Literature DB >> 2445965

The action of excitatory amino acids on chick spinal cord neurones in culture.

V Vlachová1, L Vyklický, L Vyklický, F Vyskocil.   

Abstract

1. Membrane currents evoked by N-methyl-D-aspartate (NMDA), L-aspartate, L-glutamate, quisqualate and kainate were studied in cultured neurones from the embryonic chick spinal cord by the patch-clamp technique and by employing a quasi-step microperfusion technique. 2. Application of NMDA, aspartate, glutamate and quisqualate induced currents which exhibited an initial peak which declined to a plateau level with a time constant of 2 s and then remained constant or slowly decreased. The discontinuation of the application was followed by an after-current. The individual components of the responses were insensitive to TTX (2 X 10(-6) M) and were present in neurones which did not exhibit any sign of synaptic activity. The responses induced by kainate were monophasic and declined slowly during long-lasting application. 3. The responses induced by NMDA, aspartate and glutamate were voltage dependent, while those induced by kainate were linear between -80 and +80 mV. The equilibrium potential for all components of the responses to all excitatory amino acids was close to zero. 4. From dose-response curves the half-maximum effective dose (ED50) for glutamate and kainate was 3 X 10(-5) and 2 X 10(-4) M respectively. The Hill coefficients for the glutamate and the kainate were calculated to be 1.8 +/- 0.1 (n = 4) and 1.9 +/- 0.5 (n = 4) respectively. Thus two molecules may be interacting with each of the receptor-activated ion channels. 5. Interaction between kainate and quisqualate or kainate and NMDA was studied at both negative and positive holding potentials. No summation of the responses was found when kainate at concentrations close to those required for evoking the maximum response was applied simultaneously with quisqualate or NMDA. On the contrary, a diminution of the membrane currents was observed. A marked decrease in membrane currents was also observed when glutamate (10(-4) M) was applied simultaneously with aspartate (10(-4) M). 6. Glutamate-activated single-channel currents were recorded in the cell-attached configuration with electrodes filled with glutamate (20 microM) in five neurones and a conductance approximately 50 pS was found. 7. It is suggested that differences in the potency of the different excitatory amino acids as open-channel blockers may be one of the mechanisms which contribute to the diversity in the action of excitatory amino acids and that at least some of the effects of NMDA, aspartate, glutamate, quisqualate and kainate may be mediated by a common receptor-channel complex.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2445965      PMCID: PMC1192470          DOI: 10.1113/jphysiol.1987.sp016542

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  30 in total

1.  Ion channel block by acetylcholine, carbachol and suberyldicholine at the frog neuromuscular junction.

Authors:  D C Ogden; D Colquhoun
Journal:  Proc R Soc Lond B Biol Sci       Date:  1985-09-23

Review 2.  Excitatory amino acid transmitters.

Authors:  J C Watkins; R H Evans
Journal:  Annu Rev Pharmacol Toxicol       Date:  1981       Impact factor: 13.820

Review 3.  S-Glutamate: its interactions with spinal neurons.

Authors:  E Puil
Journal:  Brain Res       Date:  1981-12       Impact factor: 3.252

4.  An analysis of the dose-response relationship at voltage-clamped frog neuromuscular junctions.

Authors:  V E Dionne; J H Steinbach; C F Stevens
Journal:  J Physiol       Date:  1978-08       Impact factor: 5.182

5.  Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.

Authors:  O P Hamill; A Marty; E Neher; B Sakmann; F J Sigworth
Journal:  Pflugers Arch       Date:  1981-08       Impact factor: 3.657

6.  A receptor for protons in the nerve cell membrane.

Authors:  O A Krishtal; V I Pidoplichko
Journal:  Neuroscience       Date:  1980       Impact factor: 3.590

7.  Drug blockade of open end-plate channels.

Authors:  P R Adams
Journal:  J Physiol       Date:  1976-09       Impact factor: 5.182

8.  L-Aspartic acid induces a region of negative slope conductance in the current-voltage relationship of cultured spinal cord neurons.

Authors:  J F MacDonald; A V Porietis; J M Wojtowicz
Journal:  Brain Res       Date:  1982-04-08       Impact factor: 3.252

9.  Life time and elementary conductance of the channels mediating the excitatory effects of acetylcholine in Aplysia neurones.

Authors:  P Ascher; A Marty; T O Neild
Journal:  J Physiol       Date:  1978-05       Impact factor: 5.182

10.  Ion channels activated by L-glutamate and GABA in cultured cerebellar neurons of the rat.

Authors:  S G Cull-Candy; D C Ogden
Journal:  Proc R Soc Lond B Biol Sci       Date:  1985-05-22
View more
  10 in total

1.  Fading and rebound of currents induced by ATP in PC12 cells.

Authors:  R Giniatullin; L Khiroug; M Talantova; A Nistri
Journal:  Br J Pharmacol       Date:  1996-11       Impact factor: 8.739

2.  N-methyl-D-aspartate activates different channels than do kainate and quisqualate.

Authors:  J Lerma; L Kushner; R S Zukin; M V Bennett
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

3.  Rapid desensitization of glutamate receptors in vertebrate central neurons.

Authors:  L O Trussell; L L Thio; C F Zorumski; G D Fischbach
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

Review 4.  Regulation of ionotropic glutamate receptors by their auxiliary subunits.

Authors:  Susumu Tomita
Journal:  Physiology (Bethesda)       Date:  2010-02

Review 5.  The expanding social network of ionotropic glutamate receptors: TARPs and other transmembrane auxiliary subunits.

Authors:  Alexander C Jackson; Roger A Nicoll
Journal:  Neuron       Date:  2011-04-28       Impact factor: 17.173

6.  Thiocyanate ions selectively antagonize AMPA-evoked responses in Xenopus laevis oocytes microinjected with rat brain mRNA.

Authors:  D Bowie; T G Smart
Journal:  Br J Pharmacol       Date:  1993-07       Impact factor: 8.739

7.  Autoinactivation of neuronal AMPA receptors via glutamate-regulated TARP interaction.

Authors:  Megumi Morimoto-Tomita; Wei Zhang; Christoph Straub; Chang-Hoon Cho; Kwang S Kim; James R Howe; Susumu Tomita
Journal:  Neuron       Date:  2009-01-15       Impact factor: 17.173

8.  Purified unitary kainate/alpha-amino-3-hydroxy-5-methylisooxazole-propionate (AMPA) and kainate/AMPA/N-methyl-D-aspartate receptors with interchangeable subunits.

Authors:  J M Henley; A Ambrosini; D Rodriguez-Ithurralde; H Sudan; P Brackley; C Kerry; I Mellor; K Abutidze; P N Usherwood; E A Barnard
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

9.  Development of L-glutamate- and glycine-activated currents in spinal cord neurones during early chick embryogenesis.

Authors:  K V Baev; K I Rusin; B V Safronov
Journal:  J Physiol       Date:  1990-04       Impact factor: 5.182

10.  Rapid desensitization of glutamate receptors in vertebrate central neurons.

Authors:  L O Trussell; L L Thio; C F Zorumski; G D Fischbach
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.