Nigral dopamine type-1 receptors are reduced in Huntington's disease: A postmortem autoradiographic study using ( sup 3 H)SCH 23390 and correlation with ( sup 3 H)forskolin binding
- Univ. of Utah, Salt Lake City (USA)
Intrastriatal injection of excitatory amino acids, particularly quinolinic acid, has been proposed as an animal model of Huntington's disease. Such neurotoxic lesions of caudate-putamen result in marked dopamine type-1 (D1) receptor losses in the injected nuclei as well as in the ipsilateral substantia nigra pars reticulata. Postmortem human substantia nigra from Huntington's disease brains and from control brains were examined using in vitro autoradiography. A marked reduction in ({sup 3}H)SCH 23390 binding (labeling D1 receptors) in the substantia nigra of postmortem brains of Huntington's patients was identified, thus paralleling the alterations seen in the animal models. A positive, statistically significant correlation was also encountered between D1 receptor binding (labeled by ({sup 3}H)SCH 23390) and ({sup 3}H)forskolin binding (which identifies adenylate cyclase, a second messenger system linked to D1 receptor activation). The results suggest that in the human--as in lower vertebrates--D1 receptors are located on striatonigral terminals and that D1 receptor loss tends to be paralleled by a reduction in adenylate cyclase. Radioactive agents selective for the D1 receptor may prove useful in future studies of Huntington's disease using positron emission tomography scanning.
- OSTI ID:
- 6068837
- Journal Information:
- Experimental Neurology; (USA), Journal Name: Experimental Neurology; (USA) Vol. 110:2; ISSN 0014-4886; ISSN EXNEA
- Country of Publication:
- United States
- Language:
- English
Similar Records
6-hydroxydopamine-induced degeneration of nigral dopamine neurons: differential effect on nigral and striatal D-1 dopamine receptors
Comparison between dopamine-stimulated adenylate cyclase and /sup 3/H-SCH 23390 binding in rat striatum
Related Subjects
59 BASIC BIOLOGICAL SCIENCES
AMINES
AMINO ACIDS
ANIMALS
AROMATICS
AUTONOMIC NERVOUS SYSTEM AGENTS
AUTORADIOGRAPHY
BIOCHEMICAL REACTION KINETICS
CARBOXYLIC ACIDS
CARDIOTONICS
CARDIOVASCULAR AGENTS
CYCLASES
DISEASES
DOPAMINE
DRUGS
ENZYMES
ESTERS
HYDROGEN COMPOUNDS
HYDROXY COMPOUNDS
KINETICS
LIPIDS
LYASES
MAMMALS
MAN
MEMBRANE PROTEINS
NERVOUS SYSTEM DISEASES
NEUROREGULATORS
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC PHOSPHORUS COMPOUNDS
PATHOGENESIS
PHENOLS
PHOSPHOLIPIDS
POLYPHENOLS
PRIMATES
PROTEINS
REACTION KINETICS
RECEPTORS
SYMPATHOMIMETICS
TRITIUM COMPOUNDS
VERTEBRATES