Birthelmer A, Stemmelin J, Jackisch R, Cassel J-C
Institut für Experimentelle und Klinische Pharmakologie und Toxikologie der Universität Freiburg, Neuropharmakologisches Labor, Hansastrasse 9A, D-79104 Freiburg, Germany.
Brain Res Bull. 2003 May 15;60(3):283-96. doi: 10.1016/s0361-9230(03)00042-x.
Aged (25-27 months) Long-Evans female rats were distinguished according to whether they showed no significant impairment (AU), moderate impairment (AMI), or severe impairment (ASI) in a spatial reference-memory task. Young (3-5 months) rats served as controls. Electrically evoked overflow of tritium was assessed in hippocampal slices preloaded with [3H]choline or [3H]serotonin (5-HT). Nicotine-evoked overflow of tritium was measured after preloading with [3H]noradrenaline (NA). Choline acetyltransferase (ChAT) and acetylcholinesterase (AChE) activity, and concentration of monoamines were assessed in homogenates. Aged rats exhibited reduced accumulation of [3H]choline and [3H]5-HT, increased accumulation of [3H]NA, and weaker electrically evoked overflow of [3H]acetylcholine ([3H]ACh) and [3H]5-HT. The overflow of [3H]NA was not altered consistently by aging. Roughly, drugs acting presynaptically had comparable effects in aged rats: oxotremorine and CP 93,129 inhibited the overflow of [3H]ACh, CP 93,129 and UK 14,304 reduced that of [3H]5-HT. ChAT or AChE activity, and 5-HT concentration were not changed by age; NA concentration was reduced. When significant, changes were comparable in AU, AMI, and ASI rats. Data show that aging alters cholinergic and serotonergic hippocampal innervations, release of ACh and 5-HT, but not presynaptic release-modulating mechanisms. These alterations do not account for variability in water-maze performance of aged rats.
根据在空间参考记忆任务中是否表现出无明显损伤(AU)、中度损伤(AMI)或重度损伤(ASI),将25 - 27月龄的长Evans雌性大鼠区分开来。3 - 5月龄的年轻大鼠作为对照。在预先加载了[3H]胆碱或[3H]5 - 羟色胺(5 - HT)的海马切片中评估电诱发的氚溢出。在预先加载[3H]去甲肾上腺素(NA)后测量尼古丁诱发的氚溢出。在匀浆中评估胆碱乙酰转移酶(ChAT)和乙酰胆碱酯酶(AChE)活性以及单胺浓度。老年大鼠表现出[3H]胆碱和[3H]5 - HT积累减少,[3H]NA积累增加,以及电诱发的[3H]乙酰胆碱([3H]ACh)和[3H]5 - HT溢出减弱。衰老并未使[3H]NA的溢出发生一致改变。大致而言,作用于突触前的药物在老年大鼠中具有类似的作用:氧化震颤素和CP 93,129抑制[3H]ACh的溢出,CP 93,129和UK 14,304降低[3H]5 - HT的溢出。ChAT或AChE活性以及5 - HT浓度不受年龄影响;NA浓度降低。当有显著变化时,AU、AMI和ASI大鼠中的变化相当。数据表明,衰老会改变海马胆碱能和5 - 羟色胺能神经支配、ACh和5 - HT的释放,但不会改变突触前释放调节机制。这些改变并不能解释老年大鼠在水迷宫实验中表现的变异性。