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多刺龙虾离体口胃神经节中胃节律产生的机制:爆发性起搏电位、突触相互作用和毒蕈碱调节

Mechanisms of gastric rhythm generation in the isolated stomatogastric ganglion of spiny lobsters: bursting pacemaker potentials, synaptic interactions, and muscarinic modulation.

作者信息

Elson R C, Selverston A I

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093-0322.

出版信息

J Neurophysiol. 1992 Sep;68(3):890-907. doi: 10.1152/jn.1992.68.3.890.

Abstract
  1. The gastric central pattern generator (CPG), located in the stomatogastric ganglion (STG) of the spiny lobster (Panulirus interruptus), is nonrhythmic when deprived of neuromodulatory inputs from anterior ganglia. Leaving these inputs intact in vitro can sustain a gastric rhythm but also introduces numerous, uncontrolled and largely unknown modulatory and synaptic influences that greatly complicate analysis of this CPG. 2. Here we induced gastric rhythms in the isolated STG, by superfusing a specific modulator, the muscarinic agonist, pilocarpine. Muscarinic agents sustain vigorous gastric rhythms in the isolated STG. Our aim was to analyze the pattern-generating functions of the restricted gastric circuit, free of complicating influences from other ganglia, and under specific (muscarinic) modulation. 3. We used combinations of multiple cell hyperpolarizations, photodeletions, and synaptic blockade by picrotoxin to assess the pattern-generating role of individual gastric neurons and to study the activity of subcircuits. 4. Four identified gastric neurons [lateral gastric (LG), dorsal gastric (DG), 2 electrically coupled lateral posterior gastric (2LPGs)] acted as pattern-generating cells. They showed bursting pacemaker potentials (BPPs), i.e., plateau (or driver) potentials that underlay bursts of axonal spikes and slow, interburst depolarizing potentials that underlay repetitive burst activity. LG and DG, at least, became conditional bursters, able to burst repetitively because of intrinsic oscillations. The other gastric neurons behaved mainly as follower cells and derived their rhythmic bursting from synaptic coupling to the pattern-generator cells and from their own intrinsic (but nonoscillatory) properties. 5. The pattern-generating neurons form a novel "kernel" circuit that works by the cooperative interaction of cellular properties and synaptic connectivity. 6. This study constitutes the first complete and fully consistent analysis of pattern generation in the gastric network of the isolated STG. These mechanisms pertain to muscarinic rhythms in particular but also, we suggest, to gastric rhythm generation and CPG function in general. We suggest that 1) rhythmicity normally depends on the induction of bursty membrane properties in at least some component neurons; 2) different subcircuits can produce rhythmic patterns and may be activated by different modulators; and 3) the gastric network shares several important "building blocks" with CPGs that have been analyzed in other systems. 7. Muscarinic inputs are implicated as an important gastric regulator. We compare these responses with the reported modulatory actions of the anterior pyloric modulator (AMP), an identified, putatively cholinergic input interneuron that may act via muscarinic mechanisms.
摘要
  1. 位于多刺龙虾(Panulirus interruptus)口胃神经节(STG)中的胃中枢模式发生器(CPG),在缺乏来自前神经节的神经调节输入时是无节律的。在体外保持这些输入完整可以维持胃节律,但也会引入许多不受控制且很大程度上未知的调节和突触影响,这使得对该CPG的分析变得极为复杂。2. 在这里,我们通过灌注一种特定的调节剂——毒蕈碱激动剂毛果芸香碱,在分离的STG中诱导胃节律。毒蕈碱剂在分离的STG中维持强烈的胃节律。我们的目的是分析受限胃回路的模式生成功能,不受来自其他神经节的复杂影响,并处于特定(毒蕈碱)调节之下。3. 我们使用了多种细胞超极化、光缺失和用苦味毒进行突触阻断的组合,以评估单个胃神经元的模式生成作用并研究子回路的活动。4. 四个已识别的胃神经元[外侧胃(LG)、背侧胃(DG)、两个电耦合的外侧后胃(2LPG)]充当模式生成细胞。它们表现出爆发性起搏电位(BPPs),即构成轴突峰电位爆发基础的平台(或驱动)电位,以及构成重复爆发活动基础的缓慢的爆发间期去极化电位。至少LG和DG成为条件性爆发神经元,能够由于内在振荡而重复爆发。其他胃神经元主要表现为跟随细胞,其节律性爆发源于与模式生成细胞的突触耦合以及它们自身的内在(但非振荡)特性。5. 模式生成神经元形成了一个新颖的“核心”回路,该回路通过细胞特性和突触连接性的协同相互作用来工作。6. 这项研究构成了对分离的STG胃网络中模式生成的首次完整且完全一致的分析。这些机制尤其适用于毒蕈碱节律,但我们认为,一般也适用于胃节律生成和CPG功能。我们认为:1)节律性通常取决于至少一些组成神经元中爆发性膜特性的诱导;2)不同的子回路可以产生节律模式,并且可能由不同的调节剂激活;3)胃网络与其他系统中已分析的CPG共享几个重要的“构建模块”。7. 毒蕈碱输入被认为是一种重要的胃调节剂。我们将这些反应与已报道的前幽门调节剂(AMP)的调节作用进行比较,AMP是一种已识别的、推测为胆碱能输入的中间神经元,可能通过毒蕈碱机制起作用。

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