Effects of Donepezil on the Musculoskeletal System in Female Rats

Int J Mol Sci. 2023 May 19;24(10):8991. doi: 10.3390/ijms24108991.

Abstract

The extension of human life makes it more and more important to prevent and treat diseases of the elderly, including Alzheimer's disease (AD) and osteoporosis. Little is known about the effects of drugs used in the treatment of AD on the musculoskeletal system. The aim of the present study was to investigate the effects of donepezil, an acetylcholinesterase inhibitor, on the musculoskeletal system in rats with normal and reduced estrogen levels. The study was carried out on four groups of mature female rats: non-ovariectomized (NOVX) control rats, NOVX rats treated with donepezil, ovariectomized (OVX) control rats and OVX rats treated with donepezil. Donepezil (1 mg/kg p.o.) was administered for four weeks, starting one week after the ovariectomy. The serum concentrations of CTX-I, osteocalcin and other biochemical parameters, bone mass, density, mineralization, histomorphometric parameters and mechanical properties, and skeletal muscle mass and strength were examined. Estrogen deficiency increased bone resorption and formation and worsened cancellous bone mechanical properties and histomorphometric parameters. In NOVX rats, donepezil decreased bone volume to tissue volume ratio in the distal femoral metaphysis, increased the serum phosphorus concentration and tended to decrease skeletal muscle strength. No significant bone effects of donepezil were observed in OVX rats. The results of the present study indicate slightly unfavorable effects of donepezil on the musculoskeletal system in rats with normal estrogen levels.

Keywords: donepezil; estrogen deficiency; musculoskeletal system; osteoporosis; rats.

MeSH terms

  • Acetylcholinesterase*
  • Aged
  • Animals
  • Bone Density
  • Bone and Bones*
  • Donepezil / pharmacology
  • Estrogens / pharmacology
  • Female
  • Humans
  • Ovariectomy
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Donepezil
  • Acetylcholinesterase
  • Estrogens