Adenosine kinase inhibitors augment release of adenosine from spinal cord slices

Krystyna Golembiowska, Thomas D. White, Jana Sawynok

Résultat de recherche: Articleexamen par les pairs

54 Citations (Scopus)

Résumé

Inhibitors of adenosine kinase, but not adenosine deaminase, produce antinociception when administered spinally. In this study, we evaluated the relative contribution of adenosine kinase and adenosine deaminase to the regulation of adenosine release into the extracellular space within the spinal cord by determining the effects of the adenosine kinase inhibitors 5'-amino-5'-deoxyadenosine and 5-iodotubercidin, and the adenosine deaminase inhibitor 2'-deoxycoformycin on adenosine release from spinal cord slices in an in vitro perfusion system. Both 5'-amino-5'-deoxyadenosine (5-50 μM) and 5-iodotubercidin (5-50 μM), but not 2'-deoxycoformycin (50 μM), augmented adenosine release. 5-Iodotubercidin was slightly more potent and effective than 5'-amino-5'-deoxyadenosine in augmenting release except at the highest concentration, where it was considerably more effective. Combinations of 2'-deoxycoformycin (50 μM) and minimally active concentrations of 5'-amino-5'-deoxyadenosine and 5-iodotubercidin (5 μM each) produced a synergistic enhancement of release. These results support a predominant involvement of adenosine kinase in regulating extracellular adenosine levels in the spinal cord, but adenosine deaminase also can play a significant role.

Langue d'origineEnglish
Pages (de-à)157-162
Nombre de pages6
JournalEuropean Journal of Pharmacology
Volume307
Numéro de publication2
DOI
Statut de publicationPublished - juin 27 1996

Note bibliographique

Funding Information:
This work was supportedb y the Medical Research Councilo f CanadaW. e thankP arkeD avisPharmaceuticals for the provisiono f 2’-deoxycoformyc(inP entostatin).

ASJC Scopus Subject Areas

  • Pharmacology

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