Hansen T D, Warner D S, Traynelis V C, Todd M M
University of Iowa, Department of Anesthesia, Iowa City.
Neurosurgery. 1994 Mar;34(3):505-11; discussion 511. doi: 10.1227/00006123-199403000-00017.
Little is known about how intravenous fluids influence peritumoral edema formation. This experiment was designed to determine, in a rat glioma model, whether changes in plasma osmolality alter water content, as assessed by specific gravity (SpGr), in normal and neoplastic cerebral tissue. Cells cultured from an ethylnitrosourea-induced rat glioma were stereotactically implanted into the right striatum of Fischer 344 rats. A tumor growth interval of 21 days was allowed. In a second experiment, rats underwent a 60-second cortical freeze injury followed by 24 hours' recovery. In both experiments, rats were assigned to one of three groups: hypotonic (100 ml/kg of 0.2 mol/L NaCl in H2O, intraperitoneally; resultant plasma osmolality approximately 268 mOsm/kg); isotonic (no treatment; plasma osmolality approximately 298 mOsm/kg); or hypertonic (10 ml/kg of 1.0 mol/L NaCl in H2O, intraperitoneally; plasma osmolality approximately 342 mOsm/kg). Thirty minutes after fluid injection, regional SpGr was determined using a kerosene-bromobenzene gradient. In subsets of rats, the tissue morphology and blood-brain barrier permeability of Evans blue dye were assessed. Tissue within the freeze lesion was stained by Evans blue dye with sharp demarcation. Evans blue dye did not stain gliomatous tissue, and central necrosis was not histologically evident. In isotonic rats, glioma SpGr was reduced (1.0411 +/- 0.0012 g/ml) relative to the contralateral striatum (1.0437 +/- 0.0008 g/ml; P < 0.001). Despite this, a strong linear relation was observed for SpGr and plasma osmolality in both neoplastic and normal tissue. Within the freeze lesion in isotonic rats, SpGr was severely reduced (1.0335 +/- 0.0008 g/ml; P < 0.0001) compared with contralateral frontal cortex.(ABSTRACT TRUNCATED AT 250 WORDS)
关于静脉输液如何影响瘤周水肿形成的了解甚少。本实验旨在通过大鼠胶质瘤模型确定血浆渗透压的变化是否会改变正常和肿瘤性脑组织中的含水量(通过比重(SpGr)评估)。将从乙基硝基脲诱导的大鼠胶质瘤培养的细胞立体定向植入Fischer 344大鼠的右侧纹状体。给予21天的肿瘤生长间隔期。在第二个实验中,大鼠接受60秒的皮层冷冻损伤,随后恢复24小时。在这两个实验中,大鼠被分为三组之一:低渗组(腹腔注射100 ml/kg的0.2 mol/L NaCl水溶液;血浆渗透压约为268 mOsm/kg);等渗组(不治疗;血浆渗透压约为298 mOsm/kg);或高渗组(腹腔注射10 ml/kg的1.0 mol/L NaCl水溶液;血浆渗透压约为342 mOsm/kg)。输液30分钟后,使用煤油-溴苯梯度测定局部SpGr。在部分大鼠中,评估伊文思蓝染料的组织形态和血脑屏障通透性。冷冻损伤内的组织被伊文思蓝染料染色,界限清晰。伊文思蓝染料未对胶质瘤组织染色,且中央坏死在组织学上不明显。在等渗大鼠中,相对于对侧纹状体(1.0437 +/- 0.0008 g/ml;P < 0.001),胶质瘤的SpGr降低(1.0411 +/- 0.0012 g/ml)。尽管如此,在肿瘤组织和正常组织中均观察到SpGr与血浆渗透压之间存在强线性关系。在等渗大鼠的冷冻损伤内,与对侧额叶皮层相比,SpGr严重降低(1.0335 +/- 0.0008 g/ml;P < 0.0001)。(摘要截断于250字)