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在离体脊髓标本中镁离子对兴奋性氨基酸诱导的去极化的选择性抑制作用

Selective depression of excitatory amino acid induced depolarizations by magnesium ions in isolated spinal cord preparations.

作者信息

Ault B, Evans R H, Francis A A, Oakes D J, Watkins J C

出版信息

J Physiol. 1980 Oct;307:413-28. doi: 10.1113/jphysiol.1980.sp013443.

Abstract
  1. The depressant actions of Mg2+ and a range of other divalent ions on synaptic excitation and on responses produced by excitatory amino acids and other putative transmitters have been investigated in hemisected isolated spinal cords of frogs and neonatal rats. Some comparative studies were also made using the rat isolated superior cervical ganglion. 2. At concentrations above 10 microM, Mg2+ selectively antagonized N-methyl-D-aspartate (NMDA)-induced motoneurone depolarization as recorded from ventral roots of tetrodotoxin-blocked spinal cords. Depolarization evoked by quisqualate (unaffected by 20 mM-Mg2+) was resistant to the depressant action of these ions, while depolarizations evoked by other excitant amino acids were depressed to intermediate degrees. 3. Mn2+, Co2+ and Ni2+ had qualitatively similar actions to Mg2+; Mn2+ was somewhat less potent and Co2+ and Ni2+ more potent than Mg2+. The alkaline earth metal ions, Ca2+, Sr2+ and Ba2+, had very weak Mg2+-like actions. Ca2+ and Mg2+ acted additively in depressing amino acid-induced responses. 4. Mg2+ also depressed motoneurone responses evoked by noradrenaline, substance P and carbachol in the neonatal rat isolated spinal cord. However, none of these effects were as marked as the depression of NMDA-induced responses by Mg2+ in this preparation. Mg2+ did not depress motoneurone depolarization produced by 5-HT in the rat spinal cord or the depolarizing action of GABA on primary afferent terminals of the isolated frog spinal cord. 5. At concentrations producing marked depression of NMDA-induced responses, Mg2+ also depressed synaptic transmission in spinal cords in the absence of an effect on ganglionic transmission. At the same concentrations, Mn2+, Co2+ and Ni2+ depressed synaptic transmission in both preparations. 6. From the similarity in action between Mg2+ and the D-alpha-aminoadipate group of NMDA antagonists, it is suggested that the central depressant action of low concentrations of Mg2+ involves predominantly a postsynaptically mediated interference with the action of an excitatory amino acid transmitter.
摘要
  1. 研究了Mg2+及一系列其他二价离子对青蛙和新生大鼠半切离体脊髓突触兴奋以及由兴奋性氨基酸和其他假定递质产生的反应的抑制作用。还使用大鼠离体颈上神经节进行了一些比较研究。2. 在浓度高于10 microM时,Mg2+选择性拮抗N-甲基-D-天冬氨酸(NMDA)诱导的运动神经元去极化,这是从河豚毒素阻断脊髓的腹根记录到的。quisqualate诱发的去极化(不受20 mM-Mg2+影响)对这些离子的抑制作用有抗性,而其他兴奋性氨基酸诱发的去极化则受到中等程度的抑制。3. Mn2+、Co2+和Ni2+的作用在性质上与Mg2+相似;Mn2+的效力稍低,Co2+和Ni2+比Mg2+更有效。碱土金属离子Ca2+、Sr2+和Ba2+具有非常微弱的类似Mg2+的作用。Ca2+和Mg2+在抑制氨基酸诱导的反应中起相加作用。4. Mg2+也抑制新生大鼠离体脊髓中去甲肾上腺素、P物质和卡巴胆碱诱发的运动神经元反应。然而,在该制剂中,这些作用均不如Mg2+对NMDA诱导反应的抑制作用明显。Mg2+不抑制大鼠脊髓中5-HT产生的运动神经元去极化或GABA对离体青蛙脊髓初级传入终末的去极化作用。5. 在产生对NMDA诱导反应明显抑制的浓度下,Mg2+在不影响神经节传递的情况下也抑制脊髓中的突触传递。在相同浓度下,Mn2+、Co2+和Ni2+在两种制剂中均抑制突触传递。6. 从Mg2+与NMDA拮抗剂的D-α-氨基己二酸基团作用的相似性来看,提示低浓度Mg2+的中枢抑制作用主要涉及对兴奋性氨基酸递质作用的突触后介导干扰。

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