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加州海兔中乳状分泌物的运动控制。

Motor controls of opaline secretion in Aplysia californica.

作者信息

Tritt S H, Byrne J H

出版信息

J Neurophysiol. 1980 Mar;43(3):581-94. doi: 10.1152/jn.1980.43.3.581.

Abstract
  1. Using combined morphological and electrophysiological techniques, we have identified motor neurons in the right pleural ganglion of Aplysia californica that contribute to the release of opaline from the opaline gland. 2. Three pleural ganglion neurons were found to meet the requirements for identification as opaline gland motor neurons by a) sending processes in nerve P5, which innervates the gland; b) producing contractions of the gland in the absence of central synaptic activity; and c) producing excitatory junctional potentials (EJPs) in cells making up the opaline gland itself. The neurons can be reliably located and have been designated PLR1, PLR2, and PLR3. 3. When gland contraction is measured by the change in luminal pressure, the gland response is a graded function of low-frequency spike activity in the motor neurons. 4. Presumptive EJPs recorded from opaline gland cells are reversibly decreased in size by high extracellular Mg2+ and reversibly increased in size by raising the concentration of extracellular Ca2+. These results suggest that the presumptive EJPs are chemically mediated. The presumptive EJPs show facilitation and posttetanic potentiation. 5. The identified opaline motor neurons may constitute a significant portion of the motor input to the opaline gland via nerve P5 since hyperpolarization of the cells prevents the opaline gland response elicited by right connective stimulation in vitro. 6. We have compared the properties of the opaline motor neurons with the previously identified properties of the ink motor neurons (6--9, 19). Like the ink motor neurons, the opaline motor neurons have high resting potentials, are electrically coupled, and have no spontaneous spike activity. They also receive a slow and long-lasting evoked depolarizing synaptic input, which appears to be mediated by a decreased conductance mechanism. The firing pattern of the opaline motor neurons produced by synaptic input shows the same delayed bursting pattern previously described for the ink motor neurons. 7. The biophysical properties and synaptic input to the ink motor neurons have been shown to affect the features of inking behavior (4, 6--9, 19). The opaline motor neurons share some of these biophysical characteristics and mediate a defensive behavior similar to ink release. Further comparisons of these behaviors and their underlying neural circuits may provide a better understanding of the extent to which cellular biophysical properties and patterns of synaptic input influence the features of the behaviors that individual neurons mediate.
摘要
  1. 运用形态学与电生理学相结合的技术,我们在加州海兔的右侧胸膜神经节中识别出了有助于从乳白色腺释放乳白色物质的运动神经元。2. 发现三个胸膜神经节神经元符合被认定为乳白色腺运动神经元的要求,具体依据如下:a) 其轴突延伸至支配该腺体的P5神经;b) 在中枢突触活动缺失的情况下能使腺体产生收缩;c) 在构成乳白色腺自身的细胞中能产生兴奋性突触后电位(EJP)。这些神经元能够被可靠定位,已被命名为PLR1、PLR2和PLR3。3. 当通过管腔内压力变化来测量腺体收缩时,腺体反应是运动神经元低频锋电位活动的分级函数。4. 从乳白色腺细胞记录到的推测性EJP,在细胞外高镁离子环境下其大小可逆性减小,而提高细胞外钙离子浓度时其大小可逆性增加。这些结果表明推测性EJP是化学介导的。推测性EJP表现出易化和强直后增强。5. 已识别出的乳白色运动神经元可能通过P5神经构成了输入到乳白色腺的运动输入的重要部分,因为这些细胞的超极化会阻止体外右侧连接刺激所引发的乳白色腺反应。6. 我们已将乳白色运动神经元的特性与先前识别出的墨汁运动神经元的特性进行了比较(参考文献6 - 9、19)。与墨汁运动神经元一样,乳白色运动神经元具有高静息电位,存在电耦合,且无自发锋电位活动。它们还会接受缓慢且持久的诱发去极化突触输入,这似乎是由电导降低机制介导的。由突触输入产生的乳白色运动神经元的放电模式显示出与先前描述的墨汁运动神经元相同的延迟爆发模式。7. 已证明墨汁运动神经元的生物物理特性和突触输入会影响喷墨行为的特征(参考文献4、6 - 9、19)。乳白色运动神经元具有其中一些生物物理特征,并介导一种类似于喷墨释放的防御行为。对这些行为及其潜在神经回路的进一步比较,可能会更好地理解细胞生物物理特性和突触输入模式在多大程度上影响单个神经元所介导行为的特征。

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