High salt-induced weakness of anti-oxidative function of natriuretic peptide receptor-C and podocyte damage in the kidneys of Dahl rats

Abstract

Background:

Atrial natriuretic peptide (ANP) and its natriuretic peptide receptors A (NPR-A) and C (NPR-C) are involved in the regulation of physiological and pathophysiological process of blood pressure. The present study aimed to determine the role of NPR-C in the development of salt-sensitive hypertension.

Methods:

The Dahl salt-sensitive (DS) and salt-resistant (DR) rats were used in this study. Animals were matched according to their age and weight, and then placed on either a high-salt (HS, 8%) or a normal-salt (NS, 0.4%) diet for 6 weeks randomly using random number table. The systolic blood pressure (SBP), plasmatic sodium concentration (PL _Na), urinary sodium excretion (UV _Na), and serum creatinine concentration (Scr) were measured. The concentration of ANP in blood and tissues (heart and kidney) was detected by enzyme-linked immunosorbent assay. The expression of ANP, NPR-A, and NPR-C in kidney was evaluated with western blot analysis. Regarding renal redox state, the concentration changes in malondialdehyde (MDA), lipofuscin, nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (Nox), and nitric oxide synthase (NOS) in kidney were detected by a spectrophotometric method. The kidney damage was evaluated using pathological techniques and the succinodehydrogenase (SDHase) examination. Furthermore, after an intra-peritoneal injection of C-atrial natriuretic peptide (ANP) _4–23 (C-ANP _4–23), an NPR-C receptor agonist, the SBP, biochemical values in blood and urine, and renal redox state were evaluated. The paired Student's t test and analysis of variance followed by the Bonferroni test were performed for statistical analyses of the comparisons between two groups and multiple groups, respectively.

Results:

The baseline SBP in all groups was within the normal range. At the end of the 6-week experiment, HS diet significantly increased the SBP in DS rats from 116.63 ± 2.90 mmHg to 162.25 ± 2.15 mmHg ( t = −10.213, P < 0.001). The changes of SBP were not significant in DS rats on an NS diet and DR rats on an NS diet or on an HS diet (all P > 0.05). The significant increase of PL _Na, UV _Na, and Scr related to an HS diet was found in both DS and DR rats (all P <  0.05). However, significant changes in the concentration ( t = −21.915, P < 0.001) and expression of renal ANP ( t = −3.566, P = 0.016) and the expression of renal NPR-C ( t = 5.864, P = 0.002) were only observed in DS hypertensive rats. The significantly higher desmin immunochemical staining score ( t = −5.715, P = 0.005) and mitochondrial injury score ( t = −6.325, P = 0.003) accompanied by the lower SDHase concentration ( t = 3.972, P = 0.017) revealed mitochondrial pathologic abnormalities in podocytes in DS rats with an HS diet. The distinct increases of MDA ( t = −4.685, P = 0.009), lipofuscin ( t = −8.195, P = 0.001), and Nox ( t = −12.733, P <  0.001) but not NOS ( t = −0.328, P = 0.764) in kidneys were also found in DS hypertensive rats. C-ANP _4–23 treatment significantly decreased the SBP induced by HS in DS rats ( P < 0.05), which was still higher than NS groups with the vehicle or C-ANP _4–23 treatment ( P < 0.05). Moreover, the HS-induced increase of MDA, lipofuscin, Nox concentrations, and Nox4 expression in DS rats was significantly attenuated by C-ANP _4–23 treatment as compared with those with HS diet and vehicle injection (all P <  0.05).

Conclusions:

The results indicated that the renal NPR-C might be involved in the salt-sensitive hypertension through the damage of mitochondria in podocytes and the reduction of the anti-oxidative function. Hence, C-ANP _4–23 might serve as a therapeutic agent in treating salt-sensitive hypertension.