Abstract. The objective of this study was to investigate the changes in secretion of inhibin and cellular localization of the inhibin α and inhibin/activin (βA and βB) subunits in male Japanese quail from 1 to 7 weeks after hatching. The posthatch profile of plasma luteinizing hormone (LH), immunoreactive (ir) inhibin and testosterone were measured by radioimmunoassay. Testes were immunostained by the avidin-biotin-peroxidase complex method (ABC) using polyclonal antisera raised against inhibin α, inhibin/activin βA and inhibin/activin βB from one week of age to sexual maturity. Testicular weight increased gradually until 4 weeks and abruptly increased from 5 weeks of age onwards. The plasma concentrations of LH and ir-inhibin increased significantly at 5 weeks of age, and the plasma concentration of testosterone increased significantly at 6 weeks of age. Pituitary contents of LH showed a steady increase until 6 weeks of age and then abruptly increased at 7 weeks of age. Coincident to the increase in plasma testosterone, the testicular contents of testosterone significantly increased from 5 weeks through sexual maturity.Immunohistochemically, localization of the inhibin/activin α, βA and βB subunts was found in the Sertoli and Leydig cells at all ages of development from one week of age to sexual maturity. These results suggest that Sertoli and Leydig cells are the major source of inhibin secretion during development in male Japanese quail. Key words: Inhibin, Japanese quail (Coturnix japonica), Luteinizing hormone (LH), Testes, Testosterone (J. Reprod. Dev. 54: [100][101][102][103][104][105][106] 2008) nhibins and activins are growth and differentiation factors that have been localized in both the reproductive and non-reproductive organs. They exert their effects through both endocrine and local (autocrine/paracrine) mechanisms [1]. Inhibins and activins are structurally related dimeric gonadal proteins with the ability to regulate follicle-stimulating hormone (FSH) secretion from the pituitary glands [2,3]. Inhibin consists of an α subunit linked by a disulfide bridge to one of the 2 highly homologous β subunits (βA and βB) to form inhibin A (α and βA) or inhibin B (α and βB) [4]. In mammalian species, apart from their action on FSH secretion, the inhibins and activins have been shown to exert paracrine/autocrine effects within the gonads [5][6][7][8] and other tissues [9] and have been proposed to have an important paracrine function during testes development [10,11]. In the male, inhibin is produced in the testis, principally by Sertoli cells. There are temporal changes in inhibin expression and secretion with the changing role of the Sertoli cell in immature and adult testes. Variations in inhibins production among species reflect the different patterns of maturation [11][12][13].In avian species, studies have confirmed a mammalian-type endocrine role for inhibins [14][15][16][17]; however, the autocrine/paracrine roles of inhibins and activins in the gonads are still being defined. The profiles of plasm...