Isolated melanophores were differentiated from aggregates of neural crest obtained from neurula stage Xenopus laevis embryos after 2 days in culture.
Condensation of pigment granules in these cells by melatonin (5‐methoxy N‐acetyltryptamine, aMT) and various novel analogues was monitored with an image analysis system to quantitate the area occupied by pigment in individual cells.
Melanophores exposed to vehicle (a maximum of 0.1% MeOH) showed little (< 5%) change in pigment area. aMT produced a dramatic condensation of pigment granules (EC50 = the concentration producing a half maximal condensation, 9 pm). The response was rapid, reached a maximum (∼80% decrease in pigmented area) by 10 min, and was reversible after removal of aMT from the culture medium.
Aggregation to aMT was blocked by treating melanophores with pertussis toxin (1 μg ml−1, 7h) indicating a role for a guanosine 5′ triphosphate (GTP)‐binding protein in transducing the aMT receptor signal.
Structure‐activity studies indicated that analogues of aMT lacking a side‐chain N‐acyl substituent (5‐methoxytryptamine, MT) or a group at the 5‐position of the indole ring (N‐acetyltryptamine, aT) were unable to induce pigment aggregation (EC50 > 10 μm).
Lengthening the side‐chain N‐acyl group (N‐propionyl, N‐butanoyl) was tolerated to some degree but eventually (N‐valeroyl and larger) activity diminished. Of the 5‐position analogues tested 5‐methoxy (aMT) was by far the most potent.
Halogen substitution in the 6‐position of the indole ring led to some loss of activity as did a 6‐OH substitution. The 6‐OCH3 compound was inactive.
These studies demonstrate the utility of this model in investigations of structure‐activity relationships at the aMT receptor and suggest that it may be a valuable system for determining the transduction mechanisms coupled to the aMT receptor.
Isolated melanophores were differentiated from aggregates of neural crest obtained from neurula stage Xenopus laevis embryos after 2 days in culture.
Condensation of pigment granules in these cells by melatonin (5‐methoxy N‐acetyltryptamine, aMT) and various novel analogues was monitored with an image analysis system to quantitate the area occupied by pigment in individual cells.
Melanophores exposed to vehicle (a maximum of 0.1% MeOH) showed little (< 5%) change in pigment area. aMT produced a dramatic condensation of pigment granules (EC50 = the concentration producing a half maximal condensation, 9 pm). The response was rapid, reached a maximum (∼80% decrease in pigmented area) by 10 min, and was reversible after removal of aMT from the culture medium.
Aggregation to aMT was blocked by treating melanophores with pertussis toxin (1 μg ml−1, 7h) indicating a role for a guanosine 5′ triphosphate (GTP)‐binding protein in transducing the aMT receptor signal.
Structure‐activity studies indicated that analogues of aMT lacking a side‐chain N‐acyl substituent (5‐methoxytryptamine, MT) or a group at the 5‐position of the indole ring (N‐acetyltryptamine, aT) were unable to induce pigment aggregation (EC50 > 10 μm).
Lengthening the side‐chain N‐acyl group (N‐propionyl, N‐butanoyl) was tolerated to some degree but eventually (N‐valeroyl and larger) activity diminished. Of the 5‐position analogues tested 5‐methoxy (aMT) was by far the most potent.
Halogen substitution in the 6‐position of the indole ring led to some loss of activity as did a 6‐OH substitution. The 6‐OCH3 compound was inactive.
These studies demonstrate the utility of this model in investigations of structure‐activity relationships at the aMT receptor and suggest that it may be a valuable system for determining the transduction mechanisms coupled to the aMT receptor.
DOI: 10.1111/j.1476-5381.1991.tb12527.x
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