Bruno V M, Goldberg M P, Dugan L L, Giffard R G, Choi D W
Department of Anesthesia, Stanford University School of Medicine, California.
J Neurochem. 1994 Oct;63(4):1398-406. doi: 10.1046/j.1471-4159.1994.63041398.x.
We examined the effect of moderate hypothermia (30 degrees C) on neuronal injury in murine cortical cell cultures. Lowering the temperature during and after a period of oxygen-glucose deprivation reduced both the release of glutamate to the bathing medium and accompanying neuronal degeneration. Hypothermia immediately after brief exposure to high concentrations of NMDA or glutamate also reduced the resulting neuronal degeneration. This protective effect was not eliminated when MK-801 and 6-cyano-7-nitroquinoxaline-2,3-dione were added immediately after washout of the exogenously added excitotoxin, suggesting that it was mediated by actions additional to reduction of endogenous late glutamate release. Hypothermia applied only during exposure to NMDA or glutamate, whether brief or prolonged, did not reduce subsequent cytosolic calcium accumulation or neuronal degeneration, suggesting that the postsynaptic induction of NMDA receptor-mediated excitotoxicity is not sensitive to temperature reduction. However, hypothermia during prolonged S-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid or kainate exposure did reduce neuronal degeneration.
我们研究了中度低温(30摄氏度)对小鼠皮质细胞培养物中神经元损伤的影响。在氧葡萄糖剥夺期间及之后降低温度,可减少谷氨酸释放到培养液中以及随之而来的神经元变性。短暂暴露于高浓度N-甲基-D-天冬氨酸(NMDA)或谷氨酸后立即进行低温处理,也可减少由此导致的神经元变性。在外源性兴奋性毒素洗脱后立即添加MK-801和6-氰基-7-硝基喹喔啉-2,3-二酮时,这种保护作用并未消除,这表明它是由除减少内源性晚期谷氨酸释放之外的其他作用介导的。仅在暴露于NMDA或谷氨酸期间(无论短暂还是延长)进行低温处理,并不会减少随后的胞质钙积累或神经元变性,这表明NMDA受体介导的兴奋性毒性的突触后诱导对温度降低不敏感。然而,在长时间暴露于α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)或红藻氨酸期间进行低温处理确实可减少神经元变性。