The present study tested the hypothesis that photoperiodic control of reproductive function in the postpubertal Djungarian hamster is associated with changes in the number, morphology, or distribution of GnRH-immunoreactive cell bodies in the brain. To initiate or arrest sexual maturation, males were reared in long (LD, 16L:8D) or short (SD, 10L:14D) days from birth. In two other groups that were chronologically past the normal onset of puberty, males were transferred at 30 days of age from LD to SD or from SD to LD to arrest or initiate reproductive function, respectively. At 40, 60, or 90 days of age, 4-6 hamsters in each of the four photoperiod treatment groups were killed by intracardiac perfusion. Testes weights were significantly increased in males exposed to long days (LD and SD-to-LD groups) compared to those treated with short days (SD and LD-to-SD groups). Serum FSH concentrations at 40 days of age were also increased in the two groups of males in long days compared to those in both groups in short days (p < 0.05, ANOVA); LH concentrations were unaffected by photoperiod treatments. Brain sections (60 microns) from the corpus callosum decussation to the suprachiasmatic nucleus in the anterior hypothalamus were processed for GnRH immunocytochemistry. In brain regions that contained the majority of GnRH neurons, i.e., the medial preoptic area and diagonal band of Broca, the numbers of GnRH-immunoreactive cell bodies were the same among the four treatment groups.(ABSTRACT TRUNCATED AT 250 WORDS)