Caspary Donald M, Ling Lynne, Turner Jeremy G, Hughes Larry F
Southern Illinois University School of Medicine, Springfield, IL 62794, USA.
J Exp Biol. 2008 Jun;211(Pt 11):1781-91. doi: 10.1242/jeb.013581.
Aging and acoustic trauma may result in partial peripheral deafferentation in the central auditory pathway of the mammalian brain. In accord with homeostatic plasticity, loss of sensory input results in a change in pre- and postsynaptic GABAergic and glycinergic inhibitory neurotransmission. As seen in development, age-related changes may be activity dependent. Age-related presynaptic changes in the cochlear nucleus include reduced glycine levels, while in the auditory midbrain and cortex, GABA synthesis and release are altered. Presumably, in response to age-related decreases in presynaptic release of inhibitory neurotransmitters, there are age-related postsynaptic subunit changes in the composition of the glycine (GlyR) and GABA(A) (GABA(A)R) receptors. Age-related changes in the subunit makeup of inhibitory pentameric receptor constructs result in altered pharmacological and physiological responses consistent with a net down-regulation of functional inhibition. Age-related functional changes associated with glycine neurotransmission in dorsal cochlear nucleus (DCN) include altered intensity and temporal coding by DCN projection neurons. Loss of synaptic inhibition in the superior olivary complex (SOC) and the inferior colliculus (IC) likely affect the ability of aged animals to localize sounds in their natural environment. Age-related postsynaptic GABA(A)R changes in IC and primary auditory cortex (A1) involve changes in the subunit makeup of GABA(A)Rs. In turn, these changes cause age-related changes in the pharmacology and response properties of neurons in IC and A1 circuits, which collectively may affect temporal processing and response reliability. Findings of age-related inhibitory changes within mammalian auditory circuits are similar to age and deafferentation plasticity changes observed in other sensory systems. Although few studies have examined sensory aging in the wild, these age-related changes would likely compromise an animal's ability to avoid predation or to be a successful predator in their natural environment.
衰老和听觉创伤可能导致哺乳动物大脑中枢听觉通路部分外周传入神经阻滞。根据稳态可塑性,感觉输入的丧失会导致突触前和突触后γ-氨基丁酸(GABA)能及甘氨酸能抑制性神经传递发生变化。正如在发育过程中所见,与年龄相关的变化可能依赖于活动。耳蜗核中与年龄相关的突触前变化包括甘氨酸水平降低,而在听觉中脑和皮层,GABA的合成和释放发生改变。据推测,由于与年龄相关的抑制性神经递质突触前释放减少,甘氨酸(GlyR)和GABA A(GABA A R)受体组成会出现与年龄相关的突触后亚基变化。抑制性五聚体受体结构亚基组成的与年龄相关的变化会导致药理学和生理学反应改变,这与功能抑制的净下调一致。与背侧耳蜗核(DCN)中甘氨酸神经传递相关的与年龄相关的功能变化包括DCN投射神经元强度编码和时间编码的改变。上橄榄复合体(SOC)和下丘(IC)中突触抑制的丧失可能会影响老年动物在自然环境中定位声音的能力。IC和初级听觉皮层(A1)中与年龄相关的突触后GABA A R变化涉及GABA A Rs亚基组成的变化。反过来,这些变化会导致IC和A1回路中神经元的药理学和反应特性出现与年龄相关的变化,这些变化共同可能会影响时间处理和反应可靠性。哺乳动物听觉回路中与年龄相关的抑制性变化的研究结果与在其他感觉系统中观察到的与年龄和传入神经阻滞可塑性变化相似。尽管很少有研究在野外研究感觉衰老,但这些与年龄相关的变化可能会损害动物在自然环境中躲避捕食或成为成功捕食者的能力。