Oberti F, Veal N, Kaassis M, Pilette C, Rifflet H, Trouvé R, Calès P
Laboratoire d'Hémodynamique Splanchnique, Université d'Angers, France.
J Hepatol. 1998 Jul;29(1):103-11. doi: 10.1016/s0168-8278(98)80184-0.
BACKGROUND/AIMS: The action sites and kinetic effects of octreotide and terlipressin may be different. Therefore, we studied the hemodynamic effects of acute administration of these drugs alone or in combination in rats with portal hypertension due to portal vein ligation.
In a first study performed in anesthetized rats, hemodynamics were measured before and after drug administration (placebo, octreotide: 8 microg x kg(-1) x h(-1) for 30 min, terlipressin: 50 microg/kg bolus, terlipressin + octreotide at the same doses). The second study, performed in conscious rats, included the same groups and drug doses; hemodynamics were measured every 10 min for 1 h. The third study tested the effect of preinfusion of octreotide on responsiveness to terlipressin.
Terlipressin produced more marked systemic effects than octreotide by decreasing heart rate and cardiac output and increasing mean arterial pressure. Terlipressin produced a greater decrease in portal pressure than octreotide: placebo: -3+/-5%, terlipressin: -42+/-8%, octreotide: -16+/-10%, combination: -44+/-8% (conscious rats at 20 min, p<10(-4)). The decrease in portal pressure was immediate and lasted at least 60 min with both drugs. Octreotide significantly decreased spleno-renal shunt blood flow (% variation): placebo: -6+/-8, terlipressin: -15.5+/-20, octreotide: -22.5+/-20, combination: -27+/-10 (p<10(-2)). Octreotide preinfusion significantly increased the responsiveness of arterial pressure and heart rate to terlipressin.
Terlipressin decreases portal pressure significantly more than octreotide, while only octreotide significantly decreases collateral blood flow. Simultaneous administration of these drugs does not have significant additive effects but has complementary effects. The preadministration of octreotide alters systemic response to terlipressin.
背景/目的:奥曲肽和特利加压素的作用部位和动力学效应可能不同。因此,我们研究了在门静脉结扎所致门静脉高压大鼠中单独或联合急性给予这些药物的血流动力学效应。
在第一项针对麻醉大鼠的研究中,于给药前及给药后(安慰剂、奥曲肽:8微克/千克/小时,持续30分钟;特利加压素:50微克/千克静脉推注;特利加压素+奥曲肽,剂量相同)测量血流动力学。第二项研究在清醒大鼠中进行,包括相同的组和药物剂量;每10分钟测量一次血流动力学,共1小时。第三项研究测试了预先输注奥曲肽对特利加压素反应性的影响。
特利加压素通过降低心率和心输出量以及增加平均动脉压,产生了比奥曲肽更显著的全身效应。特利加压素使门静脉压力的降低幅度大于奥曲肽:安慰剂:-3±5%,特利加压素:-42±8%,奥曲肽:-16±10%,联合用药:-44±8%(清醒大鼠在20分钟时,p<10⁻⁴)。两种药物使门静脉压力的降低均迅速且至少持续60分钟。奥曲肽显著降低脾肾分流血流量(%变化):安慰剂:-6±8,特利加压素:-15.5±20,奥曲肽:-22.5±20,联合用药:-27±10(p<10⁻²)。预先输注奥曲肽显著增加了动脉压和心率对特利加压素的反应性。
特利加压素降低门静脉压力的幅度明显大于奥曲肽,而只有奥曲肽能显著降低侧支血流量。同时给予这些药物没有显著的相加作用,但有互补作用。预先给予奥曲肽会改变对特利加压素的全身反应。