Inhibition and activation of the thyroidal axis by the adrenal axis in vertebrates

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 120, Issue 1, 1998, Pages 169-174

  Kühn, Eduard R ^a   Geris, Kris L ^a   Van Der Geyten, Serge ^a   Mol, Koen A ^a   Darras, Veerle M ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

Adrenal thyroid interaction; Adrenals; Deiodination; Inner ring deiodination; Iodohormones; Iodothyronine deiodinase; Outer ring deiodination; Surrenals; Thyroid; Thyroid activation; Thyroid inhibition

Indexed keywords

CORTICOTROPIN RELEASING FACTOR; GLUCOCORTICOID; IODOTHYRONINE; THYROTROPIN;

ADRENAL GLAND; AMPHIBIA; CHICK EMBRYO; CONFERENCE PAPER; DEIODINATION; FISH; METAMORPHOSIS; NONHUMAN; STRESS; THYROID FUNCTION;

AMPHIBIA; AVES; MAMMALIA; VERTEBRATA;

EID: 0344542036     PISSN: 10956433     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1095-6433(98)10026-0     Document Type: Conference Paper

References (49)

1. Berkowsky, B., Hanke, W. Interaction between thyroid and interrenal gland in carp (Cyprinus carpio). 15th Conference of European Comparative Endocrinologists, Leuven, Abstract p. 157; 1990.
2. Brown S.B., MacLatchy D.L., Hara T.J., Eales J.G. Effects of cortisol on aspects of 3,5,3′-triiodo-L-thyronine metabolism in rainbow trout (Oncorhynchus mykiss). Gen Comp Endocrinol. 81:1991;207-216.
3. Buscaglia M., Leloup J., De Luze A. The role and regulation of monodeiodination of thyroxine to 3,5,3′-triiodothyronine during amphibian metamorphosis. Balls M., Bownes M. Metamorphosis. 1985;273-293 Clarendon, Oxford.
4. Darras V.M., Kühn E.R. Increased plasma levels of thyroid hormones in a frog Rana ridibunda following intravenous administration of TRH. Gen Comp Endocrinol. 48:1982;469-475.
5. Darras V.M., Kühn E.R. Purification of frog (Rana ridibunda) thyrotropin and its identification using a specific and sensitive bioassay. Ann Soc Zool Belg. 113:1983;301-308.
6. Darras V.M., Berghman L.R., Vanderpooten A., Kühn E.R. Growth hormone acutely decreases type III iodothyronine deiodinase in chicken liver. FEBS Letts. 310:1992;5-8.
7. Darras V.M., Visser T.J., Berghman L.R., Kühn E.R. Ontogeny of type I and type III deiodinase activities in embryonic and posthatch chicks: relationship with changes in plasma triiodothyronine and growth hormone levels. Comp Biochem Physiol. 103A:1992;131-136.
8. Darras V.M., Cokelaere M., Dewil E., Arnouts S., Decuypere E., Kühn E.R. Partial food restriction increases hepatic inner ring deiodinating activity in the chicken and the rat. Gen Comp Endocrinol. 100:1995;334-338.
9. Darras V.M., Kotanen S.P., Geris K.L., Berghman L.R., Kühn E.R. Plasma thyroid hormone levels and iodothyronine-deiodinase activity following an acute glucocorticoid challenge in embryonic compared to posthatch chickens. Gen Comp Endocrinol. 104:1996;203-212.
10. Decuypere E., Kühn E.R. Effect of fasting and feeding time on circadian rhythms of serum thyroid hormone concentrations, glucose, liver monodeiodinating activity and rectal temperature in growing chickens. Dom Anim Endocrinol. 1:1984;251-262.
11. 3) and on peripheral monodeiodination in pre- and posthatching chickens. Horm Metab Res. 15:1983;233-236.
12. Decuypere E., Dewil E., Kühn E.R. The hatching process and the role of hormones. Tullett S.C. Avian Incubation. 1990;239-256 Butterworth, Guildford.
13. De Jesus E.G., Inui Y., Hirano T. Cortisol enhances the stimulating action of thyroid hormones on dorsal fin-ray resorption of flounder larvae in vitro. Gen Comp Endocrinol. 79:1990;167-173.
14. Denver R.J. Several hypothalamic peptides stimulate in vitro thyrotropin secretion by pituitaries of anuran amphibians. Gen Comp Endocrinol. 72:1988;383-393.
15. Denver R.J. Acceleration of anuran amphibian metamorphosis by corticotropin-releasing hormone-like peptides. Gen Comp Endocrinol. 91:1983;38-51.
16. Denver R.J., Licht P. Neuropeptide stimulation of thyrotropin secretion in the larval bullfrog: evidence for a common neuroregulator of thyroid and interrenal activity in metamorphosis. J Exp Zool. 252:1989;101-104.
17. Eales J.G. The influence of nutritional state on thyroid function in various vertebrates. Am Zool. 28:1988;351-362.
18. Etkin W. Metamorphosis. Moore J. Physiology of Amphibia. 1:1964;426-468 Academic Press, New York.
19. Farbridge K.J., Flett P.A., Leatherland J.F. Temporal effects of restricted diet and compensatory increased dietary intake on thyroid function, plasma growth hormone levels and tissue lipid reserves of rainbow trout, Oncorhynchus mykiss. Aquaculture. 104:1992;157-174.
20. Fisher D.A., Klein A.H. Thyroid development and disorders of thyroid function in the newborn. N Engl J Med. 304:1981;702-712.
21. Foo J.T.W., Lam T.J. Serum cortisol response to handling stress and the effect of cortisol implantation on testosterone level in the tilapia, Oreochromis mossambicus. Aquaculture. 115:1993;145-148.
22. Frith S.D., Eales J.G. Thyroid hormone deiodination pathways in brain and liver of rainbow trout, Oncorhynchus mykiss. Gen Comp Endocrinol. 101:1996;323-332.
23. Galton V.A., Hiebert A. The ontogeny of the enzyme systems for the 5′- and 5-deiodination of thyroid hormones in chick embryo liver. Endocrinology. 120:1987;2604-2610.
24. Galton V.A., Hiebert A. The ontogeny of iodothyronine 5'-monodeiodinase activity in Rana catesbeiana tadpoles. Endocrinology. 122:1988;640-645.
25. Geris K.L., Darras V.M., Berghman L.R., Kühn E.R. Influence of corticotropin-releasing factor on the in vitro thyroxine and thyrotropin secretion in newly hatched fowl. Belg J Zool. 125:1995;143-156.
26. Geris K.L., Kotanen S.P., Berghman L.R., Kühn E.R., Darras V.M. Evidence of a thyrotropin-releasing activity of ovine corticotropin-releasing factor in the domestic fowl (Gallus domesticus). Gen Comp Endocrinol. 104:1996;139-146.
27. Griffin J.E. The thyroid. Griffin J.E., Ojeda S.R. Textbook of Endocrine Physiology. 2:1992;224-246 Oxford University Press, London.
28. Gudernatsch J.F. Feeding experiments on tadpoles. I. The influence of specific organs given as food on growth and differentiation. Arch Entwick Organ. 35:1912;357-481.
29. Kanamori A., Brown D.D. The regulation of thyroid hormone receptor β genes by thyroid hormone in Xenopus laevis. J Biol Chem. 267:1992;739-745.
30. Kaplan N.M. The adrenal glands. Griffin J.E., Ojeda S.R. Textbook of Endocrine Physiology. 2:1992;247-275 Oxford University Press, London.
31. Kikuyama S., Kawamura K., Tanaka S., Yamamoto K. Aspects of amphibian metamorphosis: hormonal control. Int Rev Cytol. 145:1993;105-148.
32. Kühn E.R., Berghman L.R., Moons L., Vandesande F., Decuypere E., Darras V.M. Hypothalamic and peripheral control of thyroid function during the life cycle of the chicken. Sharp P.J. Avian Endocrinology. 1993;29-46 Journal of Endocrinology, Bristol.
33. Kühn E.R., Shimada K., Ohkubo T., Vleurick L.M., Berghman L.R., Darras V.M. Influence of recombinant chicken prolactin on thyroid hormone metabolism in the chick embryo. Gen Comp Endocrinol. 103:1996;349-358.
34. 4 concentrations in chicken serum. Gen Comp Endocrinol. 34:1978;323-327.
35. Meeuwis R., Michielsen R., Decuypere E., Kühn E.R. Thyrotropic activity of the ovine corticotropin-releasing factor in the chick embryo. Gen Comp Endocrinol. 76:1989;357-363.
36. Mitchell M.A., MacLeod M.G., Raza A. The effects of ACTH and dexamethasone upon plasma thyroid hormone levels and heat production in the domestic fowl. Comp Biochem Physiol. 85A:1986;207-215.
37. Mol K., Kaptein E., Darras V.M., de Greef W.J., Kühn E.R., Visser T.J. Different thyroid hormone-deiodinating enzymes in tilapia (Oreochromis niloticus) liver and kidney. FEBS Letts. 321:1993;140-144.
38. Redding J.M., Schreck C.B., Birks E.K., Ewing R.D. Cortisol and its effects on plasma thyroid hormone and electrolyte concentrations in fresh water and during seawater acclimation in yearling Coho salmon, Oncorhynchus kisutch. Gen Comp Endocrinol. 56:1984;146-155.
39. Redding J.M., de Luze A., Leloup-Hatey J., Leloup J. Suppression of plasma thyroid hormone concentrations by cortisol in the European eel Anguilla anguilla. Comp Biochem Physiol. 83A:1986;409-413.
40. Shields C.A., Eales J.G. Thyroxine 5′-monodeiodinase activity in hepatocytes of rainbow trout, Salmo gairdneri: distribution, effects of starvation and exogenous inhibitors. Gen Comp Endocrinol. 63:1986;334-343.
41. Sweeting R.M., Eales J.G. The effects of fasting and feeding on hepatic thyroxine 5′-monodeiodinase activity in the rainbow trout, Oncorhynchus mykiss. Can J Zool. 70:1992;1516-1525.
42. Tonon M.C., Cuet P., Lomacz M., Jégou S., Côté J., Couteux L., Ling N., Pelletier G., Vaudry H. Comparative effects of corticotrophin-releasing factor, argenine vasopressin, and related neuropeptides on the secretion of ACTH and α-MSH by frog anterior pituitary cells and neurointermediate lobes in vitro. Gen Comp Endocrinol. 61:1986;438-445.
43. Van der Geyten, S., Pluymers, W. Mol, K. Darras, V.M., Kühn, E.R. The influence of fasting and refeeding on iodothyronine deiodinases in tilapia (Oreochromis niloticus), 17th Annual Conference European Society for Comparative Physiology and Biochemistry, Antwerp 27-31, 1996;Abstract 37.
44. Vijayan M.M., Flett P.A., Leatherland J.F. Effect of cortisol on the in vitro hepatic conversion of thyroxine to triiodothyronine in brook charr (Salvelinus fontinalis Mitchill). Gen Comp Endocrinol. 70:1988;312-318.
45. Williamson R.A., Davison T.F. Effects of increased circulating corticosterone on serum and thyroidal concentrations of iodothyronines and the responses to thyrotrophin in the immature fowl (Gallus domesticus). Gen Comp Endocrinol. 65:1987;65-72.
46. Wright M.L., Cykowski L.J., Lundgren L., Hamond K.L., Kochan D.M., Faszewski E.E., Anuszewski C.M. Anterior pituitary and adrenal cortical hormones accelerate or inhibit tadpole hindlimb growth and development depending on stage of spontaneous development or thyroxine concentration in induced metamorphosis. J Exp Zool. 270:1944;175-188.
47. Wu S.Y., Klein A.H., Chopra I.J., Fisher D.A. Alterations in tissue thyroxine-5′-monodeiodinating activity in perinatal period. Endocrinology. 103:1978;235-239.
48. Yaoita Y., Shi Y.B., Brown D.D. Xenopus laevis α and β thyroid hormone receptors. Proc Natl Acad Sci USA. 87:1990;7090-7094.
49. Yoshizato K., Frieden E. Increase in binding capacity for triiodothyronine in tadpole tail nuclei during metamorphosis. Nature. 254:1975;705-706.