Abstract
Diabetic nephropathy (DN) is a long-term complication of diabetes characterized by proteinuria and loss of kidney function. Up to one third of patients with diabetes develop DN, and no new therapies targeting DN have been introduced for more than a decade. The lack of treatment options may, in part, be caused by the scarcity of translatable rodent models. We have established a surgically induced rat model of non-insulin dependent type 1-like diabetes (90% pancreatectomy, Px), displaying a stable blood glucose of >20 mmol/L. In addition, both Px and uninephrectomy (UNx) was performed simultaneously to potentially increase progression of renal pathological changes. Kidneys in the Px diabetic rat model displayed hypertrophy of glomeruli, cortex, and medulla 11 weeks post-surgery. Renal fibrosis was significantly increased in Px rats vs. nondiabetic control animals, as determined by quantitative histology following picro-sirius red staining of collagen (total kidney collagen, Px vs. controls; 127 ± 8 mg vs. 39 ± 5 mg, p
In conclusion, our data suggest that the Px model develops profound renal hypertrophy and fibrosis, and that renal hypertrophy is exacerbated in the Px-UNx model. Thus, Px alone and Px-UNx in rats may represent novel, strong alternatives to streptozotocin-induced diabetes and genetic models for the study of DN drug candidates.
Disclosure
T. Secher: Employee; Self; Gubra. Employee; Spouse/Partner; Novo Nordisk A/S. T.T. Johansen: None. M.V. Oestergaard: None. P.J. Pedersen: None. N.E. Zois: Employee; Self; Gubra. T.X. Pedersen: Employee; Self; Gubra. N. Vrang: Board Member; Self; Gubra. Employee; Self; Gubra. Stock/Shareholder; Self; Gubra. K. Fosgerau: Stock/Shareholder; Self; Novo Nordisk A/S. Employee; Self; Gubra. Stock/Shareholder; Self; Gubra. L.N. Fink: Employee; Self; Gubra. Stock/Shareholder; Self; Novo Nordisk A/S.
In conclusion, our data suggest that the Px model develops profound renal hypertrophy and fibrosis, and that renal hypertrophy is exacerbated in the Px-UNx model. Thus, Px alone and Px-UNx in rats may represent novel, strong alternatives to streptozotocin-induced diabetes and genetic models for the study of DN drug candidates.
Disclosure
T. Secher: Employee; Self; Gubra. Employee; Spouse/Partner; Novo Nordisk A/S. T.T. Johansen: None. M.V. Oestergaard: None. P.J. Pedersen: None. N.E. Zois: Employee; Self; Gubra. T.X. Pedersen: Employee; Self; Gubra. N. Vrang: Board Member; Self; Gubra. Employee; Self; Gubra. Stock/Shareholder; Self; Gubra. K. Fosgerau: Stock/Shareholder; Self; Novo Nordisk A/S. Employee; Self; Gubra. Stock/Shareholder; Self; Gubra. L.N. Fink: Employee; Self; Gubra. Stock/Shareholder; Self; Novo Nordisk A/S.
Originalsprog | Engelsk |
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Publikationsdato | 1 jul. 2018 |
Status | Udgivet - 1 jul. 2018 |
Udgivet eksternt | Ja |
Begivenhed | American Diabetes Association - Orlando, USA Varighed: 22 jun. 2018 → 26 jun. 2018 Konferencens nummer: 78 |
Konference
Konference | American Diabetes Association |
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Nummer | 78 |
Land/Område | USA |
By | Orlando |
Periode | 22/06/2018 → 26/06/2018 |