Journal article
Relaxin-2 does not ameliorate nephropathy in an experimental model of type-1 diabetes
TB Dschietzig, K Krause-Relle, M Hennequin, K Von Websky, J Rahnenführer, J Ruppert, HJ Grön, FP Armbruster, RAD Bathgate, JR Aschenbach, WG Forssmann, B Hocher
Kidney and Blood Pressure Research | KARGER | Published : 2015
DOI: 10.1159/000368484
Abstract
Background/Aims: In diabetic nephropathy (DN), the current angiotensin-II-blocking pharmacotherapy is frequently failing. For diabetic cardiomyopathy (DC), there is no specific remedy available. Relaxin-2 (Rlx)-An anti-fibrotic, anti-inflammatory, and vasoprotecting peptide-is a candidate drug for both. Methods: Low-dose (32 μg/kg/day) and high-dose (320 μg/kg/day) Rlx were tested against vehicle (n = 20 each) and non-diabetic controls (n = 14) for 12 weeks in a model of type-1 diabetes induced in endothelial nitric oxide synthase knock-out (eNOS-KO) mice by intraperitoneal injection of streptozotocin. Results: Diabetic animals showed normal plasma creatinine, markedly increased albuminuria ..
View full abstractGrants
Awarded by German Ministry for Education and Research
Funding Acknowledgements
This work was supported by a grant from the German Ministry for Education and Research (AiF KF2181502FR9) given to TBD and WGF.