(Hypertension. 2002;39:348.)
© 2002 American Heart Association, Inc.
Scientific Contributions |
From the Department of Pharmacology, University of California at San Diego (R.L.J., M.J., S.C., L.B., M.P.P.), La Jolla; Department of Pediatrics, University of California at Irvine (P.L.F., M.A.S.); Institute of Biology and Medical Genetics, Charles University (M.J., V.K., D.K.), Prague; and Institute of Physiology Czech Academy of Sciences (M.P.), Prague, Czech Republic.
Correspondence to Dr Morton P. Printz, Department of Pharmacology, University of California, San Diego, 9500 Gilman Dr 0636, La Jolla CA, 92093-0636. E-mail mprintz{at}ucsd.edu
The airpuff startle reaction is a probe of sensori-autonomic processing and is useful for studies of genetic control of stress-induced cardiovascular activity. Using a Wistar-Kyoto-Spontaneously Hypertensive Rat F2 cross, we reported an airpuff-elicited strain-dependent and trial-dependent bradycardia, the absence of which cosegregated with hypertension. Here, we use the mapping power of the HXB-BXH recombinant inbred rat strains (n=23) to locate quantitative trait loci (QTL) for this and associated cardiovascular phenotypes. Rats (12 weeks old), with indwelling femoral arterial catheters, were subjected to repeated airpuff startle stimuli (100 ms, 12.5 psi, 28 trials). Basal mean arterial pressure (MAP), delta MAP, and delta heart rate response to airpuff stimuli were analyzed as the average over 28 trials. There was a significant strain effect on the cardiovascular phenotypes measured. One QTL for the bradycardia elicited by the first airpuff stimulus was identified on chromosome 2 (D2rat 62/63; logarithm of odds [LOD] 2.9) mapping near a reported blood pressure locus. Further QTL were identified for basal MAP (RN08), stimulus-elicited tachycardia on trials 2 to 5 (RNO1 and RNO10), and delta MAP (RNO6). Our results indicate that chromosomes 1, 2, and 10 are involved in heart rate responses to airpuff startle stimulus, and chromosomes 6 and 8 are involved in pressor responses. This study is the first to identify stress-related heart rate loci and provides additional support for our prior cosegregation results. Furthermore, we have established the utility of this experimental paradigm to identify loci responsible for cardiovascular regulation during stress in genetic hypertensive models.
Key Words: behavior blood pressure bradycardia tachycardia heart rate genomics
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