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大鼠暴露于酒精一年后的血清脂质组学特征。

Lipidomic signature of serum from the rats exposed to alcohol for one year.

机构信息

National Chengdu Center for Safety Evaluation of Drugs, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.

National Chengdu Center for Safety Evaluation of Drugs, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Collaborative Innovation Center for Biotherapy, Chengdu 610041, China; Sichuan Center for Disease Control and Prevention, Chengdu 610041, China.

出版信息

Toxicol Lett. 2018 Sep 15;294:166-176. doi: 10.1016/j.toxlet.2018.05.011. Epub 2018 May 26.

Abstract

Alcohol abuse and its related diseases are the major risk factors for human health. Although the mechanism of alcohol-related disorders has been widely investigated, serum metabolites associated with long-term alcohol intake have not been well explored. In this study, we aimed to investigate the profiles of serum metabolites and lipid species of rats chronically exposed to alcohol, which may be involved in the pathogenesis of alcohol-associated disease. An H NMR-based metabolomics and Q-TOF/MS-based lipidomics approach were applied to investigate the profile of serum metabolites and lipid species of rats administrated daily with alcohol (12% vol/vol, 10 ml/kg per day, i.g.) for one year continuously. The rats administered with sterile water (10 ml/kg per day, i.g.) were used as control. We found that alcohol affected mostly the lipid species rather than small molecule metabolites in the serum of both female and male rats. Among the modified lipids, glycerophospholipid, sphingolipid and glycerolipids metabolism pathways were profoundly altered. The prominent changes in lipid profiles included diacylglycerol (DG), lysophosphatidylcholine (LysoPC), phosphatidic acid (PA), phosphatidylcholine (PC), phosphatidylethanolamine (PE) and triacylglycerol (TG). Moreover, fatty-acyl profile of lipids and total degree of unsaturation of fatty acid were also significantly altered by alcohol. The modified lipidomic profile may help to understand the pathogenesis of alcohol-associated diseases and also be of value for clinical evaluation of alcohol abuse, alcohol-associated disease diagnosis.

摘要

酗酒及其相关疾病是影响人类健康的主要危险因素。尽管酒精相关疾病的发病机制已被广泛研究,但与长期饮酒相关的血清代谢物仍未得到充分探索。在这项研究中,我们旨在研究长期饮酒的大鼠血清代谢物和脂质种类的特征,这些代谢物和脂质种类可能与酒精相关疾病的发病机制有关。我们应用基于核磁共振(1H NMR)的代谢组学和基于四极杆飞行时间质谱(Q-TOF/MS)的脂质组学方法,来研究连续一年每天经口给予酒精(12%vol/vol,10ml/kg)的大鼠和每天经口给予无菌水(10ml/kg)的大鼠的血清代谢物和脂质种类特征。我们发现,酒精主要影响雌性和雄性大鼠血清中的脂质种类,而不是小分子代谢物。在改变的脂质中,甘油磷脂、鞘脂和甘油酯代谢途径受到了深刻的影响。脂质图谱的显著变化包括二酰基甘油(DG)、溶血磷脂酰胆碱(LysoPC)、磷脂酸(PA)、磷脂酰胆碱(PC)、磷脂酰乙醇胺(PE)和三酰基甘油(TG)。此外,酒精还显著改变了脂质的脂肪酸酰基谱和脂肪酸总不饱和度。改变的脂质组学特征有助于理解酒精相关疾病的发病机制,也有助于对酒精滥用、酒精相关疾病的临床评估。

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