It has been demonstrated using Fos immunocytochemistry that copulation
activates specific cell populations in the mammalian brain. Prior to
this study, no similar work has been carried out in birds. In mammals,
Fos has identified brain circuits activated by genital (penile)/somat
osensory and by olfactory/vomeronasal stimuli. Such inputs, of course,
should play little or no role in birds (no penis, little or no role f
or olfaction) and a differential responsiveness could therefore be exp
ected. Male Japanese quail (Coturnix japonica) were allowed to interac
t freely with adult females and the presence of active sexual behavior
, including cloacal contact movements, was confirmed in each case. Con
trol subjects were exposed to a domestic chick (same size as an adult
quail) and no sexual behavior was observed. Copulation induced the app
earance of Fos-like immunoreactive (FLI) cells in the preoptic area, t
he hyperstriatum ventrale, parts of the archistriatum, and the nucleus
intercollicularis. Induction of FLI cells was observed throughout the
rostral to caudal extent of the preoptic region of males from the lev
el of the tractus septomesencephalicus to the level of the anterior co
mmissure, and in the rostral part of the hypothalamus to the level of
the supraoptic decussation. The FLI cells did not lie directly adjacen
t to the third ventricle, but were located 500-1000 mu m from the vent
ricle wall at the level of the lateral edge of the medial preoptic nuc
leus or, in more caudal sections, in a position ventrolateral to the b
ed nucleus striae terminalis. It is unlikely that the Fos induction in
males resulted from copulation-induced endocrine changes because copu
lation did not affect plasma levels of luteinizing hormone or testoste
rone. It is concluded that the responses were due to copulation-associ
ated somatosensory inputs and/or to stimuli originating from the femal
e.