Kittivanichkul Donlaporn, Charoenphandhu Narattaphol, Khemawoot Phisit, Malaivijitnond Suchinda
Department of BiologyFaculty of Science, Chulalongkorn University, Bangkok, Thailand.
Center of Calcium and Bone Research (COCAB)Faculty of Science, Mahidol University, Bangkok, Thailand.
J Endocrinol. 2016 Nov;231(2):121-133. doi: 10.1530/JOE-16-0277. Epub 2016 Sep 6.
Since the in vitro and in vivo anti-osteoporotic effects of Pueraria mirifica (PM) in rodents have been verified, its activity in menopausal monkeys was evaluated as required before it can be applicable for human use. In this study, postmenopausal osteoporotic monkeys were divided into two groups (five per group), and fed daily with standard diet alone (PMP0 group) or diet mixed with 1000 mg/kg body weight (BW) of PM powder (PMP1000 group) for 16 months. Every 2 months, the bone mineral density (BMD), bone mineral content (BMC) and bone geometry parameters (cortical area and thickness and periosteal and endosteal circumference) at the distal radius and proximal tibia were determined using peripheral quantitative computed tomography together with plasma and urinary bone markers. Compared with the baseline (month 0) values, the cortical, but not trabecular, BMDs and BMCs and the cortical area and thickness at the metaphysis and diaphysis of the radius and tibia of the PMP0 group continuously decreased during the 16-month study period. In contrast, PMP1000 treatment ameliorated the bone loss mainly at the cortical diaphysis by decreasing bone turnover, as indicated by the lowered plasma bone-specific alkaline phosphatase and osteocalcin levels. Generally, changes in the cortical bone geometry were in the opposite direction to the cortical bone mass after PMP1000 treatment. This study indicated that postmenopausal monkeys continuously lose their cortical bone compartment, and they have a higher possibility for long bone fractures. Oral PMP treatment could improve both the bone quantity (BMC and BMD) and quality (bone geometry).
由于葛根提取物(PM)在啮齿动物体内外的抗骨质疏松作用已得到验证,因此在其可应用于人类之前,需按要求评估其在绝经后猴子体内的活性。在本研究中,将绝经后骨质疏松猴子分为两组(每组五只),一组每天仅喂食标准饮食(PMP0组),另一组每天喂食含1000mg/kg体重PM粉末的饮食(PMP1000组),持续16个月。每2个月,使用外周定量计算机断层扫描技术测定桡骨远端和胫骨近端的骨密度(BMD)、骨矿物质含量(BMC)以及骨几何参数(皮质面积、厚度、骨膜和骨髓腔周长),同时检测血浆和尿液中的骨标志物。与基线(第0个月)值相比,在16个月的研究期间,PMP0组桡骨和胫骨干骺端及骨干的皮质骨(而非小梁骨)BMD、BMC、皮质面积和厚度持续下降。相比之下,PMP1000治疗通过降低骨转换改善了主要在皮质骨干处的骨质流失,血浆骨特异性碱性磷酸酶和骨钙素水平降低表明了这一点。一般来说,PMP1000治疗后皮质骨几何形状的变化与皮质骨量的变化方向相反。本研究表明,绝经后猴子的皮质骨持续流失,发生长骨骨折的可能性更高。口服PMP治疗可改善骨量(BMC和BMD)和骨质量(骨几何形状)。