Grapefruit juice exerts anti-osteoporotic activities in a prednisolone-induced osteoporosis rat femoral fracture model, possibly via the RANKL/OPG axis.

Bone density Grapefruit juice Osteoprotegerin Plasma alkaline phosphatase Ultrastructure

Journal

Cytotechnology
ISSN: 0920-9069
Titre abrégé: Cytotechnology
Pays: United States
ID NLM: 8807027

Informations de publication

Date de publication:
30 May 2019
Historique:
received: 13 08 2018
accepted: 26 05 2019
entrez: 1 6 2019
pubmed: 31 5 2019
medline: 31 5 2019
Statut: aheadofprint

Résumé

This study aimed to shed light on the protective and therapeutic anti-osteoporotic effects and mechanisms of action of grapefruit juice (GFJ) on prednisolone-induced osteoporosis a rat femoral fracture model. We found that treating rats with GFJ before and/or after prednisolone-induced osteoporosis resulted in increased bone density, total mineral content, and calcium content to counteract the osteoporotic effects of prednisolone. In parallel, the histological and ultrastructural results of the GFJ-treated groups correlated well with enhanced breaking strength of femurs subjected to a constant load. Furthermore, GFJ treatment before and after prednisolone-induced osteoporosis decreased plasma alkaline phosphatase and tartrate-resistant acid phosphatase activities and increased the level of insulin-like growth factor 1. Mechanistically, our immunohistochemistry study showed that GFJ ameliorated prednisolone-induced osteocalcin depletion, decreased receptor activator of nuclear factor kappa-B ligand (RANKL) expression, and increased osteoprotegerin (OPG) expression. GFJ showed a beneficial anti-osteoporotic effect against prednisolone-induced osteoporosis in rats, possibly via the RANKL/OPG axis, suggesting that GFJ might be a good candidate for developing anti-osteoporotic drugs.

Identifiants

pubmed: 31147813
doi: 10.1007/s10616-019-00321-6
pii: 10.1007/s10616-019-00321-6
pmc: PMC6663959
doi:

Types de publication

Journal Article

Langues

eng

Pagination

769-783

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Auteurs

Eslam Muhammad Bastawy (EM)

Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan. eslam-bastawy@hiroshima-u.ac.jp.
Zoology Department, Faculty of Science, Ain Shams University, Cairo, Egypt. eslam-bastawy@hiroshima-u.ac.jp.

Rasha Rashad Ahmed (RR)

Zoology Department, Faculty of Science, Beni-Seuif University, Beni Suef, Egypt.

Amer Ali Abd El-Hafeez (AA)

Pharmacology and Experimental Oncology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt. amer.ali@nci.cu.edu.eg.
Department of Cellular and Molecular Medicine, School of medicine, University of California, San Diego, La Jolla, CA, USA. amer.ali@nci.cu.edu.eg.

Fatma Kamal Abd El-Hady (FK)

Zoology Department, Faculty of Science, Ain Shams University, Cairo, Egypt.

Toru Hosoi (T)

Pharmacotherapy Department, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Koichiro Ozawa (K)

Pharmacotherapy Department, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Monir Ali El-Ganzuri (MA)

Zoology Department, Faculty of Science, Ain Shams University, Cairo, Egypt.

Classifications MeSH