Liu Lei, Guo Yuan-hui, Xin Hai-liang, Nie Yan, Han Ting, Qin Lu-ping, Zhang Qiao-yan
Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Zhong Xi Yi Jie He Xue Bao. 2012 Dec;10(12):1419-26. doi: 10.3736/jcim20121214.
To evaluate the antiosteoporotic effects of benzyl benzoate glucosides from Curculigo orchioides (COBG) in ovariectomized (OVX) rats.
A total of 70 female Sprague-Dawley rats were assigned to sham-operated and OVX model groups. The OVX rats were further divided into six subgroups treated by gavage with vehicle, 1 mg/kg of nylestriol, 6, 18 and 54 mg/kg of COBG and 3.0 g/kg of ethanol extract of Curculigo orchioides respectively for 12 weeks. Bone mineral density (BMD) was measured by dual-energy X-ray absorptiometry. The sections of tibia were prepared for histomorphometric analysis. The biomarkers in serum and urine were determined using reagent kits.
Ovariectomy induced the bone loss and microarchitectural deterioration of bone tissue with the activities of increased serum alkaline phosphatase and loss of calcium through the excretion in urine, and decreased levels of antioxidant in serum (P<0.05, P<0.01). Administration of 6, 18 and 54 mg/kg of COBG significantly increased the BMD, improved the microarchitecture of bone tissue, prevented the depletion of antioxidant enzymes like superoxide dismutase and glutathione peroxidase, inhibited the increase of malondialdehyde in serum and reduced the excretion of urine calcium in OVX rats (P<0.05, P<0.01).
COBG could prevent the bone loss through improving the antioxidant status, which offers a potential new therapeutic drug for postmenopausal osteoporosis.
评价仙茅苯甲酸苄酯糖苷(COBG)对去卵巢(OVX)大鼠的抗骨质疏松作用。
将70只雌性Sprague-Dawley大鼠分为假手术组和OVX模型组。将OVX大鼠进一步分为6个亚组,分别灌胃给予溶媒、1 mg/kg尼尔雌醇、6、18和54 mg/kg COBG以及3.0 g/kg仙茅乙醇提取物,持续12周。采用双能X线吸收法测量骨密度(BMD)。制备胫骨切片用于组织形态计量学分析。使用试剂盒测定血清和尿液中的生物标志物。
去卵巢导致骨组织骨量丢失和微结构破坏,血清碱性磷酸酶活性增加,尿钙排泄导致钙流失,血清抗氧化剂水平降低(P<0.05,P<0.01)。给予6、18和54 mg/kg COBG可显著增加OVX大鼠的BMD,改善骨组织微结构,防止超氧化物歧化酶和谷胱甘肽过氧化物酶等抗氧化酶的消耗,抑制血清丙二醛的增加,并减少尿钙排泄(P<0.05,P<0.01)。
COBG可通过改善抗氧化状态预防骨丢失,为绝经后骨质疏松症提供了一种潜在的新型治疗药物。