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褪黑素抑制2型糖尿病骨质疏松症中的自噬。

Melatonin suppresses autophagy in type 2 diabetic osteoporosis.

作者信息

Zhang Wei-Lin, Meng Hong-Zheng, Yang Rui-Fei, Yang Mao-Wei, Sun Guang-Hong, Liu Jun-Hua, Shi Peng-Xu, Liu Fei, Yang Bo

机构信息

Department of Orthopedics, the First Hospital of China Medical University, Shenyang, Liaoning, China.

School of Medical Applied Technology, Shenyang Medical College, Shenyang, Liaoning, China.

出版信息

Oncotarget. 2016 Aug 9;7(32):52179-52194. doi: 10.18632/oncotarget.10538.

DOI:10.18632/oncotarget.10538
PMID:27438148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5239543/
Abstract

Type 2 diabetes mellitus is often complicated by osteoporosis, a process which may involve osteoblast autophagy. As melatonin suppresses autophagy under certain conditions, we its investigated the effects on bone autophagy during diabetes. We first assessed different body parameters in a diabetic rat model treated with various concentrations of melatonin. Dynamic biomechanicalmeasurements, bone organization hard slice dyeing and micro-CT were used to observe the rat bone microstructure, and immunohistochemistry was used to determine levels of autophagy biomarkers. We also performed in vitro experiments on human fetal osteoblastic (hFOB1.19) cells cultured with high glucose, different concentrations of melatonin, and ERK pathway inhibitors. And we used Western blotting and immunofluorescence to measure the extent of osteogenesis and autophagy. We found that melatonin improved the bone microstructure in our rat diabetes model and reduced the level of autophagy(50 mg/kg was better than 100 mg/kg). Melatonin also enhanced osteogenesis and suppressed autophagy in osteoblasts cultured at high glucose levels (10 μM was better than 1 mM). This suggests melatonin may reduce the level of autophagy in osteoblasts and delay diabetes-induced osteoporosis by inhibiting the ERK signaling pathway.

摘要

2型糖尿病常并发骨质疏松症,这一过程可能涉及成骨细胞自噬。由于褪黑素在某些情况下会抑制自噬,我们研究了其在糖尿病期间对骨自噬的影响。我们首先在接受不同浓度褪黑素治疗的糖尿病大鼠模型中评估了不同的身体参数。采用动态生物力学测量、骨组织硬切片染色和显微CT观察大鼠骨微观结构,并用免疫组织化学法测定自噬生物标志物水平。我们还对用高糖、不同浓度褪黑素和ERK通路抑制剂培养的人胎儿成骨细胞(hFOB1.19)进行了体外实验。我们用蛋白质免疫印迹法和免疫荧光法测量成骨和自噬程度。我们发现褪黑素改善了我们大鼠糖尿病模型中的骨微观结构并降低了自噬水平(50毫克/千克比100毫克/千克效果更好)。褪黑素还增强了在高糖水平下培养的成骨细胞的成骨作用并抑制了自噬(10微摩尔比1毫摩尔效果更好)。这表明褪黑素可能通过抑制ERK信号通路降低成骨细胞中的自噬水平并延缓糖尿病诱导的骨质疏松症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe47/5239543/5f7fac8c1810/oncotarget-07-52179-g007.jpg
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