Chongqing Municipality Clinical Research Center for Endocrinology and Metabolic Diseases, Chongqing University Three Gorges Hospital, Chongqing, People's Republic of China.
Department of Hepatology, Chongqing University Three Gorges Hospital, Chongqing, People's Republic of China.
Int J Nanomedicine. 2024 May 27;19:4907-4921. doi: 10.2147/IJN.S462602. eCollection 2024.
, a dual-purpose food and medicine, displays limited efficacy in alcohol detoxification and liver protection, with previous research primarily focused on puerarin in its dried roots. In this study, we investigated the potential effects and mechanisms of fresh root-derived exosome-like nanovesicles (P-ELNs) for mitigating alcoholic intoxication, promoting alcohol metabolism effects and protecting the liver in C57BL/6J mice.
We isolated P-ELNs from fresh root using differential centrifugation and characterized them via transmission electron microscopy, nanoscale particle sizing, ζ potential analysis, and biochemical assays. In Acute Alcoholism (AAI) mice pre-treated with P-ELNs, we evaluated their effects on the timing and duration of the loss of the righting reflex (LORR), liver alcohol metabolism enzymes activity, liver and serum alcohol content, and ferroptosis-related markers.
P-ELNs, enriched in proteins, lipids, and small RNAs, exhibited an ideal size (150.7 ± 82.8 nm) and negative surface charge (-31 mV). Pre-treatment with 10 mg/(kg.bw) P-ELNs in both male and female mice significantly prolonged ebriety time, shortened sobriety time, enhanced acetaldehyde dehydrogenase (ALDH) activity while concurrently inhibited alcohol dehydrogenase (ADH) activity, and reduced alcohol content in the liver and serum. Notably, P-ELNs demonstrated more efficacy compared to P-ELNs supernatant fluid (abundant puerarin content), suggesting alternative active components beyond puerarin. Additionally, P-ELNs prevented ferroptosis by inhibiting the reduction of glutathione peroxidase 4 (GPX4) and reduced glutathione (GSH), and suppressing acyl-CoA synthetase long-chain family member 4 (ACSL4) elevation, thereby mitigating pathological liver lipid accumulation.
P-ELNs exhibit distinct exosomal characteristics and effectively alleviate alcoholic intoxication, improve alcohol metabolism, suppress ferroptosis, and protect the liver from alcoholic injury. Consequently, P-ELNs hold promise as a therapeutic agent for detoxification, sobriety promotion, and prevention of alcoholic liver injury.
葛根既是食品又是药品,其在解酒和保肝方面的功效有限,既往研究主要集中在其干根中的葛根素上。本研究旨在探讨新鲜葛根来源的外泌体样纳米囊泡(P-ELNs)减轻醉酒、促进酒精代谢和保护 C57BL/6J 小鼠肝脏的潜在作用及机制。
我们采用差速离心法从新鲜葛根中分离 P-ELNs,并通过透射电子显微镜、纳米粒度分析、ζ 电位分析和生化分析对其进行表征。在急性酒精中毒(AAI)小鼠中,我们评估了 P-ELNs 预处理对翻正反射潜伏期(LORR)时间和持续时间、肝酒精代谢酶活性、肝和血清中酒精含量以及铁死亡相关标志物的影响。
P-ELNs 富含蛋白质、脂质和小 RNA,具有理想的大小(150.7 ± 82.8 nm)和负表面电荷(-31 mV)。雄性和雌性小鼠预先给予 10 mg/(kg.bw)的 P-ELNs 可显著延长醉酒时间,缩短清醒时间,增强乙醛脱氢酶(ALDH)活性,同时抑制醇脱氢酶(ADH)活性,降低肝和血清中酒精含量。值得注意的是,与富含葛根素的 P-ELNs 上清液相比,P-ELNs 表现出更强的效果,这表明除了葛根素之外,还存在其他活性成分。此外,P-ELNs 通过抑制谷胱甘肽过氧化物酶 4(GPX4)和还原型谷胱甘肽(GSH)的减少以及抑制长链酰基辅酶 A 合成酶家族成员 4(ACSL4)的升高来防止铁死亡,从而减轻病理性肝脂质积累。
P-ELNs 具有明显的外泌体特征,可有效缓解醉酒,改善酒精代谢,抑制铁死亡,保护肝脏免受酒精损伤。因此,P-ELNs 有望成为一种解毒、清醒促进和预防酒精性肝损伤的治疗药物。