Literature DB >> 8201829

Cyclophosphamide induced early biochemical changes in lung lavage fluid and alterations in lavage cell function.

N Venkatesan1, G Chandrakasan.   

Abstract

The present investigation evaluated the changes in bronchoalveolar lavage fluid (BALF) biochemical constituents and indices of bronchoalveolar lavage cell functions to detect early lung injury in rats following intraperitoneal administration of cyclophosphamide (CP). Rats were exposed to a single intraperitoneal injection of CP (200 or 300 mg/kg body weight). Experimental and control rats were sacrificed at various time intervals (2, 3, 5, 7, 11, 21, and 42 days after cessation of exposure), and lung lavage was performed to examine several markers of lung injury. Biochemical analyses revealed dose-related increases in BALF angiotensin converting enzyme activity, total protein, lactate, lactate dehydrogenase, and N-acetyl-beta-D-glucosaminidase (NAG) levels on days 2, 3, 5, 7, and dose-related increases in albumin, alkaline phosphatase, acid phosphatase, and lipid peroxidation on days 2, 3, 5, 7, and 11 after CP treatment. In contrast, reduced levels of ascorbic acid and glutathione (GSH) content were observed in lung lavage fluid. We also examined bronchoalveolar lavage cells for acid hydrolases (acid phosphatase, beta-glucuronidase, NAG) and GSH content. Activity of acid hydrolases was slightly elevated on day 2 and peaked on days 3, 5, and 7. However, lavage cell GSH content was decreased. Thus, measurements of pulmonary changes by analyzing lavage fluid and lavage cell functions seems to be a useful marker for assessing the early onset and development of CP-induced lung injury.

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Year:  1994        PMID: 8201829     DOI: 10.1007/bf00175943

Source DB:  PubMed          Journal:  Lung        ISSN: 0341-2040            Impact factor:   2.584


  41 in total

1.  Pharmacokinetics, metabolic activation, and lung toxicity of cyclophosphamide in C57/B16 and ICR mice.

Authors:  S Kanekal; L Fraiser; J P Kehrer
Journal:  Toxicol Appl Pharmacol       Date:  1992-05       Impact factor: 4.219

2.  Increased lysosomal enzymes in lungs of ozone-exposed rats.

Authors:  C J Dillard; K Reddy; B Fletcher; B de Lumen; S Langberg; A L Tappel; N Urribarri
Journal:  Arch Environ Health       Date:  1972-12

3.  Adverse effects of (15S)-15-methyl-prostaglandin E1 in normal and paraquat-exposed rats.

Authors:  J H Williams; R D Fairshter; T R Ulich; S Crosby; M Chen; L Rosario; N D Vaziri
Journal:  Toxicol Appl Pharmacol       Date:  1988-02       Impact factor: 4.219

4.  Early diagnosis of bleomycin pulmonary toxicity using bronchoalveolar lavage in dogs.

Authors:  P J Fahey; M J Utell; R J Mayewski; J D Wandtke; R W Hyde
Journal:  Am Rev Respir Dis       Date:  1982-07

5.  Early damage indicators in the lung. III. Biochemical and cytological response of the lung to inhaled metals salts.

Authors:  R F Henderson; A H Rebar; J A Pickrell; G J Newton
Journal:  Toxicol Appl Pharmacol       Date:  1979-08       Impact factor: 4.219

6.  Guinea pig ozone-induced airway hyperreactivity is associated with increased N-acetyl-beta-D-glucosaminidase activity in bronchoalveolar lavage fluid.

Authors:  D B Lew; V Chodimella; C G Murlas
Journal:  Lung       Date:  1990       Impact factor: 2.584

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Authors:  V E Gould; J Miller
Journal:  Am J Pathol       Date:  1975-12       Impact factor: 4.307

8.  Glutathione depletion as a determinant of sensitivity of human leukemia cells to cyclophosphamide.

Authors:  T R Crook; R L Souhami; G D Whyman; A E McLean
Journal:  Cancer Res       Date:  1986-10       Impact factor: 12.701

9.  Cyclophosphamide-induced depression of the antioxidant defense mechanisms of the lung.

Authors:  J M Patel; E R Block
Journal:  Exp Lung Res       Date:  1985       Impact factor: 2.459

10.  Cyclophosphamide-induced lung damage in mice: protection by a small preliminary dose.

Authors:  C H Collis; C M Wilson; J M Jones
Journal:  Br J Cancer       Date:  1980-06       Impact factor: 7.640

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  1 in total

1.  Modulation of cyclophosphamide-induced early lung injury by curcumin, an anti-inflammatory antioxidant.

Authors:  N Venkatesan; G Chandrakasan
Journal:  Mol Cell Biochem       Date:  1995-01-12       Impact factor: 3.396

  1 in total

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