BACKGROUND: Circadian rhythms play an essential role in physiological function. The molecular clock that underlies circadian physiological function consists of a core group of transcription factors, including the protein PER1 (Period1). Studies in mice show that PER1 plays a role in the regulation of blood pressure and renal sodium handling; however, the results are dependent on the strain being studied. Using male Dahl salt-sensitive (SS) rats with global knockout of PER1 (SS), we aim to test the hypothesis that PER1 plays a key role in the regulation of salt-sensitive blood pressure. Per1-/-
METHODS: The model was generated using CRISPR/Cas9 and was characterized using radiotelemetry and measures of renal function and circadian rhythm.
RESULTS: SSrats had similar mean arterial pressure when fed a normal 0.4% NaCl diet but developed augmented hypertension after three weeks on a high-salt (4% NaCl) diet. Despite being maintained on a normal 12:12 light:dark cycle, SSrats exhibited desynchrony mean arterial pressure rhythms on a high-salt diet, as evidenced by increased variability in the time of peak mean arterial pressure. SSrats excrete less sodium after three weeks on the high-salt diet. Furthermore, SSrats exhibited decreased creatinine clearance, a measurement of renal function, as well as increased signs of kidney tissue damage. SSrats also exhibited higher plasma aldosterone levels. Per1-/-Per1-/-Per1-/-Per1-/-Per1-/-
CONCLUSIONS: Altogether, our findings demonstrate that loss of PER1 in Dahl SS rats causes an array of deleterious effects, including exacerbation of the development of salt-sensitive hypertension and renal damage.
