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Published on: December 2, 2014
Increased water intake reduces long-term renal and cardiovascular disease progression in experimental polycystic
Priyanka S Sagar1,2, Jennifer Zhang1,2, Magda Luciuk1,2
1Centre for Transplant and Renal Research, Westmead Institute for Medical Research, The University of Sydney, Sydney, NSW, Australia.
Insights
Increasing water intake significantly slowed kidney cyst growth and disease progression in a rat model of polycystic kidney disease (PKD). This intervention also reduced hypertension and cardiovascular issues, offering a potential new treatment strategy.
Area of Science:
- Nephrology
- Genetics
- Pharmacology
Background:
- Polycystic kidney disease (PKD) is a leading inherited cause of kidney failure with limited therapeutic options.
- Previous studies suggest increased water intake may slow cyst growth in some PKD models, but this effect requires further investigation in other models.
Purpose of the Study:
- To investigate the efficacy of high water intake (HWI) in mitigating cystic renal disease progression in Lewis polycystic kidney (LPK) rats, a model for human nephronophthisis-9.
- To evaluate the impact of HWI on renal pathology, proteinuria, blood pressure, and cardiovascular parameters in LPK rats.
Main Methods:
- LPK and control Lewis rats received either normal water intake (NWI) or HWI (water supplemented with 5% glucose) from postnatal weeks 3 to 16.
- Key parameters assessed included kidney-to-body weight ratio, renal cyst area, interstitial collagen, proteinuria, systolic blood pressure, and heart-to-body weight ratio.
Main Results:
- HWI significantly reduced kidney enlargement in LPK rats by 54% at week 10 and 42% at week 16 compared to NWI.
- HWI led to decreased renal cyst area, interstitial collagen, and proteinuria in LPK rats.
- In male LPK rats, HWI lowered systolic blood pressure by 16% and heart-to-body weight ratio by 21% at week 16.
Conclusions:
- A modest increase in water intake during early disease stages can attenuate renal cystic disease progression in LPK rats.
- HWI demonstrated secondary benefits, including reduced hypertension and cardiovascular disease markers.
- These findings support increased water intake as a potential preclinical intervention for cystic renal diseases.
Abstract:
Polycystic kidney disease (PKD) is the most common inherited cause of kidney failure and currently has limited treatment options. Increasing water intake reduces renal cyst growth in the pck rat (a genetic ortholog of autosomal recessive PKD) but it is not clear if this beneficial effect is present in other models of PKD. In this study, we tested the hypothesis that high water intake (HWI) reduces the progression of cystic renal disease in Lewis polycystic kidney (LPK) rats (a genetic ortholog of human nephronophthisis-9). Groups of female and male LPK (n = 8-10 per group) and Lewis (n = 4 per group) rats received water ad libitum supplemented with or without 5% glucose [to simulate HWI or normal water intake (NWI) respectively] from postnatal weeks 3 to 16. Water intake increased ~1.3-fold in the LPK+HWI group compared to LPK+NWI rats between weeks 3 to 10 but the differences were not significant at later timepoints. In LPK rats, HWI reduced the increases in the kidney to body weight ratio by 54% at week 10 and by 42% at week 16 compared to NWI (both p<0.01). The reduction in kidney enlargement was accompanied by decreases in the percentage renal cyst area, percentage renal interstitial collagen and proteinuria (all p<0.05). At week 16, HWI reduced systolic blood pressure and the heart to body to weight ratio by 16% and 21% respectively in males LPK rats (both p<0.01). In conclusion, a modest increase in water intake during the early phase of disease was sufficient to attenuate renal cystic disease in LPK rats, with secondary benefits on hypertension and cardiovascular disease. These data provide further preclinical evidence that increased water intake is a potential intervention in cystic renal diseases.
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