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海兔巨细胞中的异突触易化作用。

Heterosynaptic facilitation in the giant cell of Aplysia.

作者信息

Shimahara T, Tauc L

出版信息

J Physiol. 1975 May;247(2):321-41. doi: 10.1113/jphysiol.1975.sp010934.

Abstract
  1. Heterosynaptic facilitation, defined as an increase of the efficacy of synaptic transmission between a test interneurone and a post-synaptic neurone, produced by the stimulation of a separate pathway, was studied in the left pleural ganglion. The experimental procedure consisted of detecting the effects of a brief tetanus, applied to tentacular and tegumentary nerves, on the amplitude of monosynaptic and unitary post-synaptic potentials (p.s.p.s) recorded in the left giant cell and generated by stimulating the test interneurone every 10 sec. The membrane potential of the test interneurone was simultaneously recorded. 2. Following heterosynaptic stimulation, the amplitude of the test p.s.p. increased, after a delay of about 30 sec, up to 250% of its original size; this increase subsided after 2-3 min or more. 3. Only the interneurones producing in the giant cell the e.i.p.s.p. (excitatory-inhibitory post-synaptic potential) were affected by hetero-synaptic facilitation. Other interneuronal types showed no changes in their synaptic transmission on the giant cell after heterosynaptic stimulation. 4. Heterosynaptic stimulation did not produce either orthodromic or antidromic spikes in the test interneurones clearly indicating that facilitation of test p.s.p. did not result from increased spike activity in the test interneurone. 5. Often heterosynaptic facilitation of the test p.s.p. was observed due to spontaneous activity in the heterosynaptic pathway, demonstrating the normal occurrence of the phenomenon. 6. Iontophoretic injection of 5-HT at critical, presumably synaptic, sites in the neuropil, evoked a facilitation of the test p.s.p. similar to heterosynaptic facilitation. Only the e.i.p.s.p.s. were so affected by 5-HT. On the contrary, other p.s.p. types were depressed by 5-HT as a result of conductance changes in the left giant cells. 7. Both heterosynaptic facilitation and 5-HT facilitation were suppressed by the presence in the bath of 5-HT (10(-5) M) and of LSD-25 (3 X 10(-4) M). The action of injected 5-HT on the membrane conductance of the left giant cell was also depressed in the pressence of 5-HT in the bath, but was unaffected by LSD-25 (3 X 10(-4) M). 8. From the parallelism of properties of heterosynaptic and 5-HT facilitation, it is suggested that 5-HT is the probable transmitter mediating heterosynaptic facilitation. It seems likely that 5HT is released from the heterosynaptic pathway at the level of the synaptic ending of the test interneurone on to the giant cell and that it increases the efficacy of this synapse, probably acting on the quantity of synaptic transmitter liberated.
摘要
  1. 异突触易化作用被定义为通过刺激一条独立通路,使测试中间神经元与突触后神经元之间突触传递的效能增强,该作用在左侧胸膜神经节中进行了研究。实验过程包括检测施加于触手和体表神经的短暂强直刺激,对每10秒刺激一次测试中间神经元时,在左侧巨细胞中记录到的单突触和单位突触后电位(p.s.p.s)幅度的影响。同时记录测试中间神经元的膜电位。2. 异突触刺激后,测试p.s.p.的幅度在大约30秒的延迟后增加,达到其原始大小的250%;这种增加在2 - 3分钟或更长时间后消退。3. 只有那些在巨细胞中产生兴奋性 - 抑制性突触后电位(e.i.p.s.p.)的中间神经元受到异突触易化作用的影响。其他类型的中间神经元在异突触刺激后,其在巨细胞上的突触传递没有变化。4. 异突触刺激在测试中间神经元中未产生顺向或逆向动作电位,这清楚地表明测试p.s.p.的易化并非由测试中间神经元中动作电位活动增加所致。5. 由于异突触通路中的自发活动,经常观察到测试p.s.p.的异突触易化作用,这证明了该现象的正常发生。6. 在神经纤维网中关键的、推测为突触的部位进行5 - 羟色胺(5 - HT)的离子电泳注射,可诱发与异突触易化作用相似的测试p.s.p.易化。只有e.i.p.s.p.s受到5 - HT的这种影响。相反,由于左侧巨细胞中的电导变化,其他类型的p.s.p.受到5 - HT的抑制。7. 浴槽中存在5 - HT(10^(-5) M)和麦角酰二乙胺(LSD - 25,3×10^(-4) M)时,异突触易化作用和5 - HT易化作用均被抑制。浴槽中存在5 - HT时,注射的5 - HT对左侧巨细胞膜电导的作用也受到抑制,但不受LSD - 25(3×10^(-4) M)的影响。8. 从异突触易化作用和5 - HT易化作用特性的相似性来看,推测5 - HT可能是介导异突触易化作用的递质。5 - HT似乎是从异突触通路在测试中间神经元到巨细胞的突触末梢水平释放的,并且它可能通过作用于释放的突触递质数量来增加该突触的效能。

相似文献

1
Heterosynaptic facilitation in the giant cell of Aplysia.海兔巨细胞中的异突触易化作用。
J Physiol. 1975 May;247(2):321-41. doi: 10.1113/jphysiol.1975.sp010934.

本文引用的文献

4
Habituation at the synaptic level in Aplysia.海兔突触水平的习惯化。
Nature. 1966 Apr 2;210(5031):37-9. doi: 10.1038/210037a0.
6
Presynaptic inhibition in the abdominal ganglion of Aplysia.海兔腹神经节中的突触前抑制。
J Physiol. 1965 Nov;181(2):282-307. doi: 10.1113/jphysiol.1965.sp007761.

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