NKCC1 is a widely expressed isoform of the Na-2Cl-K cotransporter that mediates several direct and indirect vascular effects and regulates expression and release of renin. In this study, we used NKCC1-deficient (NKCC1^−/−) and wild-type (WT) mice to assess day/night differences of blood pressure (BP), locomotor activity, and renin release and to study the effects of high (8%) or low (0.03%) dietary NaCl intake on BP, activity, and the renin/aldosterone system. On a standard diet, 24-h mean arterial blood pressure (MAP) and heart rate determined by radiotelemetry, and their day/night differences, were not different in NKCC1^−/− and WT mice. Spontaneous and wheel-running activities in the active night phase were lower in NKCC1^−/− than WT mice. In NKCC1^−/− mice on a high-NaCl diet, MAP increased by 10 mmHg in the night without changes in heart rate. In contrast, there was no salt-dependent blood pressure change in WT mice. MAP reductions by hydralazine (1 mg/kg) or isoproterenol (10 μg/mouse) were significantly greater in NKCC1^−/− than WT mice. Plasma renin (PRC; ng ANG I·ml⁻¹·h⁻¹) and aldosterone (aldo; pg/ml) concentrations were higher in NKCC1^−/− than WT mice (PRC: 3,745 ± 377 vs. 1,245 ± 364; aldo: 763 ± 136 vs. 327 ± 98). Hyperreninism and hyperaldosteronism were found in NKCC1^−/− mice during both day and night. High Na suppressed PRC and aldosterone in both NKCC1^−/− and WT mice, whereas a low-Na diet increased PRC and aldosterone in WT but not NKCC1^−/− mice. We conclude that 24-h MAP and MAP circadian rhythms do not differ between NKCC1^−/− and WT mice on a standard diet, probably reflecting a balance between anti- and prohypertensive factors, but that blood pressure of NKCC1^−/− mice is more sensitive to increases and decreases of Na intake.