Literature DB >> 1713505

Characterization and pharmacological studies of an octopamine-sensitive adenylate cyclase from nerve cord of Locusta migratoria.

Z W Wang1, R G Downer, J W Gole, G L Orr.   

Abstract

An octopamine-sensitive adenylate cyclase that is insensitive to stimulation by dopamine (DA) and 5-hydroxytryptamine (5-HT), was studied in a homogenized nerve cord preparation of the migratory locust, Locusta migratoria. The enzyme complex is similar to catecholamine-sensitive cyclases from mammals with respect to pH-optimum, requirement for Mg++ and GTP, and sensitivity to forskolin. The octopamine-mediated elevation of adenylate cyclase activity is antagonized by a variety of drugs with the following order of potency: mianserin greater than phentolamine greater than promethazine greater than gramine greater than cyproheptadine greater than cis-flupenthixol greater than chlorpromazine greater than metoclopramide.

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Year:  1991        PMID: 1713505     DOI: 10.3109/13813459109146962

Source DB:  PubMed          Journal:  Arch Int Physiol Biochim Biophys        ISSN: 0778-3124


  2 in total

Review 1.  Octopamine receptor subtypes and their modes of action.

Authors:  P D Evans; S Robb
Journal:  Neurochem Res       Date:  1993-08       Impact factor: 3.996

2.  Characterization of insect neuronal octopamine receptors (OA3 receptors).

Authors:  T Roeder; J A Nathanson
Journal:  Neurochem Res       Date:  1993-08       Impact factor: 3.996

  2 in total

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