Airway remodeling in asthma amplifies heterogeneities in smooth muscle shortening causing hyperresponsiveness

被引:100
作者
Gillis, HL [1 ]
Lutchen, KR [1 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
关键词
inhomogeneous; lung mechanics; lung resistance; lung elastance; impedance;
D O I
10.1152/jappl.1999.86.6.2001
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Although airway remodeling and inflamation in asthma can amplify the constriction response of a single airway, their influence on the structural changes in the whole airway network is unknown. We present a morphometric model of the human lung that incorporates cross-sectional wall areas corresponding to the adventitia, airway smooth muscle (ASM), and mucosa for healthy and mildly and severely asthmatic airways and the influence of parenchymal tethering. A heterogeneous ASM percent shortening stimulus is imposed, causing distinct constriction patterns for healthy and asthmatic airways. We calculate lung resistance and elastance from 0.1 to 5 Hz. We show that, for a given ASM stimulus, the distribution of wall area in asthmatic subjects will amplify not only the mean but the heterogeneity of constriction in the lung periphery. Moreover, heterogeneous ASM shortening that would produce only mild changes in the healthy lung can cause hyperresponsive changes in lung resistance and elastance at typical breathing rates in the asthmatic lung, even with relatively small increases in airway resistance. This condition arises when airway closures occur randomly in the lung periphery. We suggest that heterogeneity is a crucial determinant of hyper-responsiveness in asthma and that; acute asthma is more a consequence of extensive airway wall inflamation and remodeling, predisposing the lung to produce an acute pattern of heterogeneous constriction.
引用
收藏
页码:2001 / 2012
页数:12
相关论文
共 26 条
[1]   PROPOSED NOMENCLATURE FOR QUANTIFYING SUBDIVISIONS OF THE BRONCHIAL WALL [J].
BAI, A ;
EIDELMAN, DH ;
HOGG, JC ;
JAMES, AL ;
LAMBERT, RK ;
LUDWIG, MS ;
MARTIN, J ;
MCDONALD, DM ;
MITZNER, WA ;
OKAZAWA, M ;
PACK, RJ ;
PARE, PD ;
SCHELLENBERG, RR ;
TIDDENS, HAWM ;
WAGNER, EM ;
YAGER, D .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (02) :1011-1014
[2]   The myth of maximal airway responsiveness in vivo [J].
Brown, RH ;
Mitzner, W .
JOURNAL OF APPLIED PHYSIOLOGY, 1998, 85 (06) :2012-2017
[3]   Airway smooth muscle, tidal stretches, and dynamically determined contractile states [J].
Fredberg, JJ ;
Inouye, D ;
Miller, B ;
Nathan, M ;
Jafari, S ;
Raboudi, SH ;
Butler, JP ;
Shore, SA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (06) :1752-1759
[4]   How heterogeneous bronchoconstriction affects ventilation distribution in human lungs: A morphometric model [J].
Gillis, HL ;
Lutchen, KR .
ANNALS OF BIOMEDICAL ENGINEERING, 1999, 27 (01) :14-22
[5]   PRESSURE-VOLUME AND LENGTH-STRESS RELATIONSHIPS IN CANINE BRONCHI INVITRO [J].
GUNST, SJ ;
STROPP, JQ .
JOURNAL OF APPLIED PHYSIOLOGY, 1988, 64 (06) :2522-2531
[6]   AIRWAY GEOMETRY AND WALL MECHANICAL-PROPERTIES ESTIMATED FROM SUBGLOTTAL INPUT IMPEDANCE IN HUMANS [J].
HABIB, RH ;
CHALKER, RB ;
SUKI, B ;
JACKSON, AC .
JOURNAL OF APPLIED PHYSIOLOGY, 1994, 77 (01) :441-451
[7]   INPUT IMPEDANCE AND PERIPHERAL INHOMOGENEITY OF DOG LUNGS [J].
HANTOS, Z ;
DAROCZY, B ;
SUKI, B ;
NAGY, S ;
FREDBERG, JJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1992, 72 (01) :168-178
[8]   MODELS OF HUMAN BRONCHIAL TREE [J].
HORSFIEL.K ;
DART, G ;
OLSON, DE ;
FILLEY, GF ;
CUMMING, G .
JOURNAL OF APPLIED PHYSIOLOGY, 1971, 31 (02) :207-&
[9]   THE MECHANICS OF AIRWAY NARROWING IN ASTHMA [J].
JAMES, AL ;
PARE, PD ;
HOGG, JC .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (01) :242-246
[10]   THE USE OF THE INTERNAL PERIMETER TO COMPARE AIRWAY SIZE AND TO CALCULATE SMOOTH-MUSCLE SHORTENING [J].
JAMES, AL ;
HOGG, JC ;
DUNN, LA ;
PARE, PD .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 138 (01) :136-139