Accumulation of Advanced Oxidation Protein Products Promotes Age-Related Decline of Type H Vessels in Bone

被引:0
作者
Zhao, Kai [1 ,2 ]
Zhu, Guo-Zheng [1 ]
Li, Hong-Zhou [1 ]
Gao, Jia-Wen [1 ]
Tu, Chen [1 ]
Wu, Di-Zheng [1 ]
Huang, Yu-Sheng [1 ]
Han, Dong [1 ]
Chen, Xing-Yu [1 ]
Wu, Long-Yan [3 ]
Zhong, Zhao-Ming [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Orthopaed, Div Spine Surg, Guangzhou, Peoples R China
[2] Gannan Med Univ, Affiliated Hosp 1, Dept Orthopaed, Ganzhou, Peoples R China
[3] Ganzhou Peoples Hosp, Dept Ultrasound Med, Ganzhou, Peoples R China
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2024年 / 80卷 / 01期
基金
中国国家自然科学基金;
关键词
Advanced oxidation protein products; Aging; Osteoporosis; Oxidative stress; Type H vessels; ENDOTHELIAL-CELLS; STRESS; ANGIOGENESIS; ATHEROSCLEROSIS; OSTEOGENESIS; VASCULOPATHY; INFLAMMATION; IMPAIRMENT; GLYCATION; VCAM-1;
D O I
10.1093/gerona/glae271
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Type H vessels have been proven to couple angiogenesis and osteogenesis. The decline of type H vessels contributes to bone loss in the aging process. Aging is accompanied by the accumulation of advanced oxidation protein products (AOPPs). However, whether AOPP accumulation is involved in age-related decline of type H vessels is unclear. Here, we show that the increase of AOPP levels in plasma and bone was correlated with the decline of type H vessels and loss of bone mass in old mice. Exposure of microvascular endothelial cells to AOPPs significantly inhibited cell proliferation, migration, and tube formation; increased NADPH oxidase activity and excessive reactive oxygen species generation; upregulated the expression of vascular cell adhesion molecule-1 and intercellular cell adhesion molecule-1; and eventually impaired angiogenesis, which was alleviated by redox modulator N-acetylcysteine and NADPH oxidase inhibitor apocynin. Furthermore, reduced AOPP accumulation by NAC treatment was able to alleviate significantly the decline of type H vessels, bone mass loss, and deterioration of bone microstructure in old mice. Collectively, these findings suggest that AOPPs accumulation contributes to the decline of type H vessels in the aging process, and illuminate a novel potential mechanism underlying age-related bone loss.
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页数:12
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