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瑞舒伐他汀治疗对INS-1 832/13细胞的基础胰岛素分泌及葡萄糖诱导的胰岛素分泌均有影响。

Rosuvastatin Treatment Affects Both Basal and Glucose-Induced Insulin Secretion in INS-1 832/13 Cells.

作者信息

Salunkhe Vishal A, Elvstam Olof, Eliasson Lena, Wendt Anna

机构信息

Unit of Islet Cell Exocytosis, Lund University Diabetes Centre, Dept. Clinical Sciences in Malmö, Lund University, Clinical Research Centre, SUS Malmö, Malmö, Sweden.

出版信息

PLoS One. 2016 Mar 17;11(3):e0151592. doi: 10.1371/journal.pone.0151592. eCollection 2016.

Abstract

Rosuvastatin is a member of the statin family. Like the other statins it is prescribed to lower cholesterol levels and thereby reduce the risk of cardiovascular events. Rosuvastatin lowers the cholesterol levels by inhibiting the key enzyme 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMG-CoA reductase) in the cholesterol producing mevalonate pathway. It has been recognized that apart from their beneficial lipid lowering effects, statins also exhibit diabetogenic properties. The molecular mechanisms behind these remain unresolved. To investigate the effects of rosuvastatin on insulin secretion, we treated INS-1 832/13 cells with varying doses (20 nM to 20 μM) of rosuvastatin for 48 h. At concentrations of 2 μM and above basal insulin secretion was significantly increased. Using diazoxide we could determine that rosuvastatin did not increase basal insulin secretion by corrupting the KATP channels. Glucose-induced insulin secretion on the other hand seemed to be affected differently at different rosuvastatin concentrations. Rosuvastatin treatment (20 μM) for 24-48 h inhibited voltage-gated Ca(2+) channels, which lead to reduced depolarization-induced exocytosis of insulin-containing granules. At lower concentrations of rosuvastatin (≤ 2 μM) the stimulus-secretion coupling pathway was intact downstream of the KATP channels as assessed by the patch clamp technique. However, a reduction in glucose-induced insulin secretion could be observed with rosuvastatin concentrations as low as 200 nM. The inhibitory effects of rosuvastatin on glucose-induced insulin secretion could be reversed with mevalonate, but not squalene, indicating that rosuvastatin affects insulin secretion through its effects on the mevalonate pathway, but not through the reduction of cholesterol biosynthesis. Taken together, these data suggest that rosuvastatin has the potential to increase basal insulin secretion and reduce glucose-induced insulin secretion. The latter is possibly an unavoidable side effect of rosuvastatin treatment as it occurs through the same mechanisms as the lipid-lowering effects of the drug.

摘要

瑞舒伐他汀是他汀类药物家族的一员。与其他他汀类药物一样,它被用于降低胆固醇水平,从而降低心血管事件的风险。瑞舒伐他汀通过抑制胆固醇生成甲羟戊酸途径中的关键酶3-羟基-3-甲基戊二酰辅酶A还原酶(HMG-CoA还原酶)来降低胆固醇水平。人们已经认识到,除了有益的降脂作用外,他汀类药物还具有致糖尿病的特性。其背后的分子机制仍未得到解决。为了研究瑞舒伐他汀对胰岛素分泌的影响,我们用不同剂量(20 nM至20 μM)的瑞舒伐他汀处理INS-1 832/13细胞48小时。在2 μM及以上浓度时,基础胰岛素分泌显著增加。使用二氮嗪我们可以确定瑞舒伐他汀不会通过破坏KATP通道来增加基础胰岛素分泌。另一方面,不同浓度的瑞舒伐他汀对葡萄糖诱导的胰岛素分泌的影响似乎有所不同。用20 μM的瑞舒伐他汀处理24至48小时会抑制电压门控Ca(2+)通道,这导致去极化诱导的含胰岛素颗粒的胞吐作用减少。通过膜片钳技术评估,在较低浓度的瑞舒伐他汀(≤2 μM)下,KATP通道下游的刺激-分泌偶联途径是完整的。然而,在低至200 nM的瑞舒伐他汀浓度下即可观察到葡萄糖诱导的胰岛素分泌减少。瑞舒伐他汀对葡萄糖诱导的胰岛素分泌的抑制作用可以被甲羟戊酸逆转,但不能被鲨烯逆转,这表明瑞舒伐他汀通过其对甲羟戊酸途径的影响来影响胰岛素分泌,而不是通过减少胆固醇生物合成。综上所述,这些数据表明瑞舒伐他汀有增加基础胰岛素分泌和减少葡萄糖诱导的胰岛素分泌的潜力。后者可能是瑞舒伐他汀治疗不可避免的副作用,因为它与药物的降脂作用通过相同的机制发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e512/4795644/120c80ee0d79/pone.0151592.g002.jpg

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