| Fluids and Barriers of the CNS | |
| Oral antioxidant therapy for juvenile rats with kaolin-induced hydrocephalus | |
| Marc R Del Bigio1  Emily Turner-Brannen2  Domenico L Di Curzio2  | |
| [1] Department of Pathology, University of Manitoba, 727 McDermot Avenue, Winnipeg, R3E 3P5, Canada;Manitoba Institute of Child Health, 715 McDermot Avenue, Winnipeg, MB R3E 3P4, Canada | |
| 关键词: Oxidative stress; Antioxidant; Hydrocephalus; Brain; Rodent model; | |
| Others : 1098239 DOI : 10.1186/2045-8118-11-23 |
|
| received in 2014-07-28, accepted in 2014-09-23, 发布年份 2014 | |
PDF
|
|
【 摘 要 】
Background
Oxidative and nitrosylative changes have been shown to occur in conjunction with the hypoxic changes and cellular/axonal damage in hydrocephalic rodent brains. We hypothesized that antioxidant therapy would improve behavioral, neurophysiological, and/or neurobiochemical outcomes in juvenile rats following induction of hydrocephalus.
Methods
Three-week old rats received an injection of kaolin (aluminum silicate) into the cisterna magna. Magnetic resonance (MR) imaging was performed two weeks later to assess ventricle size and stratify rats to four treatment conditions. Rats were treated for two weeks daily with sham therapy of either oral canola oil or dextrose or experimental therapy of a low or high dose of an antioxidant mixture containing α-tocopherol, L-ascorbic acid, coenzyme Q10 (CoQ10), reduced glutathione, and reduced lipoic acid. Behavior was examined thrice weekly.
Results
All hydrocephalic groups lagged in weight gain in comparison to non-hydrocephalic controls, all developed significant ventriculomegaly, and all exhibited white matter destruction. Canola oil with or without the antioxidant mixture normalized antioxidant capacity in brain tissue, and the dextrose-treated rats had the greatest ventricular enlargement during the treatment period. However, there were no significant differences between the four treatment groups of hydrocephalic rats for the various behavioral tasks. Glial fibrillary acidic protein and myelin basic protein quantitation showed no differences between the treatment groups or with control rats. There was increased lipid peroxidation in the hydrocephalic rats compared to controls but no differences between treatment groups.
Conclusion
The antioxidant cocktail showed no therapeutic benefits for juvenile rats with kaolin-induced hydrocephalus although canola oil might have mild benefit.
【 授权许可】
2014 Di Curzio et al.; licensee BioMed Central Ltd.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150131021359982.pdf | 1224KB | ||
| Figure 2. | 65KB | Image | |
| Figure 1. | 125KB | Image |
【 图 表 】
Figure 1.
Figure 2.
【 参考文献 】
- [1]Del Bigio M: Neuropathology and structural changes in hydrocephalus. Develop Disabil Res Rev 2010, 16:16-22.
- [2]McAllister J II: Pathophysiology of congenital and neonatal hydrocephalus. Sem Fet Neonat Med 2012, 17:285-294.
- [3]Del Bigio M, Khan OH, da Silva Lopes L, Packiasamy ARJ: Cerebral white matter oxidation and nitrosylation in young rodents with kaolin-induced hydrocephalus. J Neuropathol Exp Neurol 2012, 71(4):274-288.
- [4]Butterfield D: Oxidative stress in neurodegenerative disorders. Antioxid Redox Signal 2006, 8(11–12):1971-1973.
- [5]Emerit J, Edeas M, Bricaire F: Neurodegenerative diseases and oxidative stress. Biomed Pharmacother 2004, 58(1):39-46.
- [6]Simonian N, Coyle JT: Oxidative stress in neurodegenerative diseases. Annu Rev Pharmacol Toxicol 1996, 36:83-106.
- [7]Sun A, Chen YM: Oxidative stress and neurodegenerative disorders. J Biomed Sci 1998, 5:401-414.
- [8]Uttara B, Singh AV, Zamboni P, Mahajan RT: Oxidative stress and neurodegenerative diseases: a review of upstream and downstream antioxidant therapeutic options. Curr Neuropharm 2009, 7:65-74.
- [9]Caner H, Atasever A, Kilinç K, Durgun B, Peker S, Ozcan OE: Lipid peroxide level increase in experimental hydrocephalus. Acta Neurochir (Wien) 1993, 121(1–2):68-71.
- [10]Etus V, Gazioglu N, Belce A: N-acetylcystein reduces cerebral lipid peroxidation in a rat model of infantile hydrocephalus. J Neurol Sci (Turkish) 2001, 18(1):#2.
- [11]Etus V, Altug T, Belce A, Ceylan S: Green tea polyphenol (-)-epigallocatechin gallate prevents oxidative damage on periventricular white matter of infantile rats with hydrocephalus. Tohoku J Exp Med 2003, 200(4):203-209.
- [12]Socci D, Bjugstad KB, Jones HC, Pattisapu JV, Arendash GW: Evidence that oxidative stress is associated with the pathophysiology of inherited hydrocephalus in the H-Tx rat model. Exp Neurol 1999, 155(1):109-117.
- [13]Mori K, Miyake H, Kurisaka M, Sakamoto T: Immunohistochemical localization of superoxide dismutase in congenital hydrocephalic rat brain. Childs Nerv Syst 1993, 9:136-141.
- [14]Pudenz R: The surgical treatment of hydrocephalus: an historical review. Surg Neurol 1981, 15(1):15-26.
- [15]Del Bigio M: Cellular damage and prevention in childhood hydrocephalus. Brain Pathol 2004, 14(3):317-324.
- [16]Eskandari R, McAllister JP II, Miller JM, Ding Y, Ham SD, Shearer DM, Way JS: Effects of hydrocephalus and ventriculoperitoneal shunt therapy on afferent and efferent connections in the feline sensorimotor cortex. J Neurosurg 2004, 101(2 Suppl):196-210.
- [17]Epstein F: How to keep shunts functioning, or “the impossible dream”. Clin Neurosurg 1985, 32:608-631.
- [18]Riva D, Milani N, Giorgi C, Pantaleoni C, Zorzi C, Devoti M: Intelligence outcome in children with shunted hydrocephalus of different etiology. Childs Nerv Syst 1994, 10(1):70-73.
- [19]Del Bigio M, Massicotte EM: Protective effect of nimodipine on behavior and white matter of rats with hydrocephalus. J Neurosurg 2001, 94(5):788-794.
- [20]Khan O, Enno T, Del Bigio MR: Magnesium sulfate therapy is of mild benefit to young rats with kaolin-induced hydrocephalus. Pediatr Res 2003, 53(6):970-976.
- [21]Botfield H, Gonzalez AM, Abdullah O, Skjolding AD, Berry M, McAllister JP II, Logan A: Decorin prevents the development of juvenile communication hydrocephalus. Brain 2013, 136:2842-2858.
- [22]Del Bigio M, Crook CR, Buist R: Magnetic resonance imaging and behavioral analysis of immature rats with kaolin-induced hydrocephalus: pre- and postshunting observations. Exp Neurol 1997, 148:256-264.
- [23]Del Bigio M, Kanfer JN, Zhang YW: Myelination delay in the cerebral white matter of immature rats with kaolin-induced hydrocephalus is reversible. J Neuropathol Exp Neurol 1997, 56(9):1053-1066.
- [24]Del Bigio M, Zhang YW: Cell death, axonal damage, and cell birth in the immature rat brain following induction of hydrocephalus. Exp Neurol 1998, 154:157-169.
- [25]Romijn H, Hofman MA, Gramsbergen A: At what age is the developing cerebral cortex of the rat comparable to that of the full-term newborn human baby? Early Human Dev 1991, 26:61-67.
- [26]Tuor U, Del Bigio MR, Chumas PD: Brain damage due to cerebral hypoxia/ischemia in the neonate: pathology and pharmacological modification. Cerebrovasc Brain Metab Rev 1996, 8:159-193.
- [27]Clancy B, Darlington RB, Finlay BL: Translating developmental time across mammalian species. Neuroscience 2001, 105(1):7-17.
- [28]Littarru G, Tiano L: Bioenergetic and antioxidant properties of coenzyme Q10: recent developments. Mol Biotechnol 2007, 37(1):31-37.
- [29]Young A, Johnson S, Steffens DC, Doraiswamy PM: Coenzyme Q10: a review of its promise as a neuroprotectant. CNS Spectr 2007, 12(1):62-68.
- [30]Zhang B, Tanaka J, Yang L, Yang L, Sakanaka M, Hata R, Maeda N, Mitsuda N: Protective effect of vitamin E against focal brain ischemia and neuronal death through induction of target genes of hypoxia-inducible factor-1. Neuroscience 2004, 126:433-440.
- [31]Ibrahim W, Bhagavan HN, Chopra RK, Chow CK: Dietary coenzyme Q10 and vitamin E alter the status of these compounds in rat tissues and mitochondria. J Nutr 2000, 130:2343-2348.
- [32]Gonzalez-Perez O, Gonzalez-Castaneda RE, Huerta M, Luquin S, Gomez-Pinedo U, Sanchez-Almaraz E, Navarro-Ruiz A, Garcia-Estrada J: Beneficial effects of α-lipoic acid plus vitamin E on neurological deficit, reactive gliosis and neuronal remodeling in the penumbra of the ischemic rat brain. Neurosci Let 2002, 321:100-104.
- [33]Marriage B, Clandinin MT, Glerum DM: Nutritional cofactor treatment in mitochondrial disorders. J Am Diet Assoc 2003, 103:1029-1038.
- [34]Faria R, Abilio VC, Grassl C, Chinen CC, Negrao LT, de Castro JP, Fukushiro DF, Rodrigues MS, Gomes PH, Registro S, de Carvalho Rde C, D’Almeida V, Silva RH, Ribeiro Rde A, Frussa-Filho R: Beneficial effects of vitamin C and vitamin E on reserpine-induced oral dyskinesia in rats: Critical role of striatal catalase activity. Neuropharmacology 2005, 48(7):993-1001.
- [35]Vatassery G, Lai JC, DeMaster EG, Smith WE, Quach HT: Oxidation of vitamin E and vitamin C and inhibition of brain mitochondrial oxidative phosphorylation by peroxynitrite. J Neurosci Res 2004, 75(6):845-853.
- [36]Sharma P, Ahmad Shah Z, Kumar A, Islam F, Mishra KP: Role of combined administration of Tiron and glutathione against aluminum-induced oxidative stress in rat brain. J Trace Elem Med Biol 2007, 21(1):63-70.
- [37]Garcia-Estrada J, Gonzalez-Perez O, Gonzalez-Castaneda RE, Martinez-Contreras A, Luquin S, de la Mora PG, Navarro-Ruiz A: An alpha-lipoic acid-vitamin E mixture reduces post-embolism lipid peroxidation, cerebral infarction, and neurological deficit in rats. Neurosci Res 2003, 47(2):219-224.
- [38]Metz G, Whishaw IQ: The ladder rung walking task: a scoring system and its practical application. J Vis Exp 2009, 28:e1204.
- [39]Di Curzio D, Buist RJ, Del Bigio MR: Reduced subventricular zone proliferation and white matter damage in juvenile ferrets with kaolin-induced hydrocephalus. Exp Neurol 2013, 248:112-128.
- [40]Khan O, Enno TL, Del Bigio MR: Brain damage in neonatal rats following kaolin induction of hydrocephalus. Exp Neurol 2006, 200(2):311-320.
- [41]Ohkawa H, Ohishi N, Yagi K: Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979, 95(2):351-358.
- [42]Wakamatsu D, Morimura S, Sawa T, Kida K, Nakal C, Maeda H: Isolation, identification, and structure of a potent alkyl-peroxyl radical scavenger in crude canola oil, canolol. Biosci Biotechnol Biochem 2005, 69(8):1568-1574.
- [43]Del Bigio M, Wang X, Wilson MJ: Sodium channel-blocking agents are not of benefit to rats with kaolin-induced hydrocephalus. Neurosurgery 2002, 51:460-466.
- [44]Khan O, Enno T, Del Bigio MR: Tacrolimus and cyclosporine A are of no benefit to young rats with kaolin-induced hydrocephalus. Pediatr Neurosurg 2003, 39:309-313.
- [45]Khan O, McPhee LC, Moddemann LN, Del Bigio MR: Calcium antagonism in neonatal rats with kaolin-induced hydrocephalus. J Child Neurol 2007, 22(10):1161-1166.
- [46]McAllister J II, Miller JM: Minocycline inhibits glial proliferation in the H-Tx rat model of congenital hydrocephalus. Cerebrospinal Fluid Res 2010, 7(1):7. BioMed Central Full Text
- [47]Cabuk B, Etus V, Bozkurt SU, Sav A, Ceylan S: Neuroprotective effect of memantine on hippocampal neurons in infantile rat hydrocephalus. Turk Neurosurg 2011, 21(3):352-358.
- [48]Botsoglou N, Fletouris DJ, Papageorgiou GE, Vassilopoulos VN, Mantis AJ, Trakatellis AG: Rapid, sensitive, and specific thiobarbituric acid method for measuring lipid peroxidation in animal tissue, food, and feedstuff samples. J Agric Food Chem 1994, 42:1931-1937.
- [49]Fisher M, Feuerstein G, Howells DW, Hurn PD, Kent TA, Savitz SI, Lo EH, STAIR Group: Update of the stroke therapy academic industry roundtable preclinical recommendations. Stroke 2009, 40(6):2244-2250.
- [50](STAIR) STAIR Group: Recommendations for standards regarding preclinical neuroprotective and restorative drug development. Stroke 1999, 30:2752-2758.
- [51]Del Bigio M, Slobodian I, Schellenberg AE, Buist RJ, Kemp-Buors TL: Magnetic resonance imaging indicators of blood–brain barrier and brain water changes in young rats with kaolin-induced hydrocephalus. Fluids Barriers CNS 2011, 8:22. BioMed Central Full Text
- [52]Kannan R, Kuhlenkamp JF, Jeandidier E, Trinh H, Ookhtens M, Kaplowitz N: Evidence for carrier-mediated transport of glutathione across the blood–brain barrier in the rat. J Clin Invest 1990, 85:2009-2013.
- [53]Zhang Y, Turunen M, Appelkvist EL: Restricted uptake of coenzyme Q is in contrast to unrestricted uptake of α-tocopherol into rat organs and cells. J Nutr 1996, 126:2089-2097.
- [54]Matthews R, Yang L, Browne S, Balk M, Beal F: Coenzyme Q10 administration increases brain mitochondrial concentrations and exerts neuroprotective effects. Proc Natl Acad Sci U S A 1998, 95:8892-8897.
- [55]Zhang Y, Aberg F, Appelkvist EL, Dallner G, Ernster L: Uptake of dietary coenzyme Q supplement is limited in rats. J Nutr 1995, 125:446-453.
- [56]Li H, Klein G, Sun P, Buchan AM: CoQ10 fails to protect brain against focal and global ischemia in rats. Brain Res 2000, 877:7-11.
- [57]Sikorska M, Borowy-Borowski H, Zurakowski B, Walker PR: Derivatised α-tocopherol as a CoQ10 carrier in a novel water-soluble formulation. BioFactors 2003, 18:173-183.
- [58]Sánchez-Moreno C, Dorfman SE, Lichtenstein AH, Martín A: Dietary fat type affects vitamins C and E and biomarkers of oxidative status in peripheral and brain tissues of golden Syrian hamsters. J Nutr 2004, 134(3):655.
- [59]Kuwahara H, Kanazawa A, Wakamatsu D, Morimura S, Kida K, Akaike T, Maeda H: Antioxidative and antimutagenic activities of 4-vinyl-2,6-dimethoxyphenol (canolol) isolated from canola oil. J Agric Food Chem 2004, 52:4380-4387.
- [60]Torreilles F, Salman-Tabcheh S, Guerin M, Torreilles J: Neurodegenerative disorders: The role of peroxynitrite. Brain Res Brain Res Rev 1999, 30:153-163.
- [61]Szabo C: The pathophysiological role of peroxynitrite in shock, inflammation, and ischemia-reperfusion injury. Shock 1996, 6:79-88.
- [62]Quijano C, Romero N, Radi R: Tyrosine nitration by superoxide and nitric oxide fluxes in biological systems: modeling the impact of superoxide dismutase and nitric oxide diffusion. Free Rad Biol Med 2005, 39:728-741.
PDF