A COMPARISON OF THE EFFECTS OF ESERINE SULFATE ON THE ACTIVITY OF MEDULLARY RAPHE NEURONS IN THE ANESTHETIZED RABBIT AND RAT

Citation
Ha. Futuroneto et al., A COMPARISON OF THE EFFECTS OF ESERINE SULFATE ON THE ACTIVITY OF MEDULLARY RAPHE NEURONS IN THE ANESTHETIZED RABBIT AND RAT, Brazilian journal of medical and biological research, 27(6), 1994, pp. 1445-1454
Citations number
26
Categorie Soggetti
Medicine, Research & Experimental
ISSN journal
0100879X
Volume
27
Issue
6
Year of publication
1994
Pages
1445 - 1454
Database
ISI
SICI code
0100-879X(1994)27:6<1445:ACOTEO>2.0.ZU;2-I
Abstract
1. Medullary raphe neurons are involved in the control of sympathetic activity during desynchronized sleep (DS). Eserine sulfate induces a s tate with the somatic and visceral signs of DS in decerebrate animals. The rabbit and rat display diverse hemodynamic patterns during DS. 2. To determine whether eserine sulfate provokes different responses in the medullary raphe neuron population of these different species, the drug (100 mg/kg, iv) was administered to urethane-anesthetized (1.2 g/ kg, iv) rabbits (1.5-3.0 kg) and rats (Wistar, 260-310 g). 3. Extracel lular activity was recorded from 66 neurons in 30 rats. Cholinergic st imulation provoked an increase in discharge rate (DR) in 45 neurons (6 8%), a decrease in 8 neurons (12%) and no change in 13 neurons (20%). Recordings were obtained from 30 neurons in 11 rabbits. Stimulation of these cells provoked an increase in DR in 17 neurons (57%), a decreas e in DR in 7 neurons (23%) and no change in 6 neurons (20%). Interspik e interval and auto-correlation analysis was performed on 28 rat and r abbi t neurons. No significant difference was found between the rat an d the rabbit with respect to the number of the neurons which were eith er inhibited or excited by cholinergic stimulation (P > 0.05). Similar ly, unit response to eserine was not related to whether the unit displ ayed regular or irregular DR. 4. Therefore, we suggest that the divers e hemodynamic patterns during DS and the distinct cardiovascular respo nses to raphe nuclei stimulation are not due to differences in the org anization of the raphe nuclei themselves but to differences in their a xonal projections or in the postsynaptic receptors activated in the in termediolateral cell column or other postsynaptic targets.