Key result
Chronic ethanol ingestion doubled AT2 expression in rat alveolar epithelial cells and enhanced TNF-α- and angiotensin II-induced cytotoxicity, which was inhibited by a selective AT2 blocker.
Why the study?
Does chronic ethanol ingestion increase AT2 expression and enhance TNF-α- and angiotensin II-induced cytotoxicity via AT2 signaling in rat alveolar epithelial cells?
Does chronic ethanol ingestion increase AT2 expression and enhance TNF-α- and angiotensin II-induced cytotoxicity via AT2 signaling in rat alveolar epithelial cells?
Chronic ethanol ingestion increases AT2 receptor expression in rat alveolar epithelial cells, enhancing TNF-α- and angiotensin II-induced cytotoxicity via AT2 signaling, suggesting AT2 inhibition could limit acute lung injury in alcoholics.
Hypothesis-generating for AT2 blockade in alcohol-related lung injury; leaves open translation to human acute lung injury prevention.
Background: Alcohol abuse increases the risk of acute lung injury in critically ill patients. We have shown that alveolar epithelial cell (AEC) apoptosis in response to inflammatory mediators, including tumor necrosis factor‐α (TNF‐α), parallels endotoxin‐mediated acute lung injury in ethanol‐fed rats. Although angiotensin II mediates TNF‐α‐induced apoptosis of AECs in vitro, its role in ethanol‐mediated susceptibility to AEC apoptosis is unknown. Methods: Adult male rats were fed the Lieber‐DeCarli diet for 6 weeks. AECs were isolated, and TNF‐α‐ and angiotensin II‐induced cytotoxicity (by terminal transferase‐mediated dUTP nick end labeling staining) was determined with or without the addition of the angiotensin‐converting enzyme inhibitor (lisinopril) or a selective blocker of the angiotensin II type 1 receptor (AT1) or type 2 receptor (AT2). Finally, the relative expression of the AT1 and AT2 receptors in AECs was determined by Western blot analysis. Results: TNF‐α‐induced cytotoxicity, but not angiotensin II‐induced cytotoxicity, was prevented by lisinopril, indicating that de novo angiotensin II synthesis is required for TNF‐α‐induced apoptosis in these cells. Both TNF‐α‐ and angiotensin II‐induced cytotoxicity in AECs from control‐fed and ethanol‐fed rats were inhibited by the selective AT2 blocker, PD123319, but not by the selective AT1 blocker, losartan. In parallel, ethanol ingestion doubled AT2 expression in AECs (by Western blot) but had no significant effect on AT1 receptor expression. Conclusions: Chronic ethanol ingestion increases AT2 expression in the alveolar epithelium and enhances TNF‐α‐ and angiotensin II‐induced cytotoxicity, both of which act via AT2. Together, these findings suggest that selective AT2 receptor inhibition could limit the development of acute lung injury in alcoholic patients.
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Bechara et al. (2003) studied Acute lung injury susceptibility. Chronic ethanol ingestion vs. Control diet was evaluated on TNF-α- and angiotensin II-induced cytotoxicity and AT2 receptor expression. Chronic ethanol ingestion doubled AT2 expression in rat alveolar epithelial cells and enhanced TNF-α- and angiotensin II-induced cytotoxicity, which was inhibited by a selective AT2 blocker.
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