成年大鼠神经元功能活力的长期变化及其可能的行为后果。

Journal de physiologie Pub Date : 1988-01-01
B Peretz
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引用次数: 0

摘要

1. 在不同年龄的应用程序中,研究了三种明确的行为反应及其基础。2. 两种行为及其基础是年龄敏感,鳃退缩反射和渗透调节。它们的激活依赖于感觉。第三,鳃呼吸泵送运动(GPM)及其底物是年龄不变的。它由中枢神经系统中的网络发起,并由感觉输入调节。3.神经元的年龄敏感性似乎依赖于它的通路:介导感觉启动行为的通路比介导中枢启动行为的通路更容易受到衰老的影响。4. a)无约束动物和减量制剂中年龄敏感、GWR、鳃退缩反射符合L7功能的年龄依赖性减弱,L7是该反射的主要介质。b)然而,年龄不变的GPM符合LDG1的年龄无关功能,LDG1是GPM的主要贡献者。c)与年龄相关的渗透调节减慢与假定的水平衡神经元R15对稀释海水刺激渗透受体缺乏反应是一致的。5. L7的年龄敏感性是由其功能降低、末端易化性降低、输入阻力降低以及其支配的肌肉连接处的重塑所决定的。这与LDG1及其支配的肌肉连接处的这些特性的年龄不变性形成对比。到目前为止,R15的年龄敏感性表现为对突触输入的反应性降低,输入阻力降低,对眼球刺激的反应很小。6. GWR的年龄敏感性、渗透调节及其底物并不一定是不适应的。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term change of viability of neuron functioning and its possible behavioral consequences in the adult Aplysia.

1. In Aplysia of different ages, three well defined behavioral responses and their substrates were examined. 2. Two of the behaviors and their substrates are age-sensitive, the gill withdrawal reflex, and osmoregulation. They are sensory-dependent for their activation. The third, the gill respiratory pumping movements, GPM, and its substrates is age-invariant. It is initiated by a network in the CNS, and modulated by sensory input. 3. Age-sensitivity of a neuron appears dependent on its pathway: the pathways mediating sensory-initiated behavior are more vulnerable to aging than the pathway mediating CNS-initiated behavior. 4. a) The age-sensitive, GWR, gill withdrawal reflex, in unrestrained animals and in reduced preparations conforms to the age-dependent reduced functioning of L7, the major mediator of the reflex. b) Whereas, the age-invariant GPM conforms to the age-independent functioning of LDG1, a major contributor to GPMs. c) The age-related slowing of osmoregulation is consistent with the lack of response in the putative water balance neuron, R15, to stimulation of osmoreceptors by dilute seawater. 5. Age-sensitivity of L7 is defined by its reduced function, decreased facilitation at its terminals, reduced input resistance, and remodeling of junctions in the muscles it innervates. This is in contrast to the age-invariance of these properties in LDG1 and of the junctions in muscles it innervates. Thus far, the age-sensitivity of R15 is revealed by its reduced responsiveness to synaptic input, reduced input resistance, and little response to osphradial stimulation. 6. Age-sensitivity of the GWR, osmoregulation and of their substrates is not necessarily maladaptive.(ABSTRACT TRUNCATED AT 250 WORDS)

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