Protective effects of electroacupuncture on senile osteoporosis in rats.

Wnt/β-catenin signaling bone architecture bone loss electroacupuncture osteoporosis

Journal

Acupuncture in medicine : journal of the British Medical Acupuncture Society
ISSN: 1759-9873
Titre abrégé: Acupunct Med
Pays: England
ID NLM: 9304117

Informations de publication

Date de publication:
26 Oct 2024
Historique:
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 26 10 2024
Statut: aheadofprint

Résumé

The objectives were to explore the protective effects of electroacupuncture (EA) on senile osteoporosis in aged rats and investigate the underlying mechanisms. 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. 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. 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.

Identifiants

pubmed: 39460675
doi: 10.1177/09645284241280089
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9645284241280089

Déclaration de conflit d'intérêts

Declaration of conflicting interestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Jun Zhou (J)

Department of Rehabilitation Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Jinling Wang (J)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Mengjian Qu (M)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Qian Wang (Q)

Department of Rehabilitation Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.

Liqiong Wang (L)

Department of Rehabilitation Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.

Sijia Liu (S)

Department of Rehabilitation Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.

Jing Liu (J)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Guanghua Sun (G)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Peirui Zhong (P)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Xiarong Huang (X)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Danni Liu (D)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Linwei Yin (L)

The First Affiliated Hospital, Department of Rehabilitation, Hengyang Medical School, University of South China, Hengyang, China.
The First Affiliated Hospital, Rehabilitation Laboratory, Hengyang Medical School, University of South China, Hengyang, China.

Chengqi He (C)

Department of Rehabilitation Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
Key Laboratory of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.

Classifications MeSH