Jeong In-Kyung, Han Anna, Jun Ji Eun, Hwang You-Cheol, Ahn Kyu Jeung, Chung Ho Yeon, Kang Bo Seung, Choung Se-Young
Division of Endocrinology and Metabolism, Department of Internal Medicine, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul 05278, Republic of Korea.
Department of Food Science and Human Nutrition, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Pharmaceuticals (Basel). 2024 Aug 20;17(8):1087. doi: 10.3390/ph17081087.
This open-labeled and comparative study aimed to test the efficacy and safety of a fermented rice extract-based substance containing yeast-fermented powder having aldehyde dehydrogenase (KisLip, Pico Entech, Republic of Korea) in healthy male individuals. Healthy male subjects (n = 20) consumed 90 g of alcohol at their first visit. At the second visit, participants consumed 90 g of alcohol or alcohol with a low dose of KISLip (2000 mg, KL-L) and then 90 g of alcohol or alcohol with a high dose of KISLip (3000 mg, KL-H) at the third visit. The efficacy of KISLip depends on the mutational status of important genes related to alcohol metabolism, including alcohol dehydrogenase (), cytochrome P4502E1 ( () and ()), and aldehyde dehydrogenase (). KISLip significantly reduced the highest level (Cmax) of alcohol and overall levels of acetaldehyde compared to the alcohol-only group in a dose-dependent manner. These significant effects of KISLip on alcohol metabolism were observed independent of mutations in the four genes. In addition, hangover symptoms were significantly decreased in the KISLip treated groups. During the study, the participants did not show any adverse events after KISLip intake. This clinical study suggested that supplementation of KISLip had beneficial effects on alcohol metabolism and might ameliorate the severity of hangovers without any adverse events.
这项开放标签的对比研究旨在测试一种含有酵母发酵粉末(具有乙醛脱氢酶,KisLip,韩国Pico Entech公司)的发酵大米提取物在健康男性个体中的疗效和安全性。健康男性受试者(n = 20)在首次就诊时饮用90克酒精。在第二次就诊时,参与者饮用90克酒精或酒精与低剂量KISLip(2000毫克,KL-L),然后在第三次就诊时饮用90克酒精或酒精与高剂量KISLip(3000毫克,KL-H)。KISLip的疗效取决于与酒精代谢相关的重要基因的突变状态,包括乙醇脱氢酶()、细胞色素P4502E1(()和())以及乙醛脱氢酶()。与仅饮酒组相比,KISLip以剂量依赖的方式显著降低了酒精的最高水平(Cmax)和乙醛的总体水平。观察到KISLip对酒精代谢的这些显著影响与这四个基因的突变无关。此外,KISLip治疗组的宿醉症状显著减轻。在研究期间,参与者在摄入KISLip后未出现任何不良事件。这项临床研究表明,补充KISLip对酒精代谢有有益作用,可能会改善宿醉的严重程度且无任何不良事件。