Protective effects of electroacupuncture on senile osteoporosis in rats

医学 电针 针灸科 老年性骨质疏松症 骨质疏松症 物理疗法 传统医学 麻醉 内科学 替代医学 病理
作者
Jun Zhou,Jinling Wang,Mengjian Qu,Qian Wang,Liqiong Wang,Sijia Liu,Jing Liu,Guanghua Sun,Peirui Zhong,Xiarong Huang,Danni Liu,Linwei Yin,Chengqi He
出处
期刊:Acupuncture in Medicine [SAGE]
卷期号:42 (6): 334-341 被引量:1
标识
DOI:10.1177/09645284241280089
摘要

Objectives: The objectives were to explore the protective effects of electroacupuncture (EA) on senile osteoporosis in aged rats and investigate the underlying mechanisms. Methods: This study included aged (24-month-old; n = 16) and young (3-month-old; n = 8) male Sprague–Dawley rats. Aged rats were further randomized 1:1 to an aged control group (Aged; n = 8) and an EA treatment group (EA; n = 8). The 3-month-old rats served as young controls (Young). EA rats received EA at ST36, SP6, GB34 and SP10 bilaterally for 30 min a day, 5 days a week, for 8 weeks. Results: EA significantly increased serum markers of bone formation in Aged rats. There were no significant differences in serum markers of bone resorption between EA and Aged rats. Deterioration of bone mineral density (BMD) and trabecular bone architecture was observed in the Aged group, while EA significantly increased BMD of the left femur and L5 vertebral body in aged rats. Aging-induced deterioration of trabecular bone architecture was partially reversed in EA rats. Runx2 and Osterix mRNA and protein levels were significantly increased and peroxisome proliferator-activated receptor (PPAR)γ was significantly decreased in bone marrow cells in EA compared with Aged groups. The mRNA and protein levels of core constituents of the Wnt/β-catenin signaling pathway (Wnt3a, low-density lipoprotein receptor-related protein (LRP)5 and β-catenin) were significantly increased and Dickkopf 1 was significantly decreased in bone marrow cells in EA compared with Aged groups. Conclusion: EA may prevent bone loss and deterioration in aged rats by promoting osteogenesis via a mechanism that may involve activation of the Wnt/β-catenin signaling pathway. EA may represent a therapeutic option for senile osteoporosis.
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