Vasoactive Agents Alter the Biomechanical Properties of Aortic Heart Valve Leaflets in a Time-Dependent Manner

被引:0
作者
Warnock, James N. [1 ]
Gamez, Carol A. Pregonero [1 ]
Metzler, Scott A. [1 ]
Chen, Joseph [1 ]
Elder, Steven H. [1 ]
Liao, Jun [1 ]
机构
[1] Mississippi State Univ, Dept Agr & Biol Engn, Mississippi State, MS 39762 USA
关键词
DISEASE; CALCIFICATION; SCLEROSIS; CELLS; CONTRACTION;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aim of the study: Although the vasoactive agents, angiotensin II (Ang II) and 5-hydroxytryptamine (5-HT) are implicated in aortic heart valve disease, it is unclear how these compounds alter the biomechanical properties of valve leaflet tissue. The study aim was to characterize temporal changes in the elastic modulus of tissues incubated with these compounds. Methods: Valve leaflets were excised from fresh porcine aortic heart valves. Leaflet tissue was incubated with 10(-6) M 5-HT, or 10(-6) M Ang II. The stress and elongation of the tissue in the circumferential and radial directions was measured using a stepper motor-driven micromechanical testing machine at 0.5, 6, and 24 h, followed by calculations of strain and elastic modulus of each sample. Results: Tissue samples incubated with Ang II showed a significant increase in stiffness with time in the radial direction, but not in the circumferential direction. Regression analysis showed a correlation between time and elastic modulus for the tissue (R-2 = 0.84). Conversely, leaflets incubated in 5-HT did not show any significant change in elastic modulus over time in the radial direction; however, significant increases in stiffness were observed after 24 h in the circumferential direction. A strong correlation between the elastic modulus in the circumferential direction and time was also noted (R-2 = 0.99). Conclusion: The study results showed that vasoactive agents are capable of increasing the elastic modulus of aortic valve tissue in a time-dependent manner. Furthermore, the biomechanical changes induced by vasoactive agents are direction-specific, indicating different modes of action.
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页码:86 / 96
页数:11
相关论文
共 31 条
[1]   Aortic valve sclerosis and aortic atherosclerosis: Different manifestations of the same disease? Insights from a population-based study [J].
Agmon, Y ;
Khandheria, BK ;
Meissner, I ;
Sicks, JD ;
O'Fallon, WM ;
Wiebers, DO ;
Whisnant, JP ;
Seward, JB ;
Tajik, AJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 38 (03) :827-834
[2]   Aortic valve sclerosis is associated with preclinical cardiovascular disease in hypertensive adults: the Hypertension Genetic Epidemiology Network study [J].
Agno, FS ;
Chinali, M ;
Bella, JN ;
Liu, JE ;
Arnett, DK ;
Kitzman, DW ;
Oberman, A ;
Hopkins, PN ;
Rao, DC ;
Devereux, RB .
JOURNAL OF HYPERTENSION, 2005, 23 (04) :867-873
[3]   Cardiac valve calcification: characteristics of patients with calcification of the mitral annulus or aortic valve [J].
Boon, A ;
Cheriex, E ;
Lodder, J ;
Kessels, F .
HEART, 1997, 78 (05) :472-474
[4]  
Chester AH, 2000, J HEART VALVE DIS, V9, P250
[5]   Valvular heart disease associated with fenfluramine-phentermine [J].
Connolly, HM ;
Crary, JL ;
McGoon, MD ;
Hensrud, DD ;
Edwards, BS ;
Edwards, WD ;
Schaff, HV .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (09) :581-588
[6]   ENDOTHELIAL-CELL ORIENTATION ON AORTIC-VALVE LEAFLETS [J].
DECK, JD .
CARDIOVASCULAR RESEARCH, 1986, 20 (10) :760-767
[7]   Planar biaxial creep and stress relaxation of the mitral valve anterior leaflet [J].
Grashow, Jonathan S. ;
Sacks, Michael S. ;
Liao, Jun ;
Yoganathan, Ajit P. .
ANNALS OF BIOMEDICAL ENGINEERING, 2006, 34 (10) :1509-1518
[8]  
Hafizi S, 2000, J HEART VALVE DIS, V9, P454
[9]   Induction of local angiotensin II-producing systems in stenotic aortic valves [J].
Helske, S ;
Lindstedt, KA ;
Laine, M ;
Mäyränpää, M ;
Werkkala, K ;
Lommi, J ;
Turto, H ;
Kupari, M ;
Kovanen, PT .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 44 (09) :1859-1866
[10]   Inflammatory regulation of extracellular matrix remodeling in calcific aortic valve stenosis [J].
Kaden, JJ ;
Dempfle, CE ;
Grobholz, R ;
Fischer, CS ;
Vocke, DC ;
Kiliç, R ;
Sarikoç, A ;
Piñol, R ;
Hagl, S ;
Lang, S ;
Brueckmann, M ;
Borggrefe, M .
CARDIOVASCULAR PATHOLOGY, 2005, 14 (02) :80-87