ENDOCARDIAL ENDOTHELIUM MODULATES MYOFILAMENT CA2+ RESPONSIVENESS IN AEQUORIN-LOADED FERRET MYOCARDIUM

被引:49
作者
WANG, JX
MORGAN, JP
机构
[1] HARVARD UNIV,BETH ISRAEL HOSP,THORNDIKE LAB,BOSTON,MA 02215
[2] HARVARD UNIV,SCH MED,DEPT MED,DIV CARDIOVASC,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,CHARLES A DANA RES INST,BOSTON,MA 02115
关键词
ENDOCARDIAL ENDOTHELIUM; CA2+ TRANSIENT; CONTRACTION; RELAXATION; AEQUORIN;
D O I
10.1161/01.RES.70.4.754
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The influence of selective removal of the endocardial endothelium (by a 1-second exposure to the detergent Triton X-100, 0.5%) on myofilament Ca2+ responsiveness and intracellular Ca2+ transients was studied in ferret papillary muscles loaded with the Ca2+ -regulated bioluminescent indicator aequorin. The removal of endocardial endothelium produced three major effects: 1) a decrease in peak developed tension and an early onset in isometric relaxation without corresponding changes in the intracellular Ca2+ transient; 2) a rightward shift in the peak [Ca2+]i-peak tension relation with no change in maximum Ca2+-activated twitch tension; and 3) a decrease in steady-state tetanic force with a slight increase in the steady-state [Ca2+]i (at 4 mM [Ca2+]o) and an unchanged steady-state tetanic force with a clear increase in the steady-state [Ca2+]i (at 10 mM [Ca2+]o). These results suggest that intact endocardium may enhance performance of the heart by increasing the myofilament Ca2+ responsiveness through endothelium-derived compounds such as endothelin. This hypothesis is supported by our observations that endothelin 1) induced a leftward shift in peak [Ca2+]i-peak tension curve and 2) could reverse the characteristic changes produced by the removal of endocardium.
引用
收藏
页码:754 / 760
页数:7
相关论文
共 28 条
[1]  
Blinks J.R., 1978, Methods in Enzymology, V57, P292
[2]  
BLINKS JR, 1982, TECHNIQUES CELLULA 2
[3]  
BLINKS JR, 1984, METHODS STUDYING HEA, V2, P237
[4]  
BLOCH KD, 1989, J BIOL CHEM, V264, P18156
[5]   EFFECTS OF DAMAGING THE ENDOCARDIAL SURFACE ON THE MECHANICAL PERFORMANCE OF ISOLATED CARDIAC-MUSCLE [J].
BRUTSAERT, DL ;
MEULEMANS, AL ;
SIPIDO, KR ;
SYS, SU .
CIRCULATION RESEARCH, 1988, 62 (02) :358-366
[6]   THE ENDOCARDIUM [J].
BRUTSAERT, DL .
ANNUAL REVIEW OF PHYSIOLOGY, 1989, 51 :263-273
[7]   CHARACTERIZATION OF THE MECHANICAL-BEHAVIOR OF ISOLATED PAPILLARY-MUSCLE PREPARATIONS OF THE FERRET [J].
CHAPPELL, S ;
HENDERSON, A ;
LEWIS, M .
JOURNAL OF PHARMACOLOGICAL METHODS, 1986, 15 (01) :35-39
[8]   AUTORADIOGRAPHICAL LOCALIZATION OF BINDING-SITES FOR PORCINE [I-125] ENDOTHELIN-1 IN HUMANS, PIGS, AND RATS - FUNCTIONAL RELEVANCE IN HUMANS [J].
DAVENPORT, AP ;
NUNEZ, DJ ;
HALL, JA ;
KAUMANN, AJ ;
BROWN, MJ .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1989, 13 :S166-S170
[9]   EFFECTS OF ACID-BASE CHANGES ON EXCITATION-CONTRACTION COUPLING IN GUINEA-PIG AND RABBIT CARDIAC VENTRICULAR MUSCLE [J].
FRY, CH ;
POOLEWILSON, PA .
JOURNAL OF PHYSIOLOGY-LONDON, 1981, 313 (APR) :141-160
[10]  
GU XH, 1989, J MOL CELL CARDIO S2, V21, pS4