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内毒素会改变青蛙神经肌肉接头处的自发递质释放。

Endotoxin alters spontaneous transmitter release at the frog neuromuscular junction.

作者信息

Person R J

出版信息

J Neurosci Res. 1977;3(1):63-72. doi: 10.1002/jnr.490030107.

Abstract

The direct neurotoxic effects of E. coli endotoxin (ETX) on spontaneous transmitter release were tested at the frog sartorius muscle neuromuscular junction. Spontaneous transmitter release was monitored by intracellularly recording miniature end-plate potentials (MEPPs). Junctions were continuously exposed to standard concentrations of 10 microgram/ml of 3 ETX samples, 2 of which produced a significant elevation of MEPP frequency followed by a decline of frequency to very low rates. The third ETX sample, known to have a decreased canine lethality, was without effect on MEPP frequency. No significant changes in MEPP amplitude were evident. The rate of change in MEPP frequency, but not the peak frequency, was reduced by lowering ETX concentrations. Alterations in MEPP frequency induced by ETX were prevented by removing Ca++ and antagonized by high [K+]out. The results suggest that ETX alters ion conductance channels, particularly those for Ca++, in the presynaptic terminal membrane.

摘要

在青蛙缝匠肌神经肌肉接头处测试了大肠杆菌内毒素(ETX)对自发递质释放的直接神经毒性作用。通过细胞内记录微小终板电位(MEPPs)来监测自发递质释放。将接头连续暴露于3个ETX样品的标准浓度10微克/毫升中,其中2个样品使MEPP频率显著升高,随后频率下降至极低水平。已知第三个ETX样品对犬的致死率降低,对MEPP频率无影响。MEPP振幅无明显显著变化。降低ETX浓度可降低MEPP频率的变化率,但不影响峰值频率。去除Ca++可防止ETX诱导的MEPP频率改变,高细胞外[K+]可拮抗这种改变。结果表明,ETX改变了突触前终板膜中的离子电导通道,尤其是Ca++通道。

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