Opiates inhibit adenylate cyclase by stimulating GTP hydrolysis

التفاصيل البيبلوغرافية
العنوان: Opiates inhibit adenylate cyclase by stimulating GTP hydrolysis
المؤلفون: Greg Koski, Werner A. Klee
المصدر: Proceedings of the National Academy of Sciences. 78:4185-4189
بيانات النشر: Proceedings of the National Academy of Sciences, 1981.
سنة النشر: 1981
مصطلحات موضوعية: GTP', Adenylate kinase, GTPase, Cyclase, Adenylyl Cyclase Inhibitors, Cell Line, GTP Phosphohydrolases, Structure-Activity Relationship, Animals, heterocyclic compounds, Opioid peptide, Multidisciplinary, Chemistry, Cell Membrane, Stereoisomerism, Enkephalins, Enkephalin, Leucine-2-Alanine, Phosphoric Monoester Hydrolases, Rats, Biochemistry, Receptors, Opioid, Guanosine Triphosphate, Cyclase activity, Research Article
الوصف: Specific, GTP hydrolysis catalyzed by membranes prepared from neuroblastoma--glioma (NG108-15) hybrid cells can be measured in the presence of adenosine-5'-[beta, gamma-imido] triphosphate (p[NH]ppA), ATP, and a nucleotide triphosphate-regenerating system. Opiates and opioid peptides stimulate low Km GTP hydrolysis when measured in the presence of Na+ and Mg2+. Opiate stimulation is rapid, stereospecific, and reserved by the antagonist naloxone. Potencies of opiates as stimulators of GTP hydrolysis and as inhibitors of adenylate cyclase are closely correlated. Agents that stimulate adenylate cyclase, including prostaglandin E1, 2-Cl-adenosine, secretin, and NaF, have little or no effect upon the rate of GTP hydrolysis. Opiates have no effect upon either adenylate cyclase or GTPase activity in membranes prepared from C6-BU1 glioma cells, which lack opiate receptors. In view of the pivotal role of GTP in the activation of adenylate cyclase, we conclude that receptor-mediated stimulation of GTP hydrolysis is the mechanism by which opiates and other inhibitory hormones lower adenylate cyclase activity in NG108-15 cell membranes.
تدمد: 1091-6490
0027-8424
DOI: 10.1073/pnas.78.7.4185
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98d2488253890063448b2ed7a39ccbca
https://doi.org/10.1073/pnas.78.7.4185
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....98d2488253890063448b2ed7a39ccbca
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10916490
00278424
DOI:10.1073/pnas.78.7.4185