EFFECT OF ACUTE ADMINISTRATION OF BLEOMYCIN ON LUNG FLUID BALANCE IN SHEEP

被引:6
作者
WEIDNER, WJ [1 ]
QUAM, DA [1 ]
MCCLURE, DE [1 ]
DEFOUW, DO [1 ]
机构
[1] UNIV MED & DENT NEW JERSEY,DEPT ANAT CELL BIOL & INJURY SCI,NEWARK,NJ
关键词
LUNG; ACUTE LUNG INJURY; BLEOMYCIN; LYMPH; PULMONARY EDEMA; PULMONARY MICROCIRCULATION; ARDS;
D O I
10.3109/01902149509031763
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
This study examined the effects of acute administration of bleomycin (BLM) on lung liquid and protein exchange in anesthetized sheep prepared with caudal mediastinal lung lymph fistulas. Six sheep received BLM (15 U IV) after a baseline period, while seven others were given BLM after a steady state was obtained following elevation of left atrial pressure (P-LA) a procedure intended to minimize changes in pulmonary microvascular surface area and produce high lung lymph flow (Q(L)). Plasma and lung lymph angiotensin converting enzyme (ACE) activities were measured in order to independently assess the effects of BLM on pulmonary endothelial integrity. Q(L) rose significantly in all animals following BLM. The ratio of lymph to plasma protein concentration (C-L/C-P) did not change in the group given BLM alone, and fell continuously during the period of P-LA elevation after BLM in that group. Plasma and lung lymph ACE activities were unchanged following BLM administration in either group. The ultrastructure of the gas-exchanging region of lungs from animals in each group was examined by transmission electron microscopy. The data suggest that acute administration of a low dose of BLM does not increase pulmonary microvascular permeability, but may induce an increase in perfused pulmonary microvascular surface area responsible for increased Q(L).
引用
收藏
页码:617 / 630
页数:14
相关论文
共 27 条
  • [1] Adamson I.Y.R., Bowden D.H., The pathogenesis of bleomycin-induced pulmonary fibrosis in mice, Am J Pathol., 77, pp. 185-198, (1974)
  • [2] Lazo J.S., Catravas J.D., Dobuler K.J., Gillis C.N., Prolonged reduction in serum angiotensin converting enzyme activity after treatment of rabbits with bleomycin, Toxicol Appl Pharmacol., 69, pp. 276-282, (1983)
  • [3] Lazo J.S., Catravas J.D., Gillis C.N., Reduction in rabbit serum and pulmonary angiotensin converting enzyme activity after subacute bleomycin treatment, Biochem Pharmacol., 30, pp. 2577-2584, (1981)
  • [4] Newman R.A., Kimberly P.J., Stuart J.A., Kelley J., Assessment of bleomycin lung toxicity using angiotensin converting enzyme in pulmonary lavage, Cancer Res., 40, pp. 3621-3626, (1980)
  • [5] Aso Y., Yoneda K., Kikkawa Y., Morphologic and biochemical study of pulmonary changes induced by bleomycin in mice, Lab Invest., 35, pp. 558-568, (1976)
  • [6] Thrall R.S., McCormick J.R., Jack R.M., McReynolds R.A., Ward P.A., Bleomycin-induced pulmonary fibrosis in the rat, Am J Pathol., 95, pp. 117-130, (1979)
  • [7] Wangensteen D., Yankovich R., Hoidal J., Niewoehner D., Bleomycin-induced changes in pulmonary microvascular albumin permeability and extravascular albumin space, Am Rev Respir Dis., 127, pp. 204-208, (1983)
  • [8] Catravas J.D., Lazo J.S., Dobuler K.J., Mills L.R., Gillis C.N., Pulmonary endothelial dysfunction in the presence or absence of interstitial injury induced by intratracheally injected bleomycin in rabbits, Am Rev Respir Dis., 128, pp. 740-748, (1983)
  • [9] Sorenson P.G., Romer F.K., Cortes D., Angiotensin converting enzyme: an indicator of bleomycin-induced pulmonary toxicity in humans, Eur J Cancer Clin Oncol., 20, pp. 1405-1406, (1984)
  • [10] Hollinger M.A., Giri S.N., Patwell S., Zuckerman J.E., Gorin A.B., Parsons G., Effect of acute lung injury on angiotensin converting enzyme in serum lung lavage and effusate, Am Rev Respir Dis., 121, pp. 373-376, (1980)