Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

Holzer, P; Lippe, IT; Jocic, M; Wachter, C; Erb, R; Heinemann, A.
Nitric oxide-dependent and -independent hyperaemia due to calcitonin gene-related peptide in the rat stomach.
Br J Pharmacol. 1993; 110(1):404-410 Doi: 10.1111/j.1476-5381.1993.tb13824.x [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Holzer Peter
Co-Autor*innen der Med Uni Graz
Heinemann Akos
Lippe Irmgard Theresia
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
1. Calcitonin gene-related peptide (CGRP) potently enhances mucosal blood flow in the rat stomach. The aim of this study was to examine whether CGRP also dilates extramural arteries supplying the stomach and whether the vasodilator action of CGRP involves nitric oxide (NO). 2. Rat CGRP-alpha (0.03-1 nmol kg-1, i.v.) produced a dose-dependent increase in blood flow through the left gastric artery (LGA) as determined by an ultrasonic transit time technique in urethane-anaesthetized rats. Blockade of NO synthesis by NG-nitro-L-arginine methyl ester (L-NAME, 20 and 60 mumol kg-1, i.v.) significantly reduced basal blood flow (BF) in the LGA and attenuated the hyperaemic activity of CGRP by a factor of 2.8-4. D-NAME tended to enhance basal BF in the LGA but had no influence on the dilator activity of CGRP. The ability of vasoactive intestinal polypeptide to increase left gastric arterial blood flow remained unaltered by L-NAME. 3. L-NAME (20 and 60 mumol kg-1, i.v.) evoked a prompt and sustained rise of mean arterial blood pressure (MAP) and caused a slight decrease in the hypotensive activity of CGRP. In contrast, D-NAME induced a delayed and moderate increase in MAP and did not influence the hypotensive activity of CGRP. 4. Rat CGRP-alpha dilated the isolated perfused bed of the rat LGA precontracted with methoxamine and was 3 times more potent in this respect than rat CGRP-beta. The dilator action of rat CGRP-alpha in this preparation was not affected by L-NAME or D-NAME (40 microM).(ABSTRACT TRUNCATED AT 250 WORDS)
Find related publications in this database (using NLM MeSH Indexing)
Anesthesia -
Animals -
Arginine - analogs and derivatives
Blood Pressure - drug effects
Calcitonin Gene-Related Peptide - pharmacology
Dose-Response Relationship, Drug - pharmacology
Female - pharmacology
Gastric Mucosa - blood supply
Heart Rate - drug effects
Hyperemia - chemically induced
Muscle, Smooth, Vascular - drug effects
NG-Nitroarginine Methyl Ester - drug effects
Nitric Oxide - antagonists and inhibitors
Perfusion - antagonists and inhibitors
Rats - antagonists and inhibitors
Rats, Sprague-Dawley - antagonists and inhibitors
Regional Blood Flow - drug effects
Stomach - blood supply
Vasoactive Intestinal Peptide - pharmacology
Vasodilation - drug effects

Find related publications in this database (Keywords)
Calcitonin Gene-Related Peptide (CGRP)
Vasoactive Intestinal Polypeptide
Blood Flow
Rat Stomach
Gastric Mucosa
Left Gastric Artery
Vasodilation
Hypotension
Nitric Oxide
Ng-Nitro-L-Arginine Methyl Ester (L-Name)
D-Name
Inhibition of Nitric Oxide
© Med Uni Graz Impressum