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PMID: 10930194 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Long-term blood pressure telemetry in AT2 receptor-disrupted mice.

Journal of hypertension ·Vol. 18 ·No. 7 ·2000-07-00 ·Pages 955-61

Gross V, Milia AF, Plehm R, Inagami T, Luft FC

Abstract

The hypertension in AT2 receptor knockout mice is imperfectly defined. Therefore, we investigated the influence of dietary salt loading and deoxycorticosterone (DOCA)-salt treatment on blood pressure and diurnal patterns of blood pressure in these mice by radiotelemetry. We used telemetry in AT2 receptor knockout and wild-type mice to measure blood pressure, heart rate, aortic pressure dp/dt, locomotor activity, and circadian rhythms. Salt-related effects were studied by increasing the salt in chow to 4%, adding 1% saline in drinking water, and by DOCA-salt treatment Baseline blood pressures were higher in AT2 receptor knockout than in wild-type mice and were not affected by increasing the salt intake. The blood pressure increase was steeper and greater in AT2 receptor knockout than in wild-type mice after DOCA-salt treatment A circadian rhythm of blood pressure and heart rate, with higher values during the night, was seen in wild-type, but not in AT2 receptor knockout mice. In AT2 receptor knockout mice, this rhythm was only significant when daily salt intake was increased or when DOCA-salt hypertension was induced. The acrophase of blood pressure and heart rate was found between 2000 and 2400 h and was in accordance with the maximum physical activity. These data suggest that AT2 knockout mice display slight hypertension which is not salt-sensitive. On the other hand, the susceptibility to develop DOCA-salt hypertension is increased. The study also illustrates the power of telemetry in monitoring long-term cardiovascular changes and circadian blood pressure and heart rate rhythms in genetically engineered mice.

MeSH Terms
Animals Blood Pressure/physiology Blood Pressure Determination/methods Circadian Rhythm/physiology Desoxycorticosterone/toxicity Follow-Up Studies Heart Rate/physiology Hypertension/chemically induced,physiopathology Locomotion/physiology Male Mice Mice, Knockout Receptor, Angiotensin, Type 1 Receptor, Angiotensin, Type 2 Receptors, Angiotensin/blood Sodium, Dietary/toxicity Telemetry
Chemicals
Receptor, Angiotensin, Type 1 Receptor, Angiotensin, Type 2 Receptors, Angiotensin Sodium, Dietary Desoxycorticosterone
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Gross V
Franz Volhard Clinic and Max Delbrück Center for Molecular Medicine, Medical Faculty of the Charité, Humboldt University of Berlin, Germany.
Milia A F
Plehm R
Inagami T
Luft F C
Article Info
Journal
Journal of hypertension
Abbr.
J Hypertens
ISSN
0263-6352
Published
2000-07-00
Pages
955-61
Language
English
Region
England
NLM ID
8306882
Subset
IM
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