Effect of a Farnesoid X-receptor Agonist on Postprandial Lipemia in Rats Fed a Supraphysiological Fat Dozes

Q3 Pharmacology, Toxicology and Pharmaceutics Drug Development and Registration Pub Date : 2023-05-29 DOI:10.33380/2305-2066-2023-12-2-174-184
Yu. N. Alekhin, O. S. Popova, V. S. Ponamarev, P. A. Parshin
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Abstract

Introduction. One of the most progressive directions of the modern stage of development of biology is the deepening of knowledge about the mechanisms of regulation of metabolic processes, in particular about signal molecules that transmit information to the cell through ion channels and nuclear receptors associated with G-protein or with enzymatic activity. The nuclear Farnesoid X receptor (FXR) is mainly expressed in the liver and intestines, it regulates key genes that provide the processes of synthesis, transport and reabsorption of bile acids, and is also involved in the metabolism of lipids and carbohydrates. Aim. To evaluate the effect of a farnesoid X receptor agonist on postprandial lipemia in rats fed a supraphysiological fat diet. Materials and methods. An experimental, prospective, controlled, unblinded, randomized study was conducted to study the effect of a farnesoid X receptor agonist (obeticholic acid) on postprandial lipemia in rats receiving a diet containing a supraphysiological dose of fats. Results and discussion. It has been shown that when assessing postprandial lipemia, an oral test for tolerance to supraphysiological doses of fat with the determination of the initial lipid profile parameters and 4 hours after exercise has a sufficiently high information content. It was found that in animals that received a diet containing an increased amount of fat for 28 days, there was an imbalance in lipid metabolism with activation of their absorption in the intestine, but a "slow" reaction of the mechanisms of intermediate lipid metabolism, which was accompanied by the accumulation of triglycerides and cholesterol in the blood of hungry rats, chylomicrons and LDL. At 4 hours post-feeding, these animals showed abnormal increases in triglycerides and cholesterol. Conclusion. The use of obeticholic acid harmonizes lipid metabolism against the background of alimentary fat load, due to the activation of farnesoid X-receptors of the intestine and liver, which is manifested by a simultaneous increase in the intensity of lipid absorption processes and their intermediate metabolism. As a result, the risk of hyperchylomicronemia, hypercholesterolemia and hypertriglyceridemia is eliminated, the likelihood of developing secondary hyperlipedemia, insulin tolerance and functional overload (or pathology) of the liver is reduced.
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Farnesoid x受体激动剂对喂食超生理脂肪睡眠大鼠餐后脂血症的影响
介绍。生物学发展的现代阶段最进步的方向之一是对代谢过程调节机制的认识的深化,特别是关于通过离子通道和与g蛋白或酶活性相关的核受体向细胞传递信息的信号分子。核Farnesoid X受体(FXR)主要表达于肝脏和肠道,它调节提供胆汁酸合成、转运和重吸收过程的关键基因,也参与脂质和碳水化合物的代谢。的目标。评价一种法内甾体X受体激动剂对喂食超生理脂肪饮食的大鼠餐后血脂的影响。材料和方法。一项实验性、前瞻性、对照、非盲、随机研究旨在研究一种法内甾体X受体激动剂(奥贝胆酸)对进食含有超生理剂量脂肪的大鼠餐后血脂的影响。结果和讨论。研究表明,在评估餐后脂血症时,在运动后4小时进行口服测试,以确定对超生理剂量脂肪的耐受性,并确定初始脂质参数,具有足够高的信息量。研究发现,在连续28天增加脂肪摄入量的动物饮食中,脂质代谢失衡,肠道吸收被激活,但中间脂质代谢机制出现“缓慢”反应,伴随着甘油三酯和胆固醇在饥饿大鼠、乳糜微粒和LDL血液中的积累。在喂食后4小时,这些动物的甘油三酯和胆固醇出现异常升高。结论。由于肠道和肝脏的法脂类x受体的激活,奥贝胆酸的使用在消化脂肪负荷的背景下协调脂质代谢,这表现为脂质吸收过程及其中间代谢强度的同时增加。因此,消除了高乳糜微粒血症、高胆固醇血症和高甘油三酯血症的风险,降低了继发性高脂血症、胰岛素耐受性和肝脏功能过载(或病理)的可能性。
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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