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pmid: 4358240
SummaryAntagonism of the antinociceptive action of morphine in mice by prior parenteral administration of cAMP has been confirmed using two additional analgesic testing procedures, the hot-plate test and the stretching test. The analgesia-antagonistic property, however, is not specific for cAMP because it also occurred after pretreatment with compounds which probably increased the concentration of adenosine or adenine in the body. Preliminary indications are that an unsubstituted purine ring is a requirement for the adenine derivative that is primarily responsible for the antagonism of the analgesic action of morphine.
Male, Analgesics, Adenosine, Deoxyadenosines, Morphine, Adenine, Cytidine, Adenosine Monophosphate, Adenosine Diphosphate, Mice, Structure-Activity Relationship, Adenosine Triphosphate, Hypoxanthines, Cyclic AMP, Methods, Animals, Uridine
Male, Analgesics, Adenosine, Deoxyadenosines, Morphine, Adenine, Cytidine, Adenosine Monophosphate, Adenosine Diphosphate, Mice, Structure-Activity Relationship, Adenosine Triphosphate, Hypoxanthines, Cyclic AMP, Methods, Animals, Uridine
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 43 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |