Characterization of Musclin as a New Target for Treatment of Hypertension
Author(s) -
JiaWei Lin,
Cheng-Chia Tsai,
LiJen Chen,
Ho-Shan Niu,
Chen Kuei Chang,
Chiang-Shan Niu
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/354348
Subject(s) - phenylephrine , pathogenesis , vasoconstriction , contraction (grammar) , skeletal muscle , medicine , endocrinology , intracellular , vascular smooth muscle , calcium in biology , calcium , incubation , in vitro , pharmacology , chemistry , biology , blood pressure , smooth muscle , microbiology and biotechnology , biochemistry
Musclin is a novel skeletal muscle-derived factor found in the signal sequence trap of mouse skeletal muscle cDNAs. Recently, it has been demonstrated that musclin is involved in the pathogenesis of spontaneously hypertensive rats (SHRs). However, it is known as a genetic hypertension model. In the present study, we aim to investigate the role of musclin in another animal model of hypertension and characterize the direct effect of musclin on vascular contraction. The results show that expression of musclin was increased in arterial tissues isolated from DOCA-salt induced hypertensive rats or the normal rats received repeated vasoconstriction with phenylephrine. Additionally, direct incubation with phenylephrine did not modify the expression of musclin in the in vitro studies. Also, the direct effect of musclin on the increase of intracellular calcium was observed in a concentration-dependent manner. These results provide the evidence to support that musclin is involved in hypertension. Thus, musclin is suitable to be considered as a novel target for treatment of hypertension.
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