| Literature DB >> 6147391 |
Abstract
Low Km GTP hydrolysis in rat brain is stimulated in a concentration-dependent manner by the opiate alkaloid etorphine, and by the opioid peptide D-Ala2-leucine-enkephalinamide. The opiate antagonist naloxone inhibits the maximal D-Ala2-leucine-enkephalinamide stimulation of the GTPase, also with concentration dependency. The magnitude of maximally stimulated, opioid-sensitive, GTP hydrolysis is differentially distributed across brain regions. Opioid-stimulated GTPase may represent one means of identifying a specific type of opioid receptor.Entities:
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Year: 1984 PMID: 6147391 DOI: 10.1111/j.1471-4159.1984.tb12853.x
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372