Biomedical subjects

C M Contreras

Publications and source records attributed to C M Contreras.

49 records · Page 3Linked to original sources

PubMedDate not supplied

Cortical and septal responses to dorsal raphe nucleus stimulation in the rat: long-term clomipramine actions.

In cerebral cortex and lateral septal nuclei different serotonergic receptor subtypes coexist, thus a different action on neuronal firing may be expected depending on the receptor activated. Dorsal raphe nucleus stimulation produced an increased rate of firing in cortical layer V, and in lateral septal nuclei. However, firing rate in cortical layer VI remained unchanged after stimulating the dorsal raphe nucleus. Clomipramine is a tricyclic which exerts its main actions on serotonergic receptors, and long-term treatment with this antidepressant produced a selective increased firing rate in lateral septal neurons, but not in cortical neurons. From an electrophysiological point of view, it is concluded that the excitatory actions on firing rate elicited by dorsal raphe nucleus stimulation or clomipramine treatment are mediated by 5-HT2 receptor subtype activation which is likely to be acting as a 5-HT1A modulator in such places where both receptor subtypes coexist.

Action Potentials↗

PubMedDate not supplied

Amygdalar catecholaminergic input to septal nuclei, relation to clomipramine actions on lateral septal neurons in the rat.

Antidepressants exert mixed actions on serotonergic and catecholaminergic systems. However, it is unknown whether a catecholaminergic blockade impinge on the actions of a tricyclic with serotonergic agonist properties (clomipramine) in limbic structures. The aim of the present study is to explore the effects of a catecholaminergic lesion in the basolateral amygdala on the firing rate of lateral septal, and hippocampal neurons in rats treated with clomipramine. An amygdaline lesion with 6-OHDA resembled the actions of clomipramine on the firing rate in lateral septal neurons, i.e. an increased rate of firing. However, the lesion blocked further effects of clomipramine on septal firing. Clomipramine decreased the firing rate in hippocampal neurons; however, neither the 6-OHDA lesion nor the added treatment with clomipramine modified the firing rate. It is concluded that an intact catecholaminergic amygdaloid input to lateral septal nuclei is necessary for clomipramine actions; however, the initial action of the tricyclic may involve a catecholaminergic blockade.

Action Potentials↗

PubMedDate not supplied

Clomipramine actions on firing rate in septal nuclei of the rat are not related to anaesthesia (urethane).

An increased firing rate in lateral septal nuclei (LSN) appears in urethane-anesthetized rats after several acute drug and non-drug human antidepressant treatments. A still more pronounced increase in firing rate is produced in LSN after clomipramine (CMI) long-term treatment. In spite of urethane is a widely used anesthetic for single unit extracellular recordings, it modifies evoked potentials wave-form. Therefore, present study discards urethane interaction with CMI in LSN single unit extracellular recordings. CMI was acutely injected (1.25 mg/kg: IP) either to urethane-anesthetized, or non-anesthetized encephale-isolé rats. The CMI treated groups showed higher rates of firing in LSN regardless of the use of general anesthesia during recordings. Another group of urethane-anesthetized rats received intracerebroventricular (ICV) microinjections of CMI (100 micrograms/10 microliters/1 min). An amount of 42.8% of LSN-recorded neurons responded with a long-lasting increased firing rate. Results discard urethane and CMI interactions. Additionally, systemic actions of CMI on firing rate of LSN are reproduced by ICV/route microinjections.

Action Potentials↗

PubMedDate not supplied

Ketamine antagonizes toxic action of anticholinesterase agents.

Ketamine is an anaesthetic interacting with several neurotransmitters. Among others, ketamine exerts some cholinergic actions (ACh). This paper presents the results of studying the interaction of ketamine with ACh in two animal species. Atropine slightly increased the time of immobility produced by ketamine injections in rats. Meanwhile, neostigmine slightly decreased such immobility. Ketamine resulted similar in behavioral actions and shared some electroencephalographic (EEG) actions of scopolamine in cats. The most striking interaction consisted on an antagonism of ketamine on the action of anticholinesterase agents. In both species, ketamine blocked the EEG and the behavioral toxic effects of neostigmine and physostigmine. Notwithstanding, the anticholinesterase agents were unable in reducing the actions of ketamine. This partial cholinergic agonist action of ketamine support certain but limited use of the anesthetic against insecticidal anticholinesterase poisoning.

Animals↗

PubMedDate not supplied

Visual evoked potentials in a sample of schizophrenic patients.

Variations in evoked potentials utilizing a photic stimulus in a sample of psychiatric patients compared to a healthy sample were evaluated. A group of patients diagnosed as schizophrenic was tested against a sample of healthy volunteers in a trial combining visual evoked potentials and a simultaneous cognitive processing. The stimulus was a checkerboard pattern presented under three different conditions. The results indicate diminished P100 and lack the reactivity associated with cognitive processes in schizophrenic group. The P200 component also lacked, in the inpatient group the changes associated with the performance of the trial. Finally the multiple P300 component was shortened in latency and decreased in amplitude in the schizophrenia group. Besides, P300 interhemispheric shifts related to trials, were commonly inverted in schizophrenics. Results are interpreted as a lacked interhemispheric coordination in schizophrenics, rather than a fixed hemispheric alteration. Likewise, an attenuation in processing from specific cortical areas to association cortex is concluded.

Adult↗

PubMedDate not supplied

Effects of quipazine in evoked potentials recorded in the cingulum of the cat.

The present study describes the changes in electroencephalogram (EEG), behavior, and visual evoked potentials (VEPs) recorded in some structures of the limbic system of freely moving cats which had been administered two different doses of quipazine through different routes (5 mg/kg i.p. and 10 mg/kg i.v.). After the low dose of quipazine, the EEG from the cingulum developed a 6 c/s spike and wave activity. The amplitude of the P150 component of VEPs in the cingulum recording increased, while the VEPs recorded in visual cortex were barely affected. Simultaneously the animals displayed exploratory movements towards objects undetected by observers. The changes found in the cingulum with the tested doses may be due to specific actions of the drug on the polysensorial pathways. The high dose produced a rage reaction accompanied by a generalized spiking, intermixed with high voltage-low frequency waves, and an increase in VEPs in all recorded structures. At high doses the drug may be producing a discordance between the sensorial pathways and those in charge of the emotional processes.

Animals↗

PubMedDate not supplied

Relations between anxiety, psychophysiological variables and menstrual cycle in healthy women.

The present study was designed to explore whether changes occur in psychophysiological variables in healthy women not suffering from premenstrual tension. Variations in electroencephalogram frequencies, reaction time, somatosensory evoked potentials, and nerve conduction velocity were examined in a sample of 30 women, in relation to scores from the Hamilton Psychiatric Rating Scale for Depression and the State-Trait Anxiety Inventory. Trials and recordings were done weekly. EEG frequencies decreased before menstruation in all subjects. However, there were no significant changes for reaction time, nerve conduction velocity, HAMILTON nor State-Trait Anxiety scales associated with subperiods of the menstrual cycle. To explore the impact of anxiety, high and low anxiety groups were formed. The high anxiety group showed the highest scores in the A-Trait form, longer reaction time, enlarged latencies of the P100, but shorter nerve conduction velocity. Anxiety scores as well as reaction time increased during the premenstrual period only for the low anxiety group. The authors conclude that for some women premenstrual anxiety may be related to previous and continuous high levels of anxiety, which associated with some subtle neurological differences as compared with women who rated in low scores for anxiety.

Anxiety↗

PubMedDate not supplied