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阿扎那韦/利托那韦与洛匹那韦/利托那韦对葡萄糖摄取及胰岛素敏感性的影响:体外及临床的显著差异

Effects of atazanavir/ritonavir and lopinavir/ritonavir on glucose uptake and insulin sensitivity: demonstrable differences in vitro and clinically.

作者信息

Noor Mustafa A, Flint Oliver P, Maa Jen-Fue, Parker Rex A

机构信息

Discovery and Exploratory Clinical Research, Bristol-Myers Squibb Company, NJ 08543, USA.

出版信息

AIDS. 2006 Sep 11;20(14):1813-21. doi: 10.1097/01.aids.0000244200.11006.55.

Abstract

BACKGROUND

The HIV protease inhibitor (PI) atazanavir does not impair insulin sensitivity acutely but ritonavir and lopinavir induce insulin resistance at therapeutic concentrations.

OBJECTIVE

To test the hypothesis that atazanavir combined with a lower dose of ritonavir would have significantly less effect on glucose metabolism than lopinavir/ritonavir in vitro and clinically.

METHODS

Glucose uptake was measured following insulin stimulation in differentiated human adipocytes in the presence of ritonavir (2 micromol/l) combined with either atazanavir or lopinavir (3-30 micromol/l). These data were examined clinically using the hyperinsulinemic euglycemic clamp and oral glucose tolerance testing (OGTT) in 26 healthy HIV-negative men treated with atazanavir/ritonavir (300/100 mg once daily) and lopinavir/ritonavir (400/100 mg twice daily) for 10 days in a randomized cross-over study.

RESULTS

Atazanavir inhibited glucose uptake in vitro significantly less than lopinavir and ritonavir at all concentrations. Ritonavir (2 micromol/l) combined with either atazanavir or lopinavir (3-30 micromol/l) did not further inhibit glucose uptake. During euglycemic clamp, there was no significant change from baseline insulin sensitivity with atazanavir/ritonavir (P = 0.132), while insulin sensitivity significantly decreased with lopinavir/ritonavir from the baseline (-25%; P < 0.001) and from that seen with atazanavir/ritonavir (-18%; P = 0.023). During OGTT, the HOMA insulin resistance index significantly increased from baseline at 120 min with atazanavir/ritonavir and at 150 min with lopinavir/ritonavir. The area under the curve of glucose increased significantly with lopinavir/ritonavir but not with atazanavir/ritonavir.

CONCLUSIONS

Both glucose uptake in vitro and clinical insulin sensitivity in healthy volunteers demonstrate differential effects on glucose metabolism by the combination PI atazanavir/ritonavir and lopinavir/ritonavir.

摘要

背景

HIV蛋白酶抑制剂(PI)阿扎那韦不会急性损害胰岛素敏感性,但利托那韦和洛匹那韦在治疗浓度下会诱导胰岛素抵抗。

目的

验证阿扎那韦联合低剂量利托那韦在体外和临床上对糖代谢的影响明显小于洛匹那韦/利托那韦的假设。

方法

在分化的人脂肪细胞中,于存在利托那韦(2微摩尔/升)并联合阿扎那韦或洛匹那韦(3 - 30微摩尔/升)的情况下,测量胰岛素刺激后的葡萄糖摄取。在一项随机交叉研究中,对26名健康的HIV阴性男性进行高胰岛素正常血糖钳夹试验和口服葡萄糖耐量试验(OGTT),这些男性分别接受阿扎那韦/利托那韦(300/100毫克,每日一次)和洛匹那韦/利托那韦(400/100毫克,每日两次)治疗10天,以此对上述数据进行临床检验。

结果

在所有浓度下,阿扎那韦在体外对葡萄糖摄取的抑制作用均明显小于洛匹那韦和利托那韦。利托那韦(2微摩尔/升)联合阿扎那韦或洛匹那韦(3 - 30微摩尔/升)并未进一步抑制葡萄糖摄取。在正常血糖钳夹试验期间,阿扎那韦/利托那韦组的胰岛素敏感性与基线相比无显著变化(P = 0.132),而洛匹那韦/利托那韦组的胰岛素敏感性与基线相比显著降低(-25%;P < 0.001),与阿扎那韦/利托那韦组相比也降低(-18%;P = 0.023)。在OGTT期间,阿扎那韦/利托那韦组在120分钟时、洛匹那韦/利托那韦组在150分钟时,稳态模型评估胰岛素抵抗指数均较基线显著升高。洛匹那韦/利托那韦组葡萄糖曲线下面积显著增加,而阿扎那韦/利托那韦组未增加。

结论

健康志愿者的体外葡萄糖摄取和临床胰岛素敏感性均显示,PI联合用药阿扎那韦/利托那韦和洛匹那韦/利托那韦对糖代谢有不同影响。

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