Sikes Patricia J, Zhao Piyu, Maass David L, White Jean, Horton Jureta W
UT Southwestern Medical Center Department of Surgery, Dallas, Texas, USA.
Crit Care Med. 2005 Mar;33(3):605-15. doi: 10.1097/01.ccm.0000155910.89252.fe.
Sepsis or septic shock occurs frequently in sick and injured patients and is associated with a significant mortality. Myocardial contractile dysfunction has been proposed to be a major determinant of sepsis-related mortality. This study was directed to examine the role of Na/H exchange activity in myocardial defects after sepsis or after sepsis complicated by a previous burn injury.
Laboratory study.
University research laboratory.
Sprague-Dawley rats (300-350 g, males).
Cardiac function, cellular Na and Ca, myocardial pH, and high-energy phosphates were examined in perfused hearts harvested after sepsis alone (intratracheal Streptococcus pneumoniae, 0.4 mL of 1 x 10 CFU/mL), after sepsis complicated by previous burn injury (40% total body surface area), and after amiloride (a selective inhibitor of Na/H exchange) treatment of either sepsis alone or sepsis plus burn.
The ratio of Na signal from the intracellular compartment (Nai) compared with an external standard (monitored by Na-NMR spectroscopy, TmDOTP shift reagent) increased by 70% in sepsis alone and by 41% in sepsis complicated by previous burn injury compared with shams. Cardiac adenosine triphosphate and intracellular pH (P nuclear magnetic resonance spectroscopy) were unchanged by sepsis or sepsis plus burn. Left ventricular pressure and maximal change in pressure over time were reduced after sepsis or after sepsis plus burn injury. Amiloride treatment in either sepsis or sepsis complicated by a previous burn injury prevented myocardial Na and Ca accumulation, attenuated sepsis-related lactic acidosis, and improved left ventricular function.
Our results suggest that sepsis-related cardiac dysfunction is mediated, in part, by Na/H exchange activity, and inhibition of Na/H exchange activity improves cardiac function after sepsis alone or sepsis complicated by a previous injury.
脓毒症或脓毒性休克在伤病患者中频繁发生,且与显著的死亡率相关。心肌收缩功能障碍被认为是脓毒症相关死亡率的主要决定因素。本研究旨在探讨钠/氢交换活性在脓毒症或既往有烧伤史的脓毒症合并症后心肌损伤中的作用。
实验室研究。
大学研究实验室。
Sprague-Dawley大鼠(300 - 350克,雄性)。
在单独脓毒症(气管内注射肺炎链球菌,0.4毫升1×10 CFU/毫升)、既往有烧伤史的脓毒症合并症(全身表面积的40%)以及单独脓毒症或脓毒症加烧伤后用氨氯地平(钠/氢交换的选择性抑制剂)治疗后,对采集的灌注心脏进行心脏功能、细胞内钠和钙、心肌pH值以及高能磷酸盐的检测。
与假手术组相比,单独脓毒症组细胞内室钠信号(Nai)与外部标准(通过钠核磁共振波谱法,TmDOTP位移试剂监测)的比值增加了70%,既往有烧伤史的脓毒症合并症组增加了41%。脓毒症或脓毒症加烧伤对心脏三磷酸腺苷和细胞内pH值(磷核磁共振波谱法)无影响。脓毒症或脓毒症加烧伤后左心室压力和压力随时间的最大变化降低。单独脓毒症或既往有烧伤史的脓毒症合并症用氨氯地平治疗可防止心肌钠和钙蓄积,减轻脓毒症相关的乳酸酸中毒,并改善左心室功能。
我们的结果表明,脓毒症相关的心脏功能障碍部分由钠/氢交换活性介导,抑制钠/氢交换活性可改善单独脓毒症或既往有损伤的脓毒症合并症后的心脏功能。