Bastawy Eslam Muhammad, Ahmed Rasha Rashad, Abd El-Hafeez Amer Ali, Abd El-Hady Fatma Kamal, Hosoi Toru, Ozawa Koichiro, El-Ganzuri Monir Ali
Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Zoology Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
Cytotechnology. 2019 May 30;71(4):769-783. doi: 10.1007/s10616-019-00321-6.
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.
本研究旨在阐明葡萄柚汁(GFJ)对泼尼松龙诱导的大鼠股骨骨折骨质疏松模型的保护和治疗性抗骨质疏松作用及作用机制。我们发现,在泼尼松龙诱导骨质疏松之前和/或之后用GFJ处理大鼠,可提高骨密度、总矿物质含量和钙含量,以抵消泼尼松龙的骨质疏松作用。同时,GFJ处理组的组织学和超微结构结果与承受恒定负荷的股骨增强的断裂强度密切相关。此外,在泼尼松龙诱导骨质疏松之前和之后进行GFJ处理,可降低血浆碱性磷酸酶和抗酒石酸酸性磷酸酶活性,并提高胰岛素样生长因子1水平。从机制上讲,我们的免疫组织化学研究表明,GFJ改善了泼尼松龙诱导的骨钙素耗竭,降低了核因子κB受体活化因子配体(RANKL)表达,并增加了骨保护素(OPG)表达。GFJ对泼尼松龙诱导的大鼠骨质疏松具有有益的抗骨质疏松作用,可能是通过RANKL/OPG轴实现的,这表明GFJ可能是开发抗骨质疏松药物的良好候选物。