The Effect of ERK Signaling Pathway on the Level of Soluble RAGE (sRAGE) Peptide in AGE-Induced Oxidative Stress

Article Type:
Research/Original Article (بدون رتبه معتبر)
Abstract:
In the context of diabetes, there is a bidirectional relation between AGEs and ROS which is amplified under hyperglycemic condition. Indeed, the AGE/RAGE interaction, via triggering several signaling pathways underlies such interplay. These damaging signaling cascades could be attenuated by naturally occurring soluble form of RAGE, namely sRAGE. In the present study, the effect of AGEs on the intracellular superoxide anion level and the antioxidant defense system was studied. Moreover, the link between the level of soluble RAGE and the AGE-triggered signaling pathways, namely ERK, was also investigated. Our results demonstrated that the elevation in intracellular superoxide anion level was associated with decrease in antioxidant enzyme activities. Our data also revealed that the level of sRAGE is negatively correlated with the ERK expression in a hyperglycemia model system. Hence, the current study brings about novel evidences suggesting that the level of sRAGE would be under the influence of stress-sensitive signaling pathways.
Language:
English
Published:
Trends in Peptide and Protein Sciences, Volume:1 Issue: 3, May 2017
Pages:
115 to 122
magiran.com/p1774946  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!