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Published in: NeuroMolecular Medicine 4/2018

01-12-2018 | Original Paper

Neuroprotective Effect of Hydrogen Sulfide in Hyperhomocysteinemia Is Mediated Through Antioxidant Action Involving Nrf2

Authors: Mohit Kumar, Rajat Sandhir

Published in: NeuroMolecular Medicine | Issue 4/2018

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Abstract

Homocysteine (Hcy) is a sulfur-containing amino acid derived from methionine metabolism. Elevated plasma Hcy levels (> 15 µM) result in a condition called hyperhomocysteinemia (HHcy), which is an independent risk factor in the development of various neurodegenerative disorders. Reactive oxygen species (ROS) produced by auto-oxidation of Hcy have been implicated in HHcy-associated neurological conditions. Hydrogen sulfide (H2S) is emerging as a potent neuroprotective and neuromodulator molecule. The present study was aimed to evaluate the ability of NaHS (a source of H2S) to attenuate Hcy-induced oxidative stress and altered antioxidant status in animals subjected to HHcy. Impaired cognitive functions assessed by Y-maze and elevated plus maze in Hcy-treated animals were reversed on NaHS administration. Increased levels of ROS, lipid peroxidation, protein carbonyls, and 4-hydroxynonenal (4-HNE)-modified proteins were observed in the cortex and hippocampus of Hcy-treated animals suggesting accentuated oxidative stress. This increase in Hcy-induced oxidative stress was reversed following NaHS supplementation. GSH/GSSG ratio, activity of antioxidant enzymes viz; superoxide dismutase, glutathione peroxidase, glutathione reductase, and glutathione-S-transferase were decreased in Hcy-treated animals. NaHS supplementation, on the otherhand, restored redox ratio and activity of antioxidant enzymes in the brains of animals with HHcy. Further, NaHS administration normalized nuclear factor erythroid 2-related factor 2 expression and acetylcholinesterase (AChE) activity in the brain of Hcy-treated animals. Histopathological studies using cresyl violet indicated higher number of pyknotic neurons in the cortex and hippocampus of HHcy animals, which were reversed by NaHS administration. The results clearly demonstrate that NaHS treatment significantly ameliorates Hcy-induced cognitive impairment by attenuating oxidative stress, improving antioxidant status, and modulating AChE activity thereby suggesting potential of H2S as a therapeutic molecule.
Literature
go back to reference Blokland, A. (1995). Acetylcholine: A neurotransmitter for learning and memory? Brain Research Reviews, 21(3), 285–300.CrossRef Blokland, A. (1995). Acetylcholine: A neurotransmitter for learning and memory? Brain Research Reviews, 21(3), 285–300.CrossRef
go back to reference Boldyrev, A., Bryushkova, E., Mashkina, A., & Vladychenskaya, E. (2013). Why is homocysteine toxic for the nervous and immune systems? Current Aging Science, 6(1), 29–36.CrossRef Boldyrev, A., Bryushkova, E., Mashkina, A., & Vladychenskaya, E. (2013). Why is homocysteine toxic for the nervous and immune systems? Current Aging Science, 6(1), 29–36.CrossRef
go back to reference Butterfield, D. A., Castegna, A., Lauderback, C. M., & Drake, J. (2002). Evidence that amyloid beta-peptide-induced lipid peroxidation and its sequelae in Alzheimer’s disease brain contribute to neuronal death. Neurobiology of Aging, 23(5), 655–664.CrossRef Butterfield, D. A., Castegna, A., Lauderback, C. M., & Drake, J. (2002). Evidence that amyloid beta-peptide-induced lipid peroxidation and its sequelae in Alzheimer’s disease brain contribute to neuronal death. Neurobiology of Aging, 23(5), 655–664.CrossRef
go back to reference Carlberg, I., & Mannervik, B. (1985). Glutathione reductase. Methods in Enzymology, 113, 484–490.CrossRef Carlberg, I., & Mannervik, B. (1985). Glutathione reductase. Methods in Enzymology, 113, 484–490.CrossRef
go back to reference Dayal, S., Arning, E., Bottiglieri, T., Boger, R. H., Sigmund, C. D., Faraci, F. M., & Lentz, S. R. (2004). Cerebral vascular dysfunction mediated by superoxide in hyperhomocysteinemic mice. Stroke, 35(8), ,1957–1962.CrossRef Dayal, S., Arning, E., Bottiglieri, T., Boger, R. H., Sigmund, C. D., Faraci, F. M., & Lentz, S. R. (2004). Cerebral vascular dysfunction mediated by superoxide in hyperhomocysteinemic mice. Stroke, 35(8), ,1957–1962.CrossRef
go back to reference Flohé, L., & Günzler, W. A. (1984). Assays of glutathione peroxidase. Methods in Enzymology, 105, 114–121.CrossRef Flohé, L., & Günzler, W. A. (1984). Assays of glutathione peroxidase. Methods in Enzymology, 105, 114–121.CrossRef
go back to reference Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1974). Glutathione S-Transferases the first enzymatic step in mercapturic acid formation*. The Journal of Biological Chemistry, 249(22), 7130–7139.PubMed Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1974). Glutathione S-Transferases the first enzymatic step in mercapturic acid formation*. The Journal of Biological Chemistry, 249(22), 7130–7139.PubMed
go back to reference Hissin, P. J., & Hilf, R. (1976). A fluorometric method for determination of oxidized and reduced glutathione in tissues. Analytical Biochemistry, 74(1), 214–226.CrossRef Hissin, P. J., & Hilf, R. (1976). A fluorometric method for determination of oxidized and reduced glutathione in tissues. Analytical Biochemistry, 74(1), 214–226.CrossRef
go back to reference Hrnčić, D., -Marković, R., Stojković, A., Velimirović, T., Puškaš, M., Obrenović, N., R., et al (2014). Hyperhomocysteinemia induced by methionine dietary nutritional overload modulates acetylcholinesterase activity in the rat brain. Molecular and Cellular Biochemistry, 396(1–2), 99–105. https://doi.org/10.1007/s11010-014-2146-8.CrossRefPubMed Hrnčić, D., -Marković, R., Stojković, A., Velimirović, T., Puškaš, M., Obrenović, N., R., et al (2014). Hyperhomocysteinemia induced by methionine dietary nutritional overload modulates acetylcholinesterase activity in the rat brain. Molecular and Cellular Biochemistry, 396(1–2), 99–105. https://​doi.​org/​10.​1007/​s11010-014-2146-8.CrossRefPubMed
go back to reference Kono, Y. (1978). Generation of superoxide radical during autoxidation of hydroxylamine and an assay for superoxide dismutase. Archives of Biochemistry and Biophysics, 186(1), 189–195.CrossRef Kono, Y. (1978). Generation of superoxide radical during autoxidation of hydroxylamine and an assay for superoxide dismutase. Archives of Biochemistry and Biophysics, 186(1), 189–195.CrossRef
go back to reference Levine, R. L., Garland, D., Oliver, C. N., Amici, A., Climent, I., Lenz, A. G., et al. (1990). Determination of carbonyl content in oxidatively modified proteins. Methods in Enzymology, 186, 464–478.CrossRef Levine, R. L., Garland, D., Oliver, C. N., Amici, A., Climent, I., Lenz, A. G., et al. (1990). Determination of carbonyl content in oxidatively modified proteins. Methods in Enzymology, 186, 464–478.CrossRef
go back to reference Li, M., Zhang, P., Wei, H. J., Li, M. H., Zou, W., Li, X., et al. (2017). Hydrogen sulfide ameliorates homocysteine-induced cognitive dysfunction by inhibition of reactive aldehydes involving upregulation of ALDH2. International Journal of Neuropsychopharmacology, 20(4), 305–315. https://doi.org/10.1093/ijnp/pyw103.CrossRefPubMed Li, M., Zhang, P., Wei, H. J., Li, M. H., Zou, W., Li, X., et al. (2017). Hydrogen sulfide ameliorates homocysteine-induced cognitive dysfunction by inhibition of reactive aldehydes involving upregulation of ALDH2. International Journal of Neuropsychopharmacology, 20(4), 305–315. https://​doi.​org/​10.​1093/​ijnp/​pyw103.CrossRefPubMed
go back to reference Lipton, S. A., Kim, W. K., Choi, Y. B., Kumar, S., D’Emilia, D. M., Rayudu, P. V., et al. (1997). Neurotoxicity associated with dual actions of homocysteine at the N-methyl-D-aspartate receptor. Proceedings of the National Academy of Sciences of the United States of America, 94(11), 5923–5928.CrossRef Lipton, S. A., Kim, W. K., Choi, Y. B., Kumar, S., D’Emilia, D. M., Rayudu, P. V., et al. (1997). Neurotoxicity associated with dual actions of homocysteine at the N-methyl-D-aspartate receptor. Proceedings of the National Academy of Sciences of the United States of America, 94(11), 5923–5928.CrossRef
go back to reference Lowry, O. H., Rosebrough, N. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry, 193(1), 265–275.PubMed Lowry, O. H., Rosebrough, N. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry, 193(1), 265–275.PubMed
go back to reference Lu, M., Zhao, F.-F., Tang, J.-J., Su, C.-J., Fan, Y., Ding, J.-H., et al. (2012). The neuroprotection of hydrogen sulfide against MPTP-induced dopaminergic neuron degeneration involves uncoupling protein 2 rather than ATP-sensitive potassium channels. Antioxidants & Redox Signaling, 17(6), 849–859. https://doi.org/10.1089/ars.2011.4507.CrossRef Lu, M., Zhao, F.-F., Tang, J.-J., Su, C.-J., Fan, Y., Ding, J.-H., et al. (2012). The neuroprotection of hydrogen sulfide against MPTP-induced dopaminergic neuron degeneration involves uncoupling protein 2 rather than ATP-sensitive potassium channels. Antioxidants & Redox Signaling, 17(6), 849–859. https://​doi.​org/​10.​1089/​ars.​2011.​4507.CrossRef
go back to reference Luna-Sánchez, M., Hidalgo-Gutiérrez, A., Hildebrandt, T. M., Chaves-Serrano, J., Barriocanal-Casado, E., Santos-Fandila, Á, et al. (2017). CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated with this syndrome. EMBO Molecular Medicine, 9(1), 78–95. https://doi.org/10.15252/emmm.201606345.CrossRefPubMed Luna-Sánchez, M., Hidalgo-Gutiérrez, A., Hildebrandt, T. M., Chaves-Serrano, J., Barriocanal-Casado, E., Santos-Fandila, Á, et al. (2017). CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated with this syndrome. EMBO Molecular Medicine, 9(1), 78–95. https://​doi.​org/​10.​15252/​emmm.​201606345.CrossRefPubMed
go back to reference Matté, C., Pereira, L. O., Santos, D., Mackedanz, T. M., Cunha, V., Netto, A. A., C. A., & Wyse, A. T. S. (2009). Acute homocysteine administration impairs memory consolidation on inhibitory avoidance task and decreases hippocampal brain-derived neurotrophic factor immunocontent: Prevention by folic acid treatment. Neuroscience, 163(4), 1039–1045. https://doi.org/10.1016/j.neuroscience.2009.07.023.CrossRefPubMed Matté, C., Pereira, L. O., Santos, D., Mackedanz, T. M., Cunha, V., Netto, A. A., C. A., & Wyse, A. T. S. (2009). Acute homocysteine administration impairs memory consolidation on inhibitory avoidance task and decreases hippocampal brain-derived neurotrophic factor immunocontent: Prevention by folic acid treatment. Neuroscience, 163(4), 1039–1045. https://​doi.​org/​10.​1016/​j.​neuroscience.​2009.​07.​023.CrossRefPubMed
go back to reference Miller, J. W. (1999). Homocysteine and Alzheimer’s disease. Nutrition Reviews, 57(4), 126–129.PubMed Miller, J. W. (1999). Homocysteine and Alzheimer’s disease. Nutrition Reviews, 57(4), 126–129.PubMed
go back to reference Moreira, D. D. S., Figueiró, P. W., Siebert, C., Prezzi, C. A., Rohden, F., Guma, F. C. R., et al. (2017). Chronic mild hyperhomocysteinemia alters inflammatory and oxidative/nitrative status and causes protein/DNA damage, as well as ultrastructural changes in cerebral cortex : Is acetylsalicylic acid neuroprotective ? Neurotoxicity Research, 33(3), 580–592.CrossRef Moreira, D. D. S., Figueiró, P. W., Siebert, C., Prezzi, C. A., Rohden, F., Guma, F. C. R., et al. (2017). Chronic mild hyperhomocysteinemia alters inflammatory and oxidative/nitrative status and causes protein/DNA damage, as well as ultrastructural changes in cerebral cortex : Is acetylsalicylic acid neuroprotective ? Neurotoxicity Research, 33(3), 580–592.CrossRef
go back to reference Ogita, K., Okuda, H., Yamamoto, Y., Nishiyama, N., & Yoneda, Y. (2003). In vivo neuroprotective role of NMDA receptors against kainate-induced excitotoxicity in murine hippocampal pyramidal neurons. Journal of Neurochemistry, 85(5), 1336–1346.CrossRef Ogita, K., Okuda, H., Yamamoto, Y., Nishiyama, N., & Yoneda, Y. (2003). In vivo neuroprotective role of NMDA receptors against kainate-induced excitotoxicity in murine hippocampal pyramidal neurons. Journal of Neurochemistry, 85(5), 1336–1346.CrossRef
go back to reference Ohkawa, S., Fukatsu, K., Miki, S., Hashimoto, T., Sakamoto, J., Doi, T., et al. (1997). 5-Aminocoumarans: Dual inhibitors of lipid peroxidation and dopamine release with protective effects against central nervous system trauma and ischemia. Journal of Medicinal Chemistry, 40(4), 559–573. https://doi.org/10.1021/jm960411j.CrossRefPubMed Ohkawa, S., Fukatsu, K., Miki, S., Hashimoto, T., Sakamoto, J., Doi, T., et al. (1997). 5-Aminocoumarans: Dual inhibitors of lipid peroxidation and dopamine release with protective effects against central nervous system trauma and ischemia. Journal of Medicinal Chemistry, 40(4), 559–573. https://​doi.​org/​10.​1021/​jm960411j.CrossRefPubMed
go back to reference Pfaffl, M. W. (2001). A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research, 29(9), e45.CrossRef Pfaffl, M. W. (2001). A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research, 29(9), e45.CrossRef
go back to reference Towbin, H., Staehelint, T., & Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proceedings of the National Academy of Sciences, 76(9), 4350–4354.CrossRef Towbin, H., Staehelint, T., & Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proceedings of the National Academy of Sciences, 76(9), 4350–4354.CrossRef
go back to reference Wang, H., & Joseph, J. A. (1999). Quantifying cellular oxidative stress by dichlorofluorescein assay using microplate reader. Free Radical Biology & Medicine, 27(5–6), 612–616.CrossRef Wang, H., & Joseph, J. A. (1999). Quantifying cellular oxidative stress by dichlorofluorescein assay using microplate reader. Free Radical Biology & Medicine, 27(5–6), 612–616.CrossRef
go back to reference Zhao, H., Qu, J., Li, Q., Cui, M., Wang, J., Zhang, K., et al. (2017). Taurine supplementation reduces neuroinflammation and protects against white matter injury after intracerebral hemorrhage in rats. Amino Acids, 50(3–4), 439–451.PubMed Zhao, H., Qu, J., Li, Q., Cui, M., Wang, J., Zhang, K., et al. (2017). Taurine supplementation reduces neuroinflammation and protects against white matter injury after intracerebral hemorrhage in rats. Amino Acids, 50(3–4), 439–451.PubMed
Metadata
Title
Neuroprotective Effect of Hydrogen Sulfide in Hyperhomocysteinemia Is Mediated Through Antioxidant Action Involving Nrf2
Authors
Mohit Kumar
Rajat Sandhir
Publication date
01-12-2018
Publisher
Springer US
Published in
NeuroMolecular Medicine / Issue 4/2018
Print ISSN: 1535-1084
Electronic ISSN: 1559-1174
DOI
https://doi.org/10.1007/s12017-018-8505-y

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