CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Effect of naturally occurring catecholamines on adrenergic neuroeffector interaction in the canine saphenous vein
Authors
P Dalemans
WJ Janssens
PM Vanhoutte
TJ Verbeuren
Publication date
1 January 1979
Publisher
United Kingdom
Abstract
Experiments were performed to compare the effects of dopamine, epinine and norepinephrine on peripheral adrenergic neurotransmission. Helical strips of dog's saphenous veins were incubated in solutions containing 3H-norepinephrine and mounted for superfusion and determination of 3H-norepinephrine and metabolites in the superfusate. In control strips, but not in veins treated with cocaine, the catecholamines increased the efflux of 3H-norepinephrine and its deaminated metabolites, indicating intraneuronal displacement of transmitter. Equipotent doses (ED50 for activation of alpha receptors on the smooth muscle cells) of norepinephrine, but not of epinine and dopamine, reduced slightly the release of 3H-norepinephrine during electrical stimulation. In strips treated with cocaine, norepinephrine reduced the 3H-norepinephrine release evoked by nerve stimulation by 61.4, epinine by 44.1 and dopamine by 28.5%. The inhibitory effect of the three catecholamines was abolished by phentolamine. These experiments suggest that (1) prejunctional alpha receptors have a different affinity than postjunctional alpha receptors; (2) in the dog's saphenous vein alpha-receptor mediated feedback inhibition of norepinephrine release can be demonstrated best when neuronal uptake is inhibited. © 1979.link_to_subscribed_fulltex
Similar works
Full text
Available Versions
HKU Scholars Hub
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:hub.hku.hk:10722/171371
Last time updated on 01/06/2016