首页> 外文期刊>Revista Brasileira de Ortopedia >Perfil biométrico, histomorfométrico e bioquímico no tratamento com atorvastatina cálcica de ratas com osteoporose induzida com dexametasona
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Perfil biométrico, histomorfométrico e bioquímico no tratamento com atorvastatina cálcica de ratas com osteoporose induzida com dexametasona

机译:阿托伐他汀钙治疗地塞米松致骨质疏松大鼠的生物特征,组织形态和生化特征

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Objective To assess the effects of atorvastatin calcium in the treatment of dexamethasone‐induced osteoporosis. Methods Osteoporosis induction consisted of the administration of an intramuscular dose of 7.5?mg/kg of body weight of dexamethasone, once a week for four weeks, except for the control animals (G1). The animals were divided into the following groups: G1 (control group without osteoporosis), G2 (control group with untreated osteoporosis), G3 (control group with osteoporosis treated with sodium alendronate 0.2?mg/kg) and G4 (group with osteoporosis treated with atorvastatin calcium 1.2?mg/kg). Serum alkaline phosphatase, bone alkaline phosphatase, and biometric and bone histomorphometric assessments were performed after 30 and 60 days of treatment onset. Results In relation to the biometric and histomorphometric analyses, at 60 days of treatment, G4 presented bone density (Seedor index), bone trabecular density, and cortical thickness of 0.222 ± 0.004?g/cm, 59.167 ± 2.401%, and 387,501 ± 8,573?μm, respectively, with a positive and statistically significant difference (p 0.05), in relation to G2. At 30 and 60 days of treatment, G4 presented statistically significant serum levels of alkaline phosphatase alkaline phosphatase (p 0.05) that were higher than all groups (7.451 ± 0.173?μg/L and 7.473 ± 0.529?μg/L, respectively). Conclusion Treatment with atorvastatin calcium demonstrated the ability of this drug to increase osteoblastic activity and bone tissue repair activity, acting differently from alendronate sodium, which demonstrated predominantly antirebsorptive activity.
机译:目的评估阿托伐他汀钙在地塞米松诱发的骨质疏松症中的作用。方法诱导骨质疏松包括:肌肉注射剂量为7.5?mg / kg体重的地塞米松,每周一次,连续4周,对照组(G1)除外。将动物分为以下各组:G1(无骨质疏松症的对照组),G2(未治疗骨质疏松症的对照组),G3(骨质疏松症的对照组用阿仑膦酸钠0.2?mg / kg治疗)和G4(骨质疏松症的组用盐酸阿司匹林治疗)阿托伐他汀钙1.2?mg / kg)。在开始治疗30天和60天后进行血清碱性磷酸酶,骨碱性磷酸酶以及生物测定和骨组织形态测定评估。结果关于生物特征和组织形态分析,在治疗60天时,G4的骨密度(Seedor指数),骨小梁密度和皮质厚度分别为0.222±0.004?g / cm,59.167±2.401%和387,501±8,573相对于G2,μμm分别具有正和统计学显着性差异(p <0.05)。在治疗的30天和60天时,G4的血清碱性磷酸酶碱性磷酸酶水平具有统计学意义(p <0.05),高于所有组(分别为7.541±0.173?μg/ L和7.473±0.529?μg/ L)。结论阿托伐他汀钙治疗证明该药具有增强成骨活性和骨组织修复活性的能力,其作用不同于阿仑膦酸钠,后者主要表现出抗吸收活性。

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