Kinetic change of oxidative stress in cerebrospinal fluid of mice infected with Angiostrongylus cantonensis

Redox Report

Volumn 15, Issue 1, 2010, Pages 43-48

  Chung, Li Yu ^a   Wang, Lian Chen ^b   Chen, Chun Hsiang ^c   Lin, Hsiao Yi ^a   Yen, Chuan Min ^a  

^a KAOHSIUNG MEDICAL UNIVERSITY   (Taiwan)

^b CHANG GUNG UNIVERSITY COLLEGE OF MEDICINE   (Taiwan)

^c MEIHO UNIVERSITY   (Taiwan)

Author keywords

8 isoprostane; 8 ohdg; Angiostrongylus cantonensis; Malondialdehyde; Oxidative stress; Reactive oxygen species; Superoxide dismutase

Indexed keywords

8 HYDROXYDEOXYGUANOSINE; 8 ISOPROSTANE; CATALASE; DNA; LIPID; MALONALDEHYDE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE DISMUTASE;

ANGIOSTRONGYLIASIS; ANGIOSTRONGYLUS CANTONENSIS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CEREBROSPINAL FLUID; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DNA DAMAGE; ENZYME ACTIVITY; LIPID PEROXIDATION; MOUSE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL;

ANGIOSTRONGYLUS CANTONENSIS; ANIMALS; CATALASE; DEOXYGUANOSINE; DINOPROST; KINETICS; MALONDIALDEHYDE; MICE; MICE, INBRED C57BL; OXIDATIVE STRESS; REACTIVE OXYGEN SPECIES; STRONGYLIDA INFECTIONS; SUPEROXIDE DISMUTASE;

ANGIOSTRONGYLUS CANTONENSIS; MUS;

EID: 77949478653     PISSN: 13510002     EISSN: 17432928     Source Type: Journal    
DOI: 10.1179/174329210X12650506623203     Document Type: Article

References (33)

1. Zawia NH, Lahiri DK, Cardozo-Pelaez F. Epigenetics, oxidative stress, and Alzheimer disease. Free Radic Biol Med 2009; 46: 1241-1249.
2. van Horssen J, Schreibelt G, Drexhage J et al. Severe oxidative damage in multiple sclerosis lesions coincides with enhanced antioxidant enzyme expression. Free Radic Biol Med 2008; 45: 1729-1737.
3. Radwanska-Wala B, Buszman E, Druzba D. Reactive oxygen species in pathogenesis of central nervous system diseases. Wiad Lek 2008; 61: 67-73.
4. Koedel U, Pfister HW. Superoxide production by primary rat cerebral endothelial cells in response to pneumococci. J Neuroimmunol 1999; 96: 190-200.
5. Klein M, Koedel U, Pfister HW. Oxidative stress in pneumococcal meningitis: a future target for adjunctive therapy? Prog Neurobiol 2006; 80: 269-280.
6. Cheng CW, Sato Y, Chen ER. Epidemiological and clinical observations on eosinophilic meningitis and meningoencephalitis of children caused by infection with Angiostrongylus cantonensis in southern Taiwan. Ryukyu Med J 1984; 7: 1-9.
7. Tsai HC, Liu YC, Kunin CM et al. Eosinophilic meningitis caused by Angiostrongylus cantonensis: report of 17 cases. Am J Med 2001; 111: 109-114.
8. Hung TP, Chen ER. Angiostrongyliasis (Angiostrongylus cantonensis). In: Vinken PT, Bruyn GW, Klawans HL. (eds) Handbook of Clinical Neurology, 8th edn Amsterdam: Elsevier, 1988; 545-562.
9. Wang QP, Lai DH, Zhu XQ, Chen XG, Lun ZR. Human angiostrongyliasis. Lancet Infect Dis 2008; 8: 621-630.
10. Kittimongkolma S, Intapan PM, Laemviteevanich K, Kanpittaya J, Sawanyawisuth K, Maleewong W. Eosinophilic meningitis associated with angiostrongyliasis: clinical features, laboratory investigations and specific diagnostic IgG and IgG subclass antibodies in cerebrospinal fluid. Southeast Asian J Trop Med Public Health 2007; 38: 24-31.
11. Sugaya H, Yoshimura K. T-cell dependent eosinophilia in the cerebrospinal fluid of the mouse infected with Angiostrongylus cantonensis. Parasite Immunol 1988; 10: 127-138.
12. Chang EE, Chung LY, Yen CM. Kinetics of change in the eotaxin concentration in serum and cerebrospinal fluid of mice infected with Angiostrongylus cantonensis. Parasitol Res 2004; 92: 137-141.
13. John DT, Martinez AJ. Animal model: eosinophilic meningo encephalitis in mice infected with Angiostrongylus cantonensis. Am J Pathol 1975; 80: 345-348.
14. Burlingame JM, Esfandiari N, Sharma RK, Mascha E, Falcone T. Total antioxidant capacity and reactive oxygen species in amniotic fluid. Obstet Gynecol 2003; 101: 756-761.
15. Gawet S, Wardas M, Niedworok E, Wardas P.Malondialdehyde (MDA) as a lipid peroxidation marker. Wiad Lek 2004; 57: 453-455.
16. Greco A, Minghetti L. Isoprostanes as biomarkers and mediators of oxidative injury in infant and adult central nervous system diseases. Curr Neurovasc Res 2004; 1: 341-354.
17. Tsukahara H, Haruta T, Ono N et al. Oxidative stress in childhood meningitis: measurement of 8-hydroxy-2′-deoxyguanosine concentration in cerebrospinal fluid. Redox Rep 2000; 5: 295-298.
18. Lee JD, Tsai LY, Chen CH, Wang JJ, Hsiao JK, Yen CM. Blood-brain barrier dysfunction occurring in mice infected with Angiostrongylus cantonensis. Acta Trop 2006; 97: 204-211.
19. de Menezes CC, Dorneles AG, Sperotto RL, Duarte MMF, Schetinger MRC, Loro VL. Oxidative stress in cerebrospinal fluid of patients with aseptic and bacterial meningitis.Neurochem Res 2009; 34: 1255-1260.
20. Sasaki D, Sugaya H, Ishida K, Yoshimura K. Ablation of eosinophils with anti-IL-5 antibody enhances the survival of intracranial worms of Angiostrongylus cantonensis in mouse.Parasite Immunol 1993; 15: 349-354.
21. Inoue M. Protective mechanisms against reactive oxygen species. In: Arias IM, Boyer JL, Fausto N, Jakoby WB, Schachter DA, Shafritz DA. (eds) The liver: biology and pathobiology. New York: Raven, 1994; 443-459.
22. Pabon A, Carmona J, Burgos LC, Blair S. Oxidative stress in patients with non-complicated malaria. Clin Biochem2003; 36: 71-78.
23. Das BS, Mohanty S, Mishra SK et al. Increased cerebrospinal fluid protein and lipid peroxidation products in patients with cerebral malaria. Trans R Soc Trop Med Hyg 1991; 85: 733-734.
24. Manoli LP, Gamaro GD, Silverira PP, Dalmaz C. Effect of chronic variate stress on thiobarbituric-acid reactive species and on total radical-trapping potential in distinct regions of rat brain. Neurochem Res 2000; 25: 915-921.
25. Lindo JF, Escoffery CT, Reid B, Codrington G, Cunningham-Myrie C, Eberhard ML. Fatal autochthonous eosinophilic meningitis in a Jamaican child caused by Angiostrongylus cantonensis. Am J Trop Med Hyg 2004; 70: 425-428.
26. Wang LC, Wan DP, Jung SM, Chen CC, Waong HF, Wan YL. Magnetic resonance imaging findings in the brains of rabbits infected with Angiostrongylus cantonensis: a long-term investigation. J Parasitol 2005; 91: 1237-1239.
27. Greco A, Minghetti L, Levi G. Isoprostanes, novel markers of oxidative injury, help understanding the pathogenesis of neurodegenerative diseases. Neurochem Res 2000; 25: 1357-1364.
28. Marnett LJ. Oxyradicals and DNA damage. Carcinogenesis 2000; 21: 361-370.
29. Nakae D, Kobayashi Y, Akai H et al. Involvement of 8-hydroxyguanine formation in the initiation of rat liver carcinogenesis by low dose levels of N-nitro-sodiethylamine. Cancer Res 1997; 57: 1281-1287.
30. Shibutani S, Takeshita M, Grollman AP. Insertion of specific base during DNA synthesis past the oxidation-damaged base 8-oxodG. Nature 1991; 349: 431-434.
31. Fukuda M, Yamauchi H, Yamamoto H et al. The evaluation of oxidative DNA damage in children with brain damage using 8-hyroxy - deoxyguanosine levels. Brain Dev 2008; 30: 131-136.
32. Lee HH, Shiow SJ, Chung HC et al. Development of brain injury in mice by Angiostrongylus cantonensis infection is associated with the induction of transcription factor NF-κB, nuclear protooncogenes, and protein tyrosine phosphorylation. Exp Parasitol 2000; 95: 202-208.
33. Lan KP, Wang CJ, Hsu JD, Chen KM, Lai SC, Lee HH. Induced eosinophilia and proliferation in Angiostrongylus cantonensis-infected mouse brain are associated with the induction of JAK/STAT1, IAP/NF- κB and MEKK1/JNK signals. J Helminthol 2004, 78: 311-317.