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1Department of Biomedical Engineering, State University of New York at Stony Brook, Stony Brook, New York; 2Department of Nephrology, The Chang Gung Memorial Hospital, Taiwan, Republic of China; 3Department of Molecular Pharmacology, Physiology, and Biotechnology, Brown University, Providence, Rhode Island; and 4Department of Physiology and Biophysics, University of South Florida, Tampa, Florida
Submitted 4 May 2004 ; accepted in final form 10 October 2004
We have previously shown that there are two oscillating components in spontaneously fluctuating single-nephron blood flow obtained from Sprague-Dawley rats (Yip K-P, Holstein-Rathlou NH, and Marsh DJ. Am J Physiol Renal Physiol 264: F427F434, 1993). The slow oscillation (2030 mHz) is mediated by tubuloglomerular feedback (TGF), whereas the fast oscillation (100 mHz) is probably related to spontaneous myogenic activity. The fast oscillation is rarely detected in spontaneous tubular pressure because of its small magnitude and the fact that tubular compliance filters pressure waves. We detected myogenic oscillation superimposed on TGF-mediated oscillation when ambient tubular flow was interrupted. Two well-defined peaks are present in the mean power spectrum of stop-flow pressure (SFP) centering at 25 and 100 mHz (n = 13), in addition to a small peak at 125130 mHz. Bispectral analysis indicates that two of these oscillations (30 and 100 mHz) interact nonlinearly to produce the third oscillation at 125130 mHz. The presence of nonlinear interactions between TGF and myogenic oscillations indicates that estimates of the relative contribution of each of these mechanisms in renal autoregulation need to account for this interaction. The magnitude of myogenic oscillations was considerably smaller in the SFP measured from spontaneously hypertensive rats (SHR, n = 13); consequently, nonlinear interactions were not observed with bispectral analysis. Reduced augmentation of myogenic oscillations in SFP of SHR might account for the failure in detecting nonlinear interactions in SHR.
bispectrum; autoregressive; bicoherence; nonlinear interactions; hypertensive; tubuloglomerular feedback
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