肝神经刺激和去甲肾上腺素对灌注大鼠肝脏表面激光多普勒通量信号的影响。

A M Wheatley, N E Almond
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引用次数: 9

摘要

研究了肝神经刺激和去甲肾上腺素对灌注大鼠肝脏表面激光多普勒信号的影响。用含20%牛红细胞的Krebs-Henseleit缓冲液(37℃,pH 7.4)经门静脉原位灌注雄性Wistar大鼠肝脏,定时收集流出物测定肝脏总血流量(TLBF)。门静脉阻力(PVR)由肝脏压差计算。激光多普勒血流法(LDF)与TLBF的线性关系得到了证实。以0.5 ~ 20 Hz (n = 11)的频率刺激肝神经(2 ms, 20 V)。将NE以10(-10)和10(-6)M的浓度添加到缓冲液中(n = 8)。在肝神经刺激(基础,3.11 +/- 0.26 dyn / cm-5)和NE给药(基础,2.62 +/- 0.29 dyn / cm-5)期间,PVR出现刺激依赖性上升,分别在20 Hz(311 +/- 45%)和10(-6)M(591 +/- 72%)时效果最大。LDF和TLBF在神经刺激和NE时均下降。线性关系(r = 0.99;NE (10(-10) ~ 10(-6) M)的TLBF(%)和LDF通量(%)的变化p < 0.001)。在神经刺激时,TLBF和LDF通量的下降与刺激频率的对数呈线性关系,分别在10 Hz和20 Hz时达到最大值。在20 Hz的刺激频率下,LDF的变化与TLBF的变化有显著性差异(p < 0.001)。我们从研究结果中得出结论,在高频肝神经刺激时,LDF低估了TLBF。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of hepatic nerve stimulation and norepinephrine on the laser Doppler flux signal from the surface of the perfused rat liver.

The effect of hepatic nerve stimulation and norepinephrine (NE) on the laser Doppler signal from the surface of the perfused rat liver was tested. The livers from male Wistar rats were perfused in situ via the portal vein with Krebs-Henseleit buffer containing 20% bovine erythrocytes (37 degrees C, pH 7.4) and total liver blood flow (TLBF) was by timed collection of effluent. Portal vascular resistance (PVR) was calculated from the pressure difference across the liver. Linearity of laser Doppler flowmetry (LDF) with TLBF was confirmed in all preparations. Stimulation of the hepatic nerves (2 ms, 20 V) was performed at frequencies between 0.5 and 20 Hz (n = 11). NE was added to the buffer at concentrations between 10(-10) and 10(-6) M (n = 8). A stimulus-dependent rise in PVR occurred during hepatic nerve stimulation (basal, 3.11 +/- 0.26 dyn s cm-5) and NE administration (basal, 2.62 +/- 0.29 dyn s cm-5), with a maximum effect at 20 Hz (311 +/- 45%) and 10(-6) M (591 +/- 72%), respectively. Both LDF and TLBF fell during nerve stimulation and NE. A linear relationship (r = 0.99; p < 0.001) between change in TLBF (%) and LDF flux (%) was found for NE (10(-10) to 10(-6) M). During nerve stimulation, the fall in TLBF and LDF flux was linear with the logarithm of stimulus frequency and reached a maximum at 10 and 20 Hz, respectively. At a stimulus frequency of 20 Hz, the change in LDF was significantly different from the change in TLBF (p < 0.001). We conclude from our findings that during high-frequency hepatic nerve stimulation, LDF underestimates TLBF.

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