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小龙虾逃避行为:无巨纤维活动时的尾部翻转产生

Crayfish escape behavior: production of tailflips without giant fiber activity.

作者信息

Kramer A P, Krasne F B

出版信息

J Neurophysiol. 1984 Aug;52(2):189-211. doi: 10.1152/jn.1984.52.2.189.

Abstract

The giant interneurons of the crayfish nerve cord are well-known mediators of fast tail flexions, "tailflips," that propel animals through the water away from danger. More recent studies have revealed an additional nongiant generator of tailflips. In contrast to giant tailflips, which are stereotyped, nongiant tailflips have variable form. The operating principles and portions of the neural circuitry governing nongiant tailflips were here investigated. Whereas fast flexor motor neurons (FFs) receive excitatory postsynaptic potentials (EPSPs) with large unitary components just prior to giant tailflips, excitation of the FFs during nongiant tailflips is due to summation of many small EPSPs, and these build up for about 60 ms prior to the tailflip; we call the period of excitation prior to FF firing the preflexion phase and the period during which FFs fire, the flexion phase of the tailflip. Even FFs that will not fire during a given tailflip become depolarized during preflexion and flexion periods. Throughout the preflexion and flexion periods there is activity in dorsal nerve cord axons (DCAs) that lie below the giants. Many DCAs are interneurons that excite FFs at short latency. Some DCAs fire uniquely during the preflexion phase, while some fire only during the flexion phase. Which DCAs fire is highly variable, and in some cases firing of particular DCAs can be correlated with particular forms of tailflips. Two identified DCAs, 12 and 13, that fire during the flexion phase were studied. These interneurons originate and receive their synaptic input in the second and third abdominal ganglia, respectively, and project to the last ganglion exciting FFs caudal to their ganglion of origin en route. Their pattern of synaptic input prior to and during nongiant tailflips is indistinguishable from that of FFs. Their input to FFs is weak, but when they fire they tend to promote intersegmental synchrony of FFs in the segments they feed. It appears likely to us that nongiant tailflips are synthesized from a small library of component tailflip movements that can be combined to produce a variety of complete tailflips and that the component movements are produced by a limited group of premotor interneurons, of which 12 and 13 are members.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

小龙虾神经索中的巨型中间神经元是快速尾部弯曲(即“尾翻”)的著名介导者,尾翻可推动动物在水中远离危险。最近的研究揭示了另一种非巨型的尾翻发生器。与刻板的巨型尾翻不同,非巨型尾翻的形式多变。本文研究了控制非巨型尾翻的神经回路的工作原理和部分情况。在巨型尾翻之前,快速屈肌运动神经元(FFs)会接收到具有大的单一成分的兴奋性突触后电位(EPSPs),而在非巨型尾翻期间,FFs的兴奋是由于许多小EPSPs的总和,并且这些EPSPs在尾翻前约60毫秒逐渐增强;我们将FFs放电前的兴奋期称为预弯曲阶段,将FFs放电的时期称为尾翻的弯曲阶段。即使在给定的尾翻中不会放电的FFs在预弯曲和弯曲期间也会发生去极化。在整个预弯曲和弯曲期间,位于巨型神经元下方的背侧神经索轴突(DCAs)都有活动。许多DCA是中间神经元,它们能在短潜伏期内兴奋FFs。一些DCA仅在预弯曲阶段放电,而一些仅在弯曲阶段放电。哪些DCA放电具有高度变异性,在某些情况下,特定DCA的放电可与特定形式的尾翻相关。研究了两个在弯曲阶段放电的已鉴定DCA,即12和13。这些中间神经元分别在第二和第三腹神经节起源并接收突触输入,并投射到最后一个神经节,在途中兴奋其起源神经节尾侧的FFs。它们在非巨型尾翻之前和期间的突触输入模式与FFs无法区分。它们对FFs的输入较弱,但当它们放电时,往往会促进它们所支配节段中FFs的节间同步。在我们看来,非巨型尾翻可能是由一小套组成尾翻运动组合而成,这些组合运动可以产生各种完整的尾翻,并且组成运动是由一组有限的运动前中间神经元产生的,其中12和13是成员。(摘要截断于400字)

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