Francis Roland C E, Höhne Claudia, Klein Adrian, Kaisers Udo X, Pickerodt Philipp A, Boemke Willehad
Department of Anesthesiology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin, Germany.
Vet Anaesth Analg. 2010 May;37(3):258-68. doi: 10.1111/j.1467-2995.2010.00530.x. Epub 2010 Mar 11.
To test the compensatory role of endothelin-1 when acute blood loss is superimposed on anaesthesia, by characterizing the effect of systemic endothelin receptor subtype A (ET(A)) blockade on the haemodynamic and hormonal responses to haemorrhage in dogs anaesthetized with xenon/remifentanil (X/R) or isoflurane/remifentanil (I/R).
Prospective experimental randomized controlled study.
Six female Beagle dogs, 13.4 +/- 1.3 kg.
Animals were anaesthetized with remifentanil 0.5 microg kg(-1) minute(-1) plus either 0.8% isoflurane (I/R) or 63% xenon (X/R), with and without (Control) the systemic intravenous endothelin receptor subtype A antagonist atrasentan (four groups, n = 6 each). After 60 minutes of baseline anaesthesia, the dogs were bled (20 mL kg(-1)) over 5 minutes and hypovolemia was maintained for 1 hour. Continuous haemodynamic monitoring was performed via femoral and pulmonary artery catheters; vasoactive hormones were measured before and after haemorrhage.
In Controls, systemic vascular resistance (SVR), vasopressin and catecholamine plasma concentrations were higher with X/R than with I/R anaesthesia at pre-haemorrhage baseline. The peak increase after haemorrhage was higher during X/R than during I/R anaesthesia (SVR 7420 +/- 867 versus 5423 +/- 547 dyne seconds cm(-5); vasopressin 104 +/- 23 versus 44 +/- 6 pg mL(-1); epinephrine 2956 +/- 310 versus 177 +/- 99 pg mL(-1); norepinephrine 862 +/- 117 versus 195 +/- 33 pg mL(-1), p < 0.05). Haemorrhage reduced central venous pressure from 3 +/- 1 to 1 +/- 1 cm H(2)O (I/R, ns) and from 8 +/- 1 to 5 +/- 1 cm H(2)O (X/R, p < 0.05), but did not reduce mean arterial pressure, nor cardiac output. Atrasentan did not alter the haemodynamic and hormonal response to haemorrhage during either anaesthetic protocol.
Selective ET(A) receptor blockade with atrasentan did not impair the haemodynamic and hormonal compensation of acute haemorrhage during X/R or I/R anaesthesia in dogs.
通过描述全身性A 型内皮素受体(ET(A))阻断对接受氙气/瑞芬太尼(X/R)或异氟烷/瑞芬太尼(I/R)麻醉的犬类出血时血流动力学和激素反应的影响,来测试急性失血叠加在麻醉状态下时内皮素-1的代偿作用。
前瞻性实验随机对照研究。
6只雌性比格犬,体重13.4±1.3千克。
动物用0.5微克/千克·分钟的瑞芬太尼加0.8%异氟烷(I/R)或63%氙气(X/R)麻醉,有或没有(对照)全身性静脉注射A 型内皮素受体拮抗剂阿曲生坦(四组,每组n = 6)。在基线麻醉60分钟后,犬类在5分钟内失血(20毫升/千克),并维持低血容量1小时。通过股动脉和肺动脉导管进行连续血流动力学监测;在出血前后测量血管活性激素。
在对照组中,出血前基线时,X/R麻醉下的全身血管阻力(SVR)、血管加压素和儿茶酚胺血浆浓度高于I/R麻醉。出血后的峰值增加在X/R麻醉期间高于I/R麻醉(SVR 7420±867对5423±547达因·秒·厘米⁻⁵;血管加压素104±23对44±6皮克/毫升;肾上腺素2956±310对177±99皮克/毫升;去甲肾上腺素862±117对195±33皮克/毫升,p < 0.05)。出血使中心静脉压从3±1降至1±1厘米水柱(I/R,无统计学差异),从8±1降至5±1厘米水柱(X/R,p < 0.05),但未降低平均动脉压和心输出量。在任何一种麻醉方案中,阿曲生坦均未改变对出血的血流动力学和激素反应。
在犬类的X/R或I/R麻醉期间,用阿曲生坦选择性阻断ET(A)受体不会损害急性出血时的血流动力学和激素代偿。