RESUMO
We describe the behavior of the snail Megalobulimus abbreviatus upon receiving thermal stimuli and the effects of pretreatment with morphine and naloxone on behavior after a thermal stimulus, in order to establish a useful model for nociceptive experiments. Snails submitted to non-functional (22 degrees C) and non-thermal hot-plate stress (30 degrees C) only displayed exploratory behavior. However, the animals submitted to a thermal stimulus (50 degrees C) displayed biphasic avoidance behavior. Latency was measured from the time the animal was placed on the hot plate to the time when the animal lifted the head-foot complex 1 cm from the substrate, indicating aversive thermal behavior. Other animals were pretreated with morphine (5, 10, 20 mg/kg) or naloxone (2.5, 5.0, 7.5 mg/kg) 15 min prior to receiving a thermal stimulus (50 degrees C; N = 9 in each group). The results (means +/- SD) showed an extremely significant difference in response latency between the group treated with 20 mg/kg morphine (63.18 +/- 14.47 s) and the other experimental groups (P < 0.001). With 2.5 mg/kg (16.26 +/- 3.19 s), 5.0 mg/kg (11.53 +/- 1.64 s) and 7.5 mg/kg naloxone (7.38 +/- 1.6 s), there was a significant, not dose-dependent decrease in latency compared to the control (33.44 +/- 8.53 s) and saline groups (29.1 +/- 9.91 s). No statistically significant difference was found between the naloxone-treated groups. With naloxone plus morphine, there was a significant decrease in latency when compared to all other groups (minimum 64% in the saline group and maximum 83.2% decrease in the morphine group). These results provide evidence of the involvement of endogenous opioid peptides in the control of thermal withdrawal behavior in this snail, and reveal a stereotyped and reproducible avoidance behavior for this snail species, which could be studied in other pharmacological and neurophysiological studies.
Assuntos
Analgésicos Opioides/farmacologia , Comportamento Animal/efeitos dos fármacos , Temperatura Alta , Morfina/farmacologia , Naloxona/farmacologia , Caramujos/efeitos dos fármacos , Animais , Regulação da Temperatura Corporal/efeitos dos fármacos , Naloxona/antagonistas & inibidores , Tempo de Reação/efeitos dos fármacos , Termorreceptores/efeitos dos fármacosRESUMO
We describe the behavior of the snail Megalobulimus abbreviatus upon receiving thermal stimuli and the effects of pretreatment with morphine and naloxone on behavior after a thermal stimulus, in order to establish a useful model for nociceptive experiments. Snails submitted to non-functional (22°C) and non-thermal hot-plate stress (30°C) only displayed exploratory behavior. However, the animals submitted to a thermal stimulus (50°C) displayed biphasic avoidance behavior. Latency was measured from the time the animal was placed on the hot plate to the time when the animal lifted the head-foot complex 1 cm from the substrate, indicating aversive thermal behavior. Other animals were pretreated with morphine (5, 10, 20 mg/kg) or naloxone (2.5, 5.0, 7.5 mg/kg) 15 min prior to receiving a thermal stimulus (50°C; N = 9 in each group). The results (means ± SD) showed an extremely significant difference in response latency between the group treated with 20 mg/kg morphine (63.18 ± 14.47 s) and the other experimental groups (P < 0.001). With 2.5 mg/kg (16.26 ± 3.19 s), 5.0 mg/kg (11.53 ± 1.64 s) and 7.5 mg/kg naloxone (7.38 ± 1.6 s), there was a significant, not dose-dependent decrease in latency compared to the control (33.44 ± 8.53 s) and saline groups (29.1 ± 9.91 s). No statistically significant difference was found between the naloxone-treated groups. With naloxone plus morphine, there was a significant decrease in latency when compared to all other groups (minimum 64 percent in the saline group and maximum 83.2 percent decrease in the morphine group). These results provide evidence of the involvement of endogenous opioid peptides in the control of thermal withdrawal behavior in this snail, and reveal a stereotyped and reproducible avoidance behavior for this snail species, which could be studied in other pharmacological and neurophysiological studies.
Assuntos
Animais , Analgésicos Opioides/farmacologia , Comportamento Animal/efeitos dos fármacos , Temperatura Alta , Morfina/farmacologia , Naloxona/farmacologia , Caramujos/efeitos dos fármacos , Regulação da Temperatura Corporal/efeitos dos fármacos , Naloxona/antagonistas & inibidores , Tempo de Reação/efeitos dos fármacos , Termorreceptores/efeitos dos fármacosRESUMO
The aim of this study was to evaluate the interaction between N-methyl-D-aspartate (NMDA) receptors and the adrenergic and opioid systems in the modulation of inhibitory avoidance retention. Rats were trained and tested in the step-down inhibitory avoidance task (0.3 mA footshock). The training-test interval was 24 h. The animals received an i.p. injection of saline or MK-801 (0.0625 mg/kg) 30 min before training, and saline, epinephrine (25 micrograms/kg), or naloxone (0.4 mg/kg) i.p. immediately after training. In the saline-pretreated rats, epinephrine and naloxone enhanced memory retention. Pretraining MK-801 prevented the facilitatory effects of those treatments. The present findings suggest that the facilitation of learning by post-training epinephrine and naloxone is prevented by the pretraining NMDA receptor blockade.
Assuntos
Aprendizagem da Esquiva/efeitos dos fármacos , Maleato de Dizocilpina/farmacologia , Epinefrina/farmacologia , Antagonistas de Aminoácidos Excitatórios/farmacologia , Naloxona/farmacologia , Receptores de N-Metil-D-Aspartato/antagonistas & inibidores , Agonistas Adrenérgicos/farmacologia , Animais , Aprendizagem da Esquiva/fisiologia , Epinefrina/antagonistas & inibidores , Feminino , Memória/efeitos dos fármacos , Memória/fisiologia , Naloxona/antagonistas & inibidores , Antagonistas de Entorpecentes/farmacologia , Ratos , Ratos WistarRESUMO
Los antídotos son sustancias cuya función es contrarrestar el efecto farmacológico y tóxico de otras sustancias, teniendo en cuenta la importancia de las medidas generales en el manejo del intoxicado (baño general, emesis, lavado gástrico, carbón activado, catárticos). Cada día aparecen sustancias nuevas con dichas características. En el presente artículo se pretende dar información breve y detallada sobre las propiedades farmacológicas, indicaciones, dosificación, efectos secundarios y contraindicaciones de algunos de uso general (carbón activado, soluciones electrolíticas con polietilenglycol) y principalmente de algunos específicos de uso reciente: flumazenil, fragmentos Fab-antidigoxina, glucagón, naloxona, clonidina, N-acetil-cisteína, azul de metileno, nitrito y tiosulfato de sodio, ácido-2-3-dimercaptosuccínico, penicilina benzatínica, glicopirrolato y S-adenosil-metionina.