CONTRASTING EFFECTS OF PROPIONATE AND PROPIONYL-L-CARNITINE ON ENERGY-LINKED PROCESSES IN ISCHEMIC HEARTS

被引:22
作者
DILISA, F [1 ]
MENABO, R [1 ]
BARBATO, R [1 ]
SILIPRANDI, N [1 ]
机构
[1] CNR,CTR STUDIO FISIOL MITOCONDRIALE,I-35121 PADUA,ITALY
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1994年 / 267卷 / 02期
关键词
ISCHEMIA; MITOCHONDRIA; L-CARNITINE; COENZYME A;
D O I
10.1152/ajpheart.1994.267.2.H455
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Propionyl-L-carnitine, unlike L-carnitine, is known to improve myocardial function and metabolism altered during the course of ischemia-reperfusion. In this study, the effect of propionyl-L-carnitine has been compared with that of propionate and carnitine on the performance of rat hearts perfused with a glucose-containing medium either under normoxia, ischemia, or postischemic reperfusion. In the postischemic phase, contractile parameters were partially restored both in the control and in the propionate plus carnitine-treated hearts, were markedly impaired by propionate, and were fully recovered by propionyl-L-carnitine. In addition, propionyl-L-carnitine, but not propionate, reduced the functional decay of mitochondria prepared from the ischemic hearts. Even in normoxic conditions propionate, unlike propionyl-L-carnitine, caused a drastic reduction of free CoA and L-carnitine. The concomitant increase in lactate production and decrease in ATP content might be explained by the inhibition of pyruvate dehydrogenase caused by the accumulation of propionyl-CoA. Indeed, when pyruvate was the only oxidizable substrate, propionate induced a gradual decrease in developed pressure, which was largely prevented by L-carnitine. The protective effect of propionyl-L-carnitine may be a consequence of the anaplerotic utilization of propionate in the presence of an optimal amount of ATP and free L-carnitine.
引用
收藏
页码:H455 / H461
页数:7
相关论文
共 28 条
[21]  
Rossi C R, 1972, Adv Enzyme Regul, V10, P171, DOI 10.1016/0065-2571(72)90013-1
[22]   CHANGES IN CITRIC-ACID CYCLE FLUX AND ANAPLEROSIS ANTEDATE THE FUNCTIONAL DECLINE IN ISOLATED RAT HEARTS UTILIZING ACETOACETATE [J].
RUSSELL, RR ;
TAEGTMEYER, H .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (02) :384-390
[23]   COENZYME-A SEQUESTRATION IN RAT HEARTS OXIDIZING KETONE-BODIES [J].
RUSSELL, RR ;
TAEGTMEYER, H .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (03) :968-973
[24]   L-PROPIONYLCARNITINE INCREASES POSTISCHEMIC BLOOD-FLOW BUT DOES NOT AFFECT RECOVERY OF ENERGY-CHARGE [J].
SASSEN, LMA ;
BEZSTAROSTI, K ;
VANDERGIESSEN, WJ ;
LAMERS, JMJ ;
VERDOUW, PD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (01) :H172-H180
[25]   INTRACELLULAR AND INTRAMITOCHONDRIAL DISTRIBUTION OF SHORT-CHAIN ACYL-COA SYNTHETASES IN GUINEA PIG HEART [J].
SCHOLTE, HR ;
WITPEETE.EM ;
BAKKER, JC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1971, 231 (03) :479-+
[26]   PROPIONATE METABOLISM IN THE RAT-HEART BY C-13 NMR-SPECTROSCOPY [J].
SHERRY, AD ;
MALLOY, CR ;
ROBY, RE ;
RAJAGOPAL, A ;
JEFFREY, FMH .
BIOCHEMICAL JOURNAL, 1988, 254 (02) :593-598
[27]   ATP SYNTHASE ACTIVITY IS REQUIRED FOR FRUCTOSE TO PROTECT CULTURED-HEPATOCYTES FROM THE TOXICITY OF CYANIDE [J].
SNYDER, JW ;
PASTORINO, JG ;
THOMAS, AP ;
HOEK, JB ;
FARBER, JL .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (03) :C709-C714
[28]   STOICHIOMETRIC HYDROLYSIS OF LONG-CHAIN ACYL-COA AND MEASUREMENT OF COA FORMED WITH AN ENZYMATIC CYCLING METHOD [J].
VELOSO, D ;
VEECH, RL .
ANALYTICAL BIOCHEMISTRY, 1974, 62 (02) :449-460