Literature DB >> 29101646

S-Adenosylmethionine Promotes Oxidative Stress and Decreases Na+, K+-ATPase Activity in Cerebral Cortex Supernatants of Adolescent Rats: Implications for the Pathogenesis of S-Adenosylhomocysteine Hydrolase Deficiency.

Ângela Zanatta1, Cristiane Cecatto1, Rafael Teixeira Ribeiro1, Alexandre Umpierrez Amaral1,2, Angela Ts Wyse1,3, Guilhian Leipnitz1,3, Moacir Wajner4,5,6.   

Abstract

S-Adenosylmethionine (AdoMet) concentrations are highly elevated in tissues and biological fluids of patients affected by S-adenosylhomocysteine hydrolase deficiency, who are clinically characterized by cerebral symptoms whose pathogenesis is still unknown. In the present work, we investigated the effects of AdoMet on redox homeostasis and on the activity of Na+, K+-ATPase in the cerebral cortex of young rats. AdoMet caused lipid peroxidation (increase of malondialdehyde concentrations) and protein oxidation (increase of carbonyl formation and decrease of sulfhydryl content). AdoMet also reduced the antioxidant defenses (reduced glutathione, GSH) and Na+, K+-ATPase activity. Furthermore, AdoMet-induced lipid peroxidation was fully prevented by the antioxidants trolox, melatonin, and resveratrol, and the decrease of GSH concentrations was abolished by trolox, suggesting the involvement of reactive oxygen species in these effects. In this context, AdoMet induced reactive oxygen (increase of 2',7'-dichloroflurescein-DCFH oxidation) but not nitrogen (nitrate and nitrite levels) species generation. Finally, the decrease of Na+, K+-ATPase activity provoked by AdoMet was totally prevented by trolox, implying a possible oxidation of cysteine groups of the enzyme that are critical for its function and highly susceptible to oxidative attack. It is also noted that adenosine and methionine did not alter the parameters evaluated, suggesting selective effects of AdoMet. Our data strongly indicate that disturbance of redox homeostasis caused by a major metabolite (AdoMet) accumulating in S-adenosylhomocysteine hydrolase deficiency may represent a deleterious mechanism of brain damage in this disease. Finally, reduction of Na+, K+-ATPase activity provoked by AdoMet may lead to impaired neurotransmission, but disturbance of this system should be better clarified in future studies.

Entities:  

Keywords:  Brain damage; Na+, K+-ATPase; Redox homeostasis; S-Adenosylhomocysteine hydrolase deficiency; S-Adenosylmethionine

Mesh:

Substances:

Year:  2017        PMID: 29101646     DOI: 10.1007/s12035-017-0804-z

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  75 in total

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Journal:  FEBS Lett       Date:  2002-01-30       Impact factor: 4.124

2.  A direct colorimetric assay for Ca2+ -stimulated ATPase activity.

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Journal:  Anal Biochem       Date:  1986-09       Impact factor: 3.365

3.  Isolation of synaptic plasma membrane from brain by combined flotation-sedimentation density gradient centrifugation.

Authors:  D H Jones; A I Matus
Journal:  Biochim Biophys Acta       Date:  1974-08-09

4.  Oxidative damage to proteins: spectrophotometric method for carbonyl assay.

Authors:  A Z Reznick; L Packer
Journal:  Methods Enzymol       Date:  1994       Impact factor: 1.600

5.  Lipid composition and the lateral pressure profile in bilayers.

Authors:  R S Cantor
Journal:  Biophys J       Date:  1999-05       Impact factor: 4.033

6.  Protein carbonyl groups as biomarkers of oxidative stress.

Authors:  Isabella Dalle-Donne; Ranieri Rossi; Daniela Giustarini; Aldo Milzani; Roberto Colombo
Journal:  Clin Chim Acta       Date:  2003-03       Impact factor: 3.786

7.  S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomes.

Authors:  Randall Grubbs; Oliver Vugrek; Jeremy Deisch; Conrad Wagner; Sally Stabler; Robert Allen; Ivo Barić; Marko Rados; S Harvey Mudd
Journal:  J Inherit Metab Dis       Date:  2010-09-18       Impact factor: 4.982

8.  Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiency.

Authors:  Kevin A Strauss; Carlos Ferreira; Teodoro Bottiglieri; Xueqing Zhao; Erland Arning; Shucha Zhang; Steven H Zeisel; Maria L Escolar; Nancy Presnick; Erik G Puffenberger; Oliver Vugrek; Lucija Kovacevic; Conrad Wagner; George V Mazariegos; S Harvey Mudd; Kyle Soltys
Journal:  Mol Genet Metab       Date:  2015-06-19       Impact factor: 4.797

9.  Quinone and oxyradical scavenging properties of N-acetylcysteine prevent dopamine mediated inhibition of Na+, K+-ATPase and mitochondrial electron transport chain activity in rat brain: implications in the neuroprotective therapy of Parkinson's disease.

Authors:  Maria B Bagh; Arpan K Maiti; Sirsendu Jana; Kalpita Banerjee; Arun Roy; Sasanka Chakrabarti
Journal:  Free Radic Res       Date:  2008-06

10.  Methylmalonate inhibits succinate-supported oxygen consumption by interfering with mitochondrial succinate uptake.

Authors:  S R Mirandola; D R Melo; P F Schuck; G C Ferreira; M Wajner; R F Castilho
Journal:  J Inherit Metab Dis       Date:  2008-01-24       Impact factor: 4.982

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  2 in total

1.  S-adenosylmethionine induces mitochondrial dysfunction, permeability transition pore opening and redox imbalance in subcellular preparations of rat liver.

Authors:  Bianca Seminotti; Ana Cristina Roginski; Ângela Zanatta; Alexandre Umpierrez Amaral; Thabata Fernandes; Kaleb Pinto Spannenberger; Lucas Henrique Rodrigues da Silva; Rafael Teixeira Ribeiro; Guilhian Leipnitz; Moacir Wajner
Journal:  J Bioenerg Biomembr       Date:  2021-08-04       Impact factor: 2.945

Review 2.  Polyamine Metabolism and Gene Methylation in Conjunction with One-Carbon Metabolism.

Authors:  Kuniyasu Soda
Journal:  Int J Mol Sci       Date:  2018-10-10       Impact factor: 5.923

  2 in total

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