Inhibition of L-type calcium currents by salusin-β in rat cardiac ventricular myocytes

被引:21
作者
Shi, Jing-Song [1 ]
Li, Dong [1 ]
Li, Ning [2 ]
Lin, Li [1 ]
Yang, Yong-Ji [3 ]
Tang, Ying [3 ]
Sun, Tao [2 ]
Yuan, Wen-Jun [1 ,2 ]
Ren, An-Jing [4 ]
机构
[1] Second Mil Med Univ, Dept Physiol, Shanghai 200433, Peoples R China
[2] NingXia Med Univ, Dept Physiol & Neurobiol, Yinchuan 750004, Peoples R China
[3] Second Mil Med Univ, Dept Biophys, Shanghai 200433, Peoples R China
[4] Second Mil Med Univ, Dept Pathophysiol, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Calcium channel; Salusin-beta; Myocytes; Rat; POSTNATAL-DEVELOPMENT; CA2+; EXPRESSION; EXCHANGER; CELLS; HEART; CARDIOMYOCYTES; CHANNEL; ALPHA;
D O I
10.1016/j.peptides.2010.03.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salusin-beta is a new regulatory peptide relevant to the cardiovascular system and exerts negative inotropic effect on ventricular muscle. The purpose of the present study was to determine whether salusin-beta can inhibit cardiac L-type calcium channel current (I-Ca,I-L). Using whole-cell voltage-clamp techniques, I-Ca,I-L was measured in ventricular myocytes isolated from 12 to 16 weeks rats. Salusin-beta dose-dependently and reversibly reduced the magnitude of I-Ca,I-L in rat ventricular myocytes. Neither threshold potential nor the peak potential of current-voltage relationship was affected. Salusin-beta increased the rate of I-Ca,I-L inactivation without altering its gating properties. These results suggest salusin-beta inhibited I-Ca,I-L by increasing the rate of I-Ca,I-L inactivation and the inhibition of L-type Ca2+ channels induced by salusin-beta may contribute to its negative inotropic effect on ventricular muscle. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1146 / 1149
页数:4
相关论文
共 20 条
[1]   CHANGES IN THE CALCIUM CURRENT OF RAT-HEART VENTRICULAR MYOCYTES DURING DEVELOPMENT [J].
COHEN, NM ;
LEDERER, WJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1988, 406 :115-146
[2]   THE TRANSIENT K+ CURRENT IN RAT VENTRICULAR MYOCYTES - EVALUATION OF ITS CA2+ AND NA+ DEPENDENCE [J].
DUKES, ID ;
MORAD, M .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 435 :395-420
[3]   DEVELOPMENTAL-CHANGES IN CA2+ CURRENTS FROM NEWBORN RAT CARDIOMYOCYTES IN PRIMARY CULTURE [J].
GOMEZ, JP ;
POTREAU, D ;
BRANKA, JE ;
RAYMOND, G .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1994, 428 (3-4) :241-249
[4]   Cardiac Na+-H+ exchanger during postnatal development in the rat: Changes in mRNA expression and sarcolemmal activity [J].
Haworth, RS ;
Yasutake, M ;
Brooks, G ;
Avkiran, M .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1997, 29 (01) :321-332
[5]   Synthetic salusins as cardiac depressors in rat [J].
Izumiyama, H ;
Tanaka, H ;
Egi, K ;
Sunamori, M ;
Hirata, Y ;
Shichiri, M .
HYPERTENSION, 2005, 45 (03) :419-425
[6]   Run-down of the cardiac Ca2+ channel: Characterization and restoration of channel activity by cytoplasmic factors [J].
Kameyama, A ;
Yazawa, K ;
Kaibara, M ;
Ozono, K ;
Kameyama, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1997, 433 (05) :547-556
[7]   Expressional analysis of the cardiac Na-Ca exchanger in rat development and senescence [J].
Koban, MU ;
Moorman, AFM ;
Holtz, J ;
Yacoub, MH ;
Boheler, KR .
CARDIOVASCULAR RESEARCH, 1998, 37 (02) :405-423
[8]  
LIU QY, 1994, J PHARMACOL EXP THER, V271, P935
[9]   G-PROTEIN-MEDIATED SUPPRESSION OF L-TYPE CA2+ CURRENT BY INTERLEUKIN-1-BETA IN CULTURED RAT VENTRICULAR MYOCYTES [J].
LIU, S ;
SCHREUR, KD .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 268 (02) :C339-C349
[10]   INWARDLY RECTIFYING POTASSIUM CURRENT IN RAT FETAL AND NEONATAL VENTRICULAR CARDIOMYOCYTES [J].
MASUDA, H ;
SPERELAKIS, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (04) :H1107-H1111