Hotchkiss R S, Song S K, Ling C S, Ackerman J J, Karl I E
Department of Anesthesiology, Washington University School of Medicine, St. Louis 63110.
Am J Physiol. 1990 Jan;258(1 Pt 2):R21-31. doi: 10.1152/ajpregu.1990.258.1.R21.
The effects of sepsis on intracellular Na+ concentration ([Na+]i) and glucose metabolism were examined in rat red blood cells (RBCs) by using 23Na- and 2H-nuclear magnetic resonance (NMR) spectroscopy. Sepsis was induced in 15 halothane-anesthetized female Sprague-Dawley rats by using the cecal ligation and perforation technique; 14 control rats underwent cecal manipulation without ligation. The animals were fasted for 36 h, but allowed free access to water. At 36 h postsurgery, RBCs were examined by 23Na-NMR by using dysprosium tripolyphosphate as a chemical shift reagent. Human RBCs from 17 critically ill nonseptic patients and from 7 patients who were diagnosed as septic were also examined for [Na+]i. Five rat RBC specimens had [Na+]i determined by both 23Na-NMR and inductively coupled plasma-atomic emission spectroscopy (ICP-AES). For glucose metabolism studies, RBCs from septic and control rats were suspended in modified Krebs-Henseleit buffer containing [6,6-2H2]glucose and examined by 2H-NMR. No significant differences in [Na+]i or glucose utilization were found in RBCs from control or septic rats. There were no differences in [Na+]i in the two groups of patients. The [Na+]i determined by NMR spectroscopy agreed closely with measurements using ICP-AES and establish that 100% of the [Na+]i of the RBC is visible by NMR. Glucose measurements determined by 2H-NMR correlated closely (correlation coefficient = 0.93) with enzymatic analysis. These studies showed no evidence that sepsis disturbed RBC membrane function or metabolism.
通过使用23Na和2H核磁共振(NMR)光谱技术,研究了脓毒症对大鼠红细胞(RBC)细胞内Na +浓度([Na +] i)和葡萄糖代谢的影响。采用盲肠结扎和穿孔技术,在15只氟烷麻醉的雌性Sprague-Dawley大鼠中诱导脓毒症;14只对照大鼠仅进行盲肠操作但不结扎。动物禁食36小时,但可自由饮水。术后36小时,使用三聚磷酸镝作为化学位移试剂,通过23Na-NMR检测红细胞。还检测了17例非脓毒症重症患者和7例脓毒症患者的人红细胞的[Na +] i。5个大鼠红细胞标本通过23Na-NMR和电感耦合等离子体原子发射光谱法(ICP-AES)测定了[Na +] i。对于葡萄糖代谢研究,将脓毒症大鼠和对照大鼠的红细胞悬浮在含有[6,6-2H2]葡萄糖的改良Krebs-Henseleit缓冲液中,并通过2H-NMR进行检测。在对照或脓毒症大鼠的红细胞中,未发现[Na +] i或葡萄糖利用有显著差异。两组患者的[Na +] i无差异。通过NMR光谱测定的[Na +] i与使用ICP-AES的测量结果密切一致,并确定NMR可观察到红细胞100%的[Na +] i。通过2H-NMR测定的葡萄糖测量值与酶分析密切相关(相关系数=0.93)。这些研究表明,没有证据表明脓毒症会干扰红细胞膜功能或代谢。