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PMID: 8093099 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Nucleoside influx and efflux in guinea-pig ventricular myocytes. Inhibition by analogues of lidoflazine.

Biochemical pharmacology ·Vol. 48 ·No. 5 ·1994-08-30 ·Pages 873-80

Conant AR, Jarvis SM

Abstract

Adenosine influx and formycin B influx and efflux were characterized in guinea-pig ventricular myocytes at 22 degrees. Transport by both modes was saturable and inhibited by nitrobenzylthioinosine (NBMPR), indicating the presence of an equilibrative NBMPR-sensitive nucleoside transporter in the cardiomyocytes. The kinetic constants for influx and efflux of formycin B, a non-metabolized nucleoside, were similar, suggesting that the nucleoside transporter exhibits symmetrical kinetics (apparent Km 490 +/- 160 and 700 +/- 140 microM; Vmax 6.5 +/- 1.7 and 3.5 +/- 0.3 nmol/10(6) cells per min for influx and efflux, respectively). No evidence was found of either NBMPR-insensitive equilibrative nucleoside transport or sodium-dependent concentrative nucleoside transport. Inhibition of adenosine influx (apparent Km100 +/- 33 microM), by lidoflazine and the analogues mioflazine, soluflazine and R73-335, gave average Ki values of 730, 100, 64 and 2.9 nM, respectively. These compounds also inhibited formycin B efflux with a similar potency to that of adenosine influx. NBMPR-sensitive nucleoside transport was associated with high affinity binding of NBMPR (apparent Kd approximately 1 nM; 9.6 x 10(5) sites/cell). Specific binding of NBMPR was also inhibited by lidoflazine and its analogues. Mioflazine and soluflazine were 20-30-fold more potent at inhibiting NBMPR-sensitive nucleoside influx in guinea-pig erythrocytes than ventricular myocytes, indicating that the potency of some of the compounds studied is tissue dependent.

MeSH Terms
Adenosine/metabolism Affinity Labels Animals Biological Transport/drug effects Cells, Cultured Formycins/metabolism Guinea Pigs Heart Ventricles/drug effects,metabolism In Vitro Techniques Kinetics Lidoflazine/analogs & derivatives,pharmacology Myocardium/metabolism Thioinosine/analogs & derivatives,pharmacology
Chemicals
Affinity Labels Formycins formycin B Thioinosine 4-nitrobenzylthioinosine Lidoflazine Adenosine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Conant A R
Research School of Biosciences, University of Kent, Canterbury, U.K.
Jarvis S M
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
1994-08-30
Pages
873-80
Language
English
Region
England
NLM ID
0101032
Subset
IM
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