Back to Search
Start Over
Regulation of coronary venular barrier function by blood borne inflammatory mediators and pharmacological tools: insights from novel microvascular wall models.
- Source :
-
American journal of physiology. Heart and circulatory physiology [Am J Physiol Heart Circ Physiol] 2012 Feb 01; Vol. 302 (3), pp. H567-81. Date of Electronic Publication: 2011 Nov 11. - Publication Year :
- 2012
-
Abstract
- We hypothesized that postcapillary venules play a central role in the control of the tightness of the coronary system as a whole, particularly under inflammatory conditions. Sandwich cultures of endothelial cells and pericytes of precapillary arteriolar or postcapillary venular origin from human myocardium as models of the respective vascular walls (sandwich cultures of precapillary arteriolar or postcapillary venular origin) were exposed to thrombin and components of the acutely activatable inflammatory system, and their hydraulic conductivity (L(P)) was registered. L(P) of SC-PAO remained low under all conditions (3.24 ± 0.52·10(-8)cm·s(-1)·cmH(2)O(-1)). In contrast, in the venular wall model, PGE(2), platelet-activating factor (PAF), leukotriene B(4) (LTB(4)), IL-6, and IL-8 induced a prompt, concentration-dependent, up to 10-fold increase in L(P) with synergistic support when combined. PAF and LTB(4) released by metabolically cooperating platelets, and polymorphonuclear leucocytes (PMNs) caused selectively venular endothelial cells to contract and to open their clefts widely. This breakdown of the barrier function was preventable and even reversible within 6-8 h by the presence of 50 μM quercetin glucuronide (QG). LTB(4) synthesis was facilitated by biochemical involvement of erythrocytes. Platelets segregated in the arterioles and PMNs in the venules of blood-perfused human myocardium (histological studies on donor hearts refused for heart transplantation). Extrapolating these findings to the coronary microcirculation in vivo would imply that the latter's complex functionality after accumulation of blood borne inflammatory mediators can change rapidly due to selective breakdown of the postcapillary venular barrier. The resulting inflammatory edema and venulo-thrombosis will severely impair myocardial performance. The protection afforded by QG could be of particular relevance in the context of cardiosurgical intervention.
- Subjects :
- Actins metabolism
Arterioles drug effects
Arterioles immunology
Arterioles metabolism
Blood Platelets cytology
Blood Platelets drug effects
Blood Platelets metabolism
Capillaries drug effects
Capillaries immunology
Capillaries metabolism
Capillary Permeability drug effects
Cells, Cultured
Coronary Circulation drug effects
Dinoprostone pharmacology
Drug Synergism
Erythrocytes cytology
Erythrocytes drug effects
Erythrocytes metabolism
Hemostatics pharmacology
Humans
Interleukin-6 pharmacology
Interleukin-8 pharmacology
Leukotriene B4 pharmacology
Myocarditis immunology
Pericytes drug effects
Pericytes immunology
Pericytes metabolism
Platelet Activating Factor pharmacology
Thrombin pharmacology
Venules drug effects
Venules immunology
Venules metabolism
Blood Proteins pharmacology
Capillary Permeability immunology
Coronary Circulation immunology
Endothelial Cells cytology
Endothelial Cells drug effects
Endothelial Cells metabolism
Inflammation Mediators pharmacology
Myocarditis metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1522-1539
- Volume :
- 302
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- American journal of physiology. Heart and circulatory physiology
- Publication Type :
- Academic Journal
- Accession number :
- 22081707
- Full Text :
- https://doi.org/10.1152/ajpheart.00360.2011