Wittenberg-Voges Liza, Kästner Sabine Br, Raekallio Marja, Vainio Outi M, Rohn Karl, Hopster Klaus
Clinic for Horses, University of Veterinary Medicine Hannover, Hanover, Germany.
Clinic for Horses, University of Veterinary Medicine Hannover, Hanover, Germany.
Vet Anaesth Analg. 2018 Mar;45(2):165-174. doi: 10.1016/j.vaa.2017.08.010. Epub 2017 Sep 15.
To compare the effects of MK-467 during isoflurane anaesthesia combined with xylazine or dexmedetomidine on global and gastrointestinal perfusion parameters.
Prospective, randomized experimental trial.
A total of 15 warmblood horses.
Horses were divided into two groups for administration of either dexmedetomidine (D) or xylazine (X) for premedication (D: 3.5 μg kg; X: 0.5 mg kg) and as constant rate infusion during isoflurane anaesthesia (D: 7 μg kg hour; X: 1 mg kg hour). During anaesthesia, heart rate, mean arterial blood pressure (MAP), systemic vascular resistance index (SVRI) and cardiac index (CI) were measured. Microperfusion of the colon, jejunum and stomach was measured using laser Doppler flowmetry. After 2 hours of stabilization, MK-467 (250 μg kg) was administered, and measurements were continued for another 90 minutes. For statistical analysis, the permutation test and Wilcoxon rank-sum test were used (p < 0.05).
There were no differences in baseline measurements between groups. The MK-467 bolus resulted in a significant decrease in MAP (D: -58%; X: -48%) and SVRI (D: -68%; X: -65%) lasting longer in group D (90 minutes) compared to group X (60 minutes). While CI increased (D: +31%; X: +35%), microperfusion was reduced in the colon (D: -44%; X: -34%), jejunum (D: -26%; X: -33%) and stomach (D: -37%; X: -35%).
Alpha-2-agonist induced vasoconstriction was reversed by the MK-467 dose used, resulting in hypotension and rise in CI. Gastrointestinal microperfusion decreased, probably as a result of insufficient perfusion pressure. An infusion rate for MK-467 as well as an ideal agonist/antagonist ratio should be determined.
比较MK - 467在异氟烷麻醉联合赛拉嗪或右美托咪定作用下对全身及胃肠道灌注参数的影响。
前瞻性随机试验。
共15匹温血马。
将马分为两组,分别给予右美托咪定(D组)或赛拉嗪(X组)进行术前用药(D组:3.5μg/kg;X组:0.5mg/kg),并在异氟烷麻醉期间持续输注(D组:7μg/kg·小时;X组:1mg/kg·小时)。麻醉期间,测量心率、平均动脉血压(MAP)、全身血管阻力指数(SVRI)和心脏指数(CI)。使用激光多普勒血流仪测量结肠、空肠和胃的微灌注。稳定2小时后,给予MK - 467(250μg/kg),并继续测量90分钟。统计分析采用置换检验和Wilcoxon秩和检验(p<0.05)。
两组间基线测量无差异。与X组(60分钟)相比,MK - 467推注导致D组MAP(-58%)和SVRI(-68%)显著降低,且持续时间更长(90分钟)。虽然CI升高(D组:+31%;X组:+35%),但结肠(D组:-44%;X组:-34%)、空肠(D组:-26%;X组:-33%)和胃(D组:-37%;X组:-35%)的微灌注减少。
所用剂量的MK - 467可逆转α-2激动剂诱导的血管收缩,导致低血压和CI升高。胃肠道微灌注减少,可能是由于灌注压力不足所致。应确定MK - 467的输注速率以及理想的激动剂/拮抗剂比例。