Literature DB >> 27887949

Pharmacological effects of a recombinant hPTH(1-34) derived peptide on ovariectomized rats.

Wang Chunxiao1, Gu Chengying2, Jin Liang3, Shi Xiaoming3, Guo Feng4, Yuan Junting5, Wu Wenhui6, Wang Yu3, Liu Jingjing3.   

Abstract

A recombinant peptide Pro-Pro-[Arg11]hPTH(1-34)-Pro-Pro, was designed, biosynthesized, and purified in our lab (generated by substituting Arg for Leu at position 11 and adding -Pro-Pro to the carboxyl terminus of hPTH(1-34)-peptide), and reported to be capable of enhancing serum calcium level in chicken. In this investigation, we studied its impact on the structure, component, and biomechanical properties of rat bones. The pharmacological effect of Pro-Pro-[Arg11]hPTH(1-34)-Pro-Pro was investigated to evaluate its therapeutic potential for the treatment of osteoporosis, one of the most prevalent and rapidly spreading diseases in the world. 3-month-old normal female rats were sham-ovariectomized or ovariectomized, then fed for 14 weeks. Small doses of Pro-Pro-[Arg11]hPTH(1-34)-Pro-Pro were given to the rats afterward (daily subcutaneous injection of 0.4-0.9nmol/100g body weight for 16 weeks). Values of various parameters, including the body weight, the bone mass, the bone geometry, the bone biomechanics, the bone histology, the bone histomorphology, and the serum biochemistry, were collected before or after animal sacrifice. Daily subcutaneous injection of Pro-Pro-[Arg11]hPTH(1-34)-Pro-Pro induced 37.0-42.4% increase in vertebral BMD, 28.5-47.9% increase in femoral BMD, 30.7-43.7% decrease in marrow cavity or increase in trabecular bone area. The peptide also increased calcium, phosphorus, and collagen in bone by 52.1-59.7%, 24.5-34.7%, and 26.3-28.0%, respectively. In terms of mechanic properties, peptide administration elevated bone rigidity by 55.7-84.5%, decreased the deflection by 14.8-26.7%, and improved modulus of elasticity by 28.1-76.4%. These data suggest Pro-Pro-[Arg11]hPTH(1-34)-Pro-Pro has a positive effect on bone mass accumulation and microstructure improvement, fortifies bone strength, and possesses anti-aging capability, which may merit further investigation.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Anti-fracture capability; Biomechanic property; Histomorphologic property; Osteoporosis; Trabeculae; hPTH(1−34) derived peptide

Mesh:

Substances:

Year:  2016        PMID: 27887949     DOI: 10.1016/j.ejphar.2016.11.034

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  4 in total

1.  Pu-erh Tea Extract Ameliorates Ovariectomy-Induced Osteoporosis in Rats and Suppresses Osteoclastogenesis In Vitro.

Authors:  Titi Liu; Shihua Ding; Dan Yin; Xiangdan Cuan; Chuanqi Xie; Huanhuan Xu; Xuanjun Wang; Jun Sheng
Journal:  Front Pharmacol       Date:  2017-05-31       Impact factor: 5.810

2.  In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure.

Authors:  Sivanandane Sittadjody; Justin M Saul; John P McQuilling; Sunyoung Joo; Thomas C Register; James J Yoo; Anthony Atala; Emmanuel C Opara
Journal:  Nat Commun       Date:  2017-12-05       Impact factor: 14.919

3.  Effect of Black Tea Extract and Thearubigins on Osteoporosis in Rats and Osteoclast Formation in vitro.

Authors:  Qingqing Liang; Ming Lv; Xiaojuan Zhang; Jun Hu; Ying Wu; Yewei Huang; Xuanjun Wang; Jun Sheng
Journal:  Front Physiol       Date:  2018-09-03       Impact factor: 4.566

4.  Green tea (Camellia sinensis) aqueous extract alleviates postmenopausal osteoporosis in ovariectomized rats and prevents RANKL-induced osteoclastogenesis in vitro.

Authors:  Xin Wu; Chuan-Qi Xie; Qiang-Qiang Zhu; Ming-Yue Wang; Bin Sun; Yan-Ping Huang; Chang Shen; Meng-Fei An; Yun-Li Zhao; Xuan-Jun Wang; Jun Sheng
Journal:  Food Nutr Res       Date:  2018-10-08       Impact factor: 3.894

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.