Biomedical subjects

R M De Almeida

Publications and source records attributed to R M De Almeida.

4 recordsLinked to original sources

PubMed1998

8-OH-DPAT in the median raphe nucleus decreases while in the medial septal area it may increase anxiety in female rats.

The experiment evaluated the effects of 8-OH-DPAT on the activity of virgin female rats (diestrus) in the elevated plus maze. The 5-HT1A receptor agonist was infused into the median raphe nucleus (N = 60) and medial septal area (N = 68) 10 min before the test. Five groups for each brain area were analyzed: intact, saline (0.2 microl) and 8-OH-DPAT (0.2; 0.5 and 2.0 microg rat(-1)). The following measures were recorded: number of entries onto open and enclosed arms and time spent on the open and enclosed arms. In addition, the frequency of stretch-attend and head-dipping were also evaluated. The results showed that in the median raphe nucleus only the highest dose of 8-OH-DPAT (2.0 microg) increased the percentage of time spent on the open arms. On the other hand, in medial septal area 8-OH-DPAT in the dose of 0.5 microg decreased the percentage of time spent on the open arms, while the doses of 0.2 and 2.0 microg had no significant impact on anxiety. Data suggest that 8-OH-DPAT acting on 5-HT1A somatodendritic autoreceptors decreases anxiety. However, at a specific dosage and acting on postsynaptic receptors of the medial septal area, 8-OH-DPAT can increase anxiety.

8-Hydroxy-2-(di-n-propylamino)tetralin↗

PubMed1997

8-OH-DPAT in the median raphe, dorsal periaqueductal gray and corticomedial amygdala nucleus decreases, but in the medial septal area it can increase maternal aggressive behavior in rats.

The purpose of the present study was to analyze the role of somatodendritic autoreceptors and postsynaptic 5-HT1A receptors in the modulation of maternal aggressive behavior. The 5-HT1A receptor agonist 8-OH-DPAT (8-hydroxy-2-(di-n-propylamino)tetralin) was microinjected (0.2, 0.5 and 2.0 microg/0.2 microl) in different brain areas of female Wistar rats: median raphe nucleus (MnR); medial septal area (MS); anterior corticomedial amygdaloid nucleus (ACoM); and dorsal periaqueductal gray (DPAG). The behaviors of lactating female rats with pups against a conspecific male intruder were recorded on day 7 post-partum. Results showed that in the median raphe nuclei, in the dorsal periaqueductal gray and in the corticomedial amygdaloid nucleus 8-OH-DPAT decreased maternal aggression; while in the medial septum, the intermediate dose (0.5 microg/0.2 microl) of the 5-HT1A receptor agonist increased the aggressive behavior of the lactating female rat. It is concluded that the main role of the 5-HT1A somatodendritic autoreceptors and the post-synaptic receptors of the brain areas studied is to decrease maternal aggression, however, at a specific dosage, 8-OH-DPAT acting on postsynaptic receptors of the medial septal area can increase aggressiveness.

8-Hydroxy-2-(di-n-propylamino)tetralin↗

PubMed1994

Effects of intracerebroventricular administration of 5-HT receptor agonists on the maternal aggression of rats.

This study attempted to analyze the effects of 8-OH-DPAT (8-hydroxy-2-(di-n-propylamino)tetralin), TFMPP (1-(3-trifluoromethyl-phenyl)piperazine hydrochloride), and DOI (1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane) on maternal aggressive behavior. Female Wistar rats were divided into 4 groups of 12 animals each. They received an intracerebroventricular (i.c.v.) injection of: (1) saline, (2) 8-OH-DPAT (20 micrograms/rat), (3) TFMPP (100 micrograms/rat), and (4) DOI (100 micrograms/rat). 5-HT1A (8-OH-DPAT) and 5-HT2 (DOI) receptor agonists decreased the frequency of attack 15 but not 55 min after i.c.v. injection. The 5-HT1B/D receptor agonist (TFMPP), in the dose studied, showed no significant difference as compared to saline. Pup care and non-aggressive social interaction with the intruder were not affected by any drug. These data suggest that 5-HT1A and 5-HT2 receptor agonists can specifically inhibit maternal aggression without affecting maternal care; however, this effect is of short duration.

8-Hydroxy-2-(di-n-propylamino)tetralin↗

PubMed1994

Influence of the mother on development of aggressive behavior in male rats.

The present experiments investigated pre- and postnatal maternal effects on aggressive behavior in rats. Resident-intruder aggressive behavior of male rats in colonies (two males and two females) was studied in five experimental groups: 1 = WWY (n = 7) the two males of each colony were wild (biological father and mother were wild) fostered by a wild mother; 2 = WAY (n = 11) the two males were wild fostered by an albino Wistar mother; 3 = AAY (n = 11) the two males were albino (biological father and mother were Wistar) fostered by an albino mother; 4 = AWY (n = 12) the two males were albino fostered by a wild mother; and 5 = HWX+HAX (n = 9) one of the males was hybrid born and reared by a wild mother (the father was albino) and the other was also hybrid but born and reared by an albino mother (the father was wild). Each test lasted 10 min and the intruder was always a Wistar male. Aggression of wild rats was higher than the laboratory ones, independently of the mother (albino or wild) they were fostered by. However, hybrid males born and reared by a wild mother were more aggressive than those that were born and reared by an albino mother, in spite of the father being wild. In conclusion, crossfostering has little effect on territorial aggression, but prenatal maternal effects seem to play a major role on the ontogeny of aggressive behavior of male rats.

Aggression↗