.
PLoS One. 2025 May 8;20(5):e0323222. doi: 10.1371/journal.pone.0323222. eCollection 2025.
Long-term alcohol intake has toxic effects on osteoblasts and osteoclasts, resulting in decreased bone density, which directly disrupts the composition of the gut microbiota and affects bone metabolism and immune activity. The effects of alcohol on the bones may be closely related to sex. This study investigated the effects of long-term alcohol consumption on bone status in different sexes by examining the gut microbiota, bone metabolism, and immune activity.
Young male and female rats were administered a Bio-Serv liquid diet containing 5% alcohol. The effects of alcohol metabolism capacity, bone morphology, bone formation, bone resorption, bone marrow immune activity, gut microbiota, and metabolite differences were analyzed in male and female rats using hematoxylin and eosin staining, micro-computed tomography, enzyme-linked immunosorbent assay, western blotting, 16S rRNA sequencing, and untargeted metabolomics.
Chronic alcohol consumption resulted in excessive osteoclast activation and decreased bone mineral density. Furthermore, alcohol reduced bone metabolism and formation while increasing bone resorption. Bone loss was significantly more severe in female rats than in male rats, indicating that the effects of alcohol on rat bones are related to sex. Chronic alcohol consumption also led to polarization of bone marrow immunoreactivity toward the M1 phenotype. In addition, chronic alcohol consumption affected the composition of gut microbiota, reduced the richness and diversity of intestinal microbiota, and decreased the ratio of Firmicutes/Bacteroidetes. Long-term alcohol consumption also affected fecal metabolites, and 754 differentially expressed metabolites were identified.
Chronic alcohol consumption increased bone resorption, inhibited bone formation, and affected bone marrow immunoreactivity in young male and female rats. Alcohol can also affect gut microbiota composition and fecal metabolism. Female rats were more susceptible to alcohol, possibly because young female rats have a lower alcohol metabolism, immunomodulatory capacity, and gut microbiota diversity than young male rats.
长期饮酒对成骨细胞和破骨细胞具有毒性作用,导致骨密度降低,这直接破坏肠道微生物群的组成,并影响骨代谢和免疫活性。酒精对骨骼的影响可能与性别密切相关。本研究通过检测肠道微生物群、骨代谢和免疫活性,调查长期饮酒对不同性别的骨状态的影响。
给年轻的雄性和雌性大鼠喂食含5%酒精的Bio-Serv液体饲料。使用苏木精和伊红染色、微计算机断层扫描、酶联免疫吸附测定、蛋白质印迹法、16S rRNA测序和非靶向代谢组学分析雄性和雌性大鼠的酒精代谢能力、骨形态、骨形成、骨吸收、骨髓免疫活性、肠道微生物群和代谢物差异。
长期饮酒导致破骨细胞过度活化和骨矿物质密度降低。此外,酒精减少了骨代谢和形成,同时增加了骨吸收。雌性大鼠的骨质流失明显比雄性大鼠更严重,表明酒精对大鼠骨骼的影响与性别有关。长期饮酒还导致骨髓免疫反应向M1表型极化。此外,长期饮酒影响肠道微生物群的组成,降低肠道微生物群的丰富度和多样性,并降低厚壁菌门/拟杆菌门的比例。长期饮酒还影响粪便代谢物,共鉴定出754种差异表达的代谢物。
长期饮酒增加了年轻雄性和雌性大鼠的骨吸收,抑制了骨形成,并影响了骨髓免疫反应。酒精还可影响肠道微生物群组成和粪便代谢。雌性大鼠对酒精更敏感,可能是因为年轻雌性大鼠的酒精代谢、免疫调节能力和肠道微生物群多样性低于年轻雄性大鼠。