Titlebook: Central D1 Dopamine Receptors; Menek Goldstein,Kjell Fuxe,Irving Tabachnick Book 1988 The Editor(s) (if applicable) and The Author(s), und

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C. van Kuijk MD PhD,H. K. Genant MDransmission (VT) (Agnati et al., 1986a,b, Agnati et al., 1987; Fuxe et al., 1988). The WT is the classical type of electrochemical transmission, which rests on the physical substrate of the neuronal chain. The VT consists of chemical signals (such as paracrine and endocrine signals), diffusing in th

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Interventional Radiological Techniquesas a potent and irreversible α-adrenergic receptor antagonist. Subsequent . studies in peripheral tissues by Chang et al. (1970) and Kalsner (1973) revealed that it could also irreversibly inactivate muscarinic cholinergic and serotonergic receptors, respectively. There was relatively little interes

antiquated

https://doi.org/10.1007/978-3-642-60295-5action. Effects on conditioned avoidance responding (CAR) in rats were studied under the same conditions in which in vivo binding of the radioiodinated D. specific benzazepine .I-SCH 38840 was measured. It was found that there is very close agreement between the time-course for antagonism of CAR and

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https://doi.org/10.1007/978-3-642-60369-3g changes in basal ganglia output are not yet well defined. These receptors can be divided into different subtypes on the basis of either their pharmacological properties or their location. D-1 and D-2 subtypes have been characterized, as have dopamine cell body autoreceptors, terminal autoreceptors

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colloquial

Dopamine D1 and D2 Receptor Selectivities of Agonists and Antagonists, constants for inhibiting the binding of [.H]SCH 23390 at D. receptors (calf caudate nucleus) and at D. receptors (pig anterior pituitary tissue). The most selective agonists were SK&F 38393 (for D.) and (+)-PHNO (for D.), while the most selective antagonists were SCH 23390 (for D.) and raclopride or eticlopride (for D.).

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Advances in Experimental Medicine and Biologyhttp://image.papertrans.cn/c/image/223175.jpg