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Effects of SCH 23390 on Neurotransmitter-stimulated Cyclic AMP Accumulation in Mammalian Brain and Teleost Retina

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Dopaminergic Systems and their Regulation

Abstract

The benzazepine derivative SCH 23390[(R)−(+)−8−chloro−2,3,4,5-tetrahydro− 3−methyl−5−phenyl−1H−3−benzazepine] has recently been shown to antagonise dopamine-stimulated adenylate cyclase activity in homogenates of rat striatum at concentrations (IC50 = 0.01μM) approximately 2000 times lower than those required to displace 3H-spiperone binding (Iorio et al, 1983). These data have led to the suggestion that SCH 23390 is a selective D1 receptor antagonist. To examine further the pharmacological specificity of this compound, we have investigated the effects of SCH 23390 on other central neurotransmitter- stimulated adenylate cyclase systems.

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References:

  • Dowling, J.E. and Watling, K.J.(1981). Dopaminergic mechanisms in the teleost retina. II. Factors affecting the accumulation of cyclic AMP in pieces of intact carp retina. J. Neurochem, 36, 569–579.

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Watling, K.J., Williams, L.C., Bristow, D.R. (1986). Effects of SCH 23390 on Neurotransmitter-stimulated Cyclic AMP Accumulation in Mammalian Brain and Teleost Retina. In: Woodruff, G.N., Poat, J.A., Roberts, P.J. (eds) Dopaminergic Systems and their Regulation. Satellite Symposia of the IUPHAR 9th International Congress of Pharmacology. Palgrave Macmillan, London. https://doi.org/10.1007/978-1-349-07431-0_33

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  • DOI: https://doi.org/10.1007/978-1-349-07431-0_33

  • Publisher Name: Palgrave Macmillan, London

  • Print ISBN: 978-1-349-07433-4

  • Online ISBN: 978-1-349-07431-0

  • eBook Packages: MedicineMedicine (R0)

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