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高分子量脂肪酸混合物D-003对糖皮质激素和脂多糖(LPS)诱导的骨坏死的影响。

Effect of D-003, a Mixture of High Molecular Weight Aliphatic Acids, on Glucocorticoid- and Lipopolysaccharides (LPS)-Induced Osteonecrosis.

作者信息

Noa Miriam, Más Rosa, Valle Maikel, Mendoza Sarahí, Mendoza Nilda

机构信息

Center of Natural Products from the National Center for Scientific Research, Havana City, Cuba.

出版信息

Iran J Pharm Res. 2012 Fall;11(4):1201-8.

Abstract

Osteonecrosis (ON) is characterized through the impairment of osseous blood flow that leads to the collapse of femur head. Corticoid-induced ON in rats and lipopolysaccharide (LPS)-induced in rabbits are useful models to assess the efficacy of potential treatments on this disease. D-003 inhibits the mevalonate pathway, lipid peroxidation and prevents osteoporosis in rats through increasing the osteoclast apoptosis. This study investigated the effects of D-003 on corticoid- and LPS-induced ON in rats and rabbits. Corticoid-induced ON: Rats were randomized into five groups. A negative control and four groups treated with prednisolone 6 mg/Kg: a positive control and three treated with D-003 (5, 25 and 200 mg/Kg) for 80 days. All positive controls presented ON areas. D-003 significantly reduced the numbers and proportions of ON lesions, as compared to the positive control group. LPS-induced ON in rabbits: Rabbits were randomized into five groups: a negative control and four injected with a single intra-venous injection of LPS (10 μg/Kg) including a positive control and three with D-003 (5, 25 and 200 mg/Kg) for 30 days. ON was seen in all positive controls. The incidence of ON and the number of ON lesions in the groups treated with D-003 (25 and 200 mg/Kg) was significantly lower compared to the positive controls. LPS injection significantly increased the size of bone marrow fat cells in positive controls and such increase was significantly decreased by D-003. In conclusion, D-003 reduced ON lesions in corticoid-and LPS-induced ON and also the size of bone marrow fat cells in rabbits with LPS.

摘要

骨坏死(ON)的特征是骨血流受损,导致股骨头塌陷。大鼠的皮质类固醇诱导型ON和兔子的脂多糖(LPS)诱导型ON是评估潜在治疗方法对该疾病疗效的有用模型。D-003抑制甲羟戊酸途径、脂质过氧化,并通过增加破骨细胞凋亡来预防大鼠骨质疏松。本研究调查了D-003对大鼠和兔子皮质类固醇诱导型和LPS诱导型ON的影响。皮质类固醇诱导型ON:将大鼠随机分为五组。一个阴性对照组和四组用泼尼松龙6mg/Kg治疗:一个阳性对照组和三组用D-003(5、25和200mg/Kg)治疗80天。所有阳性对照组均出现ON区域。与阳性对照组相比,D-003显著减少了ON病变的数量和比例。兔子的LPS诱导型ON:将兔子随机分为五组:一个阴性对照组和四组单次静脉注射LPS(10μg/Kg),包括一个阳性对照组和三组用D-003(5、25和200mg/Kg)治疗30天。所有阳性对照组均出现ON。与阳性对照组相比,用D-003(25和200mg/Kg)治疗的组中ON的发生率和ON病变的数量显著降低。LPS注射显著增加了阳性对照组骨髓脂肪细胞的大小,而D-003显著降低了这种增加。总之,D-003减少了皮质类固醇和LPS诱导型ON中的ON病变,也减少了LPS诱导的兔子骨髓脂肪细胞的大小。

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