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Long-term change of viability of neuron functioning and its possible behavioral consequences in the adult Aplysia.

作者信息

Peretz B

机构信息

Department of Physiology and Biophysics, University of Kentucky Medical Center, Lexington 40536-0084.

出版信息

J Physiol (Paris). 1988;83(3):217-23.

PMID:3272293
Abstract
  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)
摘要

相似文献

1
Long-term change of viability of neuron functioning and its possible behavioral consequences in the adult Aplysia.
J Physiol (Paris). 1988;83(3):217-23.
2
Age-dependent behavioral changes and physiological changes in identified neurons in Aplysia californica.
J Neurobiol. 1981 Sep;12(5):469-78. doi: 10.1002/neu.480120506.
3
CNS control over gill reflex behaviors in Aplysia: satiation causes an increase in the suppressive control in older but not young animals.中枢神经系统对海兔鳃反射行为的控制:饱足状态会导致老年动物而非幼年动物的抑制性控制增强。
J Neurobiol. 1980 Nov;11(6):591-611. doi: 10.1002/neu.480110609.
4
The Aplysia gill-withdrawal reflex revisited: components of the network.再探海兔鳃收缩反射:神经网络的组成部分
Acta Biol Hung. 1992;43(1-4):387-98.
5
Age sensitivity of osmoregulation and of its neural correlates in Aplysia.海兔渗透压调节及其神经关联的年龄敏感性。
Am J Physiol. 1989 Apr;256(4 Pt 2):R989-96. doi: 10.1152/ajpregu.1989.256.4.R989.
6
Increased age affects properties characterizing behavioral plasticity in freely behaving Aplysia.年龄增长会影响自由活动的海兔行为可塑性的特征属性。
Neurobiol Aging. 1992 Mar-Apr;13(2):217-25. doi: 10.1016/0197-4580(92)90033-t.
7
Control of gill reflex habituation and the rate of EPSP decrement of L7 by a common source in the CNS of Aplysia.海兔中枢神经系统中一个共同来源对鳃反射习惯化和L7处兴奋性突触后电位衰减速率的控制。
J Neurobiol. 1980 Sep;11(5):425-33. doi: 10.1002/neu.480110502.
8
Behavioral adaptation of the Aplysia siphon-withdrawal response is accompanied by sensory adaptation.海兔缩鳃反应的行为适应性伴随着感觉适应性。
Behav Neurosci. 2007 Feb;121(1):200-11. doi: 10.1037/0735-7044.121.1.200.
9
In vitro classical conditioning of a gill withdrawal reflex in Aplysia: neural correlates and possible neural mechanisms.海兔鳃收缩反射的体外经典条件反射:神经关联及可能的神经机制
J Neurobiol. 1986 Mar;17(2):83-101. doi: 10.1002/neu.480170204.
10
Cellular and biophysical mechanisms contributing to regulation of reflex excitability of inking behavior in Aplysia.
Fed Proc. 1982 Apr;41(6):2147-52.

引用本文的文献

1
Phospholipase A2 - nexus of aging, oxidative stress, neuronal excitability, and functional decline of the aging nervous system? Insights from a snail model system of neuronal aging and age-associated memory impairment.磷脂酶 A2-衰老、氧化应激、神经元兴奋性和衰老神经系统功能下降的枢纽?来自神经元衰老和与年龄相关的记忆障碍蜗牛模型系统的见解。
Front Genet. 2014 Dec 4;5:419. doi: 10.3389/fgene.2014.00419. eCollection 2014.
2
Behavioral aging is associated with reduced sensory neuron excitability in Aplysia californica.行为衰老与加利福尼亚海兔感觉神经元兴奋性降低有关。
Front Aging Neurosci. 2014 May 9;6:84. doi: 10.3389/fnagi.2014.00084. eCollection 2014.
3
Age-associated bidirectional modulation of gene expression in single identified R15 neuron of Aplysia.
在单个鉴定的海兔 R15 神经元中,与年龄相关的基因表达双向调节。
BMC Genomics. 2013 Dec 14;14:880. doi: 10.1186/1471-2164-14-880.
4
Do different neurons age differently? Direct genome-wide analysis of aging in single identified cholinergic neurons.不同的神经元衰老速度不同吗?在单个鉴定的胆碱能神经元中进行全基因组范围的衰老直接分析。
Front Aging Neurosci. 2010 May 19;2. doi: 10.3389/neuro.24.006.2010. eCollection 2010.