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离体蛙脊髓中惊厥剂的研究。II. 对根电位的影响。

Studies on convulsants in the isolated frog spinal cord. II. Effects on root potentials.

作者信息

Barker J L, Nicoll R A, Padjen A

出版信息

J Physiol. 1975 Mar;245(3):537-48. doi: 10.1113/jphysiol.1975.sp010860.

Abstract
  1. In the isolated frog spinal cord picrotoxin, bicuculline, and strychnine were evaluated for their effects on synaptically induced root potentials recorded by the sucrose gap technique. 2. Picrotoxin (greater than 10- minus 4 M) completely blocked the dorsal root potential (DRP) elicited by stimulating the ventral root of the same segment (VR-DRP). Although picrotoxin antagonized the DRP elicited by stimulation of either an adjacent dorsal root (DR-DRP) or the lateral column (LC-DRP), a slower component to these potentials appeared and increased in size as the concentration of picrotoxin was increased. Thus picrotoxin brings out a later, picrotoxin resistant component to the DR-DRP and LC-DRP. 3. Strychnine (10- minus 8-10- minus 5 M) reduced and abolished the VR-DRP without prolongation and progressively increased and prolonged the DR-DRP (and LC-DRP) and the DR-VRP. Strychnine in higher concentrations (greater than 10- minus 4 M) also reduced the amplitude and prolonged the duration of the compound action potential of afferent fibres. 4. These results combined with those presented in the preceding paper (Barker, Nicoll & Padjen, 1975) suggest that (1) a GABA-like transmitter mediates the final step in the DR-DRP and LC-DRP pathways and that (2) either taurine or beta-alanine may mediate the last step in the VR-DRP pathway.
摘要
  1. 在离体青蛙脊髓中,对印防己毒素、荷包牡丹碱和士的宁进行了评估,以观察它们对采用蔗糖间隙技术记录的突触诱导根电位的影响。2. 印防己毒素(大于10的负4次方摩尔)完全阻断了刺激同一节段腹根(VR-DRP)所引发的背根电位(DRP)。尽管印防己毒素拮抗了刺激相邻背根(DR-DRP)或外侧柱(LC-DRP)所引发的DRP,但随着印防己毒素浓度的增加,这些电位出现了一个较慢的成分,且其大小增加。因此,印防己毒素使DR-DRP和LC-DRP出现了一个较晚的、对印防己毒素有抗性的成分。3. 士的宁(10的负8次方至10的负5次方摩尔)降低并消除了VR-DRP,且无延长现象,并逐渐增加并延长了DR-DRP(和LC-DRP)以及DR-VRP。更高浓度(大于10的负4次方摩尔)的士的宁也降低了传入纤维复合动作电位的幅度并延长了其持续时间。4. 这些结果与前文(Barker、Nicoll和Padjen,1975年)所呈现的结果相结合,表明:(1)一种类似GABA的递质介导了DR-DRP和LC-DRP通路的最后一步;(2)牛磺酸或β-丙氨酸可能介导了VR-DRP通路的最后一步。

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本文引用的文献

1
Strychnine- and pentylenetetrazol-induced changes of excitability in aplysia neurons.
Science. 1973 Mar 16;179(4078):1133-6. doi: 10.1126/science.179.4078.1133.
2
Action of some drugs on the dorsal root potentials of the isolated toad spinal cord.
Br J Pharmacol Chemother. 1961 Oct;17(2):224-31. doi: 10.1111/j.1476-5381.1961.tb01282.x.
3
PHARMACOLOGICAL STUDIES ON PRESYNAPTIC INHIBITION.
J Physiol. 1963 Oct;168(3):500-30. doi: 10.1113/jphysiol.1963.sp007205.
4
PHARMACOLOGICAL STUDIES ON THE PRIMARY AFFERENT DEPOLARIZATION OF THE TOAD SPINAL CORD.
Pflugers Arch Gesamte Physiol Menschen Tiere. 1963 Jul 2;277:325-46. doi: 10.1007/BF00362515.
5
The action of strychnine at cholinergic junctions.
Arch Int Pharmacodyn Ther. 1961 Apr 1;131:123-50.
6
On the effects of strychnine upon the myelinated nerve fibres of toads.
Jpn J Physiol. 1956 Jun 15;6(2):175-89. doi: 10.2170/jjphysiol.6.175.
7
Effects of strychnine with special reference to spinal afferent fibres.
Epilepsia. 1955 Nov;4:29-40. doi: 10.1111/j.1528-1157.1955.tb03171.x.
8
Biophysics of junctional transmission.
Physiol Rev. 1954 Oct;34(4):674-710. doi: 10.1152/physrev.1954.34.4.674.
9
The effect of strychnine on the neuro-muscular junction of the rat.
Life Sci. 1967 Dec 1;6(23):2515-7. doi: 10.1016/0024-3205(67)90315-3.
10
A study of the interaction between motoneurones in the frog spinal cord.
J Physiol. 1966 Feb;182(3):612-48. doi: 10.1113/jphysiol.1966.sp007841.

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