Hoyer S, Krier C
Neurobiol Aging. 1986 Jan-Feb;7(1):23-9. doi: 10.1016/0197-4580(86)90022-9.
Age has been considered to be a crucial risk factor for brain ischemic insults and their mortality. Brain ischemia has been found to cause severe abnormalities in glucose metabolism, energy metabolism and related metabolism, thus damaging the structure and function of brain cells. To study the effect of age and ischemia on brain glucose and energy metabolism, investigations were performed on one-and two-year-old male Wistar rats, the latter of which can be designated as aged. In both age groups, ischemia resulted in a depletion of glucose, OAA, ATP AND CRP, a diminution of Pyr, Citr and alpha-Keto and an accumulation of FDP, Lact, Succ, ADP and AMP in brain cortex. During ischemia, differences between the two age groups became most obvious in the concentrations of Glu, FDP, DHAP, Lact, Succ, Mal, ADP and AMP. In general, the metabolic changes in both age groups point to an increased glycolytic flux which may be less accelerated in the aged group, to an inhibition of the starting reactions of the tricarboxylic acid cycle more severe in aged animals, to a preponderance of anaplerotic reactions in this oxidative system more pronounced in the two-year-old group and to a loss of AMP in the same age group. The age-related metabolic variations measured may indicate that with age the biological plasticity of the brain may be reduced to meet emergency conditions.
年龄被认为是脑缺血性损伤及其死亡率的关键危险因素。已发现脑缺血会导致葡萄糖代谢、能量代谢及相关代谢出现严重异常,从而损害脑细胞的结构和功能。为研究年龄和缺血对脑葡萄糖及能量代谢的影响,对1岁和2岁的雄性Wistar大鼠进行了研究,后者可被视为老龄大鼠。在两个年龄组中,缺血均导致脑皮质中葡萄糖、草酰乙酸、三磷酸腺苷(ATP)和环磷腺苷(CRP)耗竭,丙酮酸、柠檬酸和α-酮戊二酸减少,以及1,6-二磷酸果糖(FDP)、乳酸、琥珀酸、二磷酸腺苷(ADP)和单磷酸腺苷(AMP)积累。在缺血期间,两个年龄组之间在谷氨酸、FDP、磷酸二羟丙酮(DHAP)、乳酸、琥珀酸、苹果酸、ADP和AMP浓度方面的差异最为明显。总体而言,两个年龄组的代谢变化表明糖酵解通量增加,老龄组可能增加得较少;三羧酸循环起始反应的抑制在老龄动物中更严重;在这个氧化系统中,回补反应在2岁组中更明显占优势;且在同一年龄组中AMP有所损失。所测得的与年龄相关的代谢变化可能表明,随着年龄增长,大脑的生物可塑性可能会降低,以应对紧急情况。