OWEN, P J and MARRIOTT, D B and BOARDER, M R (1989) Evidence for a dihydropyridine-sensitive and conotoxin-insensitive release of noradrenaline and uptake of calcium in adrenal chromaffin cells. British Journal of Pharmacology, 97 (1). pp. 133-138. ISSN 0007-1188Full text not available from this repository.
1 It has been suggested that neuronal voltage-sensitive calcium channels (VSCC) may be divided into dihydropyridine (DHP)-sensitive (L) and DHP-insensitive (N and T), and that both the L and the N type channels are attenuated by the peptide blocker ω-conotoxin. Here the effects of ω-conotoxin on release of noradrenaline and uptake of calcium in bovine adrenal chromaffin cells were investigated. 2 Release of noradrenaline in response to 25 mm K+, 65 mm K+, 10 nm bradykinin or 10 μm prostaglandin E1 was not affected by ω-conotoxin in the range 10 nm-1 μm. 3 45Ca2+ uptake stimulated by high K+ and prostaglandin was attenuated by 1 μm nitrendipine and enhanced by 1 μm Bay K 8644; these calcium fluxes were not modified by 20 nm ω-conotoxin. 4 With superfused rat brain striatal slices in the same medium as the above cell studies, release of dopamine in response to 25 mm K+ was attenuated by 20 nm ω-conotoxin. 5 These results show that in these neurone-like cells, release may be effected by calcium influx through DHP-sensitive but ω-conotoxin-insensitive VSCC, a result inconsistent with the suggestion that ω-conotoxin blocks both L-type and N-type neuronal calcium channels.
|Journal or Publication Title:||British Journal of Pharmacology|
|Subjects:||Q Science > QR Microbiology|
|Departments:||Faculty of Health and Medicine > Biomedical & Life Sciences|
|Deposited On:||24 Jul 2012 14:12|
|Last Modified:||14 Jan 2016 01:02|
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