DISTRIBUTION OF N-TYPE CA2-SITES IN RABBIT BRAIN FOLLOWING CENTRAL ADMINISTRATION OF OMEGA-CONOTOXIN GVIA( CHANNEL BINDING)

Citation
Sl. Whorlow et al., DISTRIBUTION OF N-TYPE CA2-SITES IN RABBIT BRAIN FOLLOWING CENTRAL ADMINISTRATION OF OMEGA-CONOTOXIN GVIA( CHANNEL BINDING), European journal of pharmacology, 315(1), 1996, pp. 11-18
Citations number
28
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
315
Issue
1
Year of publication
1996
Pages
11 - 18
Database
ISI
SICI code
0014-2999(1996)315:1<11:DONCIR>2.0.ZU;2-0
Abstract
Central administration of the N-type Ca2+ channel blocker omega-conoto xin GVIA in conscious rabbits has previously been shown to result in a slowly developing hypotensive and sympatholytic effect, with peak cha nges observed after 48 h. The aim of the current study was to examine the distribution of [I-125]omega-conotoxin GVIA binding in rabbit brai n alone or following a prior i.c.v. injection of omega-conotoxin GVIA to determine the site(s) of action of centrally administered omega-con otoxin GVIA. Brains were removed from rabbits 2 or 48 h after central administration of vehicle or non-labelled omega-conotoxin GVIA (30 pmo l/kg, i.c.v.). Brain sections were then incubated with [I-125]omega-co notoxin GVIA (50 pM) and the density of specific [I-125]omega-conotoxi n GVIA binding measured in dpm/mm(2) was determined by quantitative re ceptor autoradiography. In the vehicle group, highest densities of [I- 125]omega-conotoxin GVIA binding sites (> 20 dpm/mm(2)) were detected in cortex, caudate, putamen, and the stratum oriens and stratum radiat um of the hippocampus. Prior (48 h) i.c.v. injection of omega-conotoxi n GVIA resulted in a decrease in specific binding of [I-125]omega-cono toxin GVIA, particularly in cortex and some portions of the caudate an d hippocampus. Lesser effects were observed with a prior (2 h) i.c.v, injection of omega-conotoxin GVIA. Central administration of omega-con otoxin GVIA may be acting to disrupt neurotransmission in higher brain regions which may, in turn, affect cardiovascular control mechanisms in the rabbit.