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镉对青蛙运动神经末梢量子递质释放及超微结构的影响。

Effects of cadmium on quantal transmitter release and ultrastructure of frog motor nerve endings.

作者信息

Molgó J, Pécot-Dechavassine M, Thesleff S

机构信息

Laboratoire de Neurobiologie Cellulaire et Moléculaire du C.N.R.S., Gif sur Yvette, France.

出版信息

J Neural Transm. 1989;77(2-3):79-91. doi: 10.1007/BF01248924.

Abstract

Exposure of frog cutaneous pectoris nerve-muscle preparations to cadmium (0.1-1 mM) results in an increase in miniature end-plate potential (m.e.p.p.) frequency. The increase is dependent on the concentration, the time of exposure and the co-presence of other divalent cations in the extracellular fluid. The stimulatory effect of cadmium is most marked in a calcium-free medium. Increased levels of calcium (4-10 mM) or of magnesium (10 mM) reduce the stimulatory effect suggesting that those cations interfere with the entry of cadmium into nerve endings. Once the effect of cadmium on m.e.p.p. frequency is attained, washing with a cadmium-free solution fails to abolish its effect. The action of cadmium on m.e.p.p. frequency slowly declines towards zero after about 3 hrs. An ultrastructural study of nerve terminals exposed for one hr to 1 mM cadmium reveals that neither in calcium-containing nor in a nominally calcium-free medium are there any significant changes in the number of synaptic vesicles as compared to controls. However, after 3 hrs of cadmium action in a calcium-free medium there is about 65% depletion of synaptic vesicles, while in calcium-containing media there is only about 25% depletion. The results suggest that cadmium by itself can support transmitter release but not synaptic vesicle recycling which instead might depend upon calcium.

摘要

将青蛙胸皮神经 - 肌肉标本暴露于镉(0.1 - 1 mM)会导致微小终板电位(m.e.p.p.)频率增加。这种增加取决于镉的浓度、暴露时间以及细胞外液中其他二价阳离子的共存情况。镉的刺激作用在无钙培养基中最为明显。钙(4 - 10 mM)或镁(10 mM)水平的升高会降低这种刺激作用,这表明这些阳离子会干扰镉进入神经末梢。一旦镉对m.e.p.p.频率产生作用,用无镉溶液冲洗并不能消除其影响。镉对m.e.p.p.频率的作用在约3小时后会缓慢降至零。对暴露于1 mM镉一小时的神经末梢进行超微结构研究发现,与对照组相比,无论是在含钙培养基还是名义上无钙的培养基中,突触小泡的数量都没有显著变化。然而,在无钙培养基中镉作用3小时后,突触小泡约有65%耗尽,而在含钙培养基中只有约25%耗尽。结果表明,镉本身可以支持递质释放,但不能支持突触小泡的再循环,而突触小泡的再循环可能依赖于钙。

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