Mechanisms and sequelae of increased alveolar fluid clearance in hyperoxic rats

被引:72
作者
Yue, G
Matalon, S
机构
[1] UNIV ALABAMA, DEPT ANESTHESIOL, BIRMINGHAM, AL 35233 USA
[2] UNIV ALABAMA, DEPT PHYSIOL & BIOPHYS, BIRMINGHAM, AL 35233 USA
[3] UNIV ALABAMA, DEPT PEDIAT, BIRMINGHAM, AL 35233 USA
关键词
hyperoxia; amiloride; N-ethyl-N-isopropyl amiloride; sodium channels; fluid reabsorption; pulmonary edema; extravascular lung water; phenamil;
D O I
10.1152/ajplung.1997.272.3.L407
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We instilled 4 mi isotonic fluid containing trace amounts of fluorescently labeled dextran (molecular mass 150 kDa) in the lungs of rats exposed to either 85% O-2 for 7 days or to 85% O-2 for 7 days and 100% O-2 for 3 days. We withdrew the fluid every hour for a 3-h period and calculated alveolar fluid clearance (AFC) from changes in dextran concentration. Postinstillation (3 h), AFC values in the control and the two hyperoxic groups were 51 +/- 1, 63 +/- 2, and 62 +/- 3 (SE), respectively (%instilled volume; n greater than or equal to 5; P < 0.05). Addition of either 1 mM amiloride or N-ethyl-N-isopropyl amiloride (EIPA) in the instillate decreased the AFC values in all groups 3 h later to similar to 30% of instilled volume. Instillation of phenamil, an irreversible blocker of epithelial Na+ channels into the lungs of rats exposed to 85% O-2 for 7 days and 100% O-2 for 2 days, resulted in a significant increase of their extravascular lung fluid volumes 24 h later. These results demonstrate the existence of EIPA-inhibitable Na+ channels in alveolar epithelial cells in vivo and indicate that an increase in Na+ transport plays an important role in limiting the amount of alveolar edema in O-2-damaged lungs.
引用
收藏
页码:L407 / L412
页数:6
相关论文
共 37 条
  • [31] EPITHELIAL NA+ CHANNELS
    SMITH, PR
    BENOS, DJ
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1991, 53 : 509 - 530
  • [32] SODIUM-INDEPENDENT MODULATION OF NA+-K+-ATPASE ACTIVITY BY BETA-ADRENERGIC AGONIST IN ALVEOLAR TYPE-II CELLS
    SUZUKI, S
    ZUEGE, D
    BERTHIAUME, Y
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1995, 268 (06) : L983 - L990
  • [33] MECHANISMS OF LUNG LIQUID CLEARANCE DURING HYPEROXIA IN ISOLATED RAT LUNGS
    SZNAJDER, JI
    OLIVERA, WG
    RIDGE, KM
    RUTSCHMAN, DH
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 151 (05) : 1519 - 1525
  • [34] D-GLUCOSE AND L-GLUCOSE TRANSPORT ACROSS THE PULMONARY EPITHELIUM
    WANGENSTEEN, D
    BARTLETT, M
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1984, 57 (06) : 1722 - 1730
  • [35] INCREASED EXPRESSION AND ACTIVITY OF SODIUM-CHANNELS IN ALVEOLAR TYPE-II CELLS OF HYPEROXIC RATS
    YUE, G
    RUSSELL, WJ
    BENOS, DJ
    JACKSON, RM
    OLMAN, MA
    MATALON, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (18) : 8418 - 8422
  • [36] REGULATION OF LOW-AMILORIDE-AFFINITY SODIUM-CHANNELS IN ALVEOLAR TYPE-II CELLS
    YUE, G
    SHOEMAKER, RL
    MATALON, S
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01): : L94 - L100
  • [37] CULTURE-INDUCED ALTERATIONS IN ALVEOLAR TYPE-II CELL NA+ CONDUCTANCE
    YUE, G
    HU, P
    OH, YS
    JILLING, T
    SHOEMAKER, RL
    BENOS, DJ
    CRAGOE, EJ
    MATALON, S
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (03): : C630 - C640