Acrolein detection: potential theranostic utility in multiple sclerosis and spinal cord injury

References

• Hall ED. Free radicals and CNS injury. Crit Care Clin 1989;5(4):793-805
   Google Scholar
• Hall ED, Braughler JM. Free radicals in CNS injury. Res Publ Assoc Res Nerv Ment Dis 1993;71:81-105
   PubMedGoogle Scholar
• Halliwell B, Gutteridge JMC. Free radicals in biology and medicine. Clarendon Press, Oxford University Press; Oxford, NY, USA: 1999
   Google Scholar
• Coyle JT, Puttfarcken P. Oxidative stress, glutamate, and neurodegenerative disorders. Science 1993;262(5134):689-95
   PubMed Web of Science ®Google Scholar
• Gilgun-Sherki Y, Melamed E, Offen D. The role of oxidative stress in the pathogenesis of multiple sclerosis: the need for effective antioxidant therapy. J Neurol 2004;251(3):261-8
   PubMed Web of Science ®Google Scholar
• Hall ED. Lipid peroxidation. Adv Neurol 1996;71:247-57. discussion 257-48
   Google Scholar
• Bragt PC, Bonta IL. Oxidant stress during inflammation: anti-inflammatory effects of antioxidants. Agents Actions 1980;10(6):536-9
   Google Scholar
• Luo J, Shi R. Acrolein induces axolemmal disruption, oxidative stress, and mitochondrial impairment in spinal cord tissue. Neurochem Int 2004;44(7):475-86
   PubMed Web of Science ®Google Scholar
• Smith KJ, Kapoor R, Felts PA. Demyelination: the role of reactive oxygen and nitrogen species. Brain Pathol 1999;9(1):69-92
   PubMed Web of Science ®Google Scholar
• Esterbauer H, Schaur RJ, Zollner H. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes. Free Radic Biol Med 1991;11(1):81-128
   PubMed Web of Science ®Google Scholar
• Kehrer JP, Biswal SS. The molecular effects of acrolein. Toxicol Sci 2000;57(1):6-15
   PubMed Web of Science ®Google Scholar
• Lovell MA, Xie C, Markesbery WR. Acrolein, a product of lipid peroxidation, inhibits glucose and glutamate uptake in primary cultures. Free Radic Biol Med 2000;29:714-20
   PubMed Web of Science ®Google Scholar
• Burcham PC, Raso A, Thompson CA. Toxicity of smoke extracts towards A549 lung cells: role of acrolein and suppression by carbonyl scavengers. Chem Biol Interact 2010;183(3):416-24
   Google Scholar
• Feng Z, Hu W, Hu Y, Tang MS. Acrolein is a major cigarette-related lung cancer agent: preferential binding at p53 mutational hotspots and inhibition of DNA repair. Proc Natl Acad Sci U S A 2006;103(42):15404-9
   PubMed Web of Science ®Google Scholar
• Ghilarducci DP, Tjeerdema RS. Fate and effects of acrolein. Rev Environ Contam Toxicol 1995;144:95-146
   PubMed Web of Science ®Google Scholar
• Ho SS, Yu JZ, Chu KW, Yeung LL. Carbonyl emissions from commercial cooking sources in Hong Kong. J Air Waste Manag Assoc 2006;56(8):1091-8
   Google Scholar
• Magnusson R, Nilsson C, Andersson B. Emissions of aldehydes and ketones from a two-stroke engine using ethanol and ethanol-blended gasoline as fuel. Environ Sci Technol 2002;36(8):1656-64
   Web of Science ®Google Scholar
• Bai L, Wang W, Dong YL, et al. Attenuation of Mouse Somatic and Emotional Inflammatory Pain by Hydralazine Through Scavenging Acrolein and Inhibiting Neuronal Activation. Pain Physician 2012;15:311-26
   Google Scholar
• Huang YJ, Jin MH, Pi RB, et al. Acrolein induces Alzheimer’s disease-like pathologies in vitro and in vivo. Toxicol Lett 2013;217(3):184-91
   Google Scholar
• Leung G, Sun W, Zheng L, et al. Anti-acrolein treatment improves behavioral outcome and alleviates myelin damage in experimental autoimmune encephalomyelitis mouse. Neuroscience 2011;173:150-5
   PubMed Web of Science ®Google Scholar
• Pocernich CB, Cardin AL, Racine CL, et al. Glutathione elevation and its protective role in acrolein-induced protein damage in synaptosomal membranes: relevance to brain lipid peroxidation in neurodegenerative disease. Neurochem Int 2001;39(2):141-9
   PubMed Web of Science ®Google Scholar
• Lovell MA, Xie C, Markesbery WR. Acrolein is increased in Alzheimer’s disease brain and is toxic to primary hippocampal cultures. Neurobiol Aging 2001;22(2):187-94
   PubMed Web of Science ®Google Scholar
• Luo J, Shi R. Acrolein induces oxidative stress in brain mitochondria. Neurochem Int 2005;46(3):243-52
   Google Scholar
• Shi R, Luo J, Peasley M. Acrolein inflicts axonal membrane disruption and conduction loss in isolated guinea-pig spinal cord. Neuroscience 2002;115(2):337-40
   Web of Science ®Google Scholar
• Leung G, Sun W, Brookes S, et al. Potassium channel blocker, 4-aminopyridine-3-methanol, restores axonal conduction in spinal cord of an animal model of multiple sclerosis. Exp Neurol 2011;227(1):232-5
   Google Scholar
• Luo J, Uchida K, Shi R. Accumulation of acrolein-protein adducts after traumatic spinal cord injury. Neurochem Res 2005;30(3):291-5
   Google Scholar
• Hamann K, Durkes A, Ouyang H, et al. Critical role of acrolein in secondary injury following ex vivo spinal cord trauma. J Neurochem 2008;107(3):712-21
   Google Scholar
• Hamann K, Nehrt G, Ouyang H, et al. Hydralazine inhibits compression and acrolein-mediated injuries in ex vivo spinal cord. J Neurochem 2008;104(3):708-18
   PubMed Web of Science ®Google Scholar
• Hamann K, Shi R. Acrolein scavenging: a potential novel mechanism of attenuating oxidative stress following spinal cord injury. J Neurochem 2009;111(6):1348-56
   PubMed Web of Science ®Google Scholar
• Shi Y, Sun W, McBride JJ, et al. Acrolein induces myelin damage in mammalian spinal cord. J Neurochem 2011;117(3):554-64
   PubMed Web of Science ®Google Scholar
• Park J, Zheng L, Marquis A, et al. Neuroprotective role of hydralazine in rat spinal cord injury-attenuation of acrolein-mediated damage. J Neurochem 2014;129(2):339-49
   Google Scholar
• Liu-Snyder P, McNally H, Shi R, Borgens RB. Acrolein-mediated mechanisms of neuronal death. J Neurosci Res 2006;84(1):209-18
   Google Scholar
• Shields DC, Banik NL. Pathophysiological role of calpain in experimental demyelination. J Neurosci Res 1999;55(5):533-41
   Google Scholar
• Sun W, Smith D, Fu Y, et al. Novel potassium channel blocker, 4-AP-3-MeOH, inhibits fast potassium channels and restores axonal conduction in injured guinea pig spinal cord white matter. J Neurophysiol 2011;103(1):469-78
   Google Scholar
• Sinkuvene DS. [Hygienic assessment of acrolein as an air pollutant]. Gig Sanit 1970;35(3):6-10
   Google Scholar
• Osorio VM, de Lourdes Cardeal Z. Determination of acrolein in french fries by solid-phase microextraction gas chromatography and mass spectrometry. J Chromatogr A 2011;1218(21):3332-6
   Google Scholar
• Cahill TM, Charles MJ, Seaman VY; Committee HEIHR. Development and application of a sensitive method to determine concentrations of acrolein and other carbonyls in ambient air. Res Rep 2010(149):3-46
   Google Scholar
• Uchida K, Kanematsu M, Sakai K, et al. Protein-bound acrolein: potential markers for oxidative stress. Proc Natl Acad Sci U S A 1998;95(9):4882-7
   PubMed Web of Science ®Google Scholar
• Yan W, Byrd GD, Brown BG, Borgerding MF. Development and validation of a direct LC-MS-MS method to determine the acrolein metabolite 3-HPMA in urine. J Chromatogr Sci 2010;48(3):194-9
   Google Scholar
• Zheng L, Park J, Walls M, et al. Determination of urine 3-HPMA, a stable acrolein metabolite in a rat model of spinal cord injury. J Neurotrauma 2013;30(15):1334-41
   Google Scholar
• Abraham K, Andres S, Palavinskas R, et al. Toxicology and risk assessment of acrolein in food. Mol Nutr Food Res 2011;55(9):1277-90
   PubMed Web of Science ®Google Scholar
• Wang H, Manicke NE, Yang Q, et al. Direct analysis of biological tissue by paper spray mass spectrometry. Anal Chem 2011;83(4):1197-20
   PubMed Web of Science ®Google Scholar
• Waragai M, Yoshida M, Mizoi M, et al. Increased protein-conjugated acrolein and amyloid-beta40/42 ratio in plasma of patients with mild cognitive impairment and Alzheimer’s disease. J Alzheimers Dis 2012;32(1):33-41
   Google Scholar
• Shao C, Roberts KN, Markesbery WR, et al. Oxidative stress in head trauma in aging. Free Radic Biol Med 2006;41(1):77-85
   Google Scholar
• Bohnenstengel F, Eichelbaum M, Golbs E, Kroemer HK. High-performance liquid chromatographic determination of acrolein as a marker for cyclophosphamide bioactivation in human liver microsomes. J Chromatogr B Biomed Sci Appl 1997;692(1):163-8
   Google Scholar
• Gugliucci A, Tsuji M, Kinugasa E, et al. High free serum acrolein levels in bacterial infection and other disease states associated with oxidative stress: a potential biomarker? Clin Chem Lab Med 2007;45(11):1559-60
   Google Scholar
• Schettgen T, Musiol A, Kraus T. Simultaneous determination of mercapturic acids derived from ethylene oxide (HEMA), propylene oxide (2-HPMA), acrolein (3-HPMA), acrylamide (AAMA) and N,N-dimethylformamide (AMCC) in human urine using liquid chromatography/tandem mass spectrometry. Rapid Commun Mass Spectrom 2008;22(17):2629-38
   Google Scholar
• Yoshida M, Mikami T, Higashi K, et al. Inverse correlation between stroke and urinary 3-hydroxypropyl mercapturic acid, an acrolein-glutathione metabolite. Clin Chim Acta 2012;413(7-8):753-9
   Google Scholar