COMPARATIVE CARDIAC CONTRACTILE ACTIONS OF 6 NARCOTIC ANALGESICS - MORPHINE, MEPERIDINE, PENTAZOCINE, FENTANYL, METHADONE AND L-ALPHA-ACETYLMETHADOL (LAAM)

  • 1 January 1980
    • journal article
    • research article
    • Vol. 215  (1) , 259-265
Abstract
Cardiac muscle contractile responses to 6 narcotic analgesics (morphine, meperidine, pentazocine, fentanyl, methadone and l-.alpha.-acetylmethadol), at concentrations from 10-8 to 10-4 M, both in the presence and absence of the narcotic antagonist, naloxone, were studied in the isolated, isometric cat right ventricular papillary muscle preparation. Measurements of maximum developed tension (T), maximum rate of tension development (dT/dt) and time to peak tension indicated that no major changes in contractile function occurred with any narcotic at concentrations of 10-8 to 10-6 M except for small but significant (P < 0.05) increases in all 3 parameters at 10-6 M fentanyl and small but significant increases in dT/dt at 10-8 to 10-6 M meperidine. At 10-5 M narcotic, dT/dt was significantly elevated in meperidine-treated muscles (+7%), but significantly reduced in muscles exposed to pentazocine (-8%) or l-.alpha.-acetylmethadol (-11%). For all 6 narcotics, the 10-4 M drug concentration depressed contractile function that was associated with nonresponsiveness to electrical stimulation. Pretreatment of muscles with naloxone (10-4 M) did not prevent this reduction of contractile performance except at the highest concentration (10-4 M) of meperidine. Following removal of the drug, contractile performance improved to varying degrees (recovery to 72-97% of control T), except in l-.alpha.-acetylmethadol-treated muscles, in which there was no recovery of T. Isoproterenol (0.8 .times. 10-7 M) elicited a positive inotropic response whether administered in the presence of 10-4 M narcotic or following narcotic removal. Narcotic analgesics in high concentrations exert a direct myocardial depressant effect which is not prevented by naloxone and is not mediated by interaction with opiate receptors. Several effects, including myocardial depression, its reversibility by both drug removal and isoproterenol and decreased muscle excitability are consistent with the hypothesis that narcotic analgesics in high concentrations exert a nonspecific, local anesthetic effect on the myocardium.