Localization of Inhibin Alpha‐Subunit Immunoreactivity in the Rat Adrenal Cortex

Inhibin, a water soluble, non‐steroidal glycoprotein hormone that inhibits follicle‐stimulating hormone secretion, is produced by the gonads and several non‐gonadal tissues (placenta, pituitary and brain). This study describes the presence of inhibin α‐chain‐immunoreactive cells in the adrenal cortex of intact adult male rats and the effects of hypophysectomy and adrenocorticotropin treatment on the expression of inhibin in that gland. In intact rats, the majority of the immunoreactive cells were found scattered in the zona glomerulosa and reticularis. The zona fasciculata contained only a few cells immunopositive for the inhibin α‐chain. No immunoreactive cells were found in the medulla. Hypophysectomy resulted in a dramatic reduction in α‐subunit immunoreactivity with only scattered cells observed in the zona glomerulosa and reticularis (0 to 2 cells/section). No immunoreactive cells were found in the zona fasciculata or the medulla. Following supraphysiologic adrenocorticotropin administration to hypophysectomized animals, the number of inhibin α‐chain‐immunoreactive cells significantly increased in each zone of the adrenal cortex. The most prominent changes were seen in the zona reticularis. Interestingly, in the adrenocorticotropin‐treated animals scattered immunopositive cells were also present in the medulla. Our results suggest that inhibin‐related peptide(s) exist within the adrenal gland and that the expression of these peptides is regulated by adrenocorticotropin. Inhibin‐related peptide(s) may, therefore, play a paracrine and/or endocrine role in the adrenal function.

[1]  J. Vaughan,et al.  Inhibin β in central neural pathways involved in the control of oxytocin secretion , 1988, Nature.

[2]  M. Culler,et al.  Passive immunoneutralization of endogenous inhibin: sex-related differences in the role of inhibin during development , 1988, Molecular and Cellular Endocrinology.

[3]  H. Shibai,et al.  Erythroid differentiation factor is encoded by the same mRNA as that of the inhibin beta A chain. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[4]  M. Culler,et al.  Immunocytochemical localization of inhibin in rat and human reproductive tissues , 1987, Molecular and Cellular Endocrinology.

[5]  R. Richards,et al.  Alpha-inhibin gene expression occurs in the ovine adrenal cortex, and is regulated by adrenocorticotropin. , 1987, Molecular endocrinology.

[6]  P. Sawchenko,et al.  Localization, secretion, and action of inhibin in human placenta. , 1987, Science.

[7]  N. Ling,et al.  Complementary deoxyribonucleic acid (cDNA) cloning and DNA sequence analysis of rat ovarian inhibins. , 1987, Molecular endocrinology.

[8]  H. Burger,et al.  The human placenta: a novel source of inhibin. , 1986, Biochemical and biophysical research communications.

[9]  C. Crowther,et al.  Human inhibin genes , 1986, FEBS letters.

[10]  N. Ling,et al.  Complementary DNA Sequences of Ovarian Follicular Fluid Inhibin Show Precursor Structure and Homology with Transforming Growth Factor β , 1986 .

[11]  Joan Vaughan,et al.  Purification and characterization of an FSH releasing protein from porcine ovarian follicular fluid , 1986, Nature.

[12]  Naoto Ueno,et al.  Pituitary FSH is released by a heterodimer of the β-subunits from the two forms of inhibin , 1986, Nature.

[13]  M T Hearn,et al.  Cloning and sequence analysis of cDNA species coding for the two subunits of inhibin from bovine follicular fluid. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[14]  P. Seeburg,et al.  Structure of two human ovarian inhibins. , 1986, Biochemical and biophysical research communications.

[15]  R Guillemin,et al.  Isolation and partial characterization of a Mr 32,000 protein with inhibin activity from porcine follicular fluid. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[16]  K. Miyamoto,et al.  Isolation of porcine follicular fluid inhibin of 32K daltons. , 1985, Biochemical and biophysical research communications.

[17]  H. Burger,et al.  Isolation of inhibin from bovine follicular fluid. , 1985, Biochemical and biophysical research communications.

[18]  T. Joh,et al.  Optimization of tyrosine hydroxylase immunocytochemistry in paraffin sections using pretreatment with proteolytic enzymes. , 1984, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[19]  Peter Lindstrom,et al.  Four unlabeled antibody bridge techniques: a comparison. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[20]  C. Channing,et al.  Evidence for ovarian "inhibin": suppression of the secondary rise in serum follicle stimulating hormone levels in proestrous rats by injection of porcine follicular fluid. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[21]  R. Sharpe,et al.  Evidence for inhibin-like activity in bovine follicular fluid , 1976, Nature.

[22]  H. Burger,et al.  Studies on the relationship between FSH and germ cells: evidence for selective suppression of FSH by testicular extracts. , 1976, Journal of reproduction and fertility. Supplement.

[23]  H. Burger,et al.  Selective suppression of FSH by testicular extracts. , 1976, Endocrinology.

[24]  B. Setchell,et al.  Inhibin-like activity in rete testis fluid. , 1974, The Journal of endocrinology.

[25]  K. Stevens Exchange interactions in magnetic insulators , 1972 .

[26]  D. R. Mccullagh DUAL ENDOCRINE ACTIVITY OF THE TESTES. , 1932, Science.

[27]  J. Vaughan,et al.  Production and regulation of inhibin subunits in pituitary gonadotropes. , 1989, Endocrinology.

[28]  W. Vale,et al.  Gonadal and extragonadal expression of inhibin alpha, beta A, and beta B subunits in various tissues predicts diverse functions. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[29]  K. Osteen,et al.  The role of nonsteroidal regulators in control of oocyte and follicular maturation. , 1982, Recent progress in hormone research.

[30]  J. Findlay,et al.  Regulation of gonadotrophin secretion in rams from birth to sexual maturity. II. Response of the pituitary-testicular axis to LH-RH infusion. , 1976, Journal of reproduction and fertility.

[31]  F. Morley,et al.  Oestrogenic function in postmenopausal women. , 1971, Journal of reproduction and fertility.