Biology Reference
In-Depth Information
CHAPTER SEVEN
Neuroendocrinology of
Amphibian Metamorphosis
Robert J. Denver *
,1
* Department of Molecular, Cellular and Developmental Biology, The University of Michigan, Ann Arbor,
Michigan, USA
Department of Ecology and Evolutionary Biology, The University of Michigan, Ann Arbor, Michigan, USA
1
,
Corresponding author: e-mail address: rdenver@umich.edu
Contents
1. Hormonal Control of Metamorphosis
196
1.1 Thyroid hormone
196
1.2 Corticosteroids
203
2. Neuroendocrine Control of Metamorphosis
205
2.1 Thyroid-stimulating hormone
206
2.2 Adrenocorticotropic hormone
210
2.3 Growth hormone and prolactin
211
3. Role of the Neuroendocrine System in Mediating Environmental Influences on the
Timing of Metamorphosis
214
Acknowledgment
217
References
217
Abstract
The timing of metamorphosis is a central amphibian life history trait and is controlled by
the interplay of developmental progression, body size and condition, and environmen-
tal signals. These different processes and signals are integrated by the neuroendocrine
system to regulate production of hormones by the thyroid gland. Thyroid hormone (TH)
is the primary morphogen controlling metamorphosis, while corticosteroids (CSs) pro-
duced by the interrenal glands synergize with TH to promote metamorphic changes.
The actions of TH are modulated by monodeiodinase enzymes expressed in TH target
tissues. CSs act by sensitizing tissues to the actions of TH via the upregulation of TH recep-
tors andmonodeiodinases. The increase in thyroid gland activity duringmetamorphosis is
controlled by the hypothalamus and pituitary gland. The hypothalamo - pituitary - thyroid
and hypothalamo - pituitary - interrenal axes are regulated at multiple levels. Hypothalamic
corticotropin-releasing factor (CRF) functions as a common, central regulator of pituitary
thyroid-stimulating hormone (TSH) and adrenocorticotropic hormone (ACTH) secretion in
tadpoles. CRF neurons transduce the signals of environmental change (e.g., pond drying,
resource availability, etc.) on metamorphic timing by regulating TSH and ACTH secretion,
and consequently the production of TH and CS.
 
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