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Adrenal tissue in the male African catfish, Clarias gariepinus: localization and steroid hormone secretion

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Abstract

Interrenal-like tissue in male African catfish is localized in paired organs, situated retroperitoneally anterior of the kidney. Histological and enzyme-histochemical (3β-hydroxysteroid dehydrogenase) reactions were carried out on sections of these organs in order to localize steroid-producing cells. In vitro incubations were carried out to determine the steroidogenic capacity of the interrenal-like tissue. Twenty-one steroids could be identified and quantified in the incubation medium, by means of gas chromatography followed by mass spectrometry. Cortisol, 5α-and 5β-androstanedione and androstenedione together comprised about 80% of the total steroid content. In a previous study, twenty testicular steroids were detected in plasma after castration. In the present investigation we have shown that most of these steroids can be produced by the interrenal-like tissue, which thus can be considered as an extra-testicular source of gonadal steroids.

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References

  • Andò S, Canonaco M, Beribaldi E, Valenti A, Maggiolini M, Piro A, Tavolaro R, Dessì-Fulgheri F (1988) The evaluation of androgen circulating levels following castration in adult male rats. Exp Clin Endocrinol 91:37–45

    Google Scholar 

  • Andò S, Canonaco M, Valenti A, Aquila S, Tavolaro R, Maggiolini M, Panno ML, Dessì-Fulgheri F (1989) The in vitro conversion of 3H-androstenedione to testosterone and dihydrotestosterone in the adrenal gland of castrated male rat: influence of gonadal steroid administration. Exp Clin Endocrinol 93:83–89

    Google Scholar 

  • Arai R, Tajima H, Tamaoki B (1969) In vitro transformation of steroids by the head kidney, the body kidney, and the corpuscles of Stannius of the rainbow trout (Salmo gairderi). Gen Comp Endocrinol 12:99–109

    Google Scholar 

  • Balm PHM, Lambert JGD, Wendelaar Bonga SE (1989) Corticosteroid biosynthesis in the interrenal cells of the teleost fish, Oreochromis mossambicus. Gen Comp Endocrinol 76:53–62

    Google Scholar 

  • Bara G (1968) Histochemical study of 3β-, 3α-, 11β-, and 17β-hydroxysteroid dehydrogenases in the adrenocortical tissue and the corpuscles of Stannius of Fundulus heteroclitus. Gen Comp Endocrinol 10:126–137

    Google Scholar 

  • Bardin CW, Peterson RE (1967) Studies of androgen production by the rat: testosterone and androstenedione content of blood Endocrinology 80:38–44

    Google Scholar 

  • Bélanger B, Bélanger A, Labrie F, Dupont A, Cusan J, Monfette G (1989) Comparison of residual C-19 steroids in plasma and prostatic tissue of human, rat and guinea pig after castration: unique importance of extratesticular androgens in men. J Steroid Biochem 32:695–698

    Google Scholar 

  • Bélanger B, Couture J, Caron S, Bodou P, Fiet J, Bélanger A (1990) Production and secretion of C-19 steroids by rat and guinea pig adrenals. Steroids 55:360–365

    Google Scholar 

  • Bélanger B, Caron S, Bodou P, Fiet J, Bélanger A (1992) Adrenal steroidogenesis in the guinea pig: effects of androgens. Steroids 57:76–81

    Google Scholar 

  • Bhattacharyya TK, Butler DG (1979) Fine structure of the adrenocortical homologue in the North American eel and modifications following seawater adaptation. Anat Rec 193:213–232

    Google Scholar 

  • Bidlingmaier F, Dorr HG, Eisenmenger W, Kuhnle U, Knorr D (1986) Contribution of the adrenal gland to the production of androstenedione and testosterone during the first two years of life. J Clin Endocrinol Metab 62:331–335

    Google Scholar 

  • Canonaco M, Andò S, Valenti A, Tavolaro R, Panno ML, Maggioline M, Dessì-Fulgheri F (1989) The in vitro transformation of [3H]dehydroepiandrosterone into its principal metabolites in the adrenal cortex of adult castrated male rats and following steroid treatment. J Endocrinol 121:419–424

    Google Scholar 

  • Chavin W (1966) Adrenal histochemistry of some freshwater and marine teleosts. Gen Comp Endocrinol 6:183–194

    Google Scholar 

  • Hansson T, Gustafsson JÄ (1981) Sex differences in the hepatic in vitro metabolism of 4-androstene-3,17-dione in rainbow trout, Salmo gairdneri. Gen Comp Endocrinol 44:181–188

    Google Scholar 

  • Hyatt PJ, Bell JBG, Bhatt K, Tait JF (1983) Preparation and steroidogenic properties of purified zona fasciculata and zona reticularis cells from the guinea-pig adrenal gland. J Endocrinol 96:1–14

    Google Scholar 

  • Jung B, Moritz M-E, Berchtold J-P (1981) Fine structure and function of interrenal (adrenocortical) cells of dexamethasonetreated trout (Salmo fario L.). Cell Tissue Res 214:641–649

    Google Scholar 

  • Kime DE (1978) The hepatic catabolism of cortisol in teleost fish-adrenal origin of 11-oxo-testosterone precursors. Gen Comp Endocrinol 35:322–328

    Google Scholar 

  • Kitay JI, Coyne MD, Newsome W, Nelson R (1965) Relation of the ovary to adrenal corticosteroid production and adrenal enzyme activity in the rat. Endocrinology 77:902–907

    Google Scholar 

  • Mayer I, Borg B, Schulz R (1990) Conversion of 11-ketoandrostenedione to 11-ketotestosterone by blood cells of six fish species. Gen Comp Endocrinol 77:70–74

    Google Scholar 

  • Nandi J (1962) The structure of the interrenal gland in teleost fishes. Univ Calif Publ Zool 65:129–212

    Google Scholar 

  • Oguri M (1982) Interrenal gland and chromaffin cells. In: Hibiya T (ed) An atlas of fish histology. Kodansha, Tokyo and Fisher, Stuttgart, pp 126–130

    Google Scholar 

  • Schoonen WGEJ, Lambert JGD, Van Oordt PGWJ (1988) Quantitative analysis of steroids and steroid glucuronides in the seminal vesicle fluid of feral spawning and feral and cultivated non-spawning African catfish, Clarias gariepinus. Gen Comp Endocrinol 70:91–100

    Google Scholar 

  • Schreck CB, Bradford CS, Fitzpatrick MS, Patiño R (1989) Regulation of the interrenal of fishes: non-classical control mechanisms. Fish Physiol Biochem 7:259–265

    Google Scholar 

  • Schulz R (1986) In vitro metabolism of steroid hormones in the liver and in blood cells of male rainbow trout (Salmo gairdneri Richardson). Gen Comp endocrinol 64:312–319

    Google Scholar 

  • Schulz R, Blüm V (1991) Extragonadal 17β-hydroxysteroid dehydrogenase activity in raibow trout. Gen Comp Endocrinol 82:197–205

    Google Scholar 

  • Van den Hurk R (1973) The localization of steroidogenesis in the testes of oviparous and viviparous teleosts. Proc Koninkl Ned Acad Wetensch Series C 76:270–279

    Google Scholar 

  • Vermeulen GJ, Lambert JGD, Lenczowksi MJP, Goos HJT (1993) Steroid hormone secretion by testicular tissue from African catfish, Clarias gariepinus, in primary culture: identification and quantification by gas chromatography-mass spectrometry. Fish Physiol Biochem 12:21–30

    Google Scholar 

  • Vermeulen GJ, Lambert JGD, Van der Looy MJW, Goos HJTh (1994) Gas chromatographic-mass spectrometric (GC-MS) analysis of gonadal steroids in plasma of the male African catfish, Clarias gariepinus: effects of castration or treatment with gonadotropin-releasing hormone analogue. Gen Comp Endocrinol 96:288–297

    Google Scholar 

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Vermeulen, G.J., Lambert, J.G.D., Teitsma, C.A. et al. Adrenal tissue in the male African catfish, Clarias gariepinus: localization and steroid hormone secretion. Cell Tissue Res 280, 653–657 (1995). https://doi.org/10.1007/BF00318367

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  • DOI: https://doi.org/10.1007/BF00318367

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