Ciucanu Cristian I, Olariu Sonia, Vlad Daliborca C, Dumitraşcu Victor
Pharmacology and Biochemistry Department, Faculty of Medicine, University of Medicine and Pharmacy "Victor Babes" of Timişoara, Piaţa Eftimie Murgu 2, RO-300041, Timişoara, Romania.
Biochem Biophys Rep. 2020 Oct 2;24:100822. doi: 10.1016/j.bbrep.2020.100822. eCollection 2020 Dec.
Each fatty acid (FA) or class of FAs has a different behavior in the pathologies of atherosclerosis. The aim of this study was to investigate changes in the concentration of each fatty acid in the fraction of free fatty acids (FFAs) and total lipids in human plasma after short-term therapy with rosuvastatin as a cholesterol-lowering statin drug. Six hypercholesterolemic men on a habitual diet were studied in a randomized, double-blind, and crossover process. They received 20 mg rosuvastatin or placebo in random order, each for 4 weeks and after 2 weeks of washout period, they received another medication (placebo or rosuvastatin) for another period of 4 weeks. Rosuvastatin treatment significantly decreased the absolute concentrations of saturated and monounsaturated FAs in the total FAs as well as in FFAs. Long chain polyunsaturated fatty acids with 20 and 22 carbon atoms in the molecule had no significant change in the fraction of FFAs. Rosuvastatin is directly involved in cholesterol biosynthesis and indirectly through cholesterol homeostasis in the biosynthesis of other plasma lipids. In conclusion, our findings show that rosuvastatin treatment leads to significant changes in the concentration of each fatty acid, except for long-chain polyunsaturated fatty acids in FFAs. Our observations indicate that cholesterol homeostasis through its regulatory mechanisms appears to be the main cause of changes in the concentration of each plasma fatty acid during rosuvastatin treatment. These changes can be a source of beneficial consequences, in addition to lowering low-density lipoprotein cholesterol in cardiovascular diseases.
每种脂肪酸(FA)或脂肪酸类别在动脉粥样硬化病变中具有不同的表现。本研究的目的是调查瑞舒伐他汀作为一种降胆固醇他汀类药物进行短期治疗后,人血浆中游离脂肪酸(FFA)和总脂质部分中每种脂肪酸浓度的变化。在一项随机、双盲和交叉试验中,对6名日常饮食的高胆固醇血症男性进行了研究。他们随机接受20毫克瑞舒伐他汀或安慰剂,各为期4周,在2周的洗脱期后,他们再接受另一种药物(安慰剂或瑞舒伐他汀)治疗4周。瑞舒伐他汀治疗显著降低了总脂肪酸以及FFA中饱和脂肪酸和单不饱和脂肪酸的绝对浓度。分子中含有20和22个碳原子的长链多不饱和脂肪酸在FFA部分没有显著变化。瑞舒伐他汀直接参与胆固醇生物合成,并通过胆固醇稳态间接参与其他血浆脂质的生物合成。总之,我们的研究结果表明,瑞舒伐他汀治疗导致每种脂肪酸的浓度发生显著变化,但FFA中的长链多不饱和脂肪酸除外。我们的观察结果表明,通过其调节机制实现的胆固醇稳态似乎是瑞舒伐他汀治疗期间每种血浆脂肪酸浓度变化的主要原因。除了降低心血管疾病中的低密度脂蛋白胆固醇外,这些变化可能是有益结果的一个来源。