Seminario - Biotecnologie e Bioscienze - Giovedì 3 ottobre 2024, ore 16:30, edificio U3-BIOS, aula U3-08
Annarita Di Mise, Department of Biotechnology and Biosciences - University of Milano-Bicocca
Abstract
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is an inherited disorder characterized by development and growth of renal cysts, leading to kidney failure. Reduced resting cytosolic calcium and increased cAMP levels are two central defects in ADPKD. The only approved drug able to delay disease progression is the vasopressin receptor 2 (V2R) antagonist Tolvaptan, which has been reported to cause liver toxicity. Co-targeting two GPCRs, the Calcium Sensing Receptor (CaSR) and the V2R, using calcimimetics (CaSR modulators) in combination with vaptans (V2R antagonists), might represent a new application for two existing drugs which may potentiate each other and, more importantly, can be used at lower concentration to limit side effects.
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