Academic Journal

Trelagliptin succinate: DPP-4 inhibitor to improve insulin resistance in adipocytes

التفاصيل البيبلوغرافية
العنوان: Trelagliptin succinate: DPP-4 inhibitor to improve insulin resistance in adipocytes
المؤلفون: Zhenhua Liu, Lanting Xu, Meimei Xing, Xiaojie Xu, Jinfeng Wei, Jinmei Wang, Wenyi Kang
المصدر: Biomedicine & Pharmacotherapy, Vol 125, Iss , Pp 109952- (2020)
بيانات النشر: Elsevier
سنة النشر: 2020
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Trelagliptin succinate, Insulin resistance, Adipokines, Glucose intake, PI-3K/Akt, Therapeutics. Pharmacology, RM1-950
الوصف: Trelagliptin inhibits the enzyme dipeptidyl-4 (DPP-4) to treat type 2 diabetes and it may possess the potential to improve insulin resistance. However, the molecular mechanism is not known. In this study, the effect of trelagliptin succinate in improving insulin resistance was investigated. The differentiation system of 3T3-L1 mouse preadipocytes was used to determine the content of adipokines and the content of GLUT4 in the outer membrane. The expression of AKT, P-AKT, IRS-1 and P-IRS-1 in differentiated 3T3-L1 adipocytes was determined by western blotting. Our results demonstrated that trelagliptin succinate increased the expression of AKT, P-AKT, IRS-1 and P-IRS-1 in the PI-3K/AKT insulin signaling pathway. These events promote the trans-membrane function of GLUT4 and concomitant glucose intake in adipocytes. In addition, the secretion of free fatty acids and resistin were decreased. In conclusion, our study suggested that trelagliptin succinate improved insulin resistance in adipocytes via regulation of PI-3K/AKT/GLUT4 insulin signaling pathway.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0753-3322
Relation: http://www.sciencedirect.com/science/article/pii/S0753332220301426; https://doaj.org/toc/0753-3322; https://doaj.org/article/5591d0f231ee4effb6844eb88b350b11
DOI: 10.1016/j.biopha.2020.109952
الاتاحة: https://doi.org/10.1016/j.biopha.2020.109952
https://doaj.org/article/5591d0f231ee4effb6844eb88b350b11
رقم الانضمام: edsbas.7F221EF7
قاعدة البيانات: BASE
الوصف
تدمد:07533322
DOI:10.1016/j.biopha.2020.109952