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In a preceding paper we reported the evolution of chagasic cardiopathy in mice inoculated with low number of T. cruzi from 2 days to 75 days post-infection (p.i.). The present work analyzed the contractility, pharmacological response and histopathology of myocardium isolated from chronic chagasic mice from 90 days until 180 days. p.i. Myocardium contractile force reached values similar to controls until 165 days p.i. From this to the end contractility was significantly lower. At 90 days p.i. NE provoked negative inotropic effect or had no effect in 13% of the cases tested. The others had a reactivity to NE similar to normal ventricles. From 105 days until 180 days p.i. NE induced to a positive inotropic effect significantly lower than in normal. ACh effect was significantly smaller from 165 days to the end. Previously ACh ventricles responses were as control. The effects of dibenamine, propranolol and atropine (10-6M) on chagasic ventricles were similar to those observed in normal tissues. At 90 days p.i. the histopathology showed focalized inflammatory infiltrates. At 180 days p.i. fibers fragmentations and loss of typical striated characteristic of cardiac tissue. The abnormal pharmacological response described could be attributed to alterations in cardiac beta and muscarinic receptors probably due to a lower oxygen support. The present paper shows that during chronic Chagas' disease myocardial function and pharmacological reactivity are seriously and definitively compromised.

Cardiac disease is usually the most serious complication of human infection with Trypanosoma cruzi in our country. This report studies the evolution of the chagasic cardiopathy in mice inoculated with low number of parasites during acute and indeterminate stages in different aspects: contractility, histopathology and pharmacological response. From 2-45 days post infection (p.i.) (acute stage) myocardium contractile force reached higher values than in controls, but norepinephrine (NE) response was significantly lower. Acetylcholine (ACh) caused a negative inotropic effect similar to the observed in control group. In this period cardiac damage evolved to an acute interstitial myocarditis. In the indeterminate phase (45-75 days p.i.) of this parasitosis NE produced either small inotropic effect, negative inotropic effect or had no effect on the ventricles tested. A significantly low ACh effect, sub-endocardiac perivascular fibrosis and necrosis in wall bases were also observed. The abnormal pharmacological response described could be ascribed to modifications in cardiac beta and muscarinic receptors number or affinity. The present results showed that in myocardium isolated from T. cruzi infected mice the histopathology, contractility and pharmacological response were altered from 48 h p.i. reaching a maximum disorder at 60 days p.i.

In order to display some electrophysiological properties of the motoneurons, a special program for a microcomputer has been designed. The images in the monitor resemble those of an oscilloscope screen. The microelectrode penetration in the cell membrane, magnitude of the resting potential, inhibition and facilitation phenomena and the time-course of a spike potential are shown. The sequences of program's sentences (detailed in the text) can be exhibited in the screen also. Related theoretical basis of neurophysiology and a discussion of the present work are included.

The isometric developed tension (IDT) and the pharmacological response of isolated myocardium from T. cruzi infected Albino Swiss mice in the acute and chronic Chagas' disease, were studied. The animals were infected with 7 X 10(4) trypomastigotes, form of T. cruzi, Tulahuen strain for the acute infection and with 45 parasites for the chronic stage. The isolated myocardium from acute and chronic chagasic mice reached IDT levels similar to normal hearts. The addition of norepinephrine (NE) to acute ventricles led to lower IDT values than in control group; this hyporeactivity to NE was absent in the chronic stage. On the other hand, epinephrine (EPI) effects on acute and chronic ventricles lead to significantly higher IDT values when compared with their controls. Propranolol blocked the higher effect of EPI in isolated myocardium from the acute stage, but the hyperreactivity described in the chronic stage could not be inhibited by the beta receptors antagonist. The agonist and antagonist tested act on cardiac plasma membrane beta receptors and their actions modify transmembrane calcium fluxes, so that the present study shows that Chagas' disease modifies the normal behavior of adrenergic beta cardiac receptors in different degree depending on the stage of the trypanosomiasis.

Oxygen uptake and isometric developed tension (IDT) of isolated rat portal vein were simultaneously measured after glucose removal, following the readmission of metabolic substrates and addition of 2-deoxy-D-glucose (2-DG) or insulin. In control conditions, basal O2 uptake was 0.128 +/- 0.004 microliter O2/mg dry weight/min (n = 50). After 40 min of incubation in a glucose-free medium, IDT and O2 uptake decayed to a similar degree. Addition of 11 mM glucose, 5 mM pyruvate, acetate, lactate or butyrate to hypodynamic veins, elicited differential recoveries in the mechanical and metabolic parameters, pyruvate and acetate being the most effective. Insulin (0.1 U/ml) added 5 min prior to readmission of 11 mM glucose, increased the restoration of IDT without any effect on oxygen uptake. 2-DG 5.5 mM, when added in glucose-free medium, abolished IDT but only depressed the cellular respiration by 38% at 20 min; these effects were decreased in presence of glucose (11 mM). These results suggest that the oxygen uptake of this vessel depends, among other factors, on the exogenous substrate offered. They show also the relationship between peak of developed isometric force and metabolic activity as well as the relevance of glycolytic and oxidative pathways in this tissue.

The present study investigates the effects of Sodium Nitroprusside (SNP) on isometric developed tension (IDT) and tonic component of K+ induced contracture of rat portal vein. The availability of activator calcium for the contraction was modified by changing the ionic composition of the Krebs Ringer bicarbonate medium (KRB) or by using pharmacological agents such as nifedipine or KCl. In control conditions (KRB media) magnitude of IDT was 10.61 +/- 0.56 mN (n = 13). Addition of increasing concentrations of SNP (non cumulative) diminished IDT in a dose related manner. Tonic component of 60 mM KCl evoked contracture decayed 27.04 +/- 10.9% (n = 6) after 10(-4)M SNP incubation. Relaxant effect of SNP was more pronounced in the presence of nifedipine 10(-10)M (72.35 +/- 7.5% of inhibition, n = 6). The sensitivity of the preparation to SNP was strongly reduced in conditions of diminished Ca+2 efflux (slow sodium media = KRB sucrose). Experiments here presented support the hypothesis that the vasodilator effect of SNP could be attributed to an enhanced Ca+2 efflux from the vessel.