Growth hormone-releasing peptide-biotin conjugate stimulates myocytes differentiation through insulin-like growth factor-1 and collagen type I

Based on the potential beneficial effects of growth hormone releasing peptide (GHRP)-6 on muscle functions, a newly synthesized GHRP-6-biotin conjugate was tested on cultured myoblast cells. Increased expression of myogenic marker proteins was observed in GHRP-6-biotin conjugate-treated cells. Addit...

Full description

Saved in:
Bibliographic Details
Published inBMB reports Vol. 48; no. 9; pp. 501 - 506
Main Authors Lim, Chae Jin, Jeon, Jung Eun, Jeong, Se Kyoo, Yoon, Seok Jeong, Kwon, Seon Deok, Lim, Jina, Park, Keedon, Kim, Dae Yong, Ahn, Jeong Keun, Kim, Bong-Woo
Format Journal Article
LanguageEnglish
Published Korea (South) Korean Society for Biochemistry and Molecular Biology 01.09.2015
생화학분자생물학회
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Based on the potential beneficial effects of growth hormone releasing peptide (GHRP)-6 on muscle functions, a newly synthesized GHRP-6-biotin conjugate was tested on cultured myoblast cells. Increased expression of myogenic marker proteins was observed in GHRP-6-biotin conjugate-treated cells. Additionally, increased expression levels of insulin-like growth factor-1 and collagen type I were observed. Furthermore, GHRP-6-biotin conjugate-treated cells showed increased metabolic activity, as indicated by increased concentrations of energy metabolites, such as ATP and lactate, and increased enzymatic activity of lactate dehydrogenase and creatine kinase. Finally, binding protein analysis suggested few candidate proteins, including desmin, actin, and zinc finger protein 691 as potential targets for GHRP6-biotin conjugate action. These results suggest that the newly synthesized GHRP-6-biotin conjugate has myogenic stimulating activity through, at least in part, by stimulating collagen type I synthesis and several key proteins. Practical applications of the GHRP-6-biotin conjugate could include improving muscle condition.
Bibliography:G704-SER000001672.2015.48.9.006
ISSN:1976-6696
1976-670X
DOI:10.5483/BMBRep.2015.48.9.258