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NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES

Year 1999, Volume: 12 Issue: 2, 70 - 73, 03.12.2016

Abstract

Objective: We have used chemiluminescence (CL) measurements to investigate the effect of modulatory compounds on N-methyl-D-aspartate (NMDA) receptor activity in rat brain frontal cortex synaptosomes.
Methods: Freshly prepared synaptosomes (protein concentration: 5 mg/mL) were incubated with different modulatory molecules such as Zn++ (1 mM), Cd++ (1 mM), reduced glutathione, (GSH) (1 mM, 10 mM), oxidized glutathione (GSSG) (1 mM, 5 mM), dithiothreitol (DTT) (1 mM, 10 mM) and N- ethylmaleimide (NEM) (1 mM, 10 mM) for 5 minutes at room temperature. After preincubation, 0.1 mM NMDA was added either alone or in the presence of 65 mM KCI. CL measurements were taken with lucigenin as enhancer, at 10 second intervals for 1 minute.
Results: Synaptosomes showed a marked increase in CL upon addition of NMDA both in the presence and absence of KCI. When preincubated with the noncompetitive NMDA receptor antagonist (Zn++) or with the calcium channel blocker(Cd++), CL formation was suppressed. DTT, a strong sulfhydryl group reducing agent, increased the activity of NMDA receptor, whereas NEM, a sulfhydryl group alkylating agent, decreased the NMDA receptor activity. Reduced and oxidized forms of glutathione decreased the receptor activity and were protective under excitotoxicity and depolarization conditions.
Conclusion: Our results demonstrated that
endogenous and exogenous sulfhydryl compounds affect the redox modulatory site and play important roles in the generation of reactive oxygen species after activation of the NMDA receptor.
Key Words: Chemiluminescence; Cortical
synaptosomes; Excitotoxicity; NMDA receptor; Sulfhydryl group modulators

References

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  • Choi DW. Glutamate receptors and the induction of excitotoxic neuronal death. In: Bloom F, ed. neuroscience: from the molecular to the cognitive. Amsterdam: Elsevier Science, 1994:47-51.
  • Coyle JT, Pultfarcken P. Oxidative stress, glutamate and the neurodegenerative disorders. Science 1993,262:689-695.
  • Upton 5/1, Rosenberg PA. Excitatory amino acids as a final common pathway for neurologic disorders, n Engl J Med 1994;330:613-622.
  • Meldrum BS. The role of glutamate in epilepsy and other CHS disorders, neurology 1994;44:514-523.
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  • acids: novel therapeutic approaches in
  • neurodegenerative disorders. In: Racagni G,
  • Brunello A, Langer SZ, eds. Recent Advances in the Treatment of neurodegenerative Disorders and Cognitive Dysfunction. Voi. 7. BasehRarger, 1994:157-165.
  • Gozlan Ft, Ben-Ari Y. nMDA receptor redox sites: are they targets for neuronal protection. TIPS 1994,16:368-374.
  • Aizenman E, Reynolds IJ. Modulation of nMDA excitotoxicity by redox reagents. Ann nY Acad Sci 1992;648:125-131.
  • 2
  • Marmara Medical Journal Volume 12 No: 2 April 1999
  • Küçükkaya B, haklar G, Yalçın AS. hMDA excitotoxicity and free radical generation in rat brain homogenates, application of a chemiluminescence assay. heurochem Res 1996;21:1533-1536.
  • Dodd FR, hardy JA, Oakley AE, Edwardson JA, Perry ER, Delaunoy JP. A rapid method for preparing synaptosomes: comparison with alternative
  • procedures. Brain Res 1981 ;226:107-118.
  • I I. Yalçın /İS, haklar G, Küçükkaya B, Yüksel M, Dalaman G. Chemiluminescence measurements for the detection of free radical species. In: Özben T, ed. Free Radicals, Oxidative Stress, and Antioxidants, hew York: Plenum Press, 1998:189- 193.
  • hicholls DG. The glutamatergic nerve terminal. Eur J Biochem 1993;212:613-631.
  • Lafon-Cazal M, Pietri S, Culcasi M, Bockaert J. hMDA-dependent superoxide production and neurotoxicity, hature 1993;364:535-537.
  • Patel M, Day BJ, Grapo JD, Fridovich I, Me hamara JO. Requirement for superoxide in excitotoxic cell death, heuron 1996; 16:345-355.
  • Tang Lh. Aizenman A. Long-lasting modification of h-methyl-D-aspartate receptor channel by a voltage dependent sulfhydryl redox process. Molec Pharmacol 1993:44:473-478.
  • Sucher hJ, Upton SA. Redox modulatory site of the hMDA receptor channel complex: regulation by oxidized glutathione. J neuroscience Res 1991;30:582-591.
  • 7. Varga V, Jenei Zs, Janaky R, Saransaari P, Oja S5. Glutathione is an endogenous ligand of rat brain h- methyl-D-aspartate (hMDA) and 2-amino-3-hydroxy- 5-methyl-4-isoxazolepropionate (AMPA) receptors, heurochem Res I997;22:1165-1171.
Year 1999, Volume: 12 Issue: 2, 70 - 73, 03.12.2016

Abstract

References

  • /. Wroblewski JT, Danysz W. Modulation of glutamate receptors: molecular mechanisms and functional implications. Ann Rev Pharmacol Toxicol 1989;29:441-4 74.
  • Choi DW. Glutamate receptors and the induction of excitotoxic neuronal death. In: Bloom F, ed. neuroscience: from the molecular to the cognitive. Amsterdam: Elsevier Science, 1994:47-51.
  • Coyle JT, Pultfarcken P. Oxidative stress, glutamate and the neurodegenerative disorders. Science 1993,262:689-695.
  • Upton 5/1, Rosenberg PA. Excitatory amino acids as a final common pathway for neurologic disorders, n Engl J Med 1994;330:613-622.
  • Meldrum BS. The role of glutamate in epilepsy and other CHS disorders, neurology 1994;44:514-523.
  • Scatton B. Pharmacology of the excitatory amino
  • acids: novel therapeutic approaches in
  • neurodegenerative disorders. In: Racagni G,
  • Brunello A, Langer SZ, eds. Recent Advances in the Treatment of neurodegenerative Disorders and Cognitive Dysfunction. Voi. 7. BasehRarger, 1994:157-165.
  • Gozlan Ft, Ben-Ari Y. nMDA receptor redox sites: are they targets for neuronal protection. TIPS 1994,16:368-374.
  • Aizenman E, Reynolds IJ. Modulation of nMDA excitotoxicity by redox reagents. Ann nY Acad Sci 1992;648:125-131.
  • 2
  • Marmara Medical Journal Volume 12 No: 2 April 1999
  • Küçükkaya B, haklar G, Yalçın AS. hMDA excitotoxicity and free radical generation in rat brain homogenates, application of a chemiluminescence assay. heurochem Res 1996;21:1533-1536.
  • Dodd FR, hardy JA, Oakley AE, Edwardson JA, Perry ER, Delaunoy JP. A rapid method for preparing synaptosomes: comparison with alternative
  • procedures. Brain Res 1981 ;226:107-118.
  • I I. Yalçın /İS, haklar G, Küçükkaya B, Yüksel M, Dalaman G. Chemiluminescence measurements for the detection of free radical species. In: Özben T, ed. Free Radicals, Oxidative Stress, and Antioxidants, hew York: Plenum Press, 1998:189- 193.
  • hicholls DG. The glutamatergic nerve terminal. Eur J Biochem 1993;212:613-631.
  • Lafon-Cazal M, Pietri S, Culcasi M, Bockaert J. hMDA-dependent superoxide production and neurotoxicity, hature 1993;364:535-537.
  • Patel M, Day BJ, Grapo JD, Fridovich I, Me hamara JO. Requirement for superoxide in excitotoxic cell death, heuron 1996; 16:345-355.
  • Tang Lh. Aizenman A. Long-lasting modification of h-methyl-D-aspartate receptor channel by a voltage dependent sulfhydryl redox process. Molec Pharmacol 1993:44:473-478.
  • Sucher hJ, Upton SA. Redox modulatory site of the hMDA receptor channel complex: regulation by oxidized glutathione. J neuroscience Res 1991;30:582-591.
  • 7. Varga V, Jenei Zs, Janaky R, Saransaari P, Oja S5. Glutathione is an endogenous ligand of rat brain h- methyl-D-aspartate (hMDA) and 2-amino-3-hydroxy- 5-methyl-4-isoxazolepropionate (AMPA) receptors, heurochem Res I997;22:1165-1171.
There are 23 citations in total.

Details

Journal Section Original Research
Authors

Belgin Küçükkaya This is me

Goncagül Haklar This is me

Süha Yalçın This is me

Publication Date December 3, 2016
Published in Issue Year 1999 Volume: 12 Issue: 2

Cite

APA Küçükkaya, B., Haklar, G., & Yalçın, S. (2016). NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES. Marmara Medical Journal, 12(2), 70-73.
AMA Küçükkaya B, Haklar G, Yalçın S. NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES. Marmara Med J. June 2016;12(2):70-73.
Chicago Küçükkaya, Belgin, Goncagül Haklar, and Süha Yalçın. “NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES”. Marmara Medical Journal 12, no. 2 (June 2016): 70-73.
EndNote Küçükkaya B, Haklar G, Yalçın S (June 1, 2016) NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES. Marmara Medical Journal 12 2 70–73.
IEEE B. Küçükkaya, G. Haklar, and S. Yalçın, “NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES”, Marmara Med J, vol. 12, no. 2, pp. 70–73, 2016.
ISNAD Küçükkaya, Belgin et al. “NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES”. Marmara Medical Journal 12/2 (June 2016), 70-73.
JAMA Küçükkaya B, Haklar G, Yalçın S. NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES. Marmara Med J. 2016;12:70–73.
MLA Küçükkaya, Belgin et al. “NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES”. Marmara Medical Journal, vol. 12, no. 2, 2016, pp. 70-73.
Vancouver Küçükkaya B, Haklar G, Yalçın S. NMDA RECEPTOR ACTIVITY AND ITS MODULATION BY SULFHYDRYL COMPOUNDS: CHEMILUMINESCENCE MEASUREMENTS IN RAT BRAIN CORTICAL SYNAPTOSOMES. Marmara Med J. 2016;12(2):70-3.