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Articles in PresS, published online ahead of print July 18, 2002
Am J Physiol Regu Physiol, 10.1152/ajpregu.00768.2001
Submitted on January 2, 2002
Accepted on July 17, 2002
1 The Cardiovascular Center, University of Iowa, Iowa City, IA, USA
2 The Cardiovascular Center, University of Iowa, Iowa City, IA, USA; Department of Physiology & Biophysics, University of Iowa, Iowa City, IA, USA
3 The Cardiovascular Center, University of Iowa, Iowa City, IA, USA; Veterans Affairs Medical Center, Iowa City, IA, USA
* To whom correspondence should be addressed. E-mail: mark-chapleau{at}uiowa.edu.
Studies of genetically-modified mice provide a powerful approach to investigate consequences of altered gene expression in physiological and pathological states. The goal of the present study was to characterize afferent, central, and efferent components of the baroreceptor reflex in anesthetized Webster 4 mice. Baroreflex and baroreceptor afferent functions were characterized by measuring changes in renal sympathetic nerve activity (RSNA) and aortic depressor nerve activity (ADNA) in response to nitroprusside and phenylephrine induced changes in arterial pressure. The data were fit to a sigmoidal logistic function curve. Baroreflex diastolic pressure threshold (Pth), the pressure at 50% inhibition of RSNA (Pmid), and baroreflex gain (maximum slope) averaged 74±5 mmHg, 101±3 mmHg, and 2.30±0.54%/mmHg, respectively (n=6). The Pth, Pmid, and gain for the diastolic pressure-ADNA relation (baroreceptor afferents) were similar to that observed for the overall reflex averaging 79±9 mmHg, 101±4 mmHg, and 2.92±0.53%/mmHg, respectively (n=5). The central nervous system mediation of the baroreflex and the chronotropic responsiveness of the heart to vagal efferent activity were independently assessed by recording responses to electrical stimulation of the left ADN and the peripheral end of the right vagus nerve, respectively. Both ADN and vagal efferent stimulation induced frequency-dependent decreases in heart rate and arterial pressure. The heart rate response to ADN stimulation was nearly abolished in mice anesthetized with pentobarbital (n=4) compared with mice anesthetized with ketamine/acepromazine (n=4), whereas the response to vagal efferent stimulation was equivalent under both types of anesthesia. Application of these techniques to studies of genetically-manipulated mice can be used to identify molecular mechanisms of baroreflex function and localize altered function to afferent, central, or efferent sites.
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