Electroacupuncture ameliorates senile osteoporosis by promoting bone remodeling and regulating autophagy

老年性骨质疏松症 医学 骨质疏松症 骨重建 内科学 内分泌学 骨矿物 自噬 电针 骨细胞 N-末端末端肽 股骨 骨吸收 骨钙素 病理 成骨细胞 针灸科 外科 碱性磷酸酶 化学 替代医学 体外 细胞凋亡 生物化学
作者
Jing Liu,Jun Zhou,Jinlin Wang,Xiarong Huang,Mengjian Qu,Ying Liao,Guanghua Sun,Peirui Zhong,Jinqu Tan,Zhilu Sun
出处
期刊:Acupuncture in Medicine [SAGE Publishing]
卷期号:42 (5): 260-267 被引量:5
标识
DOI:10.1177/09645284241265872
摘要

OBJECTIVES: Osteoporosis is widely regarded as a typical aged-related disease caused by impaired bone remodeling. This research was designed to explore the protective effects of electroacupuncture (EA) on senile osteoporosis in a rat model and investigate the underlying mechanisms. METHODS: Three-month-old rats were randomly selected as the youth group, and 24-month-old rats were randomly assigned to the elderly and EA groups. Rats in the EA group received 30 min of EA at bilateral SP10, ST36, K13 and GB34 daily, 5 days a week for 8 weeks. Bone mineral density (BMD), microstructure of the bone tissue, bone turnover biomarkers and expression level of autophagy-related proteins were detected. RESULTS: Compared with the elderly group, EA treatment significantly increased BMD of the femur and ameliorated the microstructure. EA treatment increased trabecular bone volume ratio (= bone volume / total volume [BV/TV]) and trabecular number (Tb.N) and decreased trabecular separation (Tb.Sp) in senile osteoporosis rats. Compared with the elderly group, the serum N-terminal telopeptide of type I collagen (NTX1) level in the EA group was lower, and the serum procollagen type I N-terminal propeptide (PINP) concentration was higher. In addition, the expression of Beclin 1, microtubule-associated protein I light chain 3 (LC3B) and P62 was inhibited in the senile osteoporosis rats after EA treatment. CONCLUSIONS: EA can effectively alleviate aging-related bone loss and improve the microstructure of bone tissue in senile osteoporosis rats, and the regulation of autophagy might be one of the important mechanisms.
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