Literature DB >> 4392960

Evidence for separate receptors for melanophore stimulating hormone and catecholamine regulation of cyclic AMP in the control of melanophore responses.

J M Goldman, M E Hadley.   

Abstract

1. Skins of the lizard Anolis carolinensis darken in vitro in response to melanophore stimulating hormone (MSH), a peptide hormone, as well as to catecholamines. These hormones darken Anolis skins by dispersing the sub-cellular organelle, the melanosome, out into the dendritic processes of the dermal melanophores.2. Dibutyryl cyclic AMP and methylxanthines also darken skins. In addition, methylxanthines are synergistic with both catecholamines and MSH in causing skin darkening. These data suggest that the dispersion of melanosomes within melanophores in response to both MSH and catecholamines is mediated by cyclic AMP.3. alpha-Adrenoceptor blocking agents inhibit MSH-induced darkening but potentiate catecholamine-induced darkening. beta-Adrenoceptor blocking agents, in contrast, inhibit catecholamine-induced darkening but have no effect on MSH-induced darkening. This selective blockade of one receptor while the functional integrity of the other receptor is maintained suggests that MSH and catecholamines increase cyclic AMP levels through different receptors.4. Catecholamines exert their action through beta-adrenoceptors; MSH darkens skins through what appears to be a component of the alpha-adrenoceptor. beta-Adrenoceptor stimulation may stimulate adenyl cyclase to increase cyclic AMP levels whereas MSH may inhibit cyclic AMP phosphodiesterase thereby preventing cyclic AMP breakdown.

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Year:  1970        PMID: 4392960      PMCID: PMC1702945          DOI: 10.1111/j.1476-5381.1970.tb09565.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  18 in total

1.  Fractionation and characterization of a cyclic adenine ribonucleotide formed by tissue particles.

Authors:  E W SUTHERLAND; T W RALL
Journal:  J Biol Chem       Date:  1958-06       Impact factor: 5.157

2.  Physiological color changes in reptiles.

Authors:  M E Hadley; J M Goldman
Journal:  Am Zool       Date:  1969-05

3.  In vitro demonstration of adrenergic receptors controlling melanophore responses of the lizard, Anolis carolinensis.

Authors:  J M Goldman; M E Hadley
Journal:  J Pharmacol Exp Ther       Date:  1969-03       Impact factor: 4.030

4.  The beta adrenergic receptor and cyclic 3',5'-adenosine monophosphate: possible roles in the regulation of melanophore responses of the spadefoot toad, Scaphiopus couchi.

Authors:  J M Goldman; M E Hadley
Journal:  Gen Comp Endocrinol       Date:  1969-08       Impact factor: 2.822

5.  Some evidence for differentiation of ACTH and norepinephrine lipolytic receptors in adipose cells.

Authors:  J J Lech; D N Calvert
Journal:  Life Sci       Date:  1967-04-15       Impact factor: 5.037

Review 6.  Adenyl cyclase as an adrenergic receptor.

Authors:  G A Robison; R W Butcher; E W Sutherland
Journal:  Ann N Y Acad Sci       Date:  1967-02-10       Impact factor: 5.691

7.  Glucagon: effect on adenosine 3', 5'-monophosphate in the rat heart.

Authors:  P J Laraia; R J Craig; W J Reddy
Journal:  Am J Physiol       Date:  1968-10

8.  Evidence for separate epinephrine and glucagon responsive adenyl cyclase systems in rat liver.

Authors:  M W Bitensky; V Russell; W Robertson
Journal:  Biochem Biophys Res Commun       Date:  1968-06-10       Impact factor: 3.575

9.  Autonomic control of metabolism.

Authors:  S Ellis; B L Kennedy; A J Eusebi; N H Vincent
Journal:  Ann N Y Acad Sci       Date:  1967-02-10       Impact factor: 5.691

10.  Pharmacological characterization of adrenergic receptors.

Authors:  N C Moran
Journal:  Pharmacol Rev       Date:  1966-03       Impact factor: 25.468

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5.  Biochemical regulation of pigment motility in vertebrate chromatophores: a review of physiological color change mechanisms.

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