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Biomedical subjects

H de-Souza-Spinosa

Publications and source records attributed to H de-Souza-Spinosa.

2 recordsLinked to original sources

The diphenhydramine-induced decrease in general open-field activity of female rats is gonadal steroid dependent.

The effect of ovarian steroids on sedative effects of diphenhydramine (D), a histamine H1 receptor blocker, was determined. Seventy-five female Wistar rats were randomly divided into three groups: Group 1 (N = 54) was ovariectomized, group 2 (N = 7) was sham-operated, and group 3 (N = 14) was intact. The ovariectomized rats were then subdivided into 4 groups. Two groups received peanut oil 54 and 6 h before treatment with saline solution (group OS) or 20 mg/kg D (group OD). The other two groups received 50 micrograms/kg 17-beta-estradiol and 2 mg/kg progesterone, respectively, 54 and 6h before treatment with saline solution (group OHS) or 20 mg/kg D (group OHD). The sham-operated animals were treated as the OS group. Intact animals were injected with saline (group IS) or 20 mg/kg D (group ID) on the day of estrus, as determined by vaginal smears taken in the morning before the behavioral observations. Rats were observed for 6 min in the open field during the dark period of the cycle, 15 min after the administration of saline or D. There was a similar decrease in locomotion and rearing frequencies in OHS vs OHD and IS vs ID groups. Nevertheless, a lack of D sedative effect was observed in OD rats (locomotion and rearing frequencies, 56.0 +/- 3.3 vs 46.1 +/- 3.8 and 15.5 +/- 1.6 vs 15.2 +/- 1.6., for OS and OD groups, respectively). The results suggest that the sedative effect of diphenhydramine depends on the presence of ovarian steroids.

Animals↗

Effects of prenatal diphenhydramine administration on sexual behavior in rats.

In order to study the involvement of the brain histamine system on the sexual behavior of rats prenatally exposed to the histamine H1 receptor blockader, diphenhydramine (DPD), the female lordotic response and male sexual behavior were analyzed. The results show that the lordotic response in the prenatal DPD-treated rats was increased in relation to control animals. Impairment of male sexual behavior was indicated by an increase in ejaculation latency, in the number of mounts and a decrease in the number of ejaculations up to 30 min after the first intromission. Prenatal exposure to DPD thus appears to alter female and male sexual behavior on reaching adulthood.

Animals↗