INTERDEPENDENCE OF CORTICOSTERONE-HORMONES AND THYROID-HORMONES IN TOAD LARVAE (BUFO-BOREAS) .2. REGULATION OF CORTICOSTERONE-HORMONES AND THYROID-HORMONES

Authors
Citation
Tb. Hayes et Th. Wu, INTERDEPENDENCE OF CORTICOSTERONE-HORMONES AND THYROID-HORMONES IN TOAD LARVAE (BUFO-BOREAS) .2. REGULATION OF CORTICOSTERONE-HORMONES AND THYROID-HORMONES, The Journal of experimental zoology, 271(2), 1995, pp. 103-111
Citations number
26
Categorie Soggetti
Zoology
ISSN journal
0022104X
Volume
271
Issue
2
Year of publication
1995
Pages
103 - 111
Database
ISI
SICI code
0022-104X(1995)271:2<103:IOCATI>2.0.ZU;2-#
Abstract
Typically, the role of corticosterone(B) in metamorphosis is considere d secondary to that of thyroid hormone, with B having only enhancing e ffects. In the current study, we demonstrate that the relationship bet ween the thyroid hormones and B is much more complex and that thyroxin e (T-4) may depend on B for some of its functions. Tadpoles of the wes tern toad (Bufo boreas) were treated with various combinations of cort icosterone (B), thyroxine (T-4), triiodothyronine (T-3), a goitrogen ( thiourea; Thio), and a corticoid synthesis inhibitor (metyrapone; MTP) . Hormones were extracted from individual tadpoles and whole-body horm one levels determined by radioimmunoassay. B-treatment decreased the r atio of T-4 to T-3, suggesting that B increased the conversion of endo genous T-4 to T-3. In addition, B-treatment in combination with T-4 re sulted in high whole body-levels of T-3. B also caused a decrease in w hole body-thyroid hormone levels (T-4 and T-3), suggesting negative fe edback on the hypothalamo-pituitary-thyroid axis and T-3 had a similar effect, decreasing whole body-T-4 levels. T-4-treatment, but not T-3, increased whole body-B levels and MTP-treatment in combination with T -4 prevented the stimulatory effect of T-4 on B production. MTP-treatm ent alone blocked all steroid metabolism of [H-3]progesterone by the i nterrenal in vitro, and lowered whole body-B levels three-fold in vivo . Thio-treatment reduced thyroid hormone levels and also resulted in d ecreased B. Finally, we suggest that these results demonstrate a syste m in which T-4 may regulate its own potency: increasing T-4 stimulates B production, which increases the conversion of T-4 to its more activ e form T-3. Rising T-3 levels then cause a decrease in T-4, removing t he stimulatory effect of T-4 on B. These interactions between the thyr oid hormones and B help clarify the mechanisms underlying the morpholo gical effects of these hormones described in the previous study. (C) 1 995 Wiley-Liss, Inc.