Two types of lordosis-inhibiting systems in male rats: Dorsal raphe nucleus lesions and septal cuts

Masaki Kakeyama, Korehito Yamanouchi

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

To examine the functional relationships between the dorsal raphe nucleus and the septum in the inhibitory regulation of feminine sexual behavior in male rats, castrated male rats received destruction of the dorsal raphe nucleus (DRL), interruption of the septal outputs (ARD), or both DRL and ARD (DRL + ARD). All animals were treated with estradiol by using Silastic tubes, and feminine sexual behavior was observed every other day for 10 days. Most castrated control male rats did not show lordosis throughout the tests. In contrast, all of the males with DRL alone or ARD alone displayed lordosis, but the lordosis quotients (LQ) in these groups were lower than those of the female control group. On the other hand, DRL + ARD males showed higher LQs than the DRL or the ARD males, being comparable to control females. Thus, two types of strong inhibitory influence exist in the dorsal raphe nucleus and the septum, and resist the facilitation of feminine sexual behavior by estrogen in male rats. Furthermore, these inhibitory systems operate independently, because an additive effect of DRL and ARD in facilitating lordosis was clearly observed in DRL + ARD males.

Original languageEnglish
Pages (from-to)189-192
Number of pages4
JournalPhysiology and Behavior
Volume56
Issue number1
DOIs
Publication statusPublished - 1994
Externally publishedYes

Fingerprint

Lordosis
Sexual Behavior
Dorsal Raphe Nucleus
Estradiol
Estrogens

Keywords

  • Dorsal raphe nucleus
  • Inhibitory system
  • Lesion
  • Lordosis
  • Male rat
  • Septum

ASJC Scopus subject areas

  • Physiology (medical)
  • Behavioral Neuroscience

Cite this

Two types of lordosis-inhibiting systems in male rats : Dorsal raphe nucleus lesions and septal cuts. / Kakeyama, Masaki; Yamanouchi, Korehito.

In: Physiology and Behavior, Vol. 56, No. 1, 1994, p. 189-192.

Research output: Contribution to journalArticle

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