Phospholipase A2 and arachidonate increase in bronchoalveolar lavage fluid after inhaled antigen challenge in asthmatics

• Published in: American journal of respiratory and critical care medicine Vol. 155; no. 2; p. 421
• Main Authors: Bowton, D L, Seeds, M C, Fasano, M B, Goldsmith, B, Bass, D A
• Format: Journal Article
• Language: English
• Published: United States 01.02.1997
• Subjects: Arachidonic Acid - metabolism; Asthma - diagnosis; Asthma - metabolism; Bronchial Provocation Tests; Bronchoalveolar Lavage Fluid - chemistry; Gas Chromatography-Mass Spectrometry; Humans; Methacholine Chloride; Phospholipases A - metabolism; Phospholipases A2; Respiratory Function Tests
• ISSN: 1073-449X
• DOI: 10.1164/ajrccm.155.2.9032172

Phospholipases A2 (PLA2) hydrolyze phospholipids resulting in the release of fatty acids including arachidonic acid (AA) and lysophospholipids. AA, in turn, serves as a substrate for the synthesis of leukotrienes which can cause bronchoconstriction and airways edema and appear to be important mediators of clinical asthma. Further, lysophospholipids may be cytotoxic and/or impair the function of surfactant. We examined the release of secretory PLA2 (sPLA2) and AA into the airways after antigen challenge in 16 subjects with allergic asthma. Asthmatic subjects underwent bronchoscopy with bronchoalveolar lavage (BAL) before and after inhaled antigen challenge; in addition, a single BAL, without inhaled antigen, was performed in 10 control subjects. BAL was obtained at 4 h (n = 7), the time of the late asthmatic response (LAR) (n = 5), or 24 h (n = 4) after challenge. There was no difference between normal and asthmatic subjects in either BAL fluid (BALF) sPLA2 activity or AA concentration at baseline. Both sPLA2 and AA increased after antigen challenge (p < 0.01 and 0.05, respectively). These changes were most marked 4 h after challenge (p < 0.03 for both). sPLA2 may play an important role in the generation of AA in patients with asthma.