Fares Souha A, Habib Joseph R, Engoren Milo C, Badr Kamal F, Habib Robert H
Hariri School of Nursing, American University of Beirut, Beirut, Lebanon.
Vascular Medicine Program and Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.
Physiol Rep. 2016 Jun;4(11). doi: 10.14814/phy2.12823.
Blood pressure exhibits substantial short- and long-term variability (BPV). We assessed the hypothesis that the complexity of beat-to-beat BPV will be differentially altered in salt-sensitive hypertensive Dahl rats (SS) versus rats protected from salt-induced hypertension (SSBN13) maintained on high-salt versus low-salt diet. Beat-to-beat systolic and diastolic BP series from nine SS and six SSBN13 rats (http://www.physionet.org) were analyzed following 9 weeks on low salt and repeated after 2 weeks on high salt. BP complexity was quantified by detrended fluctuation analysis (DFA), short- and long-range scaling exponents (αS and αL), sample entropy (SampEn), and traditional standard deviation (SD) and coefficient of variation (CV(%)). Mean systolic and diastolic BP increased on high-salt diet (P < 0.01) particularly for SS rats. SD and CV(%) were similar across groups irrespective of diet. Salt-sensitive and -protected rats exhibited similar complexity indices on low-salt diet. On high salt, (1) SS rats showed increased scaling exponents or smoother, systolic (P = 0.007 [αL]) and diastolic (P = 0.008 [αL]) BP series; (2) salt-protected rats showed lower SampEn (less complex) systolic and diastolic BP (P = 0.046); and (3) compared to protected SSBN13 rats, SS showed higher αL for systolic (P = 0.01) and diastolic (P = 0.005) BP Hypertensive SS rats are more susceptible to high salt with a greater rise in mean BP and reduced complexity. Comparable mean pressures in sensitive and protective rats when on low-salt diet coupled with similar BPV dynamics suggest a protective role of low-salt intake in hypertensive rats. This effect likely reflects better coupling of biologic oscillators.
血压呈现出显著的短期和长期变异性(BPV)。我们评估了这样一个假设:在盐敏感型高血压 Dahl 大鼠(SS)与通过高盐或低盐饮食维持而免受盐诱导高血压的大鼠(SSBN13)中,逐搏血压变异性的复杂性会有不同程度的改变。在低盐饮食 9 周后,对 9 只 SS 大鼠和 6 只 SSBN13 大鼠(http://www.physionet.org)的逐搏收缩压和舒张压序列进行分析,并在高盐饮食 2 周后重复分析。通过去趋势波动分析(DFA)、短程和长程标度指数(αS 和 αL)、样本熵(SampEn)以及传统的标准差(SD)和变异系数(CV(%))对血压复杂性进行量化。高盐饮食时,平均收缩压和舒张压升高(P < 0.01),尤其是 SS 大鼠。无论饮食如何,各组间的 SD 和 CV(%)相似。盐敏感和受保护的大鼠在低盐饮食时表现出相似的复杂性指数。在高盐饮食时,(1)SS 大鼠的收缩压(P = 0.007 [αL])和舒张压(P = 0.008 [αL])序列的标度指数增加或更平滑;(2)盐保护大鼠的收缩压和舒张压的 SampEn 较低(复杂性较低)(P = 0.046);(3)与受保护的 SSBN13 大鼠相比,SS 大鼠收缩压(P = 0.01)和舒张压(P = 0.005)的 αL 更高。高血压 SS 大鼠对高盐更敏感,平均血压升高幅度更大且复杂性降低。低盐饮食时敏感和受保护大鼠的平均血压相当,且血压变异性动态相似,这表明低盐摄入对高血压大鼠具有保护作用。这种效应可能反映了生物振荡器更好的耦合。