Munshi Renuka, Patil Tanvi, Garuda Chetan, Kothari Dushyant
Department of Clinical Pharmacology, TN Medical College and BYL Nair Charitable Hospital, Mumbai, Maharashtra, India.
National Centre for Nanomaterials & Nanotechnology, Department of Physics, University of Mumbai, Mumbai, Maharashtra, India.
Indian J Pharmacol. 2016 May-Jun;48(3):298-303. doi: 10.4103/0253-7613.182881.
The study was conducted to develop the glucocorticoid-induced osteoporosis (GIO) model in Sprague-Dawley weanling rats using different doses of methylprednisolone (MP) and evaluate the antiosteoporotic effect of a classical ayurvedic formulation, Panchatikta Ghrita (PG), in this model.
Institutional Animal Ethics Committee approval was obtained. Development of model was done by subcutaneous injection of 2 doses of MP (14 and 28 mg/kg/week) for 4 weeks in 21-day old weanlings. Following confirmation of the dose of MP that induced osteoporosis, the antiosteoporotic effect of PG was tested in this model in comparison to a known antiosteoporotic agent, alendronate. Both alendronate (2.9 mg/kg/day) and PG (1.35 g/kg/day) were administered orally 2 weeks after MP - 14 mg/kg/week injection and continued for 4 weeks. Serum and urine calcium and inorganic phosphate were analyzed at weekly intervals. Animals were sacrificed after 6 weeks, and femur bones were processed to measure bone hardness and elasticity and for histological studies.
Rats treated with MP - 14 mg/kg/week showed optimum osteoporotic effect with no mortality as compared to MP - 28 mg/kg/week; hence, this dose of MP was used further for the efficacy study. Osteoporotic rats treated with PG 1.35 g/kg showed increase in serum calcium and inorganic phosphate levels, whereas urine calcium and phosphate levels were significantly reduced. A significant decrease in a number of osteoclasts, whereas an increase in bone hardness and elasticity was observed as compared to diseased group demonstrating antiosteoporotic effect of PG.
PG has an antiosteoporotic effect in GIO rat model.
本研究旨在利用不同剂量的甲泼尼龙(MP)在斯普拉格-道利断奶大鼠中建立糖皮质激素诱导的骨质疏松症(GIO)模型,并评估一种经典阿育吠陀配方药潘查蒂卡塔酥油(PG)在此模型中的抗骨质疏松作用。
获得了机构动物伦理委员会的批准。在21日龄的断奶大鼠中,通过皮下注射2种剂量的MP(14和28毫克/千克/周),持续4周来建立模型。在确认诱导骨质疏松症的MP剂量后,在此模型中测试PG与一种已知抗骨质疏松药物阿仑膦酸钠相比的抗骨质疏松作用。在注射MP - 14毫克/千克/周2周后,口服给予阿仑膦酸钠(2.9毫克/千克/天)和PG(1.35克/千克/天),并持续4周。每周分析血清和尿液中的钙和无机磷。6周后处死动物,对股骨进行处理以测量骨硬度和弹性,并进行组织学研究。
与MP - 28毫克/千克/周相比,用MP - 14毫克/千克/周治疗的大鼠显示出最佳的骨质疏松症效果且无死亡;因此,该剂量的MP进一步用于疗效研究。用PG 1.35克/千克治疗的骨质疏松症大鼠血清钙和无机磷水平升高,而尿钙和磷水平显著降低。与患病组相比,破骨细胞数量显著减少,同时观察到骨硬度和弹性增加,证明了PG的抗骨质疏松作用。
PG在GIO大鼠模型中具有抗骨质疏松作用。