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[Effect of local and systemic desipramine administration on extracellular noradrenaline in the myocardium of rats].

Evaluation of a local activity of the sympathetic system on the basis of norepinephrine (NE) level in the blood of myocardial vessels depends on at least three processes: NE release by sympathetic neurons, its reuptake and spillover of NE into the blood. The relations between these processes are different in various organs. Direct investigations of changes in the myocardial NE level under the effect of reuptake blockade by desmethylimipramine (DMI) were performed after appearance of the microdialysis technology. In this work the effects of local (through microdialysis membrane) and systemic administration of DMI on the NE release in a rat myocardium, were compared. Local DMI delivery increased myocardial NE level to 153 +/- 13% of the control level (0.17 +/- 0.026 ng/ml dialysate). NE concentration increased to 582 +/- 84% of control as a result of i.m. administration of 5 mg/kg DMI. No changes of the NE level in the venous blood were registered after systemic DMI. It is suggested that a relatively weak effect of local DMI is determined by saturation of DMI receptors adjacent to the probe and/or progressive diminution of the DMI effect with an increasing of the distance from the probe. Effect of systemic DMI administration depends on uniform blockade of all myocardial DMI receptors as well as the DMI influence on higher levels of the sympathetic system.

Adrenergic Uptake Inhibitors↗

Serotonergic neurons do not influence the regulation of beta adrenoceptors induced by either desipramine or isoproterenol.

It has been suggested that 5-hydroxytryptamine (serotonin)-containing neurons influence the regulation of central beta adrenoceptors caused by antidepressants. [3H]Dihydroalprenolol ( [3H] DHA) was the radioligand used in these previous studies to measure beta adrenoceptors. In this study, we compared the binding characteristics of [3H]DHA with those of [125I]iodopindolol ( [125I]PIN) and used [125I]IPIN to study effects of lesioning serotonergic nerves on the regulation of beta adrenoceptors. A comparison was made in homogenates prepared from rat frontal cortex of the specific binding of [3H]DHA with that of [125I]IPIN to beta adrenoceptors. Nonlinear regression analysis of saturation experiments of [3H]DHA binding to cortical homogenates indicated that a two-component binding model fit the data significantly better than a one-component model. A dissociation constant value of 0.47 +/- 0.16 nM and a Bmax value of 62 +/- 7 fmol/mg protein were obtained for the high-affinity site. The low-affinity site was poorly defined. Rosenthal transformations of the saturation isotherms for [3H]DHA binding were clearly curvilinear. By contrast, nonlinear regression analysis of saturation experiments of the binding of [125I]IPIN indicated that the binding of this radioligand was described adequately by a one-component model and yielded a dissociation constant value of 147 +/- 10 pM with a Bmax of 80 +/- 5 fmol/mg protein. Rosenthal transformations of the [125I]IPIN data were linear. From such data, it was inferred that [3H]DHA binds to some site in addition to beta adrenoceptors, whereas [125I]IPIN does not.(ABSTRACT TRUNCATED AT 250 WORDS)

5,7-Dihydroxytryptamine↗