Zhang Emily Q, Knight Cameron G, Pang Daniel Sj
Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Canada.
Faculty of Veterinary Medicine, University of Calgary, Calgary, Canada.
J Am Assoc Lab Anim Sci. 2017 Nov 1;56(6):786-791.
Anesthetic agents depress thermoregulatory mechanisms, causing hypothermia within minutes of induction of general anesthesia. The consequences of hypothermia include delayed recovery and increased experimental variability. Even when normothermia is maintained during anesthesia, hypothermia may occur during recovery. The primary aim of this study was to identify an effective warming period for maintaining normothermia during recovery. Adult male (n = 8) and female (n = 9) Sprague-Dawley rats were randomized to 30 min (post30) or 60 min (post60) of warming after recovery from anesthesia. During a 40-min anesthetic period, normothermia (target, 37.5 ± 1.1 °C) was maintained by manual adjustment of an electric heating pad in response to measured rectal temperatures (corrected to estimate core body temperature). Warming was continued in a recovery cage according to treatment group. Rectal temperature was measured for a total of 120 min after anesthesia. Heating pad performance was assessed by measuring temperatures at various sites over its surface. One female rat in the post30 group was excluded from analysis. Normothermia was effectively maintained during and after anesthesia without significant differences between groups. In the post60 group, core temperature was slightly but significantly increased at 90 and 100 min compared with baseline. One rat in each treatment group became hyperthermic (>38.6 °C) during recovery. During recovery, the cage floor temperature required approximately 30 min to stabilize. The heating pad produced heat unevenly over its surface, and measured temperatures frequently exceeded the programmed temperature. Providing 30 min of warming immediately after anesthesia effectively prevented hypothermia in rats. Shorter warming periods may be useful when recovery cages are preheated.
麻醉剂会抑制体温调节机制,在全身麻醉诱导后几分钟内就会导致体温过低。体温过低的后果包括恢复延迟和实验变异性增加。即使在麻醉期间维持正常体温,恢复过程中也可能发生体温过低。本研究的主要目的是确定一个有效的升温期,以在恢复过程中维持正常体温。将成年雄性(n = 8)和雌性(n = 9)Sprague-Dawley大鼠随机分为麻醉恢复后升温30分钟(post30组)或60分钟(post60组)。在40分钟的麻醉期内,根据测量的直肠温度(校正后估计核心体温),通过手动调节电加热垫来维持正常体温(目标温度为37.5±1.1°C)。根据治疗组在恢复笼中继续升温。麻醉后共测量直肠温度120分钟。通过测量加热垫表面不同部位的温度来评估其性能。post30组中的一只雌性大鼠被排除在分析之外。麻醉期间及之后均有效维持了正常体温,各组之间无显著差异。在post60组中,与基线相比,90分钟和100分钟时核心温度略有但显著升高。每个治疗组中有一只大鼠在恢复过程中体温过高(>38.6°C)。在恢复过程中,笼底温度大约需要30分钟才能稳定下来。加热垫在其表面产生的热量不均匀,测量的温度经常超过设定温度。麻醉后立即提供30分钟的升温可有效预防大鼠体温过低。当恢复笼预先加热时,较短的升温期可能会有用。