How Does Circadian Rhythm Impact Salt Sensitivity of Blood Pressure in Mice? A Study in Two Close C57Bl/6 Substrains

PLoS One. 2016 Apr 18;11(4):e0153472. doi: 10.1371/journal.pone.0153472. eCollection 2016.

Abstract

Background: Mouse transgenesis has provided the unique opportunity to investigate mechanisms underlying sodium kidney reabsorption as well as end organ damage. However, understanding mouse background and the experimental conditions effects on phenotypic readouts of engineered mouse lines such as blood pressure presents a challenge. Despite the ability to generate high sodium and chloride plasma levels during high-salt diet, observed changes in blood pressure are not consistent between wild-type background strains and studies.

Methods: The present work was designed in an attempt to determine guidelines in the field of salt-induced hypertension by recording continuously blood pressure by telemetry in mice submitted to different sodium and potassium loaded diets and changing experimental conditions in both C57BL/6N and C57BL/6J mice strain (Normal salt vs. Low salt vs. High-salt/normal potassium vs. High salt/low potassium, standard vs. modified light cycle, Non-invasive tail cuff blood pressure vs. telemetry).

Results: In this study, we have shown that, despite a strong blood pressure (BP) basal difference between C57BL/6N and C57BL/6J mice, High salt/normal potassium diet increases BP and heart rate during the active phase only (dark period) in the same extent in both strains. On the other hand, while potassium level has no effect on salt-induced hypertension in C57BL/6N mice, high-salt/low potassium diet amplifies the effect of the high-salt challenge only in C57BL/6J mice. Indeed, in this condition, salt-induced hypertension can also be detected during light period even though this BP increase is lower compared to the one occurring during the dark period. Finally, from a methodological perspective, light cycle inversion has no effect on this circadian BP phenotype and tail-cuff method is less sensitive than telemetry to detect BP phenotypes due to salt challenges.

Conclusions: Therefore, to carry investigations on salt-induced hypertension in mice, chronic telemetry and studies in the active phase are essential prerequisites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure / drug effects*
  • Blood Pressure / physiology*
  • Blood Pressure Determination / methods
  • Circadian Rhythm / physiology*
  • Diet, Sodium-Restricted
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Hypertension / chemically induced
  • Hypertension / physiopathology*
  • Male
  • Mice, Inbred C57BL / genetics
  • Potassium / blood
  • Potassium / pharmacology
  • Potassium / urine
  • Sodium / blood
  • Sodium / urine
  • Sodium Chloride, Dietary / adverse effects
  • Sodium Chloride, Dietary / pharmacology*
  • Sodium, Dietary / adverse effects
  • Sodium, Dietary / pharmacology
  • Telemetry

Substances

  • Sodium Chloride, Dietary
  • Sodium, Dietary
  • Sodium
  • Potassium

Grants and funding

This work was financed by the Mouse Clinical Institute (MCI) in collaboration with Merck Research Laboratories (MRL). This study has been performed in the frame of a provision service by MCI for MRL. The billing of this specific service included part of the material resources that have been recruited to conduct this study. Apart from this financial support for MCI, MRL did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. It is noteworthy that MRL had to validate the study design and the manuscript before publication, but no revisions were asked by MRL. The specific roles of these authors are articulated in the ‘author contributions’ section.