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Electroacupuncture ameliorates subchondral bone deterioration and inhibits cartilage degeneration in ovariectomised rats. | LitMetric

AI Article Synopsis

  • The study aimed to assess the impact of electroacupuncture (EA) on bone mass and cartilage deterioration in a rat model of osteoarthritis created by ovariectomy (OVX).
  • Ninety female rats were divided into three groups: a control group, an OVX group without treatment, and an EA group receiving electroacupuncture following OVX, with various measurements taken over 12 weeks.
  • Results indicated that EA improved bone density and reduced cartilage degradation compared to the OVX group by influencing specific biochemical pathways, including increased osteoprotegerin (OPG) and decreased levels of MMP-13.

Article Abstract

Objectives: To investigate the effects of electroacupuncture (EA) on subchondral bone mass and cartilage degeneration in an experimental animal model of osteoarthritis (OA) induced by ovariectomy (OVX).

Methods: Ninety 3-month-old female Sprague-Dawley rats were randomly divided into the following three groups (n = 30 each): sham operation without treatment (control group); OVX without treatment (OVX group);, and ovariectomy with EA treatment (EA group). Rats in the EA group received EA treatment from the day of OVX. Ten rats in each group were randomly killed at 4, 8 and 12 weeks after operation.

Results: EA reduced urine C-terminal cross-linking telopeptide of type I collagen from 4 weeks after OVX, reduced C-terminal cross-linking telopeptide of type II collagen and body weight from 8 weeks after OVX, and increased serum 17β-oestradiol from 4 weeks after OVX compared with the OVX group (all p<0.01). In the EA group, trabecular bone volume ratio, trabecular thickness and trabecular number increased, and trabecular separation were reduced at each time point compared with the OVX group (p<0.05, p<0.01, respectively). In the EA group, osteoprotegerin (OPG) expression was increased and receptor activator of nuclear factor kappa-B ligand (RANKL) expression was reduced at each time point compared with the OVX group (p<0.05, p<0.01, respectively). Mankin scores and mRNA expression of matrix metalloproteinase-13 (MMP-13) were lower in EA versus OVX groups at 12 weeks after OVX (both p<0.01).

Conclusion: The results suggest that EA inhibits subchondral bone loss by regulating RANK/RANKL/OPG signalling and protects articular cartilage by inhibiting MMP-13 in OVX rats.

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Source
http://dx.doi.org/10.1136/acupmed-2016-011258DOI Listing

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