(Hypertension. 2000;35:538.)
© 2000 American Heart Association, Inc.
Introductory Commentary |
From the Department of Cell Biology, University of Alabama at Birmingham, Birmingham, Ala.
Correspondence to Scott H. Carlson, PhD, Department of Cell Biology, 1670 University Boulevard, VH 601 Box 302, Birmingham, AL 35294-0019. E-mail scarlson{at}uab.edu
| Introduction |
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Our current paper is the first to describe long-term telemetric recording in mice. Telemetry has become the "gold standard" for recording blood pressure and heart rate in rats for several reasons. First, the probes are completely contained within the animal and remove the stress of tethering, restraint, arousal, and handling that is associated with catheterization and tail-cuff monitoring. Second, radiotelemetry facilitates continuous 24-hour recording of arterial pressure, heart rate, and activity. Because rats are nocturnal, the nighttime represents the active period; however, because it is relatively impractical to conduct experiments at night, and inconvenient to reverse the light/dark cycle in most animal facilities, most researchers have opted to monitor arterial pressure during the daytime period when the rats normally sleep. Radiotelemetric monitoring has made nighttime monitoring much more accessible to the researcher and facilitated circadian rhythm analysis of the cardiovascular system. By exploiting these advantages, research using this method has elucidated several important aspects of blood pressure control.
The recent development of smaller telemetry probes opens the door for long-term monitoring of arterial pressure and heart rate in mice, thus facilitating the characterization of the mechanisms underlying cardiovascular regulation in the species from which almost all transgenic models are derived. However, the use of newly developed telemetry probes in mice has largely been frustrating and unsuccessful for most researchers. The newly developed probes were not recommended for mice under 30 grams body weight (a size heavier than most transgenic mice) because of the high probability that the probe would occlude the aorta in smaller mice. Even with larger mice, the success rate was relatively poor for most research groups. The present study describes an implantation protocol that has a very high success rate even in mice as small as 19 grams. The results also demonstrate that the probes are highly responsive to arterial pressure challenges; in the present study mice were challenged with a high (8%) NaCl diet. By rapidly distributing this new method via electronic publishing, we hope that it will assist hypertension researchers in unlocking the potential offered by transgenic models.
| Footnotes |
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