RRC ID 41497
著者 Nishina K, Mikawa K, Morikawa O, Obara H, Mason RJ.
タイトル The effects of intravenous anesthetics and lidocaine on proliferation of cultured type II pneumocytes and lung fibroblasts.
ジャーナル Anesth Analg
Abstract UNLABELLED:Type II pneumocytes synthesize surfactant and differentiate into type I pneumocytes to maintain the epithelium (1). Alveolar type II cell proliferation is required for reepithelization after acute lung injury (ALI) and is thought to minimize the subsequent fibrotic response (1). Keratinocyte growth factor (KGF) and hepatocyte growth factor (HGF) are among the most potent mitogen for type II epithelial cells, but not for fibroblasts in the lung (1). These growth factors attenuate several experimental ALI models by promoting epithelial repair (2,3). Thus, KGF and HGF may be a promising therapeutic approach to ALI. Critically ill patients with ALI often receive IV anesthetics or sedatives to facilitate mechanical ventilation. Furthermore, these patients sometimes undergo bronchoscopy under local anesthesia to obtain bronchoalveolar lavage fluid or to remove respiratory secretions. Several IV and local anesthetics inhibit proliferation of various cells including epithelium (4,5). If these anesthetics impede proliferation of type II pneumocytes, this suppressive effect may be a disadvantage for alveolar reepithelization in the course of recovery from ALI. In this study, we examined the effects of midazolam, propofol, ketamine, thiopental, and lidocaine on proliferation of type II alveolar epithelial cells using in vitro culture system. Because fibroblast proliferation is a key event in late phase of ALI, inhibition of this fibroproliferation is probably beneficial. Thus, we further determined whether these anesthetics could regulate proliferation of lung fibroblasts. In the current study, rolipram was used as a positive control. In our previous preliminary experiment, we found that rolipram, a phosphodiesterase inhibitor type IV, augments spontaneous or KGF-/HGF-promoted type II cell proliferation (6).
IMPLICATIONS:Midazolam, ketamine, thiopental, propofol, or lidocaine did not inhibit proliferation of cultured rat type II pneumocytes. Our findings suggest that these anesthetics do not impede alveolar reepithelization after acute lung injury.
巻・号 94(2)
ページ 385-8, table of contents
公開日 2002-2-1
DOI 10.1097/00000539-200202000-00029
PMID 11812704
MeSH Anesthetics, Dissociative / pharmacology Anesthetics, Intravenous / pharmacology* Anesthetics, Local / pharmacology* Animals Cell Division / drug effects Cells, Cultured Dimethyl Sulfoxide / pharmacology Fibroblast Growth Factor 7 Fibroblast Growth Factors / pharmacology Fibroblasts / cytology* Fibroblasts / drug effects Hepatocyte Growth Factor / pharmacology Ketamine / pharmacology Lidocaine / pharmacology* Lung / cytology* Lung / drug effects Male Midazolam / pharmacology Phosphodiesterase Inhibitors / pharmacology Rats Rats, Sprague-Dawley Rolipram / pharmacology Thiopental / pharmacology
IF 4.305
引用数 14
WOS 分野 ANESTHESIOLOGY
リソース情報
ヒト・動物細胞