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胃饥饿素通过NO/cGMP信号通路保护人脐静脉内皮细胞免受晚期糖基化终产物诱导的细胞凋亡。

Ghrelin protects human umbilical vein endothelial cells against advanced glycation end products-induced apoptosis via NO/cGMP signaling.

作者信息

Li Pengjie, Liu Ying, Xiang Ying, Lin Miao, Gao Jinling

机构信息

Department of Endocrinology, The 2nd Affiliated Hospital of Harbin Medical University Harbin 150086, China.

Department of Endocrinology, China General Hospital of Shenyang Military Region Shenyang 110000, China.

出版信息

Int J Clin Exp Med. 2015 Sep 15;8(9):15269-75. eCollection 2015.

Abstract

OBJECTIVES

The aim of this study was to investigate the intracellular mechanism involved in the anti-apoptotic effect of ghrelin on human umbilical vein endothelial cells (HUVECs).

METHODS

HUVECs were pretreated with ghrelin before exposure to 200 μg/ml advanced glycation end products (AGEs)-BSA for 48 h. Cell viability and apoptosis were determined by MTT assay and Annexin V/PI staining. Intracellular cGMP levels evaluation and cGMP analogs were employed to explore possible mechanisms.

RESULTS

The inhibitory effect on AGEs induced HUVECs apoptosis could be exerted by ghrelin and co-incubation with growth hormone secretagogue receptor (GHSR)-1a antagonist [D-Lys(3)]-GHRP-6 abolished this inhibition. Decreased cGMP level in AGEs induced HUVECs apoptosis was restored by ghrelin pretreatment and abolished by [D-Lys(3)]-GHRP-6 co-incubation. cGMP analogs (8 Br-cGMP and DB-cGMP) pretreatment also exhibited inhibitory effect on AGEs induced HUVECs apoptosis.

CONCLUSIONS

Our results demonstrated that ghrelin produces a protective effect on HUVECs through GHS-R1a and cGMP/NO signaling pathway mediates the effect of ghrelin. These observations suggest a novel intracellular mechanism in the process of AGEs induced HUVECs apoptosis.

摘要

目的

本研究旨在探讨胃饥饿素对人脐静脉内皮细胞(HUVECs)抗凋亡作用的细胞内机制。

方法

在将HUVECs暴露于200μg/ml晚期糖基化终产物(AGEs)-牛血清白蛋白(BSA)48小时之前,先用胃饥饿素对其进行预处理。通过MTT法和Annexin V/PI染色来测定细胞活力和凋亡情况。采用细胞内cGMP水平评估和cGMP类似物来探究可能的机制。

结果

胃饥饿素可对AGEs诱导的HUVECs凋亡产生抑制作用,与生长激素促分泌素受体(GHSR)-1a拮抗剂[D-Lys(3)]-GHRP-6共同孵育可消除这种抑制作用。胃饥饿素预处理可恢复AGEs诱导的HUVECs凋亡中降低的cGMP水平,而与[D-Lys(3)]-GHRP-6共同孵育则可消除这种恢复作用。cGMP类似物(8-Br-cGMP和DB-cGMP)预处理也对AGEs诱导的HUVECs凋亡表现出抑制作用。

结论

我们的结果表明,胃饥饿素通过GHS-R1a对HUVECs产生保护作用,且cGMP/NO信号通路介导了胃饥饿素的作用。这些观察结果提示了AGEs诱导HUVECs凋亡过程中的一种新的细胞内机制。

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