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Additional info for Advances in Dopamine Research. Proceedings of a Satellite Symposium to the 8th International Congress of Pharmacology, Okayama, Japan, July 1981
163, 188197. I. and Toda, N. (1975). Dopamine induced relaxation of isolated canine renal, mesenteric, and femoral arteries contracted with prostaglandin F 2 . Circ. Res. Supple. I, 1-97 - 1-102. D. (1978). A comparison of the vascular dopamine receptor with other dopamine receptors. Ann. Rev. Pharmacol. Toxicol. 18, 57-79. A. , Jr. (1980). Renal vascular activity of SK&F 38393 and dopamine in anesthetized dogs. J. Cardiovasc. Pharmacol. 2, 583593. Hilditch, A. M. (1981). Characteristics of the dopamine receptors in the rabbit isolated splenic artery.
I. D. (1981). Specific dopamine receptors in vascular smooth muscle. M. Vanhoutte and I. ), Vasodilatation, Raven Press, New York, pp. 131-140. I. D. (1981). Agonists and antagonists of peri pheral pre- and post-synaptic dopamine receptors: Clinical implications. L. U. ), Apomorphine and Other Dopamino mimetics, Raven Press, New York, pp. 273-284. D. (1979). Structure activity relationships of pre- and post-synaptic dopamine recep tors mediating vasodilation. In E. J. Kopin, and J. ), Catecholamines: Basic and Clinical Frontiers, Vol.
Apomorphine is a very weak, partial agonist; isoapomorphine is inactive; and 6-npropyl norapomorphi ne is somewhat more active than apomorphine (Crumly and col leagues, 1976). More recently, several benzazepine derivatives have been found to be either full or partial agonists of the DAi receptor (Pendleton and col leagues, 1978; Hahn and Wardell, 1980; Weinstock and colleagues, 1980). These compounds are interesting because the spatial relationship of the nitrogen atom 44 L. I. Goldberg and J.