Adenosine kinase inhibitors augment release of adenosine from spinal cord slices

Krystyna Golembiowska, Thomas D. White, Jana Sawynok

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

54 Citas (Scopus)

Resumen

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.

Idioma originalEnglish
Páginas (desde-hasta)157-162
Número de páginas6
PublicaciónEuropean Journal of Pharmacology
Volumen307
N.º2
DOI
EstadoPublished - jun. 27 1996

Nota bibliográfica

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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