Manalis R S, Cooper G P, Pomeroy S L
Brain Res. 1984 Feb 27;294(1):95-109. doi: 10.1016/0006-8993(84)91313-1.
The acute effects of Pb2+ on synaptic transmission at the frog neuromuscular junction were measured using conventional microelectrode techniques. Experiments were performed on preparations bathed in high magnesium/low calcium Ringer solution in order to record subthreshold endplate potentials (EPPs). The effects of Pb2+ on the muscle membrane and postsynaptic membrane were minimal since relatively high doses of Pb2+ caused no significant change in the input resistance of the muscle fiber and in the amplitude of the acetylcholine (ACh) iontophoteric potential when the ACh micropipette was highly localized. However, when the ACh micropipette was moved away from the receptors, the resulting ACh potential was reduced significantly by Pb2+. Pb2+ is a potent blocker of the EPP. Extracellular recordings from motor nerve terminals showed that endplate currents (EPCs) were reduced by Pb2+ while the nerve terminal potentials were unaffected. Therefore, Pb2+ blocks evoked transmitter release at a step following the depolarization of the nerve terminal. The blocking effect on the EPP was overcome when [Ca2+]o was raised. The log-log relationship between [Ca2+]o (abscissa) and EPP amplitude was shifted to the right in the presence of 1 microM Pb2+; the mean +/- S.E. slopes were 4.16 +/- 0.12 (control) and 4.05 +/- 0.13 (Pb2+). Reciprocal plots relating [Ca2+]o-1 to (EPP)-1/5 confirmed that Pb2+ competitively antagonized the action of Ca2+. The dissociation constant between Pb2+ and the Ca2+ receptor site was found to be 0.99 microM. Pb2+ is about 3 X 10(3) times more potent than is Mg2+, about 150 times more potent than is either Mn2+ or Co2+, and about 3 times more potent than Cd2+ is in blocking evoked release of ACh. After Pb2+ decreased the EPP, the MEPP frequency began to increase; this was probably the result of intracellular Pb2+ disrupting the Ca2+ sequestering activity of mitochondria and/or other intraterminal organelles. [Ca2+]i was thereby increased and an increase in MEPP frequency followed. Decreased MEPP amplitudes were observed when the MEPP frequency had been increased by Pb2+. Pb2+ may affect most chemical synapses in a manner which is similar to its effects on the neuromuscular junction and that this may be one of its important neurotoxic effects.
采用传统微电极技术测定了Pb2+对青蛙神经肌肉接头处突触传递的急性效应。实验在浸泡于高镁/低钙任氏液的标本上进行,以记录阈下终板电位(EPP)。Pb2+对肌膜和突触后膜的影响极小,因为当乙酰胆碱(ACh)微电极高度定位时,相对高剂量的Pb2+并未引起肌纤维输入电阻和ACh离子电泳电位幅度的显著变化。然而,当ACh微电极远离受体时,所产生的ACh电位会被Pb2+显著降低。Pb2+是EPP的强效阻断剂。运动神经末梢的细胞外记录显示,终板电流(EPC)被Pb2+降低,而神经末梢电位未受影响。因此,Pb2+在神经末梢去极化后的一个步骤中阻断诱发的递质释放。当细胞外[Ca2+]升高时,对EPP的阻断作用被克服。在存在1 microM Pb2+的情况下,细胞外[Ca2+](横坐标)与EPP幅度之间的对数-对数关系向右移动;平均±标准误斜率分别为4.16±0.12(对照)和4.05±0.13(Pb2+)。将[Ca2+]o-1与(EPP)-1/5相关的倒数图证实,Pb2+竞争性拮抗Ca2+的作用。发现Pb2+与Ca2+受体位点之间的解离常数为0.99 microM。在阻断ACh的诱发释放方面,Pb2+的效力比Mg2+高约3×10(3)倍,比Mn2+或Co2+高约150倍,比Cd2+高约3倍。在Pb2+降低EPP后,微小终板电位(MEPP)频率开始增加;这可能是细胞内Pb2+破坏线粒体和/或其他末梢内细胞器的Ca2+螯合活性的结果。由此细胞内[Ca]增加,随后MEPP频率增加。当MEPP频率因Pb2+而增加时,观察到MEPP幅度降低。Pb2+可能以与其对神经肌肉接头的影响类似的方式影响大多数化学突触,这可能是其重要的神经毒性作用之一。