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In vitro protective effects of nicorandil on hypothermic injury to immature cardiac myocytes : comparison with nitroglycerin

The purpose of the present study was to evaluate the functional and biochemical effects of nicorandil and nitroglycerin on cardiac myocytes incubated under hypothermic conditions. Nicorandil is a coronary vasodilator with mixed nitrate-potassium channel agonist activity. Cardiac myocytes were isolat...

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Published in:Cardiovascular drugs and therapy 1994-02, Vol.8 (1), p.129-135
Main Authors: ORITA, H, FUKASAWA, M, HIROOKA, S, FUKUI, K, KOHI, M, WASHIO, M
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creator ORITA, H
FUKASAWA, M
HIROOKA, S
FUKUI, K
KOHI, M
WASHIO, M
description The purpose of the present study was to evaluate the functional and biochemical effects of nicorandil and nitroglycerin on cardiac myocytes incubated under hypothermic conditions. Nicorandil is a coronary vasodilator with mixed nitrate-potassium channel agonist activity. Cardiac myocytes were isolated from neonatal rat ventricles and cultured for 4 days with MCDB 197 medium. Myocytes (12.5 x 10(5) myocytes/flask) were then incubated at 4 degrees C for 24 hours in media containing various concentrations of nicorandil (NRD) or nitroglycerin (NTG). After hypothermic incubation, CPK and LDH were measured. The myocytes were cultured for an additional 24 hours at 37 degrees C to evaluate the recovery of the myocyte beating rate. In the nicorandil group, 10(-4) M NRD showed a significant beating rate recovery compared to control (44.2% vs. 24.6%, respectively, as a percent of control; i.e., beating rate prior to hypothermic incubation). Nitroglycerin treatment had no effect on either beating rate recovery or release of CPK and LDH from myocytes. However, the release of CPK and LDH was significantly suppressed by 10(-4) M nicorandil compared to the control (10(-4) M NRD: 24.1, 257.2; control: 125.4 mIU/flask, 459.5 mIU/flask, respectively). Thus nicorandil showed an approximate two-fold recovery of myocyte functional activity after hypothermic incubation with only minor biochemical effects, and therefore may be suitable for cardiac preservation.
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However, the release of CPK and LDH was significantly suppressed by 10(-4) M nicorandil compared to the control (10(-4) M NRD: 24.1, 257.2; control: 125.4 mIU/flask, 459.5 mIU/flask, respectively). Thus nicorandil showed an approximate two-fold recovery of myocyte functional activity after hypothermic incubation with only minor biochemical effects, and therefore may be suitable for cardiac preservation.</description><identifier>ISSN: 0920-3206</identifier><identifier>EISSN: 1573-7241</identifier><identifier>DOI: 10.1007/BF00877101</identifier><identifier>PMID: 8086323</identifier><identifier>CODEN: CDTHET</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Animals ; Antianginal agents. 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Nicorandil is a coronary vasodilator with mixed nitrate-potassium channel agonist activity. Cardiac myocytes were isolated from neonatal rat ventricles and cultured for 4 days with MCDB 197 medium. Myocytes (12.5 x 10(5) myocytes/flask) were then incubated at 4 degrees C for 24 hours in media containing various concentrations of nicorandil (NRD) or nitroglycerin (NTG). After hypothermic incubation, CPK and LDH were measured. The myocytes were cultured for an additional 24 hours at 37 degrees C to evaluate the recovery of the myocyte beating rate. In the nicorandil group, 10(-4) M NRD showed a significant beating rate recovery compared to control (44.2% vs. 24.6%, respectively, as a percent of control; i.e., beating rate prior to hypothermic incubation). Nitroglycerin treatment had no effect on either beating rate recovery or release of CPK and LDH from myocytes. 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Coronary vasodilator agents</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Creatine Kinase - metabolism</subject><subject>Heart - drug effects</subject><subject>Hypothermia - metabolism</subject><subject>Hypothermia - pathology</subject><subject>Hypothermia - prevention &amp; control</subject><subject>L-Lactate Dehydrogenase - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocardial Contraction - drug effects</subject><subject>Myocardium - metabolism</subject><subject>Niacinamide - analogs &amp; derivatives</subject><subject>Niacinamide - pharmacology</subject><subject>Nicorandil</subject><subject>Nitroglycerin - pharmacology</subject><subject>Organ Preservation</subject><subject>Pharmacology. 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Coronary vasodilator agents</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular system</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Creatine Kinase - metabolism</topic><topic>Heart - drug effects</topic><topic>Hypothermia - metabolism</topic><topic>Hypothermia - pathology</topic><topic>Hypothermia - prevention &amp; control</topic><topic>L-Lactate Dehydrogenase - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocardial Contraction - drug effects</topic><topic>Myocardium - metabolism</topic><topic>Niacinamide - analogs &amp; derivatives</topic><topic>Niacinamide - pharmacology</topic><topic>Nicorandil</topic><topic>Nitroglycerin - pharmacology</topic><topic>Organ Preservation</topic><topic>Pharmacology. 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Nicorandil is a coronary vasodilator with mixed nitrate-potassium channel agonist activity. Cardiac myocytes were isolated from neonatal rat ventricles and cultured for 4 days with MCDB 197 medium. Myocytes (12.5 x 10(5) myocytes/flask) were then incubated at 4 degrees C for 24 hours in media containing various concentrations of nicorandil (NRD) or nitroglycerin (NTG). After hypothermic incubation, CPK and LDH were measured. The myocytes were cultured for an additional 24 hours at 37 degrees C to evaluate the recovery of the myocyte beating rate. In the nicorandil group, 10(-4) M NRD showed a significant beating rate recovery compared to control (44.2% vs. 24.6%, respectively, as a percent of control; i.e., beating rate prior to hypothermic incubation). Nitroglycerin treatment had no effect on either beating rate recovery or release of CPK and LDH from myocytes. However, the release of CPK and LDH was significantly suppressed by 10(-4) M nicorandil compared to the control (10(-4) M NRD: 24.1, 257.2; control: 125.4 mIU/flask, 459.5 mIU/flask, respectively). Thus nicorandil showed an approximate two-fold recovery of myocyte functional activity after hypothermic incubation with only minor biochemical effects, and therefore may be suitable for cardiac preservation.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>8086323</pmid><doi>10.1007/BF00877101</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0920-3206
ispartof Cardiovascular drugs and therapy, 1994-02, Vol.8 (1), p.129-135
issn 0920-3206
1573-7241
language eng
recordid cdi_proquest_miscellaneous_76719191
source SpringerLink_过刊(NSTL购买)
subjects Animals
Antianginal agents. Coronary vasodilator agents
Biological and medical sciences
Cardiovascular system
Cell Survival - drug effects
Cells, Cultured
Creatine Kinase - metabolism
Heart - drug effects
Hypothermia - metabolism
Hypothermia - pathology
Hypothermia - prevention & control
L-Lactate Dehydrogenase - metabolism
Male
Medical sciences
Myocardial Contraction - drug effects
Myocardium - metabolism
Niacinamide - analogs & derivatives
Niacinamide - pharmacology
Nicorandil
Nitroglycerin - pharmacology
Organ Preservation
Pharmacology. Drug treatments
Rats
Rats, Wistar
Vasodilator Agents - pharmacology
title In vitro protective effects of nicorandil on hypothermic injury to immature cardiac myocytes : comparison with nitroglycerin
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