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首页> 外文期刊>AIDS >Effect of atazanavir and ritonavir on the differentiation and adipokine secretion of human subcutaneous and omental preadipocytes.
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Effect of atazanavir and ritonavir on the differentiation and adipokine secretion of human subcutaneous and omental preadipocytes.

机译:阿扎那韦和利托那韦对人皮下和网膜前脂肪细胞的分化和脂肪因子分泌的影响。

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BACKGROUND: Treatment of HIV with some protease inhibitors has been associated with dyslipidemia, insulin resistance and fat redistribution. It has been hypothesized that some protease inhibitors may alter the differentiation of subcutaneous and visceral adipocytes in a disparate manner. The aim of this study was to investigate whether isolated human preadipocytes display regio-specific sensitivity to the effects of ritonavir and atazanavir by examining differentiation, as well as adipokine secretion, following a 10-day drug exposure. METHODS: Paired subcutaneous and omental human preadipocytes (n = 8) were induced to differentiate for 6 days, before being exposed to atazanavir or ritonavir (1-10 micromol/l) for 10 days. Lipid metabolism was assessed by Oil Red O staining and glycerol 3-phosphate dehydrogenase enzyme activity, whereas leptin and adiponectin secretion were assessed by enzyme-linked immunosorbent assay. RESULTS: There was no difference in differentiation between subcutaneous and omental adipocytes. Repeated exposure to ritonavir, but not to atazanavir, led to significant reductions in adipocyte differentiation. There were no differences in adiponectin secretion for any of the atazanavir treatments in both subcutaneous and omental adipocytes, whereas significant reductions were evident at 10 mumol/l for ritonavir exposed subcutaneous adipocytes. In contrast, both atazanavir and ritonavir were associated with altered leptin secretion. CONCLUSIONS: Ritonavir, but not atazanavir exposure, can inhibit differentiation of subcutaneous and omental adipocytes to a similar extent. Regio-specific differences, however, were apparent for adiponectin and leptin secretion. The role of region-specific alterations in adipokine secretion and apoptosis in the pathogenesis of HIV-lipodystrophy requires further attention.
机译:背景:用某些蛋白酶抑制剂治疗HIV与血脂异常,胰岛素抵抗和脂肪重新分布有关。假设某些蛋白酶抑制剂可能以不同的方式改变皮下和内脏脂肪细胞的分化。这项研究的目的是通过在10天的药物暴露后检查分化以及脂肪因子的分泌,研究分离的人类前脂肪细胞是否对ritonavir和atazanavir的作用表现出区域特异性敏感性。方法:将配对的皮下和网膜人类前脂肪细胞(n = 8)诱导分化6天,然后再暴露于阿扎那韦或利托那韦(1-10 micromol / l)10天。通过油红O染色和3-磷酸甘油脱氢酶活性评估脂质代谢,而通过酶联免疫吸附测定评估瘦蛋白和脂联素分泌。结果:皮下和网膜脂肪细胞的分化没有差异。反复暴露于利托那韦而不是阿扎那韦,导致脂肪细胞分化显着降低。在皮下和网膜脂肪细胞中,任何阿扎那韦治疗的脂联素分泌均无差异,而利托那韦暴露的皮下脂肪细胞以10μmol/ l明显降低。相反,阿扎那韦和利托那韦均与瘦素分泌改变有关。结论:利托那韦(但不接受阿扎那韦)可在相似程度上抑制皮下和网膜脂肪细胞的分化。然而,脂联素和瘦素分泌的区域特异性差异是明显的。在HIV-脂肪营养不良的发病机理中,区域特异性改变在脂肪因子分泌和凋亡中的作用需要进一步关注。

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