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Effects of d-003, a new hypocholesterolaemic and antiplatelet compound, on lipid profile and lipid peroxidation in healthy volunteers.新型调血脂、抗血小板化合物 d-003 对健康志愿者血脂谱和脂质过氧化的影响。
Clin Drug Investig. 2003;23(3):193-203. doi: 10.2165/00044011-200323030-00005.
2
Management of avascular necrosis of femoral head at pre-collapse stage.股骨头缺血性坏死塌陷前期的治疗
Indian J Orthop. 2009 Jan;43(1):6-16. doi: 10.4103/0019-5413.45318.
3
Risk factors for developing osteonecrosis after prophylaxis in steroid-treated rabbits.类固醇治疗兔预防性治疗后发生骨坏死的危险因素。
J Rheumatol. 2008 Dec;35(12):2391-4. doi: 10.3899/jrheum.080416. Epub 2008 Nov 1.
4
Treatment of early stage osteonecrosis of the femoral head.早期股骨头坏死的治疗
J Bone Joint Surg Am. 2008 Nov;90 Suppl 4:175-87. doi: 10.2106/JBJS.H.00671.
5
The effects of alendronate in the treatment of experimental osteonecrosis of the hip in adult rabbits.阿仑膦酸盐对成年兔实验性股骨头坏死的治疗作用。
Osteoarthritis Cartilage. 2009 Mar;17(3):362-70. doi: 10.1016/j.joca.2008.07.013. Epub 2008 Sep 10.
6
Lovastatin inhibits adipogenesis and prevents osteonecrosis in steroid-treated rabbits.洛伐他汀可抑制类固醇治疗兔的脂肪生成并预防骨坏死。
Joint Bone Spine. 2008 Dec;75(6):696-701. doi: 10.1016/j.jbspin.2007.12.008. Epub 2008 Jul 11.
7
Long-term effects of D-003, a mixture of high molecular weight acids from sugarcane wax, on bones of ovariectomized rats: a one year study.甘蔗蜡中高分子量酸混合物D-003对去卵巢大鼠骨骼的长期影响:一项为期一年的研究。
Pharmazie. 2008 Jun;63(6):486-8.
8
Preventive effects of puerarin on alcohol-induced osteonecrosis.葛根素对酒精性骨坏死的预防作用。
Clin Orthop Relat Res. 2008 May;466(5):1059-67. doi: 10.1007/s11999-008-0178-7. Epub 2008 Mar 19.
9
[Oxidative stress on idiopathic osteonecrosis].[氧化应激与特发性骨坏死]
Clin Calcium. 2007 Jun;17(6):887-91.
10
[Animal models for steroid-induced osteonecrosis].[类固醇诱导性骨坏死的动物模型]
Clin Calcium. 2007 Jun;17(6):879-86.

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.

PMID:24250554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3813174/
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。