Unbound MEDLINE

Beta-adrenoceptor blockade delays granulation tissue formation in polyurethane sponge implants. Journal of cutaneous pathology [J Cutan Pathol] Journal article

 
TitleBeta-adrenoceptor blockade delays granulation tissue formation in polyurethane sponge implants.
Author(s)Romana-Souza B, Santos JS, Desmoulière A, Monte-Alto-Costa A 
InstitutionDepartment of Histology and Embryology, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
SourceJ Cutan Pathol 2009 May; 36(5):522-8.
AbstractBACKGROUND: The role of adrenoceptors in granulation tissue formation is not well understood. The aim of this study was to investigate the effects of alpha- and beta-adrenoceptor blockade on granulation tissue development using polyurethane (PU) implants in the rat.
METHODS: Animals were treated orally with propranolol (beta1- and beta2-antagonist), atenolol (beta1-antagonist) or phentolamine (alpha1- and alpha2-antagonist) until euthanasia. The control group received only water. All animals received subcutaneous implants of PU sponges. After 14 days, implants were collected, formalin-fixed and paraffin-embedded. Sections were stained with hematoxylin and eosin and Sirius red and immunostained for CD68 and alpha-smooth muscle actin.
RESULTS: The number of inflammatory cells and the volume density of myofibroblasts and blood vessels were lower in the control group than in the propranolol- and atenolol-treated groups. The collagen fiber score was greater in the control group than in the propranolol- and atenolol-treated groups. The inflammatory infiltrate, collagen fiber score, blood vessel density or myofibroblast differentiation was not affected by phentolamine. The percentage of fibrovascular invasion was greater in the antagonist-treated groups than in the control group.
CONCLUSIONS: Blockade of beta1- and beta2-adrenoceptors, but not alpha-adrenoceptors, impairs granulation tissue development in PU implants due to interference with the inflammatory response.
Languageeng
Pub Type(s)Journal Article
Research Support, Non-U.S. Gov't
PubMed ID19476519
  
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