Yang Keungmo, Ryu Tom, Chung Beom Sun
Division of Gastroenterology and Hepatology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Department of Internal Medicine, Institute for Digestive Research, Digestive Disease Center, Soonchunhyang University College of Medicine, Seoul, Republic of Korea.
Front Pharmacol. 2024 Jun 28;15:1378653. doi: 10.3389/fphar.2024.1378653. eCollection 2024.
Excessive alcohol intake often results in hangovers and inflammatory liver damage, posing a significant health concern. Current treatment options for hangovers are still insufficient, highlighting the urgent need for new therapeutic approaches. Psyllium fiber (PF) is well-known for its gastrointestinal benefits, but its effect on hangovers is less explored. We utilized a mouse model with a single binge drinking (4 g/kg) to induce hangover and inflammatory liver injury. Intestine and liver injury were serologically and histologically estimated. Hangover symptoms were assessed using cylinder and footprint tests to objectively quantify hangover symptoms in mice. Binge drinking significantly activated alcohol-metabolizing enzymes in the small intestine and liver, leading to inflammatory damage. Concurrently, there was a rise in alcohol metabolites such as acetaldehyde and acetone, which exhibited a positive correlation with hangover symptoms in mice. Interestingly, the oral administration of PF (100 mg/kg) alongside alcohol consumption significantly reduced the activity of these enzymes and lowered the levels of alcohol metabolites. Mice treated with PF exhibited a considerable improvement in hangover symptoms and a reduction in hepatic inflammation, compared to control groups. Furthermore, experiments using HepG2 cell lines and semipermeable membranes demonstrated that PF effectively inhibits alcohol absorption into the body. In conclusion, PF demonstrates a potential protective effect against alcohol-induced hangover and liver injury by inhibiting the absorption of alcohol and lowering hangover-related alcohol metabolites. This study suggests that PF could serve as an effective therapeutic option for mitigating the adverse effects of excessive alcohol consumption.
过量饮酒常常会导致宿醉和肝脏炎症性损伤,这对健康构成了重大威胁。目前针对宿醉的治疗方法仍然不足,凸显了对新治疗方法的迫切需求。洋车前子纤维(PF)因其对胃肠道有益而闻名,但其对宿醉的影响却鲜有人研究。我们利用单次暴饮酒精(4克/千克)的小鼠模型来诱发宿醉和肝脏炎症性损伤。通过血清学和组织学方法评估肠道和肝脏损伤情况。使用圆筒试验和足迹试验评估宿醉症状,以客观量化小鼠的宿醉症状。暴饮酒精显著激活了小肠和肝脏中的酒精代谢酶,导致炎症性损伤。与此同时,乙醛和丙酮等酒精代谢产物有所增加,且与小鼠的宿醉症状呈正相关。有趣的是,在饮酒的同时口服PF(100毫克/千克)可显著降低这些酶的活性,并降低酒精代谢产物的水平。与对照组相比,接受PF治疗的小鼠宿醉症状有显著改善,肝脏炎症也有所减轻。此外,使用HepG2细胞系和半透膜进行的实验表明,PF能有效抑制酒精吸收进入体内。总之,PF通过抑制酒精吸收和降低与宿醉相关的酒精代谢产物,对酒精诱导的宿醉和肝脏损伤显示出潜在的保护作用。这项研究表明,PF可作为减轻过量饮酒不良影响的有效治疗选择。