Meyer E M, Judkins J H, Momol A E, Hardwick E O
Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville 32610-0267.
Neurobiol Aging. 1994 Jan-Feb;15(1):63-7. doi: 10.1016/0197-4580(94)90145-7.
Cerebral cortical synaptosomes were prepared from 2- or 24-month-old Fischer 344 rats and exposed to a peroxidizing condition (50 microM ferrous ions and 2 microM ascorbate ions) before measuring either the release of newly synthesized [3H]acetylcholine (ACh) or protein kinase C activity (PKC). Several secretagogues with different mechanisms of action and different responses to aging were used to trigger release: K+ depolarization (5 mM-60 mM), calcium ionophore A23187 (1-10 micrograms/ml), and 4-aminopyridine (0.1-10 mM). Aging reduced K+ depolarization-induced release at every K+ concentration studied, reduced A23187-induced release at low but not high concentrations and did not affect 4-aminopyridine-induced release. Membrane peroxidation of synaptosomes from 2-month-old rats altered the response to secretagogues to match that seen in 24-month-old rats. Membrane peroxidation also attenuated the A23187-stimulated translocation of free to bound synaptosomal PKC activity in 2-month-old but not 24-month-old animals. These results suggest that membrane peroxidation may mimic some age-related deficits in secretagogue-induced [3H]ACh release.
从2个月或24个月大的费希尔344大鼠制备大脑皮质突触体,并在测量新合成的[3H]乙酰胆碱(ACh)释放或蛋白激酶C活性(PKC)之前,将其暴露于过氧化条件(50微摩尔亚铁离子和2微摩尔抗坏血酸离子)下。使用几种具有不同作用机制和对衰老有不同反应的促分泌剂来触发释放:钾离子去极化(5毫摩尔 - 60毫摩尔)、钙离子载体A23187(1 - 10微克/毫升)和4 - 氨基吡啶(0.1 - 10毫摩尔)。在研究的每个钾离子浓度下,衰老都会降低钾离子去极化诱导的释放,在低浓度而非高浓度下降低A23187诱导的释放,并且不影响4 - 氨基吡啶诱导的释放。2个月大大鼠突触体的膜过氧化改变了对促分泌剂的反应,使其与24个月大大鼠中观察到的反应相匹配。膜过氧化还减弱了2个月大动物中A23187刺激的游离突触体PKC活性向结合形式的转位,但在24个月大动物中未减弱。这些结果表明,膜过氧化可能模拟了促分泌剂诱导的[3H]ACh释放中一些与年龄相关的缺陷。