Circulation, Vol 76, 383-393, Copyright © 1987 by American Heart Association
JJ Kammerling, FJ Green, AM Watanabe, H Inoue, MJ Barber, DP Henry and DP Zipes
Denervation supersensitivity was demonstrated in anesthetized dogs 5 to 10
days after transmural myocardial infarction produced by latex embolization
of a diagonal branch of the left anterior descending coronary artery.
Sympathetic efferent denervation in noninfarcted myocardium apical to the
infarction was demonstrated by a 90% depletion of myocardial norepinephrine
content in the apical (45 +/- 15 pg norepinephrine/g tissue) vs basal (437
+/- 76 pg/g tissue) regions and by the lack of effective refractory period
(ERP) shortening during bilateral ansae subclaviae stimulation in 34% of
sites apical to the infarction. Supersensitivity in the area apical to the
infarction was manifested by an exaggerated shortening of the ERP during
both norepinephrine and isoproterenol infusions, with an upward and
leftward shift in the dose-response curves in the apical vs basal regions
(p less than .001). The cellular mechanism for denervation supersensitivity
did not involve detectable changes in the beta- adrenergic receptor
adenylate cyclase system. There was no difference in the density of
beta-adrenergic receptors ([125I]-cyanopindolol) in the apical (268.6 +/-
22.7 fmol/mg protein) vs the basal (253.5 +/- 24.8 fmol/mg protein)
regions. Adenylate cyclase activity stimulated by guanosine triphosphate
plus isoproterenol was slightly greater in the apical (58.7 +/- 17.4%) than
in the basal (49.6 +/- 10.9%) region, but this difference did not reach
statistical significance (p = .068). Muscarinic modulation of beta-receptor
coupling (oxotremorine attenuation of guanosine triphosphate plus
isoproterenol-stimulated adenylate cyclase activity) also was not
significantly different at the apical (31.6 +/- 17.5% inhibition) and basal
(21.4 +/- 20.9% inhibition) sites. These data show that a transmural
myocardial infarction produces denervation supersensitivity in areas apical
to the infarction, but in this preparation no differences in the total
number or a redistribution of beta-adrenergic receptors or adenylate
cyclase activity were detected.
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Denervation supersensitivity of refractoriness in noninfarcted areas apical to transmural myocardial infarction
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