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Tau Hyperphosphorylation is Associated with Spatial Learning and Memory After Exposure to Benzo[a]pyrene in SD Rats

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Abstract

As a representative substance of the polycyclic aromatic hydrocarbons, benzo[a]pyrene (B[a]P) is a widely distributed environmental contaminant. Several studies have indicated that B[a]P exposure could impair learning and memory function in human population and animal models. Abnormal hyperphosphorylation and aggregation of microtubule-associated protein tau play a crucial role in neurodegenerative diseases manifesting deficits of learning and memory. In the present study, we investigated the involvement of tau hyperphosphorylation in memory impairment after espousing to B[a]P in SD rats. Male SD rats were randomly divided into five groups: the blank control group received no treatment and the others received intraperitoneal injection of B[a]P (0, 1.0, 2.5, 6.25 mg/kg bw) for 1, 2, and 3 months, respectively. Morris water maze was employed to observe the learning and memory impairment. To find the relationship between cognitive functions and tau protein, we measured the site-specific phosphorylation of tau at Ser199, Ser396, Thr181, and Thr231, which are related with spatial and memory deficits in the brain of rats. The spatial and learning of rats were impaired after exposing to B[a]P for 1 month, so as 2 and 3 months compared to blank control groups, respectively. Rats exposed to 2.5 and 6.25 mg/kg bw B[a]P for either 2 or 3 months had modified behavior compared to control as indicated by the increased latencies, increased the first time arriving at the target space and decreased number crossing the platform and time in target quadrant. B[a]P led to tau hyperphosphorylation at Ser199, Thr181, and Thr231 epitopes. And with time and dose expanded, tau protein, Ser199, Thr181, and Thr231 expression increased. However, the differences in expression of Ser396 at different doses or points were not statistically significant. Moreover, we observed a correlation between memory impairments and tau phosphorylation levels. The present results indicate that Tau hyperphosphorylation is associated with the observed deficits in spatial learning and memory following exposure to B[a]P in SD rats.

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References

  • Alonso Adel C, Mederlyova A, Novak M, Grundke-Iqbal I, Iqbal K (2004) Promotion of hyperphosphorylation by frontotemporal dementia tau mutations. J Biol Chem 279:34873–34881

    Article  PubMed  Google Scholar 

  • Alonso AD, Di Clerico J, Li B, Corbo CP, Alaniz ME, Grundke-Iqbal I, Iqbal K (2010) Phosphorylation of tau at Thr212, Thr231, and Ser262 combined causes neurodegeneration. J Biol Chem 285:30851–30860

    Article  PubMed  CAS  Google Scholar 

  • Aries E, Anderson DR, Fisher R (2008) Exposure assessment of workers to airborne PCDD/Fs, PCBs and PAHs at an electric arc furnace steelmaking plant in the UK. Ann Occup Hyg 52:213–225

    Article  PubMed  CAS  Google Scholar 

  • Armstrong BG, Gibbs G (2009) Exposure-response relationship between lung cancer and polycyclic aromatic hydrocarbons (PAHs). Occup Environ Med 66:740–746

    Article  PubMed  CAS  Google Scholar 

  • Augustinack JC, Schneider A, Mandelkow EM, Hyman BT (2002) Specific tau phosphorylation sites correlate with severity of neuronal cytopathology in Alzheimer’s disease. Acta Neuropathol 103:26–35

    Article  PubMed  CAS  Google Scholar 

  • Bibow S, Mukrasch MD, Chinnathambi S, Biernat J, Griesinger C, Mandelkow E, Zweckstetter M (2011) The dynamic structure of filamentous tau. Angew Chem Int Ed Engl 50:11520–11524

    Article  PubMed  CAS  Google Scholar 

  • Boffetta P, Jourenkova N, Gustavsson P (1997) Cancer risk from occupational and environmental exposure to polycyclic aromatic hydrocarbons. Cancer Causes Control 8:444–472

    Article  PubMed  CAS  Google Scholar 

  • Bolte G, Heitmann D, Kiranoglu M, Schierl R, Diemer J, Koerner W, Fromme H (2008) Exposure to environmental tobacco smoke in German restaurants, pubs and discotheques. J Expo Sci Environ Epidemiol 18:262–271

    Article  PubMed  CAS  Google Scholar 

  • Bondareff W, Harrington CR, Wischik CM, Hauser DL, Roth M (1995) Absence of abnormal hyperphosphorylation of tau in intracellular tangles in Alzheimer’s disease. J Neuropathol Exp Neurol 54:657–663

    Article  PubMed  CAS  Google Scholar 

  • Bramblett GT, Goedert M, Jakes R, Merrick SE, Trojanowski JQ, Lee BM (1993) Abnormal tau phosphorylation at Ser396 in Alzheimer’s disease recapitulates development and contributes to reduced microtubule binding. Neuron 10:1089–10991

    Article  PubMed  CAS  Google Scholar 

  • Brandeis R, Brandys Y, Yehuda S (1989) The use of the Morris Water Maze in the study of memory and learning. Int J Neurosci 48:29–69

    Article  PubMed  CAS  Google Scholar 

  • Buerger K, Teipel SJ, Zinkowski R, Blennow K, Arai H, Engel R, Hofmann-Kiefer K, McCulloch C, Ptok U, Heun R, Andreasen N, DeBernardis J, Kerkman D, Moeller H, Davies P, Hampel H (2002a) CSF tau protein phosphorylated at threonine 231 correlates with cognitive decline in MCI subjects. Neurology 59:627–629

    Article  PubMed  CAS  Google Scholar 

  • Buerger K, Zinkowski R, Teipel SJ, Tapiola T, Arai H, Blennow K, Andreasen N, Hofmann-Kiefer K, DeBernardis J, Kerkman D, McCulloch C, Kohnken R, Padberg F, Pirttila T, Schapiro MB, Rapoport SI, Moller HJ, Davies P, Hampel H (2002b) Differential diagnosis of Alzheimer disease with cerebrospinal fluid levels of tau protein phosphorylated at threonine 231. Arch Neurol 59:1267–1272

    Article  PubMed  Google Scholar 

  • Cai T, Che H, Yao T, Chen Y, Huang C, Zhang W, Du K, Zhang J, Cao Y, Chen J, Luo W (2011) Manganese induces tau hyperphosphorylation through the activation of ERK MAPK pathway in PC12 cells. Toxicol Sci 119:169–177

    Article  PubMed  CAS  Google Scholar 

  • Cai Y, Lv J, Zhang W, Zhang L (2012) Dietary exposure estimates of 16 polycyclic aromatic hydrocarbons (PAHs) in Xuanwei and Fuyuan, counties in a high lung cancer incidence area in China. J Environ Monit 14:886–892

    Article  PubMed  CAS  Google Scholar 

  • Cardenas AM, Ardiles AO, Barraza N, Baez-Matus X, Caviedes P (2012) Role of tau protein in neuronal damage in Alzheimer’s disease and down syndrome. Arch Med Res 43:645–654

    Article  PubMed  CAS  Google Scholar 

  • Chang SH, Hsieh MY, Yang HJ, Chen MC, Kuo CY (2009) Effects of diesel vehicle emissions of polycyclic aromatic hydrocarbons on the surrounding environment and residents. J Environ Sci Health C 27:141–154

    Article  CAS  Google Scholar 

  • Charlesworth G, Gandhi S, Bras JM, Barker RA, Burn DJ, Chinnery PF, Gentleman SM, Guerreiro R, Hardy J, Holton JL, Lees A, Morrison K, Sheerin UM, Williams N, Morris H, Revesz T, Wood NW (2012) Tau acts as an independent genetic risk factor in pathologically proven PD. Neurobiol Aging 33(838):e7–11

    PubMed  Google Scholar 

  • Chen YG (2005) Specific tau phosphorylation sites in hippocampus correlate with impairment of step-down inhibitory avoidance task in rats. Behav Brain Res 158:277–284

    Article  PubMed  CAS  Google Scholar 

  • Cho JH, Johnson GV (2004) Primed phosphorylation of tau at Thr231 by glycogen synthase kinase 3beta (GSK3beta) plays a critical role in regulating tau’s ability to bind and stabilize microtubules. J Neurochem 88:349–358

    Article  PubMed  CAS  Google Scholar 

  • Crepeaux G, Bouillaud-Kremarik P, Sikhayeva N, Rychen G, Soulimani R, Schroeder H (2012) Late effects of a perinatal exposure to a 16 PAH mixture: Increase of anxiety-related behaviours and decrease of regional brain metabolism in adult male rats. Toxicol Lett 211:105–113

    Article  PubMed  CAS  Google Scholar 

  • de Vos RH, van Dokkum W, Schouten A, de Jong-Berkhout P (1990) Polycyclic aromatic hydrocarbons in Dutch total diet samples (1984–1986). Food Chem Toxicol 28:263–268

    Article  PubMed  Google Scholar 

  • del C, Alonso A, Iqbal K (2005) Tau-induced neurodegeneration: a clue to its mechanism. J Alzheimers Dis 8:223–226

    Google Scholar 

  • D’Hooge R, De Deyn PP (2001) Applications of the Morris water maze in the study of learning and memory. Brain Res Brain Res Rev 36:60–90

    Article  PubMed  Google Scholar 

  • Edwards SC, Jedrychowski W, Butscher M, Caman D, Kieltyka A, Mroz E, Flak E, Li Z, Wang S, Rauh V, Perera F (2010) Prenatal exposure to airborne polycyclic aromatic hydrocarbons and children’s intelligence at 5 years of age in a prospective cohort study in Poland. Environ Health Perspect 118:1326–1331

    Article  PubMed  CAS  Google Scholar 

  • Falco G, Domingo JL, Llobet JM, Teixido A, Casas C, Muller L (2003) Polycyclic aromatic hydrocarbons in foods: human exposure through the diet in Catalonia, Spain. J Food Prot 66:2325–2331

    PubMed  CAS  Google Scholar 

  • Goedert M, Jakes R, Crowther RA, Cohen P, Vanmechelen E, Vandermeeren M, Cras P (1994) Epitope mapping of monoclonal antibodies to the paired helical filaments of Alzheimer’s disease: identification of phosphorylation sites in tau protein. Biochem J 301:871–877

    PubMed  CAS  Google Scholar 

  • Grimmer G, Naujack KW, Dettbarn G (1987) Gas chromatographic determination of polycyclic aromatic hydrocarbons, aza-arenes, aromatic amines in the particle and vapor phase of mainstream and side stream smoke of cigarettes. Toxicol Lett 35:117–124

    Article  PubMed  CAS  Google Scholar 

  • Grova N, Valley A, Turner JD, Morel A, Muller CP, Schroeder H (2007) Modulation of behavior and NMDA-R1 gene mRNA expression in adult female mice after sub-acute administration of benzo(a)pyrene. Neurotoxicology 28:630–636

    Article  PubMed  CAS  Google Scholar 

  • Guadagna S, Esiri MM, Williams RJ, Francis PT (2012) Tau phosphorylation in human brain: relationship to behavioral disturbance in dementia. Neurobiol Aging 33:2798–2806

    Article  PubMed  CAS  Google Scholar 

  • Guo S (2004) Linking genes to brain, behavior and neurological diseases: what can we learn from zebrafish? Genes Brain Behav 3:63–74

    Article  PubMed  CAS  Google Scholar 

  • Hanger DP, Seereeram A, Noble W (2009) Mediators of tau phosphorylation in the pathogenesis of Alzheimer’s disease. Expert Rev Neurother 9:1647–1666

    Article  PubMed  CAS  Google Scholar 

  • Hernandez F, Avila J (2007) Tauopathies. Cell Mol Life Sci 64:2219–2233

    Article  PubMed  CAS  Google Scholar 

  • Iijima-Ando K, Zhao L, Gatt A, Shenton C, Iijima K (2010) A DNA damage-activated checkpoint kinase phosphorylates tau and enhances tau-induced neurodegeneration. Hum Mol Genet 19:1930–1938

    Article  PubMed  CAS  Google Scholar 

  • Jaworski J, Psujek M, Bartosik-Psujek H (2009) Total-tau and phospho-tau(181Thr) in cerebrospinal fluid of neurologically intact population increase with age. Folia Biol (Praha) 55:126–131

    CAS  Google Scholar 

  • Kilburn KH, Warshaw RH (1995) Neurotoxic effects from residential exposure to chemicals from an oil reprocessing facility and superfund site. Neurotoxicol Teratol 17:89–102

    Article  PubMed  CAS  Google Scholar 

  • Kriek E, Van Schooten FJ, Hillebrand MJ, Van Leeuwen FE, Den Engelse L, De Looff AJ, Dijkmans AP (1993) DNA adducts as a measure of lung cancer risk in humans exposed to polycyclic aromatic hydrocarbons. Environ Health Perspect 99:71–75

    Article  PubMed  CAS  Google Scholar 

  • Li N, Yu ZL, Wang L, Zheng YT, Jia JX, Wang Q, Zhu MJ, Liu XL, Xia X, Li WJ (2010) Increased tau phosphorylation and beta amyloid in the hippocampus of mouse pups by early life lead exposure. Acta Biol Hung 61:123–134

    Article  PubMed  Google Scholar 

  • Lodovici M, Akpan V, Evangelisti C, Dolara P (2004) Sidestream tobacco smoke as the main predictor of exposure to polycyclic aromatic hydrocarbons. J Appl Toxicol 24:277–281

    Article  PubMed  CAS  Google Scholar 

  • Majchrzak R, Sroczynski J, Chelmecka E (1990) Evaluation of the nervous system in workers in the furnace and coal divisions of the coke-producing plants. Med Pr 41:108–113

    PubMed  CAS  Google Scholar 

  • McCallister MM, Maguire M, Ramesh A, Aimin Q, Liu S, Khoshbouei H, Aschner M, Ebner FF, Hood DB (2008) Prenatal exposure to benzo(a)pyrene impairs later-life cortical neuronal function. Neurotoxicology 29:846–854

    Article  PubMed  CAS  Google Scholar 

  • Metcalfe MJ, Figueiredo-Pereira ME (2010) Relationship between tau pathology and neuroinflammation in Alzheimer’s disease. Mt Sinai J Med 77:50–58

    Article  PubMed  Google Scholar 

  • Mitchell CE (1982) Distribution and retention of benzo(a)pyrene in rats after inhalation. Toxicol Lett 11:35–42

    Article  PubMed  CAS  Google Scholar 

  • Morgan D (2007) Amyloid, memory and neurogenesis. Exp Neurol 205:330–335

    Article  PubMed  CAS  Google Scholar 

  • Niu Q, Zhang H, Li X, Li M (2010) Benzo[a]pyrene-induced neurobehavioral function and neurotransmitter alterations in coke oven workers. Occup Environ Med 67:444–448

    Article  PubMed  CAS  Google Scholar 

  • Nozaki I, Arai M, Takahashi K, Hamaguchi T, Yoshikawa H, Muroishi T, Noguchi-Shinohara M, Ito H, Itokawa M, Akiyama H, Kawata A, Yamada M (2010) Familial ALS with G298S mutation in TARDBP: a comparison of CSF tau protein levels with those in sporadic ALS. Intern Med 49:1209–1212

    Article  PubMed  CAS  Google Scholar 

  • Omland O, Sherson D, Hansen AM, Sigsgaard T, Autrup H, Overgaard E (1994) Exposure of iron foundry workers to polycyclic aromatic hydrocarbons: benzo(a)pyrene-albumin adducts and 1-hydroxypyrene as biomarkers for exposure. Occup Environ Med 51:513–518

    Article  PubMed  CAS  Google Scholar 

  • Pan CH, Shih TS, Chen CJ, Hsu JH, Wang SC, Huang CP, Kuo CT, Wu KY, Hu H, Chan CC (2011) Reduction of cooking oil fume exposure following an engineering intervention in Chinese restaurants. Occup Environ Med 68:10–15

    Article  PubMed  CAS  Google Scholar 

  • Perera F (1981) Carcinogenicity of airborne fine particulate benzo(a)pyrene: an appraisal of the evidence and the need for control. Environ Health Perspect 42:163–185

    Article  PubMed  CAS  Google Scholar 

  • Perera FP, Tang DL, O’Neill JP, Bigbee WL, Albertini RJ, Santella R, Ottman R, Tsai WY, Dickey C, Mooney LA (1993) HPRT and glycophorin A mutations in foundry workers: relationship to PAH exposure and to PAH-DNA adducts. Carcinogenesis 14:969–973

    Article  PubMed  CAS  Google Scholar 

  • Perera FP, Rauh V, Whyatt RM, Tang D, Tsai WY, Bernert JT, Tu YH, Andrews H, Barr DB, Camann DE, Diaz D, Dietrich J, Reyes A, Kinney PL (2005) A summary of recent findings on birth outcomes and developmental effects of prenatal ETS, PAH, and pesticide exposures. Neurotoxicology 26:573–587

    Article  PubMed  CAS  Google Scholar 

  • Perera FP, Li Z, Whyatt R, Hoepner L, Wang S, Camann D, Rauh V (2009) Prenatal airborne polycyclic aromatic hydrocarbon exposure and child IQ at age 5 years. Pediatrics 124:e195–e202

    Article  PubMed  Google Scholar 

  • Perera F, Li TY, Lin C, Tang D (2012a) Effects of prenatal polycyclic aromatic hydrocarbon exposure and environmental tobacco smoke on child IQ in a Chinese cohort. Environ Res 114:40–46

    Article  PubMed  CAS  Google Scholar 

  • Perera FP, Tang DL, Wang S, Vishnevetsky J, Zhang B, Diaz D, Camann D, Rauh V (2012b) Prenatal polycyclic aromatic hydrocarbon (PAH) exposure and child behavior at age 6–7 years. Environ Health Perspect 120:921–926

    Article  PubMed  CAS  Google Scholar 

  • Perez-Tur J, Buee L, Morris HR, Waring SC, Onstead L, Wavrant-De Vrieze F, Crook R, Buee-Scherrer V, Hof PR, Petersen RC, McGeer PL, Delacourte A, Hutton M, Siddique T, Ahlskog JE, Hardy J, Steele JC (1999) Neurodegenerative diseases of Guam: analysis of TAU. Neurology 53:411–413

    Article  PubMed  Google Scholar 

  • Phillips DH (1999) Polycyclic aromatic hydrocarbons in the diet. Mutat Res 443:139–147

    Article  PubMed  CAS  Google Scholar 

  • Pickering-Brown S, Baker M, Yen SH, Liu WK, Hasegawa M, Cairns N, Lantos PL, Rossor M, Iwatsubo T, Davies Y, Allsop D, Furlong R, Owen F, Hardy J, Mann D, Hutton M (2000) Pick’s disease is associated with mutations in the tau gene. Ann Neurol 48:859–867

    Article  PubMed  CAS  Google Scholar 

  • Qiu C, Cheng S, Xia Y, Peng B, Tang Q, Tu B (2011) Effects of subchronic benzo(a)pyrene exposure on neurotransmitter receptor gene expression in the rat hippocampus related with spatial learning and memory change. Toxicology 289:83–90

    Article  PubMed  CAS  Google Scholar 

  • Rahman A, Khan KM, Al-Khaledi G, Khan I, Attur S (2012) Early postnatal lead exposure induces tau phosphorylation in the brain of young rats. Acta Biol Hung 63:411–425

    Article  PubMed  CAS  Google Scholar 

  • Ramesh A, Knuckles ME (2006) Dose-dependent benzo(a)pyrene [B(a)P]-DNA adduct levels and persistence in F-344 rats following subchronic dietary exposure to B(a)P. Cancer Lett 240:268–278

    Article  PubMed  CAS  Google Scholar 

  • Reddy PH (2011) Abnormal tau, mitochondrial dysfunction, impaired axonal transport of mitochondria, and synaptic deprivation in Alzheimer’s disease. Brain Res 1415:136–148

    Article  PubMed  CAS  Google Scholar 

  • Reed GA, Jones BC (1996) Enhancement of benzo[a]pyrene diol epoxide mutagenicity by sulfite in a mammalian test system. Carcinogenesis 17:1063–1068

    Article  PubMed  CAS  Google Scholar 

  • Roseiro LC, Gomes A, Patarata L, Santos C (2012) Comparative survey of PAHs incidence in Portuguese traditional meat and blood sausages. Food Chem Toxicol 50:1891–1896

    Article  PubMed  CAS  Google Scholar 

  • Saunders CR, Ramesh A, Shockley DC (2002) Modulation of neurotoxic behavior in F-344 rats by temporal disposition of benzo(a)pyrene. Toxicol Lett 129:33–45

    Article  PubMed  CAS  Google Scholar 

  • Saunders CR, Das SK, Ramesh A, Shockley DC, Mukherjee S (2006) Benzo(a)pyrene-induced acute neurotoxicity in the F-344 rat: role of oxidative stress. J Appl Toxicol 26:427–438

    Article  PubMed  CAS  Google Scholar 

  • Sheppard O, Plattner F, Rubin A, Slender A, Linehan JM, Brandner S, Tybulewicz VL, Fisher EM, Wiseman FK (2012) Altered regulation of tau phosphorylation in a mouse model of down syndrome aging. Neurobiol Aging 33(828):e31–e44

    PubMed  Google Scholar 

  • Stowers SJ, Anderson MW (1985) Formation and persistence of benzo(a)pyrene metabolite-DNA adducts. Environ Health Perspect 62:31–39

    Article  PubMed  CAS  Google Scholar 

  • Vorhees CV, Williams MT (2006) Morris water maze: procedures for assessing spatial and related forms of learning and memory. Nat Protoc 1:848–858

    Article  PubMed  Google Scholar 

  • Walton JR (2007) An aluminum-based rat model for Alzheimer’s disease exhibits oxidative damage, inhibition of PP2A activity, hyperphosphorylated tau, and granulovacuolar degeneration. J Inorg Biochem 101:1275–1284

    Article  PubMed  CAS  Google Scholar 

  • Wang JZ, Grundke-Iqbal I, Iqbal K (2007) Kinases and phosphatases and tau sites involved in Alzheimer neurofibrillary degeneration. Eur J Neurosci 25:59–68

    Article  PubMed  Google Scholar 

  • Wang JZ, Xia YY, Grundke-Iqbal I, Iqbal K (2012) Abnormal hyperphosphorylation of tau: sites, regulation, and molecular mechanism of neurofibrillary degeneration. J Alzheimers Dis 33:123–139

    Google Scholar 

  • Xia Y, Cheng S, He J, Liu X, Tang Y, Yuan H, He L, Lu T, Tu B, Wang Y (2011) Effects of subchronic exposure to benzo[a]pyrene (B[a]P) on learning and memory, and neurotransmitters in male Sprague-Dawley rat. Neurotoxicology 32:188–198

    Article  PubMed  CAS  Google Scholar 

  • Yu Y, Run X, Liang Z, Li Y, Liu F, Liu Y, Iqbal K, Grundke-Iqbal I, Gong CX (2009) Developmental regulation of tau phosphorylation, tau kinases, and tau phosphatases. J Neurochem 108:1480–1494

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

This study has been supported by the National Natural Science Foundation of China (81072279 and 30800899) and the Shanxi Province Natural Science Foundation of China (2010021034-3) and Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi (20081014).

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The authors declare that there are no conflicts of interest.

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Correspondence to Qiao Niu.

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Nie Jisheng and Duan Lei have contributed equally to this study.

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Nie, J., Duan, L., Yan, Z. et al. Tau Hyperphosphorylation is Associated with Spatial Learning and Memory After Exposure to Benzo[a]pyrene in SD Rats. Neurotox Res 24, 461–471 (2013). https://doi.org/10.1007/s12640-013-9387-2

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