Ling L L, Hughes L F, Caspary D M
Department of Pharmacology, Southern Illinois University School of Medicine, Springfield, 62794, USA.
Neuroscience. 2005;132(4):1103-13. doi: 10.1016/j.neuroscience.2004.12.043.
Age-related changes within the auditory brainstem typically include alterations in inhibitory neurotransmission and coding mediated by GABA and glycinergic circuits. As part of an effort to evaluate the impact of aging on neurotransmission in the higher auditory centers, the present study examined age-related changes in the GABA synthetic enzyme, glutamic acid decarboxylase (GAD), in rat primary auditory cortex (AI), which contains a vast network of intrinsic and extrinsic GABAergic circuits throughout its layers. Message levels of the two GAD isoforms found in brain, GAD(65) and GAD(67), and GAD(67) protein levels were compared in young adult, middle-aged and aged rats using in situ hybridization and quantitative immunocytochemistry, respectively. For comparison, age-related GAD changes were also assessed in the parietal cortex and hippocampus. Significant age-related decreases in GAD(65&67) messages were observed in AI layers II-VI of aged rats relative to their young adult cohorts. The largest changes were identified in layer II (GAD(65): -26.6% and GAD(67): -40.1%). GAD(67) protein expression decreased significantly in parallel with mRNA decreases in all layers of AI. Adjacent regions of parietal cortex showed no significant GAD(67) protein changes among the age groups, except in layer IV. As previously described, GAD(67) message and protein levels in selected hippocampal regions were significantly reduced in aged rats. Age-related GAD reductions likely reflect decreases in both metabolic and pre-synaptic GABA levels suggesting a plastic down-regulation of normal adult inhibitory GABA neurotransmission. Consistent with the present findings, functional studies in primate visual cortex and preliminary studies in AI find coding changes suggestive of altered inhibitory processing in aged animals. An age-related loss of normal adult GABA neurotransmission in AI would likely alter temporal coding properties and could contribute to the loss in speech understanding observed in the elderly.
听觉脑干内与年龄相关的变化通常包括由γ-氨基丁酸(GABA)和甘氨酸能回路介导的抑制性神经传递和编码的改变。作为评估衰老对高级听觉中枢神经传递影响的一部分,本研究检测了大鼠初级听觉皮层(AI)中GABA合成酶谷氨酸脱羧酶(GAD)与年龄相关的变化,该皮层在其各层中包含大量内在和外在的GABA能回路网络。分别使用原位杂交和定量免疫细胞化学方法,比较了年轻成年、中年和老年大鼠脑中发现的两种GAD同工型GAD(65)和GAD(67)的信使水平以及GAD(67)蛋白水平。为作比较,还评估了顶叶皮层和海马体中与年龄相关的GAD变化。相对于年轻成年组,老年大鼠AI层II-VI中观察到GAD(65&67)信使显著的年龄相关下降。最大的变化出现在II层(GAD(65):-26.6%,GAD(67):-40.1%)。GAD(67)蛋白表达在AI的所有层中与mRNA下降同时显著降低。顶叶皮层的相邻区域在各年龄组中除IV层外,GAD(67)蛋白没有显著变化。如先前所述,老年大鼠中选定海马区域的GAD(67)信使和蛋白水平显著降低。与年龄相关的GAD减少可能反映了代谢和突触前GABA水平的下降,提示正常成年抑制性GABA神经传递的可塑性下调。与本研究结果一致,灵长类视觉皮层的功能研究和AI的初步研究发现编码变化提示老年动物抑制性处理改变。AI中正常成年GABA神经传递与年龄相关的丧失可能会改变时间编码特性,并可能导致老年人言语理解能力的丧失。