Effect of pinacidil on rat myocardial calcium regulation / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences
; (6): 215-218, 2003.
Artículo
en Chino
| WPRIM (Pacífico Occidental)
| ID: wpr-231083
Biblioteca responsable:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To understand the effect of pinacidil on rat myocardial Ca(2+)regulation.</p><p><b>METHODS</b>After baseline measurement and a period of equilibrium, myocytes were randomly allocated to one of 4 treatment groups Control group (8 myocytes) incubation in Lactate Ringer's solution at 24 degrees C for 2 hours; K group (8 myocytes) incubation in Lactate Ringer's solution containing 16 mmol/L potassium at 24 degrees C for 2 hours; K+P group (8 myocytes) incubation in Lactate Ringer's solution containing potassium 16 mmol/L and pinacidil 50 micromol/L at 24 degrees C for 2 hours; K+P+G group (8 myocytes) incubation in Lactate Ringer's solution containing potassium 16 mmol/L, pinacidil 50 micromol/L and glibenclamide 10 micromol/L at 24 degrees C for 2 hours. After each incubation, myocytes were resuspended in cell culture media at the same temperature and intracellular [Ca(2+)](i) and SR Ca(2+) release were measured.</p><p><b>RESULTS</b>The amplitude percent of [Ca(2+)](i) transient evoked by electrical stimulation in the K group was significantly decreased to 67.05% - 80.11% compared to 90.27% - 95.57% in the K+P group during reperfusion after ischemia (P<0.01). The percent amplitude of the [Ca(2+)](i) transient evoked by the rapid application of 10 mmol caffeine in the K group myocyte was approximately 112.00%+/-16.93% compared with that of the [Ca(2+)](i) transient evoked by electrical stimulation. However, in the K+P group myocyte the peak amplitude of the caffeine induced Ca(2+) release was 173.15%+/-26.01% compared with electrical stimulation (P<0.01). The duration of transient evoked by caffeine in K+P group (3.20+/-0.71 ms was significantly shorter than that in K group (3.93+/-0.46) ms (P<0.05).</p><p><b>CONCLUSION</b>Cardioplegic arrest with simultaneous activation of KATP channels preserves rat myocardial Ca2+ by inducing sarcoplasmic reticulum Ca(2+) release and by alteration of Na(+)-Ca(2+) exchanger to better maintain [Ca(2+)](i) homeostasis.</p>
Texto completo:
Disponible
Base de datos:
WPRIM (Pacífico Occidental)
Asunto principal:
Farmacología
/
Sodio
/
Calcio
/
Ratas Sprague-Dawley
/
Pinacidilo
/
Corazón
/
Metabolismo
/
Miocardio
Límite:
Animales
Idioma:
Chino
Revista:
Journal of Zhejiang University. Medical sciences
Año:
2003
Tipo del documento:
Artículo