Lung tissue mechanics as an emergent phenomenon

被引:115
作者
Suki, Bela [1 ]
Bates, Jason H. T. [2 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[2] Univ Vermont, Dept Med, Burlington, VT USA
基金
美国国家卫生研究院;
关键词
pressure-volume curve; viscoelasticity; pulmonary fibrosis; emphysema; EXCISED CAT LUNG; IDIOPATHIC PULMONARY-FIBROSIS; ALVEOLAR SURFACE-TENSION; PRESSURE-VOLUME DATA; EXTRACELLULAR-MATRIX; OSCILLATORY MECHANICS; CONSTITUTIVE EQUATION; DYNAMIC PROPERTIES; STRIP MECHANICS; ELASTIN FIBERS;
D O I
10.1152/japplphysiol.01244.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The mechanical properties of lung parenchymal tissue are both elastic and dissipative, as well as being highly nonlinear. These properties cannot be fully understood, however, in terms of the individual constituents of the tissue. Rather, the mechanical behavior of lung tissue emerges as a macroscopic phenomenon from the interactions of its microscopic components in a way that is neither intuitive nor easily understood. In this review, we first consider the quasi-static mechanical behavior of lung tissue and discuss computational models that show how smooth nonlinear stress-strain behavior can arise through a percolation-like process in which the sequential recruitment of collagen fibers with increasing strain causes them to progressively take over the load-bearing role from elastin. We also show how the concept of percolation can be used to link the pathologic progression of parenchymal disease at the micro scale to physiological symptoms at the macro scale. We then examine the dynamic mechanical behavior of lung tissue, which invokes the notion of tissue resistance. Although usually modeled phenomenologically in terms of collections of springs and dash-pots, lung tissue viscoelasticity again can be seen to reflect various types of complex dynamic interactions at the molecular level. Finally, we discuss the inevitability of why lung tissue mechanics need to be complex.
引用
收藏
页码:1111 / 1118
页数:8
相关论文
共 72 条
[1]   Effect of glycosaminoglycan degradation on lung tissue viscoelasticity [J].
Al Jamal, R ;
Roughley, PJ ;
Ludwig, MS .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 280 (02) :L306-L315
[2]   PRESSURE-VOLUME CURVES OF AIR-FILLED AND LIQUID-FILLED EXCISED LUNGS-SURFACE TENSION IN-SITU [J].
BACHOFEN, H ;
HILDERBR.J ;
BACHOFEN, M .
JOURNAL OF APPLIED PHYSIOLOGY, 1970, 29 (04) :422-&
[3]   Linking Parenchymal disease progression to changes in lung mechanical function by percolation [J].
Bates, Jason H. T. ;
Davis, Gerald S. ;
Majumdar, Arnab ;
Butnor, Kelly J. ;
Suki, Bela .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 176 (06) :617-623
[4]   A recruitment model of quasi-linear power-law stress adaptation in lung tissue [J].
Bates, Jason H. T. .
ANNALS OF BIOMEDICAL ENGINEERING, 2007, 35 (07) :1165-1174
[5]   A micromechanical model of lung tissue rheology [J].
Bates, JHT .
ANNALS OF BIOMEDICAL ENGINEERING, 1998, 26 (04) :679-687
[6]  
Bates JHT, 2009, LUNG MECHANICS: AN INVERSE MODELING APPROACH, P1, DOI 10.1017/CBO9780511627156
[7]   LUNG-TISSUE RHEOLOGY AND 1/F NOISE [J].
BATES, JHT ;
MAKSYM, GN ;
NAVAJAS, D ;
SUKI, B .
ANNALS OF BIOMEDICAL ENGINEERING, 1994, 22 (06) :674-681
[8]  
Baydur A, 1996, Curr Opin Pulm Med, V2, P370, DOI 10.1097/00063198-199609000-00005
[9]   Lung and alveolar wall elastic and hysteretic behavior in rats: effects of in vivo elastase treatment [J].
Brewer, KK ;
Sakai, H ;
Alencar, AM ;
Majumdar, A ;
Arold, SP ;
Lutchen, KR ;
Ingenito, EP ;
Suki, B .
JOURNAL OF APPLIED PHYSIOLOGY, 2003, 95 (05) :1926-1936
[10]   Mechanical interactions between collagen and proteoglycans: implications for the stability of lung tissue [J].
Cavalcante, FSA ;
Ito, S ;
Brewer, K ;
Sakai, H ;
Alencar, AM ;
Almeida, MP ;
Andrade, JS ;
Majumdar, A ;
Ingenito, EP ;
Suki, B .
JOURNAL OF APPLIED PHYSIOLOGY, 2005, 98 (02) :672-679