کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1912049 | 1046857 | 2006 | 14 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A novel SOD-mimetic permeability transition inhibitor agent protects ischemic heart by inhibiting both apoptotic and necrotic cell death
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کلمات کلیدی
ANTPTPcyt-cMPT3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide - 3- (4،5-dimethyl-2-thiazolyl) -2،5-difenyl-2H-tetrazolium bromideROS - ROSPermeability transition pore - افت فشار نفوذ پذیریmitochondrial permeability transition - انتقال نفوذپذیری میتوکندریCSA - ایالات مؤتلفهٔ آمریکاischemia–reperfusion - ایسکمی-رپرفیوژنadenine nucleotide translocase - ترانسکوز نوکلئوتید آدنینNMR - تشدید مغناطیسی هستهای Apoptosis - خزان یاختهایcytochrome c - سیتوکروم سیcyclosporin A - سیکلوسپورین ANecrosis - نکروز یا بافتمردگیMitochondrial membrane potential - پتانسیل غشای میتوکندریcreatine phosphate - کراتین فسفاتReactive oxygen species - گونههای فعال اکسیژن
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
سالمندی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: A novel SOD-mimetic permeability transition inhibitor agent protects ischemic heart by inhibiting both apoptotic and necrotic cell death A novel SOD-mimetic permeability transition inhibitor agent protects ischemic heart by inhibiting both apoptotic and necrotic cell death](/preview/png/1912049.png)
چکیده انگلیسی
In ischemia-reperfusion injuries, elevated calcium and reactive oxygen species (ROS) induce mitochondrial permeability transition (mPT), which plays a pivotal role in mediating damages and cell death. Inhibition of mPT decreases necrotic cell death; however, during reperfusion, the continuous production of ROS may contribute to the temporary opening of the pore and thus the onset of the delayed apoptotic cell death. Based on amiodarone structure, we developed the first SOD-mimetic mPT inhibitor (HO-3538) that can eliminate ROS in the microenvironment of the permeability pore. In isolated mitochondria, HO-3538 inhibited mPT and the release of proapoptotic mitochondrial proteins. It had a ROS scavenging effect and antiapoptotic effect in a cardiomyocyte line and it diminished release of mitochondrial proapoptotic proteins. Furthermore, HO-3538 significantly enhanced the recovery of mitochondrial energy metabolism and functional cardiac parameters; decreased infarct size, lipid peroxidation, and protein oxidation; and suppressed necrotic as well as apoptotic cell death pathways in Langendorff-perfused hearts. In these respects it was somewhat superior to its two constituents, amiodarone and a pyrrol-derivative free radical scavenger. These data suggest that the SOD-mimetic mPT inhibitors are ideal candidates for drug development for the alleviation of postinfarct myocardial injuries.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Free Radical Biology and Medicine - Volume 41, Issue 5, 1 September 2006, Pages 835-848
Journal: Free Radical Biology and Medicine - Volume 41, Issue 5, 1 September 2006, Pages 835-848
نویسندگان
Zita Bognar, Tamas Kalai, Anita Palfi, Katalin Hanto, Balazs Bognar, Laszlo Mark, Zoltan Szabo, Antal Tapodi, Balazs Radnai, Zsolt Sarszegi, Arpad Szanto, Ferenc Jr., Kalman Hideg, Balazs Sumegi, Gabor Varbiro,