Abstract
Highly purified synthetic salmonid melanin concentrating hormone (MCH) and some analogs were investigated for their ability (1) to concentrate the pigment in scale melanophores of the Chinese grass carp, Ctenopharyngodon idellus, (2) to produce melanin dispersion in frog or lizard melanophores and (3) to inhibit α-MSH in its action on mouse melanoma and rat adrenal glomerulosa cells in vitro. In the grass carp, MCH produced half-maximal pigment aggregation at 6×10 −11 M and its oxidized form at 7×10 −11 M. Replacement of the two methionines at position 3 and 6 with norvaline lowered the potency by a factor of 2.7 and with propargylglycine by a factor of about 7. Linear, Cys 5,14-Acm-protected MCH was a full agonist of MCH but with a 345-fold lower potency. Iodinated MCH showed similar, low activity. In tetrapods, salmonid MCH and its analogs displayed only marginal pigment dispersion at concentrations >10 −5 M. Alkali-treatment of MCH increased the pigment-dispersing potency by a factor of about 30 whereas the activity for pigment aggregation in the grass carp was destroyed. At high concentrations (10 −6, 10 −5 M) MCH also stimulated tyrosinase activity in B-16 mouse melanoma cells but did not modify the effects of α-MSH in this system. By contrast, when tested on rat adrenal glomerulosa cells, salmonid MCH had no effect alone but at a concentration of >10 −10 M it slightly reduced corticosterone production by an α-MSH concentration of 10 −7 M. Aldosterone production was not affected and MCH did not influence the response to ACTH.
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