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Lidocaine induces endoplasmic reticulum stress-associated apoptosis in vitro and in vivo
Authors:Hong Dae Young  Kwon Kisang  Lee Kyeong Ryong  Choi Young Jin  Goo Tae-Won  Yu Kweon  Kim Seung-Whan  Kwon O-Yu
Affiliation:Department of Emergency Medicine, Konkuk University Medical Center, Seoul 143-729, Korea; E-Mails: sean1011@daum.net (D.Y.H.); lkrer@kuh.ac.kr (K.R.L.).
Abstract:We demonstrated that upregulation of both gene expression of endoplasmic reticulum (ER) stress chaperones (BiP, calnexin, calreticulin, and PDI) and ER stress sensors (ATF6, IRE1 and PERK) was induced by lidocaine, a local anesthetic, in PC12 cells. In addition to gene regulation, lidocaine also induced typical ER stress phenomena such as ART6 proteolytic cleavage, eIF2 alpha phosphorylation, and XBP1 mRNA splicing. In in vivo experiments, while lidocaine downregulated gene expression of antiapoptotic factors (Bcl-2 and Bcl-xl), pro-apoptotic factor (Bak and Bax) gene expression was upregulated. Furthermore, lidocaine induced apoptosis, as measured histochemically, and upregulated PARP1, a DNA damage repair enzyme. These results are the first to show that lidocaine induces apoptosis through ER stress in vitro and in vivo.
Keywords:lidocaine   endoplasmic reticulum (ER) stress   ER chaperone   ER stress sensor   apoptosis
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