Department of Spinal Surgery, Nanfang Hospital, Southern Medical University, 1838 North Guangzhou Avenue, Guangzhou, 510515, China.
Department of Spinal Surgery, The Second Affiliated Hospital of Luohe Medical College, Luohe, Henan, China.
Calcif Tissue Int. 2019 Jan;104(1):59-69. doi: 10.1007/s00223-018-0468-3. Epub 2018 Aug 22.
Metformin (Met), an anti-diabetes drug, has also shown therapeutic effects for ovariectomy-induced (OVX) osteoporosis. However, similar effects against bone loss induced by a ketogenic diet (KD) have not been tested. This study was aimed to evaluate the microarchitectures and biomechanics of KD-induced osteoporosis with and without administration of Met, and compare the effect of Met on bone loss induced by KD with OVX. Forty female C57BL/6J mice were randomly divided into Sham, OVX, OVX + Met (100 mg/kg/day), KD (3:1 ratio of fat to carbohydrate and protein), and KD + Met (100 mg/kg/day) groups. After 12 weeks, the bone mass and biomechanics were measured in distal cancellous bone and in mid-shaft cortical bone of the femur. The activities of serum alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRAP), together with immunohistochemistry staining of osteocalcin (OCN) and TRAP, were evaluated. Both OVX and KD induced significant bone loss and compromised biomechanical properties in the cancellous bone, but no effect was found in cortical bone. The administration of Met increased the cancellous bone volume fraction (BV/TV) from 3.78 to 5.23% following the OVX and from 4.04 to 6.33% following the KD, it also enhanced the compressive stiffness from 47 to 160 N/mm following the OVX and from 35 to 340 N/mm with the KD. Met effectively increased serum ALP in the KD group while decreased serum TRAP in the OVX group, but up-regulated expression of OCN and down-regulated expression of TRAP in both OVX and KD groups. The present study demonstrated that Met effectively attenuated the cancellous bone loss induced by KD and maintained the biomechanical properties of long bones, providing evidence for Met as a treatment of by KD-induced osteoporosis in teenage skeleton.
二甲双胍(Met)是一种抗糖尿病药物,也显示出对去卵巢(OVX)诱导的骨质疏松症的治疗效果。然而,尚未测试其对生酮饮食(KD)引起的骨丢失的类似作用。本研究旨在评估 KD 诱导的骨质疏松症以及给予 Met 治疗时的微结构和生物力学,并比较 Met 对 KD 诱导的骨丢失和 OVX 的影响。将 40 只 C57BL/6J 雌性小鼠随机分为 Sham、OVX、OVX+Met(100mg/kg/天)、KD(脂肪与碳水化合物和蛋白质的比例为 3:1)和 KD+Met(100mg/kg/天)组。12 周后,测量股骨远端松质骨和中段皮质骨的骨量和生物力学。评估血清碱性磷酸酶(ALP)和抗酒石酸酸性磷酸酶(TRAP)的活性,以及骨钙素(OCN)和 TRAP 的免疫组织化学染色。OVX 和 KD 均导致松质骨骨量显著丢失和生物力学性能受损,但对皮质骨无影响。Met 的给予使 OVX 后松质骨的体积分数(BV/TV)从 3.78%增加到 5.23%,KD 后从 4.04%增加到 6.33%,使 OVX 后压缩刚度从 47N/mm 增加到 160N/mm,KD 后从 35N/mm 增加到 340N/mm。Met 有效增加了 KD 组的血清 ALP,降低了 OVX 组的血清 TRAP,但上调了 OVX 和 KD 两组的 OCN 表达,下调了 TRAP 表达。本研究表明,Met 有效减轻了 KD 引起的松质骨丢失,并维持了长骨的生物力学性能,为 Met 治疗青少年骨骼 KD 诱导的骨质疏松症提供了证据。