The anti-inflammatory effect of catecholamines in the peritoneal cavity and hind paw of the mouse.
Journal: 1972/September - British Journal of Pharmacology
ISSN: 0007-1188
PUBMED: 5048650
Abstract:
1. Carrageenin or 5-hydroxytryptamine-induced oedema of the mouse hind paw was antagonized by catecholamines acting on both alpha- and beta-adrenoceptors.2. Increased permeability of the mouse peritoneum induced by the local injection of acetic acid or pro-inflammatory mediators was antagonized by catecholamines acting predominantly on beta-adrenoceptors.3. The anti-inflammatory effect of catecholamines was due neither to hyperglycaemia nor to the release of adrenal cortical hormones.
Relations:
Content
Citations
(13)
References
(18)
Conditions
(1)
Drugs
(10)
Chemicals
(9)
Organisms
(2)
Processes
(1)
Anatomy
(2)
Similar articles
Articles by the same authors
Discussion board
Br J Pharmacol 45(2): 322-332

The anti-inflammatory effect of catecholamines in the peritoneal cavity and hind paw of the mouse

Abstract

1. Carrageenin or 5-hydroxytryptamine-induced oedema of the mouse hind paw was antagonized by catecholamines acting on both α- and β-adrenoceptors.

2. Increased permeability of the mouse peritoneum induced by the local injection of acetic acid or pro-inflammatory mediators was antagonized by catecholamines acting predominantly on β-adrenoceptors.

3. The anti-inflammatory effect of catecholamines was due neither to hyperglycaemia nor to the release of adrenal cortical hormones.

Full text

Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (1.0M), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.

Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Bhalla TN, Sinha JN, Tangri KK, Bhargava KP. Role of catecholamines in inflammation. Eur J Pharmacol. 1970;13(1):90–96. [PubMed] [Google Scholar]
  • Black JW, Duncan WA, Shanks RG. Comparison of some properties of pronethalol and propranolol. Br J Pharmacol Chemother. 1965 Dec;25(3):577–591.[PMC free article] [PubMed] [Google Scholar]
  • Blinks JR. Evaluation of the cardiac effects of several beta adrenergic blocking agents. Ann N Y Acad Sci. 1967 Feb 10;139(3):673–685. [PubMed] [Google Scholar]
  • Brown JH, Kissel JW, Lish PM. Studies on the acute inflammatory response. I. Involvement of the central nervous system in certain models of inflammation. J Pharmacol Exp Ther. 1968 Mar;160(1):231–242. [PubMed] [Google Scholar]
  • Brown JH, Mackey HK, Riggilo DA, Schwartz NL. Studies on the acute inflammatory response. II. Influence of antihistaminics and catecholamines on formaldehyde-induced edema. J Pharmacol Exp Ther. 1968 Mar;160(1):243–248. [PubMed] [Google Scholar]
  • BROWN RA, WEST GB. SYMPATHOMIMETIC AMINES AND VASCULAR PERMEABILITY. J Pharm Pharmacol. 1965 Feb;17:119–120. [PubMed] [Google Scholar]
  • Lish PM, Weikel JH, Dungan KW. Pharmacological and toxicological properties of two new beta-adrenergic receptor antagonists. J Pharmacol Exp Ther. 1965 Aug;149(2):161–173. [PubMed] [Google Scholar]
  • Majno G, Shea SM, Leventhal M. Endothelial contraction induced by histamine-type mediators: an electron microscopic study. J Cell Biol. 1969 Sep;42(3):647–672.[PMC free article] [PubMed] [Google Scholar]
  • MCKINNEY GR, LISH PM. ON THE ANTI-INFLAMMATORY ACTIVITY OF AMINOPHYLLINE. Proc Soc Exp Biol Med. 1964 Oct;117:280–283. [PubMed] [Google Scholar]
  • McKinney GR, Lish PM. Interaction of beta adrenergic blockade and certain vasodilators in dextran-induced rat paw edema. Proc Soc Exp Biol Med. 1966 Feb;121(2):494–496. [PubMed] [Google Scholar]
  • Meester WD, Hardman HF, Barboriak JJ. Evaluation of various adrenergic blocking agents in isolated rabbit and turtle hearts. J Pharmacol Exp Ther. 1965 Oct;150(1):34–40. [PubMed] [Google Scholar]
  • NORTHOVER BJ. The permeability to plasma proteins of the peritoneal blood vessels of the mouse, and the effect of substances that alter permeability. J Pathol Bacteriol. 1963 Apr;85:361–370. [PubMed] [Google Scholar]
  • Northover AM, Northover BJ. The effects of histamine, 5-hydroxytryptamine and bradykinin on rat mesenteric blood vessels. J Pathol. 1969 Aug;98(4):265–275. [PubMed] [Google Scholar]
  • Patil PN. Steric aspects of adrenergic drugs. 8. Optical isomers of beta adrenergic receptor antagonists. J Pharmacol Exp Ther. 1968 Apr;160(2):308–314. [PubMed] [Google Scholar]
  • Piper PJ, Collier HO. Release of catecholamines in the guinea-pig by substances involved in anaphylaxis. Nature. 1967 Feb 25;213(5078):838–840. [PubMed] [Google Scholar]
  • Riesterer L, Jaques R. Interference, by beta-adrenergic blocking agents, with the anti-inflammatory action of various drugs. Helv Physiol Pharmacol Acta. 1968;26(3):287–293. [PubMed] [Google Scholar]
  • Stanton HC, Kirchgessner T, Parmenter K. Cardiovascular pharmacology of two new beta-adrenergic receptor antagonists. J Pharmacol Exp Ther. 1965 Aug;149(2):174–182. [PubMed] [Google Scholar]
  • WILLOUGHBY DA, SPECTOR WG. ADRENALINE PRECURSORS IN THE INFLAMMATORY REACTION. J Pathol Bacteriol. 1964 Jul;88:159–166. [PubMed] [Google Scholar]
Abstract
1. Carrageenin or 5-hydroxytryptamine-induced oedema of the mouse hind paw was antagonized by catecholamines acting on both α- and β-adrenoceptors.
2. Increased permeability of the mouse peritoneum induced by the local injection of acetic acid or pro-inflammatory mediators was antagonized by catecholamines acting predominantly on β-adrenoceptors.
3. The anti-inflammatory effect of catecholamines was due neither to hyperglycaemia nor to the release of adrenal cortical hormones.
Collaboration tool especially designed for Life Science professionals.Drag-and-drop any entity to your messages.