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The correlation between oxidative stress markers and increasing intracranial pressure: a study of Malondialdehyde (MDA), Superoxide Dismutase (MnSOD), Nicotinamide Adenine Dinucleotide Phosphate Hydrogen (NADPH), and catalase

  • Wismaji Sadewo ,
  • Septelia Inawati Wanandi ,
  • Zuherman Rustam ,
  • Kevin Gunawan ,
  • Setyo Widi Nugroho ,

Abstract

Link of Video Abstract: https://youtu.be/nINFPi4uVow

 

Background: Abnormalities in the neurosurgical field concerning cranial structure are almost always followed by increased intracranial pressure (ICP), which causes cerebral hypoxia and disrupts the whole cellular system. This study analyzes the correlation between ICP changes and oxidative stress markers, in subjects with various anatomical pathology abnormalities who underwent surgery.

Methods: This was a cross sectional study of 24 subjects with ICP conducted in the Department of Neurosurgery, Cipto Mangunkusumo Hospital, Jakarta, from November to December 2009. In this study, ANOVA analysis has been done to measure the mean difference oxidative stress (MnSOD, NADPH, MDA, and catalase) in subjects with various changes in ICP who have undergone surgery and Spearman analysis to measure the correlation between each oxidative stress markers. Oxidative stress markers were measured from normal brain tissue taken intra-operatively, cerebrospinal fluid (CSF) taken while doing ventriculostomy, and peripheral blood taken from a central vein catheter (CVC).

Results: The results showed that MDA concentrations in blood were significantly correlated with MDA in brain tissue (P = 0.029) in all of the ICP groups, CSF MnSOD concentration and CSF NADPH concentrations correlated with brain tissue NAPDH (p= 0.000) in congenital group and CSF catalase concentration correlated with brain tissue catalase (p = 0.00) in congenital group.

Conclusion: Increased ICP caused by various pathological conditions causes changes in oxidative stress markers in brain cells, CSF and blood. Oxidative stress markers in blood and CSF are correlated strongly with the brain. It is suggested that it could be used to predict intracranial high pressure in all cases with intracranial abnormalities.

References

  1. Silver J, McAllister T, Arciniegas D. Textbook of Traumatic Brain Injury 3rd edition. American Psychiatric Association Publishing: Washington, 2019.
  2. Stevens RD, Shoykhet M, Cadena R. Emergency Neurological Life Support: Intracaial Hypertension and Herniation. Neurocrit Care. 2015;23(2):76-82
  3. Rodríguez-Boto G, Rivero-Garvía M, Gutiérrez-González R, Márquez-Rivas J. Basic concepts about brain pathophysiology and intracranial pressure monitoring. Neurología (English Edition). 2015;30(1):16–22.
  4. Dias C, Maia I, Cerejo A, Smielewski P, Paiva JA, Czosnyka M. Plateau Waves of Intracranial Pressure and Multimodal Brain Monitoring. Acta Neurochir Suppl. 2016;122(1):143-6
  5. Radolph W. Evans. Textbook of Neurology and Trauma: Head Trauma. WB Saunders. 2009:27-85.
  6. Schimmel SJ, Acosta S, Lozano D. Neuroinflammation in traumatic brain injury: A chronic response to an acute injury. Brain Circ. 2017;3(3):135–142
  7. Skinner RA, Gibson RM, Rothwell NJ, Pinteaux E, Penny JI. Transport of interleukin-1 across cerebromicrovascular endothelial cells. Br J Pharmacol, 2009;156(7):1115-1123.
  8. Semple BD, Bye N, Ziebell JM, Morganti-Kossmann MC. Deficiency of the chemokine receptor CXCR2 attenuates neutrophil infiltration and cortical damage following closed head injury. Neurobiol Dis, 2010;40(2):394-403
  9. Paban V, Ogier M, Chambon C, Fernandez N, Davidsson J, Risling M, et al. Molecular gene expression following blunt and rotational models of traumatic brain injury parallel injuries associated with stroke and depression. J Transl Sci, 2016;2(1):208-219
  10. Wang HC, Yang TM, Lin YJ, Chen WF, Chen WF, Ho JT, Lin YT, et al. Serial serum leukocyte apoptosis levels as predictors of outcome in acute traumatic brain injury. Biomed Res Int. 2014;4(1):334-343
  11. Krajewska M, You Z, Rong J, Kress C, Huang X, Yang J, et al. Neuronal Deletion of Caspase 8 Protects against Brain Injury in Mouse Models of Controlled Cortical Impact and Kainic Acid-Induced Excitotoxicity. PLoS ONE, 2011;6(9):e24341
  12. Antoniou X, Borsello T, Lüscher TF, Camici GG. Antioxidants and Neuroprotection. In: Laher I. (eds) Systems Biology of Free Radicals and Antioxidants. Springer, Berlin. 2014;1:2175-2189
  13. Yang J, Liu C, Du X, Liu M, Ji X, Du H, et al. Hypoxia Inducible Factor 1α Plays a Key Role in Remote Ischemic Preconditioning Against Stroke by Modulating Inflammatory Responses in Rats. J Am Heart Assoc. 2018;7(5):e007589.
  14. Majmundar A, Wong W, Simon M. Hypoxia inducible factors and the response to hypoxic stress. Mol Cell. 2010;40(2):294-309.
  15. Zimna A, Kurpisz M. Hypoxia-Inducible Factor-1 in Physiological and Pathophysiological Angiogenesis: Applications and Therapies. BioMed Research International, 2015;3(2):1–13.
  16. Chen H, Wei A, He J, Yu M, Mang J, Xu Z. Changes of hypoxia-inducible factor-1 signaling and the effect of cilostazol in chronic cerebral ischemia. Neural Regen Res. 2013;8(19):1803-13
  17. Gadoth, N. Chapter 3 Free radicals: their role in brain function and dysfunction. In: D. Armstrong and R. D. Stratton (eds). Oxidative Stress and Antioxidant Protection. John Wiley & Sons: Washington. 2016.
  18. Mates J, Perez-Gomez C, De Castro I. Antioxiant Enzymes and Human Diseases. Clinical Biochemistry, 1999;32(8):595-603.
  19. Kil HN, Eom SY, Park JD, Kawamoto T, Kim YD, Kim H. A rapid method for estimating the levels of urinary thiobarbituric Acid reactive substances for environmental epidemiologic survey. Toxicol Res. 2014;30(1):7-11.
  20. Lorente L. Biomarkers Associated with the Outcome of Traumatic Brain Injury Patients. Brain Sci. 2017;7(11):142.
  21. Chen H, Yoshioka H, Kim GS, Jung JE, Okami N, Sakata H, et al. Oxidative Stress in Ischemic Brain Damage: Mechanisms of Cell Death and Potential Molecular Targets for Neuroprotection. Antiovid Redox Signal. 2011;14(8):1505-1517.
  22. Zeiger SL, Musiek ES, Zanoni G, Vidari G, Morrow JD, Milne GJ, et al. Neurotoxic lipid peroxidation species formed by ischemic stroke increase injury. Free Radic Biol Med. 2010;47(10):1422-1431.
  23. Sentosa KW, Yehezkiel. Neurocritical care for traumatic brain injury in intensive care unit of Dr H. Andi Abdurahman Noor Hospital, Indonesia. Bali Medical Journal. 2019;8(1):134-137.
  24. Arifianto MR, Ma’ruf AZ, Ibrahim A. Efficacy comparison of mannitol and hypertonic saline for Traumatic Brain Injury (TBI) treatment. Bali Medical Journal. 2016;5(3):516-521.
  25. Wijanarko B, Sumartono C, Wirabuana B, Hardiono, Semedi BP, Airlangga PS. Effects of Tourniquet Inflation on Blood Pressure, Mean Arterial Pressure, and Pulse Rate during the Maintenance of Anesthesia Using a Combination of Dexmedetomidine and Isoflurane for Patients Undergoing Lower Extremity Surgery. Bali Medical Journal. 2023;12(1):1033-1040.

How to Cite

Sadewo, W., Wanandi, S. I., Rustam, Z., Gunawan, K., & Nugroho, S. W. (2023). The correlation between oxidative stress markers and increasing intracranial pressure: a study of Malondialdehyde (MDA), Superoxide Dismutase (MnSOD), Nicotinamide Adenine Dinucleotide Phosphate Hydrogen (NADPH), and catalase. Bali Medical Journal, 12(3), 2696–2702. https://doi.org/10.15562/bmj.v12i3.4654

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Wismaji Sadewo
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Septelia Inawati Wanandi
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Zuherman Rustam
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Kevin Gunawan
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Setyo Widi Nugroho
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