ANTIOSTEOPOROTIC ACTIVITY OF ANTHRAQUINONE ISOLATED FROM MORINDA CITRIFOLIA FRUITS IN RATS

Authors

  • Abin Joy PG SCHOLAR, PES COLLEGE OF PHARMACY
  • Chaitra N
  • Ashok M
  • Handral M

DOI:

https://doi.org/10.22159/ajpcr.2016.v9i5.13269

Abstract

Objectives: This study was designed to investigate the antiosteoporotic activity of isolated anthraquinones from Morinda citrifolia fruit extract in
ovariectomy (OVX) induced osteoporotic rats.

Methods: All the rats were divided into 4 groups (n=6 each). Group I (sham control) received vehicle, p.o., Group II OVX control (vehicle, p.o.),
Group III was OVX+standard raloxifene (5.4 mg/kg, p.o.), and Group IV was OVX+Physcion (100 mg/kg, p.o.) for 90 days.

Results: The daily oral administration of isolated compound physcion (100 mg/kg) for 12 weeks to the rats prevented OVX-induced osteoporosis.
This was examined by serum biomarkers such as alkaline phosphatase, calcium, and tartrate resistant acid phosphatase and showed significant
effects (p<0.0001). The femur bone strength assessed by three-point bending test showed improved bone strength in physcion treated rats, and
this was supported by enhanced bone mineral density (p<0.05). The ash parameters of femur bone studied from physcion treated rats exhibited a
significant (p<0.0001) value of ash weight followed by ash calcium content. Further, femur bone histological examination revealed the protective
effect of the compound physcion (100 mg/kg) against OVX-induced bone loss in rats, where it showed mineralization of trabecular spaces, improved
bone compactness thereby intact bone architecture.
Conclusion: This study concludes that the isolated anthraquinone physcion had a preventive effect against OVX-induced bone loss in rats.

Keywords: Morinda citrifolia, Physcion, Osteoporosis, Bone mineral density, Ash mineral content.

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Published

01-09-2016

How to Cite

Joy, A., C. N, A. M, and H. M. “ANTIOSTEOPOROTIC ACTIVITY OF ANTHRAQUINONE ISOLATED FROM MORINDA CITRIFOLIA FRUITS IN RATS”. Asian Journal of Pharmaceutical and Clinical Research, vol. 9, no. 5, Sept. 2016, pp. 209-13, doi:10.22159/ajpcr.2016.v9i5.13269.

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