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Modulation of intestinal gut barrier permeability by dipeptidyl peptidase IV inhibition in a model of rat septicemia /

Doaa Abdallah Zaky

Modulation of intestinal gut barrier permeability by dipeptidyl peptidase IV inhibition in a model of rat septicemia / تعديل نفاذية الحاجز المعوي بتثبيط ثنائي ببتيديل ببتيداز 4 في نموذج لتسمم الدم في الجرذان Doaa Abdallah Zaky B.Pharm ; Supervised Dalaal Moustafa Abdallah , Noha Nagah Nassar , Muhammad Yusuf Alshorbagy - Cairo : Doaa Abdallah Zaky B.Pharm , 2017 - 158 P. : charts , facsimiles ; 25cm

Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy- Department of Pharmacology and Toxicology

BThe preferential role of the underlying PI3K/Akt (PKB) axis in triggering enterocytic proliferation/differentiation signaling and AJ assembly is still controversial. The involvement of CD26/DPP-IV in obstructive jaundice (OJ)-induced sepsis has not been yet reported VLD3/10/30 dose dependently modulated CD26/DPP-IV, GLP-1, IGF-1, PI3K, pS473-Akt, pS9-GSK-3Ý, pS133-CREB, and CD1. VLD3/10 increased E-cadherin and NPSH, however, they reduced pY654-Ý-catenin, portal and aortic endotoxin, NF-mB, TNF-Ü, MPO, TBARS, subepithelial/pericryptal and submucosal collagen deposition as well as vimentin immunoreactivity, effects that were quite opposed with VLD30.



Adherens junctions Oxidative stress Vildagliptin