Exposure to Cigarette Smoke Impairs Alveolar Macrophage Functions during Halothane and Isoflurane Anesthesia in Rats

Author:

Kotani Naoki1,Hashimoto Hiroshi1,Sessler Daniel I.2,Yatsu Yuichi3,Muraoka Masatoshi1,Matsuki Akitomo4

Affiliation:

1. Assistant Professor, Department of Anesthesiology, University of Hirosaki School of Medicine.

2. Professor, Department of Anesthesia and Perioperative Care, University of California–San Francisco; Professor, Ludwig Boltzmann Institute for Clinical Anesthesia and Intensive Care; Director, Outcomes Research™; Professor and Vice Chair, Department of Anesthesia and General Intensive Care, University of Vienna.

3. Instructor, Department of Anesthesiology, University of Hirosaki School of Medicine.

4. Professor and Chair, Department of Anesthesiology, University of Hirosaki School of Medicine.

Abstract

Background Smoking alters numerous alveolar macrophage functions and is an important risk factor for postoperative pulmonary complications. The authors therefore tested the hypothesis that smoke exposure impairs antimicrobial and proinflammatory responses in alveolar macrophages during halothane and isoflurane anesthesia with mechanical ventilation. Methods Thirty control rats and 30 rats exposed to cigarette smoke were mechanically ventilated with 1.5 minimum alveolar concentration halothane and isoflurane. Ten smoke-exposed and control animals were assigned to one of three different anesthetic durations (0, 2, and 6 h). The fraction of aggregated cells and cell distribution were determined. Opsonized and unopsonized phagocytosis was measured. Microbicidal activity was determined as the ability to kill Listeria monocytogenes. The expression of interleukin (IL)-1alpha, IL-1beta, IL-6, macrophage inflammatory protein-2, interferon-gamma, and tumor necrosis factor-alpha was measured by semiquantitative reverse-transcription polymerase chain reaction. Pulmonary lavage concentrations of these cytokines were measured by enzyme-linked immunosorbent assay. Results During both halothane and isoflurane anesthesia, the fraction of aggregated macrophages increased, whereas unopsonized and opsonized phagocytosis and microbicidal activity decreased significantly over time in both groups. Responses observed in smoke-exposed rats were almost twice as great as those observed in the control rats. Gene expression and production of all proinflammatory cytokines except IL-6 increased 2-20-fold during anesthesia. The increases in IL-1beta, interferon-gamma, and tumor necrosis factor-alpha in the control rats were 1.5-8 times greater than those in the smoke-exposed rats. Conclusion Antimicrobial and proinflammatory responses of alveolar macrophages during anesthesia were markedly suppressed by smoke exposure. Our data suggest that smoke exposure reduces the efficacy of immune defenses during anesthesia.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

Reference38 articles.

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