Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 europrotection mediated by βNF and EtOH may be carried out by the metabolic activity of CYP 2D6 in mitochondria and by the role of CYP 2E1 in the efflux and the accumulation of MPP+
Jesus Fernandez-Abascal
 + 845 word(s) 845 2020-06-03 10:17:45 |
2 format correct
Nora Tang
 -7 word(s) 838 2020-11-02 03:23:46 |

Video Upload Options

We provide professional Video Production Services to translate complex research into visually appealing presentations. Would you like to try it?
No, upload directly Yes

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Fernandez-Abascal, J.; Chiaino, E.; Frosini, M.; Davey, G.P.; Valoti, M. β-Naphthoflavone, Ethanol Reverse Mitochondrial Dysfunction. Encyclopedia. Available online: https://encyclopedia.pub/entry/1000 (accessed on 16 November 2024).
Fernandez-Abascal J, Chiaino E, Frosini M, Davey GP, Valoti M. β-Naphthoflavone, Ethanol Reverse Mitochondrial Dysfunction. Encyclopedia. Available at: https://encyclopedia.pub/entry/1000. Accessed November 16, 2024.
Fernandez-Abascal, Jesus, Elda Chiaino, Maria Frosini, Gavin P. Davey, Massimo Valoti. "β-Naphthoflavone, Ethanol Reverse Mitochondrial Dysfunction" Encyclopedia, https://encyclopedia.pub/entry/1000 (accessed November 16, 2024).
Fernandez-Abascal, J., Chiaino, E., Frosini, M., Davey, G.P., & Valoti, M. (2020, June 04). β-Naphthoflavone, Ethanol Reverse Mitochondrial Dysfunction. In Encyclopedia. https://encyclopedia.pub/entry/1000
Fernandez-Abascal, Jesus, et al. "β-Naphthoflavone, Ethanol Reverse Mitochondrial Dysfunction." Encyclopedia. Web. 04 June, 2020.
β-Naphthoflavone, Ethanol Reverse Mitochondrial Dysfunction
Edit
This entry is adapted from the peer-reviewed paper 10.3390/ijms21113955

The 1-methyl-4-phenylpyridinium (MPP+) is a parkinsonian-inducing toxin that promotes neurodegeneration of dopaminergic cells by directly targeting complex I of mitochondria. Recently, it was reported that some Cytochrome P450 (CYP) isoforms, such as CYP 2D6 or 2E1, may be involved in the development of this neurodegenerative disease. In order to study a possible role for CYP induction in neurorepair, we designed an in vitro model where undifferentiated neuroblastoma SH-SY5Y cells were treated with the CYP inducers β-naphthoflavone (βNF) and ethanol (EtOH) before and during exposure to the parkinsonian neurotoxin, MPP+. The toxic effect of MPP+ in cell viability was rescued with both βNF and EtOH treatments. We also report that this was due to a decrease in reactive oxygen species (ROS) production, restoration of mitochondrial fusion kinetics, and mitochondrial membrane potential. These treatments also protected complex I activity against the inhibitory effects caused by MPP+, suggesting a possible neuroprotective role for CYP inducers. These results bring new insights into the possible role of CYP isoenzymes in xenobiotic clearance and central nervous system homeostasis.

Cytochrome P-450 System neuroprotection CYP induction

1. Introduction

Degeneration of dopaminergic neurons in the substantia nigra is a main feature of Parkinson’s disease (PD). Genetic and environmental factors are known to give rise to differential proteostatic states in the brain. Additionally, cell specific energy metabolism defects and reactive oxygen species (ROS) production can enhance neurodegeneration rates[1]. ROS can also be generated by exposure to environmental xenobiotics or drug metabolism. In addition, genetic predisposition contributes to selective neurodegeneration of these cells[2][3][4][5]. High oxidative stress and disruptors of mitochondrial membrane potential (ψm) lead to a change in morphology and alteration in mitochondrial fusion-fission dynamics[6]. These events disrupt the overall mitochondrial homeostasis, promoting apoptosis, the release of pro-apoptotic factors, and contributing to neurodegeneration in PD and other diseases[7][8]. In this context, xenobiotics have emerged as one important source of oxidative stress that may lead to mitochondrial dysfunction in the brain[8][9].

2. Mechanism

A mechanism by which the cells clear xenobiotics is by the Cytochrome P-450 system (CYP), which metabolize a wide variety of molecules[10]. In the brain, CYP represents a 0.5–2% of the total amount of CYP found in the liver, but it still plays an important role in the metabolism of drugs and some endogenous compounds in the central nervous system (CNS)[11]. This superfamily has several isoforms with specific expression patterns depending on the brain area and the cell type[12][13]. In particular, the isoform CYP 2D6 has been related with the development of PD due to its ability to metabolize several xenobiotics in dopaminergic cells and other areas[14]. Moreover, in dopaminergic cells, the induction of CYP 2E1 by nicotine or coffee has been related with less susceptibility to PD[15][16]. However, the contributions of CYPs isoforms to neurodegeneration and neuroprotection toward xenobiotic insult are still poorly understood.

Induction of CYP isoforms have been generally used for the study of drug metabolism and neuroprotection in vivo and in vitro[11]. Ethanol (EtOH) and β-naphthoflavone (βNF) are two well-known inducers of CYP isoforms[17][18][19]. We previously reported that both compounds promote the induction of CYP 2D6 and 2E1, and that CYP 2D6 can be localized in mitochondria in SH-SY5Y cells[20]. The objective of the present study is to elucidate whether treatments with both inducers protect mitochondria towards the neurotoxic effect of MPP+. Our results suggest that, in parallel with induction of CYP isoforms 2D6 and 2E1, the two compounds reverse the mitochondrial impairment promoted by MPP+.

Exposure to xenobiotics is one of the major causes of oxidative stress and apoptosis in the CNS and increases the risk of developing neurodegenerative diseases such as PD [21]. A mechanism by which the cells eliminate xenobiotics is the CYP system, which is involved in the metabolism of the drugs and toxins that cross the blood-brain barrier. Among the several isoforms that can be found in this super-family, most of them can be upregulated by at least a few xenobiotics[11]. In our previous publication, we demonstrated that βNF and EtOH are able to induce the expression of two isoforms in SH-SY5Y cells, CYP 2D6 and 2E1[20]. However, the mechanisms by which CYP isoforms can influence the overall homeostasis of the brain are poorly understood. In this study, we used SH-SY5Y cells to induce the expression of CYPs prior to exposure to MPP+, with the aim to study how these two isoforms protect mitochondria against MPP+ toxicity. Other publication has also shown that the apoptosis caused by MPP+ is mediated by ROS production[22]. We showed that both βNF and EtOH treatments rescue the decrease in cell viability promoted by MPP+. Additionally, we presented evidence that the observed neuroprotection is linked to a reduction of ROS formation, restoration of ψm and mitochondrial fusion kinetics. Finally, we showed that the toxic effect is avoided before MPP+ affects the mitochondrial complex I activity. Taken together, these results suggest that induction of CYPs by βNF and EtOH may contribute to neuroprotection of SH-SY5Y against MPP+ toxicity; however, other molecular mechanisms involving neuroprotection pathways not related with CYPs may not be discarded.

References

  1. Joshua M. Shulman; Philip L. De Jager; Mel B. Feany; Parkinson's Disease: Genetics and Pathogenesis. Annual Review of Pathology: Mechanisms of Disease 2011, 6, 193-222, 10.1146/annurev-pathol-011110-130242.
  2. Zhi-Xu He; Xiao-Wu Chen; Zhi-Wei Zhou; Shu-Feng Zhou; Impact of physiological, pathological and environmental factors on the expression and activity of human cytochrome P450 2D6 and implications in precision medicine. Drug Metabolism Reviews 2015, 47, 470-519, 10.3109/03602532.2015.1101131.
  3. Yu Lu; Qiliu Peng; Zhiyu Zeng; Jian Wang; Yan Deng; Li Xie; Cuiju Mo; Jie Zeng; Xue Qin; Shan Li; et al. CYP2D6 phenotypes and Parkinson's disease risk: A meta-analysis. Journal of the Neurological Sciences 2013, 336, 161-168, 10.1016/j.jns.2013.10.030.
  4. Chaoran Ma; Yesong Liu; Samantha Neumann; Xiang Gao; Nicotine from cigarette smoking and diet and Parkinson disease: a review. Translational Neurodegeneration 2017, 6, 18, 10.1186/s40035-017-0090-8.
  5. Natalia Palacios; Air pollution and Parkinson’s disease – evidence and future directions. Reviews on Environmental Health 2017, 32, 303-313, 10.1515/reveh-2017-0009.
  6. Sudhakar Raja Subramaniam; Marie-Françoise Chesselet; Mitochondrial dysfunction and oxidative stress in Parkinson's disease.. Progress in Neurobiology 2013, 106, 17-32, 10.1016/j.pneurobio.2013.04.004.
  7. Sandra Franco Iborra; Miquel Vila; Celine Perier; Mitochondrial Quality Control in Neurodegenerative Diseases: Focus on Parkinson's Disease and Huntington's Disease. Frontiers in Neuroscience 2018, 12, 342, 10.3389/fnins.2018.00342.
  8. Erich Gulbins; Stephan Dreschers; Jürgen Bock; Role of mitochondria in apoptosis.. Experimental Physiology 2002, 88, 85-90, 10.1113/eph8802503.
  9. Michael T. Lin; M. Flint Beal; Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature 2006, 443, 787-795, 10.1038/nature05292.
  10. Francesca Toselli; Peter R. Dodd; Elizabeth M. J. Gillam; Emerging roles for brain drug-metabolizing cytochrome P450 enzymes in neuropsychiatric conditions and responses to drugs. Drug Metabolism Reviews 2016, 48, 379-404, 10.1080/03602532.2016.1221960.
  11. Douglas McMillan; Rachel F. Tyndale; CYP-mediated drug metabolism in the brain impacts drug response. Pharmacology & Therapeutics 2018, 184, 189-200, 10.1016/j.pharmthera.2017.10.008.
  12. Charmaine S. Ferguson; Rachel F. Tyndale; Cytochrome P450 enzymes in the brain: emerging evidence of biological significance. Trends in Pharmacological Sciences 2011, 32, 708-14, 10.1016/j.tips.2011.08.005.
  13. R P Meyer; M. Gehlhaus; R. Knoth; B. Volk; Expression and function of cytochrome p450 in brain drug metabolism.. Current Drug Metabolism 2007, 8, 297-306, 10.2174/138920007780655478.
  14. Mohd Sami Ur Rasheed; Abhishek Kumar Mishra; Mahendra Pratap Singh; Cytochrome P450 2D6 and Parkinson’s Disease: Polymorphism, Metabolic Role, Risk and Protection. Neurochemical Research 2017, 42, 3353-3361, 10.1007/s11064-017-2384-8.
  15. S. Miksys; Rachel F. Tyndale; Nicotine induces brain CYP enzymes: relevance to Parkinson’s disease. Parkinson’s Disease and Related Disorders 2005, 70, 177-180, 10.1007/978-3-211-45295-0_28.
  16. Ana Carolina Valencia-Olvera; Julio Morán; Rafael Camacho-Carranza; Oscar Prospéro-García; Jesús Javier Espinosa-Aguirre; CYP2E1 induction leads to oxidative stress and cytotoxicity in glutathione-depleted cerebellar granule neurons. Toxicology in Vitro 2014, 28, 1206-1214, 10.1016/j.tiv.2014.05.014.
  17. Bent H. Hellum; Odd Georg Nilsen; The in vitro Inhibitory Potential of Trade Herbal Products on Human CYP2D6-Mediated Metabolism and the Influence of Ethanol. Basic Clinical Pharmacology Toxicology 2007, 101, 350-358, 10.1111/j.1742-7843.2007.00121.x.
  18. R T Miller; S Miksys; E Hoffmann; Rachel F. Tyndale; Ethanol self-administration and nicotine treatment increase brain levels of CYP2D in African green monkeys. British Journal of Pharmacology 2014, 171, 3077-3088, 10.1111/bph.12652.
  19. Carlo Pretti; Alessandra Salvetti; Vincenzo Longo; Mario Giorgi; Pier G. Gervasi; Effects of β-naphthoflavone on the cytochrome P450 system, and phase II enzymes in gilthead seabream (Sparus aurata). Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 2001, 130, 133-144, 10.1016/s1532-0456(01)00231-9.
  20. Jesús Fernández Abascal; Mariantonia Ripullone; Aurora Valeri; Cosima Leone; Massimo Valoti; β-Naphtoflavone and Ethanol Induce Cytochrome P450 and Protect towards MPP+ Toxicity in Human Neuroblastoma SH-SY5Y Cells. International Journal of Molecular Sciences 2018, 19, 3369, 10.3390/ijms19113369.
  21. Rona R. Ramsay; Magdalena Majekova; Milagros Medina; Massimo Valoti; Key Targets for Multi-Target Ligands Designed to Combat Neurodegeneration. Frontiers in Neuroscience 2016, 10, 375, 10.3389/fnins.2016.00375.
  22. Javier G. Pizarro; Felix Junyent; Ester Verdaguer; Joaquin Jordan; C. Beas-Zárate; Mercè Pallàs; Antoni Camins; Jaume Folch; Effects of MPP+ on the molecular pathways involved in cell cycle control in B65 neuroblastoma cells. Pharmacological Research 2010, 61, 391-399, 10.1016/j.phrs.2010.01.003.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Pharmacology & Pharmacy
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Jesus Fernandez-Abascal
,
Elda Chiaino
,
Maria Frosini
,
Gavin P. Davey
,
Massimo Valoti
View Times: 975
Revisions: 2 times (View History)
Update Date: 02 Nov 2020
Table of Contents
    1000/1000
    Hot Most Recent
    ScholarVision Creations
    Feedback