Suzuki Takeshi, Morisaki Hiroshi, Serita Ryohei, Yamamoto Michiko, Kotake Yoshifumi, Ishizaka Akitoshi, Takeda Junzo
Department of Anesthesiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Crit Care Med. 2005 Oct;33(10):2294-301. doi: 10.1097/01.ccm.0000182796.11329.3b.
Since beta-blocker therapy is known to be effective in patients with an injured heart, such as infarction, we designed the present study to examine the protective effects of infusion of the beta1-selective blocker esmolol on myocardial function in peritonitis-induced septic rats using an isolated working heart preparation.
Randomized animal study.
University research laboratory.
Thirty-one rats treated with cecal ligation and perforation to evoke peritonitis.
After cecal ligation and perforation, rats were randomly allocated to the control group (normal saline 2 mL/hr, n = 11), low-dose esmolol group (10 mg/kg/hr, n = 10), or high-dose esmolol group (20 mg/kg/hr, n = 10). After obtaining blood samples for measurement of arterial lactate and tumor necrosis factor-alpha at 24 hrs, we assessed cardiac output, myocardial oxygen consumption, and cardiac efficiency (cardiac output x peak systolic pressure/myocardial oxygen consumption) at various preloads in an isolated perfused heart preparation.
Esmolol infusion did not cause an elevation of arterial lactate levels but reduced tumor necrosis factor-alpha concentrations vs. the control group (p < .05). Both cardiac output and cardiac efficiency in the esmolol-treated rats were significantly higher throughout the study periods vs. the control group (p < .05).
Esmolol infusion in sepsis improved oxygen utilization of myocardium and preserved myocardial function.
由于已知β受体阻滞剂疗法对心脏受损患者(如心肌梗死患者)有效,我们设计了本研究,以使用离体工作心脏制备方法,研究输注β1选择性阻滞剂艾司洛尔对腹膜炎诱导的脓毒症大鼠心肌功能的保护作用。
随机动物研究。
大学研究实验室。
31只接受盲肠结扎和穿孔以诱发腹膜炎的大鼠。
盲肠结扎和穿孔后,将大鼠随机分为对照组(生理盐水2 mL/小时,n = 11)、低剂量艾司洛尔组(10 mg/kg/小时,n = 10)或高剂量艾司洛尔组(20 mg/kg/小时,n = 10)。在24小时采集血样以测量动脉血乳酸和肿瘤坏死因子-α后,我们在离体灌注心脏制备中,于不同前负荷下评估心输出量、心肌耗氧量和心脏效率(心输出量×收缩压峰值/心肌耗氧量)。
与对照组相比,输注艾司洛尔未导致动脉血乳酸水平升高,但降低了肿瘤坏死因子-α浓度(p < 0.05)。在整个研究期间,艾司洛尔治疗组大鼠的心输出量和心脏效率均显著高于对照组(p < 0.05)。
脓毒症时输注艾司洛尔可改善心肌氧利用并保护心肌功能。