Myocardial microvascular permeability, interstitial oedema, and compromised cardiac function

被引:141
作者
Dongaonkar, Ranjeet M. [1 ]
Stewart, Randolph H. [1 ]
Geissler, Hans J. [2 ]
Laine, Glen A. [1 ]
机构
[1] Texas A&M Univ, Michael E DeBakey Inst, College Stn, TX 77843 USA
[2] Univ Freiburg, Dept Cardiovasc Surg, D-79106 Freiburg, Germany
基金
美国国家卫生研究院;
关键词
Myocardial oedema; Oedemagenic gain; Interstitial compliance; Lymphatics; LEFT-VENTRICULAR FUNCTION; TUMOR-NECROSIS-FACTOR; NUCLEAR-MAGNETIC-RESONANCE; COLLOID OSMOTIC-PRESSURE; CARDIOPULMONARY BYPASS; WATER-CONTENT; TRANSCAPILLARY EXCHANGE; CAPILLARY-PERMEABILITY; DIASTOLIC PROPERTIES; CARDIOPLEGIC ARREST;
D O I
10.1093/cvr/cvq145
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The heart, perhaps more than any other organ, is exquisitely sensitive to increases in microvascular permeability and the accumulation of myocardial interstitial oedema fluid. Whereas some organs can cope with profound increases in the interstitial fluid volume or oedema formation without a compromise in function, heart function is significantly compromised with only a few percent increase in the interstitial fluid volume. This would be of little consequence if myocardial oedema were an uncommon pathology. On the contrary, myocardial oedema forms in response to many disease states as well as clinical interventions such as cardiopulmonary bypass and cardioplegic arrest common to many cardiothoracic surgical procedures. The heart's inability to function effectively in the presence of myocardial oedema is further confounded by the perplexing fact that the resolution of myocardial oedema does not restore normal cardiac function. We will attempt to provide some insight as to how microvascular permeability and myocardial oedema formation compromise cardiac function and discuss the acute changes that might take place in the myocardium to perpetuate compromised cardiac function following oedema resolution. We will also discuss compensatory changes in the interstitial matrix of the heart in response to chronic myocardial oedema and the role they play to optimize myocardial function during chronic oedemagenic disease.
引用
收藏
页码:331 / 339
页数:9
相关论文
共 82 条
[1]   Edema as a Very Early Marker for Acute Myocardial Ischemia A Cardiovascular Magnetic Resonance Study [J].
Abdel-Aty, Hassan ;
Cocker, Myra ;
Meek, Cheryl ;
Tyberg, John V. ;
Friedrich, Matthias G. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2009, 53 (14) :1194-1201
[2]   3D evaluation of myocardial edema:: Experimental study on 22 pigs using magnetic resonance and tissue analysis [J].
Albers, J ;
Schroeder, A ;
de Simone, R ;
Möckel, R ;
Vahl, CF ;
Hagl, S .
THORACIC AND CARDIOVASCULAR SURGEON, 2001, 49 (04) :199-203
[3]   Augmenting cardiac contractility hastens myocardial edema resolution after cardiopulmonary bypass and cardioplegic arrest [J].
Allen, SJ ;
Geissler, HJ ;
Davis, KL ;
Gogola, GR ;
Warters, RD ;
deVivie, ER ;
Mehlhorn, U .
ANESTHESIA AND ANALGESIA, 1997, 85 (05) :987-992
[4]   Iatrogenic myocardial edema: Increased diastolic compliance and time course of resolution in vivo [J].
Amirhamzeh, MMR ;
Dean, DA ;
Jia, CX ;
Cabreriza, SE ;
Starr, JP ;
Sardo, MJ ;
Chalik, N ;
Dickstein, ML ;
Spotnitz, HM .
ANNALS OF THORACIC SURGERY, 1996, 62 (03) :737-743
[5]  
[Anonymous], 1977, AM J PHYSIOL
[6]   INTERSTITIAL-LYMPHATIC MECHANISMS IN THE CONTROL OF EXTRACELLULAR FLUID VOLUME [J].
AUKLAND, K ;
REED, RK .
PHYSIOLOGICAL REVIEWS, 1993, 73 (01) :1-78
[7]  
BASSINGTHWAIGHTE JB, 1975, BIBL ANAT, P24
[8]   ALTERATIONS IN COLLAGEN CROSS-LINKING IMPAIR MYOCARDIAL-CONTRACTILITY IN THE MOUSE HEART [J].
CAPASSO, JM ;
ROBINSON, TF ;
ANVERSA, P .
CIRCULATION RESEARCH, 1989, 65 (06) :1657-1664
[9]   Endotoxin-induced heart dysfunction in rats: Assessment of myocardial perfusion and permeability and the role of fluid resuscitation [J].
Chagnon, F ;
Bentourkia, M ;
Lecomte, R ;
Lessard, M ;
Lesur, O .
CRITICAL CARE MEDICINE, 2006, 34 (01) :127-133
[10]   COMPLEMENT ACTIVATION DURING CARDIOPULMONARY BYPASS - EVIDENCE FOR GENERATION OF C3A AND C5A ANAPHYLATOXINS [J].
CHENOWETH, DE ;
COOPER, SW ;
HUGLI, TE ;
STEWART, RW ;
BLACKSTONE, EH ;
KIRKLIN, JW .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (09) :497-503