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贝特类药物对大鼠微粒体磷脂酰基组成的不同影响。

Differential effects of fibrates on the acyl composition of microsomal phospholipids in rats.

作者信息

Vázquez M, Muñoz S, Alegret M, Adzet T, Merlos M, Laguna J C

机构信息

Dept. Farmacología y Química Terapeutica, Facultad de Farmacia, Núcleo Universitario de Pedralbes, Barcelona, Spain.

出版信息

Br J Pharmacol. 1995 Oct;116(3):2067-75. doi: 10.1111/j.1476-5381.1995.tb16413.x.

Abstract
  1. The time-course and comparative effects of treatment with clofibrate (CFB), bezafibrate (BFB), and gemfibrozil (GFB) on the acyl composition of the main microsomal phospholipids, i.e. phosphatidylcholine and phosphatidylethanolamine, have been studied in male Sprague-Dawley rats. 2. The administration of the three fibrates caused a strong peroxisomal induction and a hypolipidaemic effect. Concerning the changes in acyl composition, CFB and BFB behaved in a similar way, with differences which could be attributed to their different potency as peroxisome inducers, whereas GFB showed a somewhat distinct profile. 3. The three drugs increased the relative content of palmitic, palmitoleic and oleic acids, whereas the levels of stearic acid and also those of long chain, highly unsaturated fatty acids docosatetraenoic, docosapentaenoic and docosahexaenoic acids were reduced. In general, these effects appeared from the first day of treatment and were highly correlated with peroxisomal proliferation. In addition, they were more evident in the phosphatidylcholine than in the phosphatidylethanolamine fraction. 4. Fibrates increased total monounsaturated fatty acids, whereas a decrease in total polyunsaturated fatty acids in the phosphatidylcholine fraction was observed in CFB- and BFB-, but not in GFB-treated rats. Clear differences appeared between CFB and BFB on the one hand, and GFB on the other when the influence of fibrate treatment on the molar percentages of linoleic, eicosatrienoic, arachidonic and mead acids was analyzed. 5. GFB increased linoleic acid content in phosphatidylethanolamine, whereas CFB and BFB decreased its level in both phospholipid fractions. In contrast, CFB and BFB enhanced eicosatrienoic and mead acids in both fractions and arachidonic acid in phosphatidylethanolamine, whereas GFB had practically no effect.
摘要
  1. 已在雄性斯普拉格-道利大鼠中研究了氯贝丁酯(CFB)、苯扎贝特(BFB)和吉非贝齐(GFB)治疗对主要微粒体磷脂即磷脂酰胆碱和磷脂酰乙醇胺的酰基组成的时间进程及比较效应。2. 三种贝特类药物的给药引起了强烈的过氧化物酶体诱导和降血脂作用。关于酰基组成的变化,CFB和BFB表现相似,其差异可归因于它们作为过氧化物酶体诱导剂的不同效力,而GFB显示出 somewhat distinct profile。3. 这三种药物增加了棕榈酸、棕榈油酸和油酸的相对含量,而硬脂酸以及长链高度不饱和脂肪酸二十二碳四烯酸、二十二碳五烯酸和二十二碳六烯酸的水平降低。一般来说,这些效应从治疗第一天就出现了,并且与过氧化物酶体增殖高度相关。此外,它们在磷脂酰胆碱中比在磷脂酰乙醇胺部分更明显。4. 贝特类药物增加了总单不饱和脂肪酸,而在CFB和BFB治疗的大鼠中观察到磷脂酰胆碱部分的总多不饱和脂肪酸减少,但在GFB治疗的大鼠中未观察到。当分析贝特类药物治疗对亚油酸、二十碳三烯酸、花生四烯酸和廿碳五烯酸摩尔百分比的影响时,一方面CFB和BFB与另一方面GFB之间出现了明显差异。5. GFB增加了磷脂酰乙醇胺中亚油酸的含量,而CFB和BFB在两个磷脂部分中均降低了其水平。相反,CFB和BFB在两个部分中均提高了二十碳三烯酸和廿碳五烯酸以及磷脂酰乙醇胺中花生四烯酸的水平,而GFB几乎没有影响。

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