首页> 外文期刊>Toxicology and Applied Pharmacology >The fibrate drug gemfibrozil disrupts lipoprotein metabolism in rainbow trout.
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The fibrate drug gemfibrozil disrupts lipoprotein metabolism in rainbow trout.

机译:贝特类药物吉非贝齐可破坏虹鳟鱼的脂蛋白代谢。

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Gemfibrozil (GEM) is a fibrate drug consistently found in effluents from sewage treatment plants. This study characterizes the pharmacological effects of GEM on the plasma lipoproteins of rainbow trout (Oncorhynchus mykiss). Our goals were to quantify the impact of the drug on: 1) lipid constituents of lipoproteins (phospholipids (PL), triacylglycerol (TAG), and cholesterol), 2) lipoprotein classes (high, low and very low density lipoproteins), and 3) fatty acid composition of lipoproteins. Potential mechanisms of GEM action were investigated by measuring lipoprotein lipase activity (LPL) and the hepatic gene expression of LPL and of the peroxisome proliferator-activated receptor (PPAR) alpha, beta, and gamma isoforms. GEM treatment resulted in decreased plasma lipoprotein levels (-29%) and a reduced size of all lipoprotein classes (lower PL:TAG ratios). However, the increase in HDL-cholesterol elicited by GEM in humans failed to be observed in trout. Therefore, HDL-cholesterol cannot be used to assess the impact of the drug on fish. GEM also modified lipoprotein composition by reducing the abundance of long-chain n-3 fatty acids, thereby potentially reducing the nutritional quality of exposed fish. The relative gene expression of LPL was increased, but the activity of the enzyme was not, and we found no evidence for the activation of PPAR pathways. The depressing effects of GEM on fish lipoproteins demonstrated here may be a concern in view of the widespread presence of fibrates in aquatic environments. Work is needed to test whether exposure to environmental concentrations of these drugs jeopardizes the capacity of fish for reproduction, temperature acclimation or migratory behaviors.
机译:吉非贝齐(GEM)是一种贝特类药物,一直存在于污水处理厂的废水中。这项研究的特点是GEM对虹鳟鱼(Oncorhynchus mykiss)血浆脂蛋白的药理作用。我们的目标是量化药物对以下方面的影响:1)脂蛋白的脂质成分(磷脂(PL),三酰甘油(TAG)和胆固醇),2)脂蛋白类别(高,低和非常低密度脂蛋白),和3 )脂蛋白的脂肪酸组成。通过测量脂蛋白脂肪酶活性(LPL)和LPL以及过氧化物酶体增殖物激活受体(PPAR)α,β和γ亚型的肝基因表达,研究了GEM作用的潜在机制。 GEM治疗导致血浆脂蛋白水平降低(-29%),所有脂蛋白类别的大小降低(PL:TAG比例降低)。然而,在鳟鱼中未观察到由GEM在人中引起的HDL-胆固醇的增加。因此,HDL-胆固醇不能用于评估药物对鱼类的影响。 GEM还通过减少长链n-3脂肪酸的含量来修饰脂蛋白组成,从而潜在地降低了裸露鱼类的营养质量。 LPL的相对基因表达增加,但酶的活性没有,并且我们没有发现激活PPAR途径的证据。考虑到水生环境中贝特类物质的广泛存在,GEM对鱼脂蛋白的抑制作用可能是一个令人担忧的问题。需要开展工作来测试暴露于这些药物的环境浓度是否会危害鱼类繁殖,温度适应或迁徙行为的能力。

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