Lien Y H, Shapiro J I, Chan L
Department of Medicine, University of Colorado Health Sciences Center, Denver 80262.
J Clin Invest. 1990 May;85(5):1427-35. doi: 10.1172/JCI114587.
We studied the effects of varying degrees and durations of hypernatremia on the brain concentrations of organic compounds believed to be important, so-called "idiogenic" osmoles in rats by means of conventional biochemical assays, nuclear magnetic resonance spectroscopy, and high-performance liquid chromatography. There were no changes in the concentrations of these osmoles (specifically myoinositol, sorbitol, betaine, glycerophosphorylcholine [GPC], phosphocreatine, glutamine, glutamate, and taurine) in rats with acute (2 h) hypernatremia (serum Na 194 +/- 5 meq/liter). With severe (serum Na 180 +/- 4 meq/liter) chronic (7 d) hypernatremia, the concentrations of each of these osmoles except sorbitol increased significantly: myoinositol (65%), betaine (54%), GPC (132%), phosphocreatine (73%), glutamine (143%), glutamate (84%), taurine (78%), and urea (191%). Together, these changes account for 35% of the change in total brain osmolality. With moderate (serum Na 159 +/- 3 meq/liter) hypernatremia, more modest but significant increases in the concentrations of each of these osmoles except betaine and sorbitol were noted. When rats with severe chronic hypernatremia were allowed to drink water freely, their serum sodium as well as the brain concentrations of all of these organic osmoles except myoinositol returned to normal within 2 d. It is concluded that: idiogenic osmoles play an important role in osmoregulation in the brain of rats subjected to hypernatremia; the development of these substances occur more slowly than changes in serum sodium; and the decrease in concentration of myoinositol occurs significantly more slowly than the decrease in serum sodium which occurs when animals are allowed free access to water. These observations may be relevant to the clinical management of patients with hypernatremia.
我们通过传统生化分析、核磁共振光谱法和高效液相色谱法,研究了不同程度和持续时间的高钠血症对大鼠脑中被认为重要的有机化合物(即所谓的“内生性”渗透溶质)浓度的影响。急性(2小时)高钠血症(血清钠194±5毫当量/升)的大鼠,这些渗透溶质(具体为肌醇、山梨醇、甜菜碱、甘油磷酸胆碱[GPC]、磷酸肌酸、谷氨酰胺、谷氨酸和牛磺酸)的浓度没有变化。严重(血清钠180±4毫当量/升)慢性(7天)高钠血症时,除山梨醇外,这些渗透溶质的浓度均显著升高:肌醇(65%)、甜菜碱(54%)、GPC(132%)、磷酸肌酸(73%)、谷氨酰胺(143%)、谷氨酸(84%)、牛磺酸(78%)和尿素(191%)。这些变化共同占总脑渗透压变化的35%。中度(血清钠159±3毫当量/升)高钠血症时,除甜菜碱和山梨醇外,这些渗透溶质的浓度也有更适度但显著的升高。当严重慢性高钠血症的大鼠自由饮水时,它们的血清钠以及除肌醇外所有这些有机渗透溶质的脑浓度在2天内恢复正常。得出以下结论:内生性渗透溶质在高钠血症大鼠的脑渗透压调节中起重要作用;这些物质的产生比血清钠的变化更慢;当动物自由饮水时,肌醇浓度的降低比血清钠的降低明显更慢。这些观察结果可能与高钠血症患者的临床管理有关。