Animal Biochemistry Division, ICAR-National Dairy Research Institute, Karnal, India; Department of Biochemistry, Ahmadu Bello University, Zaria, Nigeria.
Animal Biochemistry Division, ICAR-National Dairy Research Institute, Karnal, India.
Nutrition. 2017 Nov-Dec;43-44:21-31. doi: 10.1016/j.nut.2017.06.010. Epub 2017 Jul 10.
Oxidative stress has been implicated as a crucial pathogenic factor in the development of postmenopausal osteoporosis. Milk-derived antioxidative peptides are gaining much attention toward the development of prodrugs for alleviating several human diseases, including osteoporosis. The aim of the present study was to determine whether antioxidant peptides are good candidates for alleviating postmenopausal osteoporosis.
In the present study, an ovariectomized (OVX) osteoporotic rat model was used to investigate the protective effects of buffalo milk casein-derived novel peptide VLPVPQK (PEP) against OVX-induced bone loss and the related mechanisms.
Results of the present study indicated that daily administration of antioxidative peptide PEP at 50 and 100 μg/kg for 8 wk prevents body weight gain, uterine weight loss, and atrophy of endometrial lumen. Moreover, PEP increased femur dry weight, ash weight, bone ash calcium, and serum calcium and phosphorus level. Interestingly, PEP increased bone mineral density and improved trabecular microarchitecture in both femur and tibia of OVX rats. Additionally, PEP increased bone strength, reduced serum bone turnover markers, inhibited bone resorbing cytokines and decreased malondialdehyde level in OVX rat. Furthermore, PEP-elevated serum transforming growth factor-β, increased, reduced glutathione levels, superoxide dismutase, and catalase activity altered by OVX.
We demonstrated that PEP exhibits antiosteopenic effects via enhancement of antioxidant activity and reduction of bone-resorbing cytokines expression.
氧化应激被认为是绝经后骨质疏松症发展的关键致病因素。乳源抗氧化肽在开发治疗包括骨质疏松症在内的多种人类疾病的前药方面受到越来越多的关注。本研究旨在确定抗氧化肽是否是缓解绝经后骨质疏松症的候选药物。
本研究采用去卵巢(OVX)骨质疏松症大鼠模型,研究水牛乳酪蛋白衍生新型肽 VLPVPQK(PEP)对 OVX 诱导的骨丢失的保护作用及其相关机制。
本研究结果表明,每天给予抗氧化肽 PEP 50 和 100μg/kg 治疗 8 周可预防体重增加、子宫重量减轻和子宫内膜管腔萎缩。此外,PEP 增加了股骨干重、骨灰重、骨灰钙和血清钙磷水平。有趣的是,PEP 增加了 OVX 大鼠股骨和胫骨的骨矿物质密度,并改善了小梁微结构。此外,PEP 增加了骨强度,降低了血清骨转换标志物,抑制了 OVX 引起的破骨细胞因子,并降低了丙二醛水平。此外,PEP 还可提高血清转化生长因子-β水平,增加、降低谷胱甘肽水平,超氧化物歧化酶和过氧化氢酶活性。
我们证明 PEP 通过增强抗氧化活性和降低破骨细胞因子表达来发挥抗骨质疏松作用。