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• W2153710818 endingPage "198" @default.
• W2153710818 startingPage "193" @default.
• W2153710818 abstract "The selective kappa-opioid agonist trans-(+/-)-3, 4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl) cyclohexyl] benzenacetamidemethansulfonate (U50,488) potentiates both basal and depolarization-evoked [3H]dopamine release from NMB cells. The potentiation of dopamine release by U50,488 is mediated by N-type voltage-dependent calcium channels since it is blocked by omega-conotoxin, and is resistant to pertussis toxin (PTX)-treatment. When the stimulation of release by U50,488 is blocked by the N-channel antagonist omega-conotoxin, an inhibitory effect on dopamine release is revealed, suggesting that stimulatory and inhibitory effects of U50,488 are exerted in parallel." @default.
• W2153710818 created "2016-06-24" @default.
• W2153710818 creator A5023759426 @default.
• W2153710818 creator A5034907298 @default.
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• W2153710818 date "1999-10-01" @default.
• W2153710818 modified "2023-09-27" @default.
• W2153710818 title "Potentiation of transmitter release from NMB human neuroblastoma cells by kappa-opioids is mediated by N-type voltage-dependent calcium channels" @default.
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• W2153710818 doi "https://doi.org/10.1016/s0006-8993(99)01904-6" @default.
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