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Potential role of leptin against glucocorticoid-induced secondary osteoporosis in adult female rats

机译:瘦素对成年雌性大鼠糖皮质激素诱发的继发性骨质疏松症的潜在作用

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OBJECTIVES: The present study assessed the potential role of leptin administration in the protection and intervention against glucocorticoid-induced secondary osteoporosis in female rats. MATERIALS AND METHODS: For this purpose five groups of female Sprague Dawley rats were classified into: (1) negative control group in which the healthy rats received saline as vehicle, (2) a group orally administered with prednisolone (5 mg kg b.wt.-1) daily for six months (osteoporotic group), (3) a group subcutaneously administered with leptin (400 microg kg b.wt.-1) three times weekly for six months (positive control), (4) a group orally administered with prednisolone daily with simultaneous subcutaneous administration of leptin three times weekly for six months (protective group), and (5) a group orally administered with prednisolone daily for six months then subcutaneously administered with leptin three times weekly for other six months (therapeutic group). RESULTS: The obtained data revealed that prednisolone administration resulted in significant decrease in serum osteoprotegerin (OPG) level accompanied with significant increase in serum receptor activator of nuclear factor-κB ligand (RANKL) and beta2-microglobulin levels in comparison with the negative control group. Moreover, prednisolone significantly decreased bone mineral density and content of different areas of the right femur bones as compared to the negative control group. Furthermore, administration of leptin with/after stopping prednisolone administration resulted in a marked modulation in the majority of bone biomarkers as well as improvement in bone mineral density and content. CONCLUSIONS: Leptin provided promising effect on bone through its direct action on bone and matrix mineralization.
机译:目的:本研究评估了瘦素给药在雌性大鼠糖皮质激素诱导的继发性骨质疏松症的保护和干预中的潜在作用。材料与方法:为此,将五组Sprague Dawley雌性大鼠分为:(1)阴性对照组,健康大​​鼠接受生理盐水作为媒介;(2)口服泼尼松龙(5 mg kg b.wt)。 .-1)每天六个月(骨质疏松症组),(3)每周三次皮下注射瘦素(40​​0 microg kg b.wt.-1)的组,六个月一次(阳性对照组),(4)口服一组每天一次泼尼松龙,同时每周三次皮下注射瘦素,持续六个月(保护组);(5)每天一次口服泼尼松龙,一次连续六个月,然后皮下注射瘦素,其余六个月,连续六个月(治疗组) )。结果:与阴性对照组相比,泼尼松龙的给药导致血清骨保护素(OPG)水平显着降低,同时血清核因子-κB配体受体激活剂(RANKL)和β2-微球蛋白水平显着增加。此外,与阴性对照组相比,泼尼松龙可显着降低右股骨不同区域的骨矿物质密度和含量。此外,在泼尼松龙停药后/停止使用瘦素后,大多数骨生物标志物均发生显着调节,并改善了骨矿物质密度和含量。结论:瘦素通过直接作用于骨骼和基质矿化作用而对骨骼产生有希望的作用。

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