Pulsinelli W A, Waldman S, Rawlinson D, Plum F
Neurology. 1982 Nov;32(11):1239-46. doi: 10.1212/wnl.32.11.1239.
We compared the effects of glucose injection with those of saline or mannitol on ischemic brain damage and brain water content in a four-vessel occlusion (4-VO) rat model, which simultaneously causes severe forebrain ischemia and moderate hindbrain ischemia. Glucose given before onset of ischemia was followed by severe brain injury, with necrosis of the majority of neocortical neurons and glia, substantial neuronal damage throughout the remainder of forebrain, and severe brain edema. By comparison, saline injection before forebrain ischemia resulted in only scattered ischemic damage confined to neurons and no change in the brain water content. Mannitol injection before 4-VO or D-glucose injection during or after 4-VO produced no greater forebrain damage than did the saline injection. Morphologic damage in the cerebellum, however, was increased by D-glucose injection given either before or during 4-VO. The results demonstrate that hyperglycemia before severe brain ischemia or during moderate ischemia markedly augments morphologic brain damage.
我们在四动脉闭塞(4-VO)大鼠模型中比较了葡萄糖注射与生理盐水或甘露醇注射对缺血性脑损伤和脑含水量的影响,该模型可同时导致严重的前脑缺血和中度的后脑缺血。在缺血发作前给予葡萄糖会导致严重的脑损伤,大多数新皮质神经元和神经胶质细胞坏死,前脑其余部分存在大量神经元损伤,以及严重的脑水肿。相比之下,在前脑缺血前注射生理盐水仅导致局限于神经元的散在缺血性损伤,且脑含水量无变化。在4-VO前注射甘露醇或在4-VO期间或之后注射D-葡萄糖,所造成的前脑损伤并不比注射生理盐水更严重。然而,在4-VO前或期间注射D-葡萄糖会增加小脑的形态学损伤。结果表明,在严重脑缺血前或中度缺血期间的高血糖会显著加剧脑形态学损伤。