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Purpose The aim of this study is to evaluate the cytotoxic and antiproliferating effects of intravenous anesthetics on an mouse fibroblast in vitro cell culture system. Methods The cells were exposed to the usual clinical plasma concentration of intravenous anesthetics, i.e., midazolam (0.15 µg/ml), propofol (2 µg/ml), remifentanil (2 µg/ml), thiopental (10 µg/ml), for 4, 8, or 24 h. Cell proliferation (n = 6 for each) under intravenous anesthetics was analyzed using the MTT (3-(4,5-dimethylthiazol-2yl)-2,5-diphenyltetrazolium bromide) assay. Cytotoxicity (n = 6 for each) of intravenous anesthetics was investigated using a LIVE/DEAD viability assay kit. Results Intravenous anesthetic exposure time did not affect the proliferation rate of mouse fibroblasts. The cytotoxicity of intravenous anesthetics did not differ in accordance with exposure time. Conclusion Our results showed that intravenous anesthetics may not affect mouse fibroblast proliferation and viability. Keywords Fibroblast * Midazolam * Propofol * Remifentanil * Sedation * Transplantation, Introduction A fibroblast is a type of connective tissue cell that synthesizes the extracellular matrix rich in collagen and other macromolecules which maintain the structural framework (stroma) for many tissues [...]

Author(s): Hiroyuki Kinoshita[sup.1] Author Affiliations: (1) Department of Anesthesiology, Wakayama Medical University, 811-1 Kimiidera, 641-0012, WakayamaJapan H. Kinoshita The roles of reactive oxygen species and oxidative stress continue to be [...]

The roles of reactive oxygen species and oxidative stress continue to be an area of interest in vascular biology and pathology [1]. Oxidative stress can be defined as imbalance between [...]