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Positive and negative modulation of Bombyx mori adenylate cyclase by 5‐phenyloxazoles: Identification of octopamine and tyramine receptor agonists
Author(s) -
Khan Md. Anwar Arfien,
Nakane Toshiya,
Ohta Hiroto,
Ozoe Yoshihisa
Publication year - 2003
Publication title -
archives of insect biochemistry and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.576
H-Index - 66
eISSN - 1520-6327
pISSN - 0739-4462
DOI - 10.1002/arch.10058
Subject(s) - octopamine (neurotransmitter) , cyclase , tyramine , yohimbine , biogenic amine , biology , adenylate kinase , receptor , endocrinology , medicine , agonist , biochemistry , antagonist , neurotransmitter , serotonin
Nineteen 5‐phenyloxazoles (5POs) were examined for their ability to modulate adenylate cyclase by measuring cAMP produced in head membrane homogenates of fifth instar larvae of the silkworm Bombyx mori . Among the compounds tested, 5‐(4‐methoxyphenyl)oxazole ( 9 ) and the 2,6‐dichlorophenyl congener showed the highest activation of adenylate cyclase; both compounds produced approximately half the level of cAMP produced by the action of octopamine (OCT). The OCT receptor antagonists chlorpromazine, mianserin, and metoclopramide attenuated 9 ‐stimulated cAMP production. In contrast, 5‐(4‐hydroxyphenyl)oxazole ( 8 ) and the 4‐cyanophenyl congener attenuated both OCT‐stimulated and basal cAMP production. The tyramine (TYR) receptor antagonist yohimbine inhibited the negative effect of 8 . These findings indicate that the 5PO class of compounds includes both positive and negative modulators of adenylate cyclase in the heads of B. mori larvae, and that 9 and 8 are OCT and TYR receptor agonists, respectively. These compounds might prove useful for a pharmacological dissection of biogenic amine receptors. Arch. Insect Biochem. Physiol. 52:7–16, 2003. © 2003 Wiley‐Liss, Inc.
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