Mitigation of ROS Insults by Streptomyces Secondary Metabolites in Primary Cortical Neurons

Marta Leirós, Eva Alonso, Jon A Sanchez, Mostafa Ezzat Mohamed Rateb, Rainer Ebel, Wael E Houssen, Marcel Jaspars, Amparo Alfonso, Luis M Botana

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Oxidative stress is a common point in neurodegenerative diseases, widely connected with mitochondrial dysfunction. In this study, we screened seven natural products from Streptomyces sources against hydrogen peroxide insult in primary cortical neurons, an oxidative stress in vitro model. We showed the ability of these compounds to inhibit neuronal cytotoxicity and to reduce ROS release after 12 h treatment. Among the tested compounds, the quinone anhydroexfoliamycin and the red pyrrole-type pigment undecylprodigiosin stand out. These two compounds displayed the most complete protection against oxidative stress with mitochondrial function improvement, ROS production inhibition, and increase of antioxidant enzyme levels, glutathione and catalase. Further investigations confirmed that anhydroexfoliamycin acts over the Nrf2-ARE pathway, as a Nrf2 nuclear translocation inductor, and is able to strongly inhibit the effect of the mitochondrial uncoupler FCCP over cytosolic Ca(2+), pointing to mitochondria as a cellular target for this molecule. In addition, both compounds were able to reduce caspase-3 activity induced by the apoptotic enhancer staurosporine, but undecylprodigiosin failed to inhibit FCCP effects and it did not act over the Nrf2 pathway as was the case for anhydroexfoliamycin. These results show that Streptomyces metabolites could be useful for the development of new drugs for prevention of neurodegenerative disorders such as Parkinson's and Alzheimer's diseases and cerebral ischemia.
Original languageEnglish
Pages (from-to)71-80
Number of pages10
JournalACS Chemical Neuroscience
Volume5
Issue number1
Early online date12 Nov 2013
DOIs
Publication statusPublished - 15 Jan 2014

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Oxidative stress
Streptomyces
Metabolites
Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
Neurons
Oxidative Stress
Neurodegenerative Diseases
Neurodegenerative diseases
Pyrroles
Mitochondria
Aptitude
Staurosporine
Cytotoxicity
Biological Products
Brain Ischemia
Pigments
Caspase 3
Catalase
Hydrogen Peroxide
Glutathione

Keywords

  • marine natural products
  • streptomyces
  • oxidative stress
  • Nrf2
  • neuroprotection
  • neurodegenerative diseases

Cite this

Mitigation of ROS Insults by Streptomyces Secondary Metabolites in Primary Cortical Neurons. / Leirós, Marta; Alonso, Eva; Sanchez, Jon A; Rateb, Mostafa Ezzat Mohamed; Ebel, Rainer; Houssen, Wael E; Jaspars, Marcel; Alfonso, Amparo; Botana, Luis M.

In: ACS Chemical Neuroscience, Vol. 5, No. 1, 15.01.2014, p. 71-80.

Research output: Contribution to journalArticle

Leirós, Marta ; Alonso, Eva ; Sanchez, Jon A ; Rateb, Mostafa Ezzat Mohamed ; Ebel, Rainer ; Houssen, Wael E ; Jaspars, Marcel ; Alfonso, Amparo ; Botana, Luis M. / Mitigation of ROS Insults by Streptomyces Secondary Metabolites in Primary Cortical Neurons. In: ACS Chemical Neuroscience. 2014 ; Vol. 5, No. 1. pp. 71-80.
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abstract = "Oxidative stress is a common point in neurodegenerative diseases, widely connected with mitochondrial dysfunction. In this study, we screened seven natural products from Streptomyces sources against hydrogen peroxide insult in primary cortical neurons, an oxidative stress in vitro model. We showed the ability of these compounds to inhibit neuronal cytotoxicity and to reduce ROS release after 12 h treatment. Among the tested compounds, the quinone anhydroexfoliamycin and the red pyrrole-type pigment undecylprodigiosin stand out. These two compounds displayed the most complete protection against oxidative stress with mitochondrial function improvement, ROS production inhibition, and increase of antioxidant enzyme levels, glutathione and catalase. Further investigations confirmed that anhydroexfoliamycin acts over the Nrf2-ARE pathway, as a Nrf2 nuclear translocation inductor, and is able to strongly inhibit the effect of the mitochondrial uncoupler FCCP over cytosolic Ca(2+), pointing to mitochondria as a cellular target for this molecule. In addition, both compounds were able to reduce caspase-3 activity induced by the apoptotic enhancer staurosporine, but undecylprodigiosin failed to inhibit FCCP effects and it did not act over the Nrf2 pathway as was the case for anhydroexfoliamycin. These results show that Streptomyces metabolites could be useful for the development of new drugs for prevention of neurodegenerative disorders such as Parkinson's and Alzheimer's diseases and cerebral ischemia.",
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note = "Funding Funding is gratefully acknowledged from the following. From Ministerio de Ciencia y Tecnologia, Spain: [SAF2009-12581 ́ (subprograma NEF)], [AGL2009-13581-CO2-01], [ TRA2009-0189, AGL2010-17875]. From Xunta de Galicia, Spain: [GRC 2010/10] [PGDIT 07MMA006261PR], [PGIDIT (INCITE) 09MMA003261PR], [PGDIT (INCITE) 09261080PR], [2009/XA044], and [10PXIB261254 PR]. Funding by the EU FP7 program: [211326 - CP (CON- ffIDENCE)], [265896 BAMMBO], [265409 μAQUA], [262649 BEADS], and [312184 PharmaSea]. Through the Atlantic Area Programme (Interreg IVB Trans-national): [2009-1/117 Pharmatlantic]. M.E.R. thanks the Government of the Arab Republic of Egypt for a Ph.D. Scholarship. M.J. thanks the Scottish University Life Science Alliance which provided funding to set up the compound library.",
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N1 - Funding Funding is gratefully acknowledged from the following. From Ministerio de Ciencia y Tecnologia, Spain: [SAF2009-12581 ́ (subprograma NEF)], [AGL2009-13581-CO2-01], [ TRA2009-0189, AGL2010-17875]. From Xunta de Galicia, Spain: [GRC 2010/10] [PGDIT 07MMA006261PR], [PGIDIT (INCITE) 09MMA003261PR], [PGDIT (INCITE) 09261080PR], [2009/XA044], and [10PXIB261254 PR]. Funding by the EU FP7 program: [211326 - CP (CON- ffIDENCE)], [265896 BAMMBO], [265409 μAQUA], [262649 BEADS], and [312184 PharmaSea]. Through the Atlantic Area Programme (Interreg IVB Trans-national): [2009-1/117 Pharmatlantic]. M.E.R. thanks the Government of the Arab Republic of Egypt for a Ph.D. Scholarship. M.J. thanks the Scottish University Life Science Alliance which provided funding to set up the compound library.

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N2 - Oxidative stress is a common point in neurodegenerative diseases, widely connected with mitochondrial dysfunction. In this study, we screened seven natural products from Streptomyces sources against hydrogen peroxide insult in primary cortical neurons, an oxidative stress in vitro model. We showed the ability of these compounds to inhibit neuronal cytotoxicity and to reduce ROS release after 12 h treatment. Among the tested compounds, the quinone anhydroexfoliamycin and the red pyrrole-type pigment undecylprodigiosin stand out. These two compounds displayed the most complete protection against oxidative stress with mitochondrial function improvement, ROS production inhibition, and increase of antioxidant enzyme levels, glutathione and catalase. Further investigations confirmed that anhydroexfoliamycin acts over the Nrf2-ARE pathway, as a Nrf2 nuclear translocation inductor, and is able to strongly inhibit the effect of the mitochondrial uncoupler FCCP over cytosolic Ca(2+), pointing to mitochondria as a cellular target for this molecule. In addition, both compounds were able to reduce caspase-3 activity induced by the apoptotic enhancer staurosporine, but undecylprodigiosin failed to inhibit FCCP effects and it did not act over the Nrf2 pathway as was the case for anhydroexfoliamycin. These results show that Streptomyces metabolites could be useful for the development of new drugs for prevention of neurodegenerative disorders such as Parkinson's and Alzheimer's diseases and cerebral ischemia.

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