Effects of adrenaline administration on the interrenal gland of the newt, Triturus carnifex: Evidence of intraadrenal paracrine interactions

The existence of paracrine control of steroidogenic activity by adrenochromaffin cells in Triturus carnifex was investigated by in vivo adrenaline (A) administration. The effects were evaluated by examination of the ultrastructural morphological and morphometrical features of the tissues as well as the serum levels of aldosterone, noradrenaline (NA), and adrenaline. In March and July, adrenaline administration reduced aldosterone release (from 187.23 ± 2.93 pg/ml to 32.28 ± 1.85 pg/ml in March; from 314.60 ± 1.34 pg/ml to 87.51 ± 2.57 pg/ml in July) from steroidogenic cells. The cells showed clear signs of lowered activity: they appeared full of lipid, forming large droplets. Moreover, adrenaline administration decreased the mean total number of secretory granules in the chromaffin cells in July (from 7.74 ± 0.74 granules/μm2 to 5.14 ± 1.55 granules/μm2). In this period T. carnifex chromaffin cells contain almost exclusively NA granules (NA: 7.42 ± 0.86 granules/μm2; A: 0.32 ± 0.13 granules/μm2). Adrenaline administration reduced noradrenaline content (4.36 ± 1.40 granules/μm2) in the chromaffin cells, enhancing noradrenaline secretion (from 640.19 ± 1.65 pg/ml to 1030.16 ± 3.03 pg/ml). In March, adrenaline administration did not affect the mean total number of secretory vesicles (from 7.24 ± 0.18 granules/μm2 to 7.25 ± 1.97 granules/μm2). In this period the chromaffin cells contain both catecholamines, noradrenaline (3.88 ± 0.13 granules/μm2), and adrenaline (3.36 ± 0.05 granules/μm2), in almost equal quantities; adrenaline administration reduced adrenaline content (1.74 ± 0.84 granules/μm2), increasing adrenaline release (from 681.27 ± 1.83 pg/ml to 951.77 ± 4.11 pg/ml). The results of this study indicate that adrenaline influences the steroidogenic cells, inhibiting aldosterone release. Adrenaline effects on the chromaffin cells (increase of noradrenaline or adrenaline secretion) vary according to the period of chromaffin cell functional cycle. The existence of intraadrenal paracrine interactions in T. carnifex is discussed. J. Morphol. 261:18–25, 2004. © 2004 Wiley‐Liss, Inc.

[1]  A. Capaldo,et al.  Influence of acetylcholine administration on the interrenal gland of Triturus carnifex (Amphibia, Urodela) , 2004 .

[2]  A. Epple,et al.  Effects of exogenous catecholamines on plasma catecholamines and glucose in the sea lamprey,Petromyzon marinus , 1983, Journal of comparative physiology.

[3]  B. Nibbio,et al.  Catecholaminotropic effects of catecholamines in a teleost fish,Anguilla rostrata , 2004, Journal of Comparative Physiology B.

[4]  R. Wurtman Stress and the adrenocortical control of epinephrine synthesis. , 2002, Metabolism: clinical and experimental.

[5]  S. Perry,et al.  Adrenergic regulation of catecholamine secretion from trout (Oncorhynchus mykiss) chromaffin cells. , 2002, The Journal of endocrinology.

[6]  A. Hodel Effects of glucocorticoids on adrenal chromaffin cells. , 2001 .

[7]  S. Perry,et al.  Neuronal control of catecholamine secretion from chromaffin cells in the rainbow trout (Oncorhynchus mykiss). , 1999, The Journal of experimental biology.

[8]  S. Shepherd,et al.  Frog chromaffin and Adrenocortical Cell Co‐Cultures: A Model for the Study of Medullary Control of Corticosteroidogenesis , 1998, Journal of neuroendocrinology.

[9]  S. G. Reid,et al.  The adrenergic stress response in fish: control of catecholamine storage and release. , 1998, Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology.

[10]  S. Bornstein,et al.  Basal Steroidogenic Activity of Adrenocortical Cells Is Increased 10-Fold by Coculture with Chromaffin Cells. , 1998, Endocrinology.

[11]  G. Mazzocchi,et al.  Paracrine control of steroid hormone secretion by chromaffin cells in the adrenal gland of lower vertebrates. , 1998, Histology and histopathology.

[12]  W. Kloas,et al.  Neuroendocrine effects on adrenal hormone secretion in carp (Cyprinus carpio). , 1997, General and comparative endocrinology.

[13]  A. Krętowski,et al.  Increased in vitro interleukin-12 production by peripheral blood in high-risk IDDM first degree relatives. , 1997, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[14]  W. Scherbaum,et al.  Morphological and functional studies of the paracrine interaction between cortex and medulla in the adrenal gland , 1997, Microscopy research and technique.

[15]  G. Nussdorfer Paracrine control of adrenal cortical function by medullary chromaffin cells. , 1996, Pharmacological reviews.

[16]  W. Kloas,et al.  Comparative Aspects of Regulation and Function of the Adrenal Complex in Different Groups of Vertebrates , 1995, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[17]  W. Kloas,et al.  Hormonal regulation of osmomineral content in amphibia , 1994 .

[18]  H. Vaudry,et al.  In vitro study of catecholamine release from perifused frog adrenal slices. , 1993, General and comparative endocrinology.

[19]  M. Zerani,et al.  Corticosterone during the Annual Reproductive Cycle and in Sexual Behavior in the Crested Newt, Triturus carnifex , 1993, Hormones and Behavior.

[20]  W. Kloas,et al.  Effects of atrial natriuretic factor on corticosteroid and catecholamine secretion by the adrenals of Xenopus laevis. , 1992, General and comparative endocrinology.

[21]  A. Capaldo,et al.  The interrenal gland of Triturus cristatus after insulin administration during the annual cycle , 1992, Journal of morphology.

[22]  A. Capaldo,et al.  Annual cycle of the chromaffin cells of Triturus cristatus , 1991, Journal of morphology.

[23]  H. Vaudry,et al.  Dopamine inhibits corticosteroid secretion from frog adrenal gland, in vitro. , 1990, Endocrinology.

[24]  J. Bertoni,et al.  Physiological doses of epinephrine in the human: chronotropic but not hyperglycemic or catecholaminotropic. , 1989, The Journal of experimental zoology.

[25]  H. Vaudry,et al.  Neuronal and paracrine regulation of adrenal steroidogenesis: interactions between acetylcholine, serotonin and vasoactive intestinal peptide (VIP) on corticosteroid production by frog interrenal tissue , 1988, Brain Research.

[26]  A. Fasolo,et al.  Anatomical organization of CRF- and AVT-like systems in the newt hypothalamus and the effects of localized lesion to the posterior hypothalamus on serum aldosterone and corticosterone , 1988 .

[27]  K. Heim,et al.  Single doses of catecholamines in the rat: catecholaminotropic, but not hyperglycemic. , 1988, Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology.

[28]  S. I. Perry,et al.  The effects of prolonged epinephrine infusion on the physiology of the rainbow trout, Salmo gairdneri. I. Blood respiratory, acid-base and ionic states. , 1987, The Journal of experimental biology.

[29]  F. Accordi,et al.  Evolutionary trends in adrenal gland of anurans and urodeles , 1986, Journal of morphology.

[30]  W. Hanke The Adrenal Cortex of Amphibia , 1978 .

[31]  I. Henderson,et al.  General, comparative and clinical endocrinology of the adrenal cortex , 1976 .

[32]  J. M. Hunt,et al.  Inhibition of phenethanolamine Neethyl transferase by its product, epinephrine. , 1967, Life sciences.