Noa Miriam, Valle M, Mendoza Sarahí, Mas Rosa, Mendoza Nilda
Department of Pharmacology, Laboratory of Histology, Center of Natural Products, National Center for Scientific Research, P.O. Box 6990, Havana City, Cuba.
Indian J Pharm Sci. 2011 Sep;73(5):537-42. doi: 10.4103/0250-474X.99003.
D-003, a mixture of high molecular weight acids, inhibits cholesterol synthesis prior to mevalonate and prevents osteoporosis induced by ovariectomy in rats, and both osteoporosis and osteonecrosis induced by corticoids in rats. The aim of this study was to investigate effects of D-003 on lipopolysaccharides-induced osteonecrosis in rabbits. Animals were randomized into 5 groups: a sham and four groups injected with lipopolysaccharides: one treated orally with vehicle and three with D-003 (5, 25 and 200 mg/kg, respectively) during four weeks. We assessed the effects of treatments on the incidence of osteonecrosis (number of animals with osteonecrosis lesions/animals per group), the mean numbers and areas of osteonecrosis per animal and on the mean sizes of the bone marrow fat cells. The incidence of osteonecrosis in the groups of D-003 25 and 200 mg/kg was significantly lower than in the positive controls. The reduction of osteonecrosis increased with the doses, but significant dose-dependence relationship was not achieved. D-003 significantly and dose-dependently decreased the number of osteonecrosis lesions per animal as compared to the positive controls. Likewise, the mean osteonecrosis areas in the proximal femoral and humeral bones were significantly decreased by D-003. The injection of lipopolysaccharides significantly increased the average size of bone marrow fat cells as compared to the negative controls, and such increase was significantly and markedly reduced with D-003. It is concluded that D-003 reduced the incidence, number and percent areas of osteonecrosis lesions, and the size of bone marrow fat cells, a marker of adipogenesis, in rabbits with lipopolysaccharides-induced ostenonecrosis.
D-003是一种高分子量酸的混合物,在甲羟戊酸之前抑制胆固醇合成,并预防大鼠卵巢切除诱导的骨质疏松以及大鼠皮质激素诱导的骨质疏松和骨坏死。本研究的目的是调查D-003对脂多糖诱导的兔骨坏死的影响。将动物随机分为5组:假手术组和4个注射脂多糖的组:一组口服赋形剂,另外三组在四周内分别给予D-003(5、25和200mg/kg)。我们评估了治疗对骨坏死发生率(有骨坏死病变的动物数量/每组动物数量)、每只动物骨坏死的平均数量和面积以及骨髓脂肪细胞平均大小的影响。D-003 25mg/kg组和200mg/kg组的骨坏死发生率显著低于阳性对照组。骨坏死的减少随剂量增加,但未达到显著的剂量依赖性关系。与阳性对照组相比,D-003显著且剂量依赖性地减少了每只动物的骨坏死病变数量。同样,D-003使股骨近端和肱骨的平均骨坏死面积显著减少。与阴性对照组相比,注射脂多糖显著增加了骨髓脂肪细胞的平均大小,而D-003显著且明显地降低了这种增加。结论是,D-003降低了脂多糖诱导的骨坏死兔的骨坏死病变的发生率、数量和面积百分比以及骨髓脂肪细胞的大小(脂肪生成的标志物)。