Corrigendum to “Exposure to As, Cd and Pb-mixture impairs myelin and axon development in rat brain, optic nerve and retina” [Toxicology and Applied Pharmacology 273 (2013) 242–258, (Toxicology and Applied Pharmacology (2013) 273(242-258) (S0041008X13001920), (10.1016/j.taap.2013.05.003));Exposure to As, Cd and Pb-mixture impairs myelin and axon development in rat brain, optic nerve and retina

Toxicology and Applied Pharmacology

Volumn 273, Issue 2, 2013, Pages 242-258

  Rai, Nagendra Kumar ^a,b   Ashok, Anushruti ^a,b   Rai, Asit ^b   Tripathi, Sachin ^b   Nagar, Geet Kumar ^c   Mitra, Kalyan ^d   Bandyopadhyay, Sanghamitra ^a,b  

^a ACADEMY OF SCIENTIFIC AND INNOVATIVE RESEARCH ACSIR   (India)

^b CSIR INDIAN INSTITUTE OF TOXICOLOGY RESEARCH   (India)

^c CSIR Central Drug Research Institute   (India)

^d CENTRAL DRUG RESEARCH INSTITUTE   (India)

Author keywords

Brn3b; CNS disruption; Demyelination; MBP; Metal mixture; NF

Indexed keywords

2',3' CYCLIC NUCLEOTIDE 3' PHOSPHODIESTERASE; ARSENIC; BRAIN DERIVED NEUROTROPHIC FACTOR; CADMIUM; GLUTAMATE AMMONIA LIGASE; LEAD; MYELIN; MYELIN ASSOCIATED GLYCOPROTEIN; MYELIN BASIC PROTEIN; PROTEOLIPID PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANTIBODY LABELING; ARTICLE; ASTROCYTE; BRAIN CORTEX; BRAIN DEVELOPMENT; CONTROLLED STUDY; FEMALE; IMMUNOHISTOCHEMISTRY; IMMUNOPEROXIDASE STAINING; INDIA; MYELIN SHEATH; MYELINATION; NERVE GROWTH; NEUROFILAMENT; NEUROTOXICITY; NONHUMAN; OPTIC NERVE; RADIOIMMUNOASSAY; RAT; RETINA; THICKNESS; TRANSMISSION ELECTRON MICROSCOPY; WHITE MATTER;

RATTUS;

EID: 84888198567     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2022.116165     Document Type: Erratum

References (73)

1. Acosta G.B., et al. Glutamine synthetase activity and glutamate uptake in hippocampus and frontal cortex in portal hypertensive rats. World J. Gastroenterol. 2009, 15(23):2893-2899.
2. Baumann N., Pham-Dinh D. Biology of oligodendrocyte and myelin in the mammalian central nervous system. Physiol. Rev. 2001, 81(2):871-927.
3. Behari J.R., Prakash R. Determination of total arsenic content in water by atomic absorption spectroscopy (AAS) using vapour generation assembly (VGA). Chemosphere 2006, 63(1):17-21.
4. Brubaker C.J., et al. Altered myelination and axonal integrity in adults with childhood lead exposure: a diffusion tensor imaging study. Neurotoxicology 2009, 30(6):867-875.
5. Camp A.S., et al. Structural correlation between the nerve fiber layer and retinal ganglion cell loss in mice with targeted disruption of the Brn3b gene. Invest. Ophthalmol. Vis. Sci. 2011, 52(8):5226-5232.
6. Cavalcante L.A., Barradas P.C., Martinez A.M. Patterns of myelination in the opossum superior colliculus with additional reference to the optic tract. Anat. Embryol. (Berl) 1991, 183(3):273-285.
7. Cecil K.M., et al. Proton magnetic resonance spectroscopy in adults with childhood lead exposure. Environ. Health Perspect. 2011, 119(3):403-408.
8. Cellerino A., Maffei L. The action of neurotrophins in the development and plasticity of the visual cortex. Prog. Neurobiol. 1996, 49(1):53-71.
9. Chen H., Weber A.J. Expression of glial fibrillary acidic protein and glutamine synthetase by Muller cells after optic nerve damage and intravitreal application of brain-derived neurotrophic factor. Glia 2002, 38(2):115-125.
10. Chen M.K., et al. Peripheral benzodiazepine receptor imaging in CNS demyelination: functional implications of anatomical and cellular localization. Brain 2004, 127(Pt 6):1379-1392.
11. Chow E.S., et al. Cadmium affects retinogenesis during zebrafish embryonic development. Toxicol. Appl. Pharmacol. 2009, 235(1):68-76.
12. Colello R.J., Pott U., Schwab M.E. The role of oligodendrocytes and myelin on axon maturation in the developing rat retinofugal pathway. J. Neurosci. 1994, 14(5 Pt 1):2594-2605.
13. Das A.V., et al. SWI/SNF chromatin remodeling ATPase Brm regulates the differentiation of early retinal stem cells/progenitors by influencing Brn3b expression and Notch signaling. J. Biol. Chem. 2007, 282(48):35187-35201.
14. DeMaman A.S., et al. Effectiveness of iron repletion in the diet for the optic nerve development of anaemic rats. Eye (Lond) 2010, 24(5):901-908.
15. Deng W., Poretz R.D. Lead exposure affects levels of galactolipid metabolic enzymes in the developing rat brain. Toxicol. Appl. Pharmacol. 2001, 172(2):98-107.
16. Deng W., McKinnon R.D., Poretz R.D. Lead exposure delays the differentiation of oligodendroglial progenitors in vitro. Toxicol. Appl. Pharmacol. 2001, 174(3):235-244.
17. Di Polo A., et al. Prolonged delivery of brain-derived neurotrophic factor by adenovirus-infected Muller cells temporarily rescues injured retinal ganglion cells. Proc. Natl. Acad. Sci. U. S. A. 1998, 95(7):3978-3983.
18. Donofrio P.D., et al. Acute arsenic intoxication presenting as Guillain-Barre-like syndrome. Muscle Nerve 1987, 10(2):114-120.
19. Edwards A.M., et al. Interaction of myelin basic protein and proteolipid protein. J. Neurosci. Res. 1989, 22(1):97-102.
20. Farsetti A., et al. Molecular basis of thyroid hormone regulation of myelin basic protein gene expression in rodent brain. J. Biol. Chem. 1991, 266(34):23226-23232.
21. Fischer A.H., et al. Hematoxylin and eosin staining of tissue and cell sections 2008, CSH Protoc (2008, pdb prot4986).
22. Fressinaud C., et al. Glutamine synthetase expression in rat oligodendrocytes in culture: regulation by hormones and growth factors. J. Cell. Physiol. 1991, 149(3):459-468.
23. Fulton D., Paez P.M., Campagnoni A.T. The multiple roles of myelin protein genes during the development of the oligodendrocyte. ASN Neuro 2010, 2(1):e00027.
24. Gaur S., Agrawal S., et al. Biological effect of heavy metal in drinking water samples of western Uttar Pradesh region in India. J. Appl. Pharma. Sci. 2012, 02(07):177-181.
25. Georg Kuhn H., Blomgren K. Developmental dysregulation of adult neurogenesis. Eur. J. Neurosci. 2011, 33(6):1115-1122.
26. Hardin-Pouzet H., et al. Glutamate metabolism is down-regulated in astrocytes during experimental allergic encephalomyelitis. Glia 1997, 20(1):79-85.
27. Huth A.G., et al. A continuous semantic space describes the representation of thousands of object and action categories across the human brain. Neuron 2012, 76(6):1210-1224.
28. Jadhav S.H., et al. Effects of subchronic exposure via drinking water to a mixture of eight water-contaminating metals: a biochemical and histopathological study in male rats. Arch. Environ. Contam. Toxicol. 2007, 53(4):667-677.
29. Johnson S. The possible role of gradual accumulation of copper, cadmium, lead and iron and gradual depletion of zinc, magnesium, selenium, vitamins B2, B6, D, and E and essential fatty acids in multiple sclerosis. Med. Hypotheses 2000, 55(3):239-241.
30. Jones L.G., et al. Lead exposure during development results in increased neurofilament phosphorylation, neuritic beading, and temporal processing deficits within the murine auditory brainstem. J. Comp. Neurol. 2008, 506(6):1003-1017.
31. Ju W.K., et al. Elevated hydrostatic pressure triggers release of OPA1 and cytochrome C, and induces apoptotic cell death in differentiated RGC-5 cells. Mol. Vis. 2009, 15:120-134.
32. Kugler P., Beyer A. Expression of glutamate transporters in human and rat retina and rat optic nerve. Histochem. Cell Biol. 2003, 120(3):199-212.
33. Kumar N.I., et al. Characterization of heavy metals in vegetables using inductive coupled plasma analyzer (ICPA). J. Appl. Sci. Environ. Manage. 2007, 11(3):75-79.
34. Lee C.C., Surtees R., Duchen L.W. Distal motor axonopathy and central nervous system myelin vacuolation caused by cycloleucine, an inhibitor of methionine adenosyltransferase. Brain 1992, 115(Pt 3):935-955.
35. Lemke G., Reber M. Retinotectal mapping: new insights from molecular genetics. Annu. Rev. Cell Dev. Biol. 2005, 21:551-580.
36. Lidsky T.I., Schneider J.S. Lead neurotoxicity in children: basic mechanisms and clinical correlates. Brain 2003, 126(Pt 1):5-19.
37. MacLaren R.E. Expression of myelin proteins in the opossum optic nerve: late appearance of inhibitors implicates an earlier non-myelin factor in preventing ganglion cell regeneration. J. Comp. Neurol. 1996, 372(1):27-36.
38. Marignier R., et al. Oligodendrocytes are damaged by neuromyelitis optica immunoglobulin G via astrocyte injury. Brain 2010, 133(9):2578-2591.
39. Marita Golla K., Ramaswamy Raju T., Chatterji S. Brain derived neurotrophic factor and superior collicular extract regulate the expression of the 1.6 subfamily of voltage-gated potassium channels in the developing rat retina in vitro. J. Ophthal. Vis. Res. 2012, 7(2):139-147.
40. Meyer-Franke A., et al. Characterization of the signaling interactions that promote the survival and growth of developing retinal ganglion cells in culture. Neuron 1995, 15(4):805-819.
41. Meyer-Franke A., Shen S., Barres B.A. Astrocytes induce oligodendrocyte processes to align with and adhere to axons. Mol. Cell. Neurosci. 1999, 14(4-5):385-397.
42. Ola M.S., et al. Reduced levels of brain derived neurotrophic factor (BDNF) in the serum of diabetic retinopathy patients and in the retina of diabetic rats. Cell. Mol. Neurobiol. 2013, 33(3):359-367.
43. Ong W.Y., et al. Increased uptake of divalent metals lead and cadmium into the brain after kainite-induced neuronal injury. Exp. Brain Res. 2006, 173(3):468-474.
44. Otani A., et al. Expressions of angiopoietins and Tie2 in human choroidal neovascular membranes. Invest. Ophthal. Vis. Sci. 1999, 40(9):1912-1920.
45. Pan L., et al. Functional equivalence of Brn3 POU-domain transcription factors in mouse retinal neurogenesis. Development 2005, 132(4):703-712.
46. Petzold A., et al. In vivo monitoring of neuronal loss in traumatic brain injury: a microdialysis study. Brain 2011, 134(Pt 2):464-483.
47. Pons-Vazquez S., et al. Combined pre- and postnatal ethanol exposure in rats disturbs the myelination of optic axons. Alcohol Alcohol 2011, 46(5):514-522.
48. Prasad S., Galetta S.L. Anatomy and physiology of the afferent visual system. Handb. Clin. Neurol. 2011, 102:3-19.
49. Pun P.B., et al. Low level primary blast injury in rodent brain. Front. Neurol. 2011, 2:19.
50. Quarles R.H. Myelin-associated glycoprotein (MAG): past, present and beyond. J. Neurochem. 2007, 100(6):1431-1448.
51. Rai A., et al. Characterization of developmental neurotoxicity of As, Cd, and Pb mixture: synergistic action of metal mixture in glial and neuronal functions. Toxicol. Sci. 2010, 118(2):586-601.
52. Rios R., et al. Decreased nitric oxide markers and morphological changes in the brain of arsenic-exposed rats. Toxicology 2009, 261(1-2):68-75.
53. Rodier P.M. Developing brain as a target of toxicity. Environ. Health Perspect. 1995, 103(Suppl. 6):73-76.
54. Rowe, et al. Methods Enzymol. 1970, A17:900.
55. Saggu S.K., et al. Wallerian-like axonal degeneration in the optic nerve after excitotoxic retinal insult: an ultrastructural study. BMC Neurosci. 2010, 11:97.
56. Sanchez I., et al. Local control of neurofilament accumulation during radial growth of myelinating axons in vivo. Selective role of site-specific phosphorylation. J. Cell Biol. 2000, 151(5):1013-1024.
57. Schneider A.M., et al. Dominant-negative action of the jimpy mutation in mice complemented with an autosomal transgene for myelin proteolipid protein. Proc. Natl. Acad. Sci. U. S. A. 1995, 92(10):4447-4451.
58. Singh S., Rana S.V. Amelioration of arsenic toxicity by l-ascorbic acid in laboratory rat. J. Environ. Biol. 2007, 28(2 Suppl.):377-384.
59. Sinha R.A., et al. Anti-apoptotic role of omega-3-fatty acids in developing brain: perinatal hypothyroid rat cerebellum as apoptotic model. Int. J. Dev. Neurosci. 2009, 27(4):377-383.
60. Snodgress A.B., Dorsey C.H., Lacey L.B. Luxol fast blue staining of degenerating myelinated fibers. Anat. Rec. 1961, 140:83-90.
61. Sternberger N.H., et al. Myelin-associated glycoprotein demonstrated immunocytochemically in myelin and myelin-forming cells of developing rat. Proc. Natl. Acad. Sci. U. S. A. 1979, 76(3):1510-1514.
62. Struzynska L., Chalimoniuk M., Sulkowski G. The role of astroglia in Pb-exposed adult rat brain with respect to glutamate toxicity. Toxicology 2005, 212(2-3):185-194.
63. Sullivan S.M., et al. Morphological changes in white matter astrocytes in response to hypoxia/ischemia in the neonatal pig. Brain Res. 2010, 1319:164-174.
64. Takasaki C., et al. Cytochemical and cytological properties of perineuronal oligodendrocytes in the mouse cortex. Eur. J. Neurosci. 2010, 32(8):1326-1336.
65. Tauber H., Waehneldt T.V., Neuhoff V. Myelination in rabbit optic nerves is accelerated by artificial eye opening. Neurosci. Lett. 1980, 16(3):235-238.
66. Tennekoon G., et al. Chronic lead intoxication: effects on developing optic nerve. Ann. Neurol. 1979, 5(6):558-564.
67. Wang Q., et al. Iron supplement prevents lead-induced disruption of the blood-brain barrier during rat development. Toxicol. Appl. Pharmacol. 2007, 219(1):33-41.
68. Yang R.S., Rauckman E.J. Toxicological studies of chemical mixtures of environmental concern at the National Toxicology Program: health effects of groundwater contaminants. Toxicology 1987, 47(1-2):15-34.
69. Yang Y., Lewis R., Miller R.H. Interactions between oligodendrocyte precursors control the onset of CNS myelination. Dev. Biol. 2011, 350(1):127-138.
70. Zawia N.H., Harry G.J. Exposure to lead-acetate modulates the developmental expression of myelin genes in the rat frontal lobe. Int. J. Dev. Neurosci. 1995, 13(6):639-644.
71. Zhang Z.Z., et al. Valproate promotes survival of retinal ganglion cells in a rat model of optic nerve crush. Neuroscience 2012, 224:282-293.
72. Zhao L., Wientjes M.G., Au J.L. Evaluation of combination chemotherapy: integration of nonlinear regression, curve shift, isobologram, and combination index analyses. Clin. Cancer Res. 2004, 10(23):7994-8004.
73. Zhao F., et al. Effects of arsenite on glutamate metabolism in primary cultured astrocytes. Toxicol. In Vitro 2012, 26(1):24-31.