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1 September 2003 Effects of Highly or Relatively Selective 5-HT1A Receptor Agonists on Lordosis in Female Rats
Miki Kishitake, Korehito Yamanouchi
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Abstract

To investigate the role of serotonin (5-HT) receptor 1A or 7 in regulating lordosis behavior in female rats, ovariectomized rats were treated with 3 kinds of receptor agonists and lordosis behavior was observed. The injected agents were the selective 5-HT1A receptor agonist, buspirone (BUS), the highly selective 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetralin ((±)8-OH-DPAT), and the 5-HT1A and 5-HT7 receptor agonist, (R)-8-hydroxy-2-(di-n-propylamino)tetralin (( )8-OH-DPAT). A behavioral test was performed after ovariectomy and subcutaneous implantation of a silicon tube containing estradiol. Female rats in which the lordosis quotient (LQ) was over 70 were intraperitoneally injected with several doses of these agents. As a result, in the BUS group, the dose of 3 mg/kg bw, but not 1 mg/kg was effective for suppressing lordosis. On the other hand, an inhibitory effect was observed from 0.25 mg/kg and 0.5 mg/kg in the ( )8-OH-DPAT and (±)8-OH-DPAT groups, respectively. In the time-course experiment, in all drug-treated groups, LQ decreased to lower than 20 after 15 min and low LQ continued for 1 hr at least. Measurement of locomotor activity using an infrared sensor system showed no relation between the decrease in lordosis by these agents and spontaneous locomotion. These results indicate that 5-HT1A is strongly involved in the lordosis-inhibiting circuit of the serotonin neurons.

Miki Kishitake and Korehito Yamanouchi "Effects of Highly or Relatively Selective 5-HT1A Receptor Agonists on Lordosis in Female Rats," Zoological Science 20(9), 1133-1138, (1 September 2003). https://doi.org/10.2108/zsj.20.1133
Received: 5 February 2003; Accepted: 1 June 2003; Published: 1 September 2003
KEYWORDS
5-HT1A receptor
8-OH-DPAT
Buspirone
female rat
lordosis
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