Time-dependent effect of clonidine on microvascular permeability during endotoxemia.

Abstract

BACKGROUND:

Endothelial leakage with accompanying tissue edema and increased leukocyte adhesion are characteristics of the vascular inflammatory response. Tissue edema formation is a key mechanism in sepsis pathophysiology contributing to impaired tissue oxygenation and the development of shock. Sepsis mortality is directly associated with the severity of these microcirculatory alterations. Dysfunction of the sympathetic nervous system can have deleterious effects in generalized inflammation. This study evaluated the effect of the adrenergic alpha 2 agonist clonidine on microvascular permeability and leukocyte adhesion during endotoxemia.

METHODS:

Macromolecular leakage, leukocyte adhesion, and venular wall shear rate were examined in mesenteric postcapillary venules of rats by using intravital microscopy (IVM). Lipopolysaccharide (LPS) (4mg/kg/h) or equivalent volumes of saline were continuously infused following baseline IVM at 0min. IVM was repeated after 60 and 120min in endotoxemic and nonendotoxemic animals. Clonidine (10μg/kg) was applied as an i.v. bolus. Animals received either (i) saline alone, (ii) clonidine alone, (iii) clonidine 45min prior to LPS, (iv) clonidine 10min prior to LPS, (v) clonidine 30min after LPS, or (vi) LPS alone. Due to nonparametric data distribution, Wilcoxon test and Dunn's multiple comparisons test were used for data analysis. Data were considered statistically significant at p<0.05.

RESULTS:

LPS significantly increased microvascular permeability and leukocyte adhesion and decreased venular wall shear rate. Clonidine significantly reduced microvascular permeability when applied 45min before or 30min after LPS administration. Leukocyte adhesion and venular wall shear rate were not affected by clonidine during endotoxemia.

CONCLUSION:

Clonidine reduces microvascular permeability in endotoxemic animals in a time-dependent manner. Adrenergic alpha 2 agonists might prove beneficial in stabilizing capillary leakage during inflammation.

• Authors: Karsten Schmidt, Jochen Frederick Hernekamp, Christoph Philipsenburg, Aleksandar R Zivkovic, Thorsten Brenner, Stefan Hofer
• Journal: Microvascular research (Microvasc Res) Vol. 101 Pg. 111-7 (Sep 2015) ISSN: 1095-9319 [Electronic] United States
• PMID: 26177515 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2015 Elsevier Inc. All rights reserved.

Chemical References

• Lipopolysaccharides
• Sympatholytics
• Clonidine

Topics

• Animals
• Capillary Permeability (drug effects)
• Cell Adhesion
• Clonidine (administration & dosage)
• Endothelial Cells (cytology)
• Endotoxemia (drug therapy)
• Inflammation
• Intravital Microscopy
• Leukocytes (cytology)
• Lipopolysaccharides (chemistry)
• Male
• Microcirculation
• Permeability
• Rats
• Rats, Wistar
• Shear Strength
• Stress, Mechanical
• Sympathetic Nervous System (pathology)
• Sympatholytics (administration & dosage)
• Time Factors