McGahon B, Clements M P, Lynch M A
Department of Physiology, Trinity College, Dublin, Ireland.
Neuroscience. 1997 Nov;81(1):9-16. doi: 10.1016/s0306-4522(97)00116-4.
The ability of aged rats to sustain long-term potentiation in the dentate gyrus of the hippocampus is impaired and this impairment correlates with decreased release of glutamate and a decrease in membrane arachidonic acid concentration. Twenty-two-month-old rats receiving a diet supplemented with arachidonic acid and its precursor, gamma-linolenic acid, sustained long-term potentiation in a manner indistinguishable from four-month-old controls. Dietary supplementation also restored arachidonic acid concentrations in membranes prepared from hippocampus of these aged animals to levels observed in hippocampus of four-month-old rats. Glutamate release stimulated by depolarization was similar in dentate gyrus prepared from young rats and aged rats which received the experimental diet, but was markedly reduced in aged animals which received the control diet. In addition, the synergism between arachidonic acid and the metabotropic glutamate receptor agonist, trans-1-amino-cyclopentyl-1,3-dicarboxylate, on glutamate release, which was observed in hippocampal synaptosomes prepared from four-month-old rats, was also observed in hippocampal preparations obtained from aged rats which had been fed with the experimental diet, but was absent in hippocampal preparations obtained from aged animals which were fed with control diet. Thus, reversing the age-related decrease in membrane arachidonic acid concentration restored ability of aged animals to sustain long-term potentiation and reversed age-related changes in glutamate release.
老年大鼠在海马齿状回维持长时程增强的能力受损,这种损害与谷氨酸释放减少和膜花生四烯酸浓度降低相关。接受补充花生四烯酸及其前体γ-亚麻酸饮食的22月龄大鼠,维持长时程增强的方式与4月龄对照大鼠无法区分。饮食补充还将这些老年动物海马制备的膜中花生四烯酸浓度恢复到4月龄大鼠海马中观察到的水平。由去极化刺激的谷氨酸释放在接受实验饮食的年轻大鼠和老年大鼠制备的齿状回中相似,但在接受对照饮食的老年动物中显著降低。此外,在4月龄大鼠制备的海马突触体中观察到的花生四烯酸与代谢型谷氨酸受体激动剂反式-1-氨基环戊基-1,3-二羧酸对谷氨酸释放的协同作用,在喂食实验饮食的老年大鼠获得的海马制剂中也观察到,但在喂食对照饮食的老年动物获得的海马制剂中不存在。因此,逆转与年龄相关的膜花生四烯酸浓度降低可恢复老年动物维持长时程增强的能力,并逆转与年龄相关的谷氨酸释放变化。