Abstract
1. The effects of reactive blue 2 and brilliant blue G, which have been shown to block extracellular ATP-evoked responses, were investigated to discover whether these compounds act as P2-purinoceptor antagonists in PC12 phaeochromocytoma cells. 2. Reactive blue 2 (10 to 100 microM) suppressed the ATP-stimulated dopamine secretion from PC12 cells in a dose-dependent manner. The concentration-response curve for ATP was shifted to the right and the maximal response was decreased by reactive blue (30 and 100 microM). Brilliant blue G (up to 100 microM) did not significantly affect the secretion. 3. Reactive blue 2 (10 to 100 microM) suppressed the ATP-activated inward current recorded from the voltage-clamped cells in a concentration-dependent manner. Brilliant blue G (up to 100 microM) did not affect the current. 4. The results suggest that reactive blue 2 but not brilliant blue G is a P2-purinoceptor antagonist in PC12 cells. The purinoceptors in these cells may be the same type as those involved in ATP-evoked smooth muscle relaxation, judging from the antagonism by reactive blue 2.
MeSH Terms
Adenosine Triphosphate/antagonists & inhibitors
Adrenal Gland Neoplasms/physiopathology
Benzenesulfonates/pharmacology
Calcium/metabolism
Catecholamines/metabolism
Dopamine/metabolism
Electrophysiology
Membrane Potentials/drug effects
Pheochromocytoma/physiopathology
Protein Synthesis Inhibitors/pharmacology
Receptors, Purinergic/drug effects
Triazines/pharmacology
Tumor Cells, Cultured/drug effects
Chemicals
Benzenesulfonates
Catecholamines
Protein Synthesis Inhibitors
Receptors, Purinergic
Triazines
Cibacron Blue F 3GA
Adenosine Triphosphate
brilliant blue
Calcium
Dopamine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Inoue K
Division of Pharmacology, National Institute of Hygienic Sciences, Tokyo, Japan.
Nakazawa K
Ohara-Imaizumi M
Obama T
Fujimori K
Takanaka A
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