Beregi J P, Lahoche A, Willoteaux S, McFadden E, Bordet R, Gautier C, Etchrivi T
Service de Radiologie Vasculaire, CHRU de Lille, France.
Fundam Clin Pharmacol. 1998;12(6):613-8. doi: 10.1111/j.1472-8206.1998.tb00994.x.
Intravascular Doppler is widely used for experimental studies in the coronary circulation. We designed this study to assess baseline bloodflow and arteriolar resistance in the porcine renal circulation and to study the vasomotor responses of vasoactive drugs. In anesthesized piglets (n = 15), renal arterial diameter was measured with quantitative angiography and blood flow velocity with a Doppler wire (Cardiometrics). Bloodflow and resistances were calculated at baseline and after injection of vasoactive drugs (isosorbide dinitrate, papaverine). This allowed us to determine the renal bloodflow reserve (the capacity of the kidney to augment basal bloodflow). Injection of isosorbide dinitrate was associated with an increase in average peak velocity of 64% (P < 0.01) and a small (from 4.5 to 4.74, P < 0.01) but significant increase in renal artery diameter, resulting in an increase in bloodflow of 82% (P < 0.01) and a decrease in arteriolar resistance of 46% (P < 0.01). Bloodflow returned to baseline (4.76 +/- 1.48 mL/s) approximately 5 min after isosorbide injection. Average Peak Velocity increased almost twofold after papaverine injection (60 +/- 10 to 108 +/- 24 cm/sec, P < 0.01). There was a significant (P < 0.01) increase in arterial bloodflow of 96% in the right and 79% in the left renal artery after injection of papaverine with a corresponding significant (P < 0.01) decrease in arteriolar resistance of 49% in the right and 44% in the left renal artery. Using a combination of quantitative angiography and intravascular Doppler allows easy measurement of baseline renal blood flow and of the effects of vasodilator drugs on bloodflow and resistance. The results show that a vasodilatator reserve exists in the renal circulation but is less marked than that reported in the coronary circulation.
血管内多普勒广泛应用于冠状动脉循环的实验研究。我们设计本研究以评估猪肾循环的基础血流和小动脉阻力,并研究血管活性药物的血管舒缩反应。在15只麻醉仔猪中,用定量血管造影术测量肾动脉直径,用多普勒导丝(Cardiometrics)测量血流速度。在基础状态及注射血管活性药物(硝酸异山梨酯、罂粟碱)后计算血流和阻力。这使我们能够确定肾血流储备(肾脏增加基础血流的能力)。注射硝酸异山梨酯后,平均峰值速度增加64%(P<0.01),肾动脉直径有小幅增加(从4.5增加至4.74,P<0.01)但有显著意义,导致血流增加82%(P<0.01),小动脉阻力降低46%(P<0.01)。注射硝酸异山梨酯后约5分钟血流恢复至基础水平(4.76±1.48 mL/s)。注射罂粟碱后平均峰值速度几乎增加两倍(从60±10增至108±24 cm/秒,P<0.01)。注射罂粟碱后,右肾动脉血流显著增加96%,左肾动脉血流显著增加79%(P<0.01),相应地,右肾动脉小动脉阻力显著降低49%,左肾动脉小动脉阻力显著降低44%(P<0.01)。联合使用定量血管造影术和血管内多普勒可轻松测量基础肾血流以及血管扩张剂药物对血流和阻力的影响。结果表明,肾循环中存在血管扩张储备,但不如冠状动脉循环中报道的那样明显。