کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5685562 | 1598228 | 2017 | 15 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Heme Oxygenase 1 as a Therapeutic Target in Acute Kidney Injury
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کلمات کلیدی
HMOX1acute kidney injury (AKI) - آسیب حاد کلیه (AKI)inflammation - التهاب( توروم) Biomarker - بیومارکرOxidative stress - تنش اکسیداتیوCell cycle regulation - تنظیم چرخه سلولیCytoprotection - حفاظت از سیتوReview - مرورRenal failure - نارسایی کلیهPathophysiology - پاتوفیزیولوژیTranslational research - پژوهشهای کاربردی سازی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماریهای کلیوی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
A common clinical condition, acute kidney injury (AKI) significantly influences morbidity and mortality, particularly in critically ill patients. The pathophysiology of AKI is complex and involves multiple pathways, including inflammation, autophagy, cell-cycle progression, and oxidative stress. Recent evidence suggests that a single insult to the kidney significantly enhances the propensity to develop chronic kidney disease. Therefore, the generation of effective therapies against AKI is timely. In this context, the cytoprotective effects of heme oxygenase 1 (HO-1) in animal models of AKI are well documented. HO-1 modulates oxidative stress, autophagy, and inflammation and regulates the progression of cell cycle via direct and indirect mechanisms. These beneficial effects of HO-1 induction during AKI are mediated in part by the by-products of the HO reaction (iron, carbon monoxide, and bile pigments). This review highlights recent advances in the molecular mechanisms of HO-1âmediated cytoprotection and discusses the translational potential of HO-1 induction in AKI.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: American Journal of Kidney Diseases - Volume 69, Issue 4, April 2017, Pages 531-545
Journal: American Journal of Kidney Diseases - Volume 69, Issue 4, April 2017, Pages 531-545
نویسندگان
Subhashini PhD, Abolfazl MD, PhD, Anupam MD,