A Vegetable, Launaea taraxacifolia, Mitigated Mercuric Chloride Alteration of the Microanatomy of Rat Brain

References

• Abramoff MD, Magalhaes PJ, Ram SJ. Image processing with ImageJ. Biophotonics International. 2004;11(7):36–42.
   Google Scholar
• Adejuwon SA, Aina OO, Femi-Akinlosotu OM, Omirinde JO. Anti-clastogenic effects of Launaea taraxacifolia leaf extract on cisplatin-induced micronuclei in bone marrow erythrocytes. J Bio Innov. 2014;3(2):86–92.
   Google Scholar
• Afifi AK, Bergman RA. Functional neuroanatomy: Text and atlas (2nd ed). New York, NY: McGraw-Hill, 2005.
   Google Scholar
• Arawande JO, Amoo IA, Lajide L. Chemical and phytochemical composition of Wild Lettuce (Launaea taraxacifolia). J App Phytotechn in Environ Sanitation. 2013;2(1):25–30.
   Google Scholar
• Augusti PR, Conterato GMM, Somacal S, Einsfeld L, Ramos AT, Fernando YM, et al. Effect of lycopene on nephrotoxicity induced by mercuric chloride in rats. Basic Clin Pharmacol Toxicol. 2007;100:398–402.
   Google Scholar
• Bancroft JD, Gamble M. Theory and practice of histology techniques (6th ed). Philadelphia, PA: Churchill Livingstone Elsevier. 2008;83–134.
   Google Scholar
• Bernhoft RA. Mercury toxicity and treatment: A review of the literature. J Environ and Pub Health. 2012;2012, Article ID 460508, doi:10.1155/2012/460508.
   Google Scholar
• Clarkson TW, Magos L, and Myers GJ. The toxicology of mercury—current exposures and clinical manifestation. N Engl J Med. 2003;349:1731–1737.
   Google Scholar
• Coccine Y, Randin G, Candura S, Nappi R, Procko PL, Luigi M. Low level of exposure of methyl mercury modifies muscarinic cholinergic receptor binding characteristic in rat brain and lymphocyte: Physiologic implication and new opportunities in biological monitoring. Environ Health Perspec. 2000;108:29.
   Google Scholar
• Eto K, Yasutake A, Kuwana T, Korogi Y, Akima M, Shimozeki T, et al. Methylmercury poisoning in common marmosets—a study of selective vulnerability within the cerebral cortex. Toxicol Pathol. 2001;29(5):565–573.
   Google Scholar
• Ferraro L, Tomasini MC, Tanganelli S, Mazza R, Coluccia A, Carratu MR, et al. Developmental exposure to methylmercury elicits early cell death in the cerebral cortex and long-term memory deficits in the rat. Int J Dev Neurosci. 2009;27:165–174.
   Google Scholar
• Fonfria E, Vilaro MT, Babot Z, Rodriguez-Farre E, Sunol C. Mercury compounds disrupt neuronal glutamate transport in cultured mouse cerebellar granule cells. J Neurosci Res. 2005;79:545–553.
   Google Scholar
• Guzzi G, Pigatto PD, Spadari F, Laporta CAM. Effect of thimerosal, methylmercury, and mercuric chloride in Jurkat T cell line. Interdiscip Toxicol. 2012;5(3):159–161.
   Google Scholar
• Hussain S, Rodgers DA, Duhart HM, Ali SF. Mercuric chloride-induced reactive oxygen species and its effect on antioxidant enzymes in different regions of rat brain. J Environ Sci Health B. 1997;32:395–409.
   Google Scholar
• Kreider JC, Blumberg MS. Geotaxis in 2-week-old Norway rats (Rattus norvegicus): A reevaluation. Dev Psychobiol. 1999;35(1):35–42.
   Google Scholar
• Mensah JK, Okoli RI, Ohaju-Obodo JO, Eifediyi K. Phytochemical nutritional and medical properties of some leafy vegetables consumed by Edo people of Nigeria. Afri J Biotech. 2008;7(14):2304–2309.
   Google Scholar
• National Research Council (NRC). Toxicological effects of methylmercury. Washington, DC: National Academy Press, 2000.
   Google Scholar
• Owoeye O, Adesida A, Onwuka SK, Farombi EO. Gamma radiation effects on the brain of rats: Antioxidant and radioprotective properties of Vernonia amygdalina leaf extract. Int J Biol Chem Sci. 2010;4(6):2324–2336.
   Google Scholar
• Olopade FE, Shokunbi MT, Sirén AL. The relationship between ventricular dilatation, neuropathological and neurobehavioural changes in hydrocephalic rats. Fluids and barriers of the CNS. 2012;9:19, http://www.fluidsbarrierscns.com/content/9/1/19.
   Google Scholar
• Public Health Service (PHS). Public Health Service Policy on Humane Care and User of Laboratory Animals. Washington, DC: US Department of Health and Human Services, 1996; 99–158.
   Google Scholar
• Rao MV, Purohit AR. Neuroprotection by Melatonin on mercury induced toxicity in the rat brain. Pharmacol Pharmacy. 2011;2:375–385.
   Google Scholar
• Scharfman HE. The CA3 “backprojection” to the dentate gyrus. Prog Brain Res. 2007;163:627–637.
   Google Scholar
• Sheikh TJ, Patel BJ, Joshi DV, Patel RB, Jegoda MD. Repeated dose oral toxicity of inorganic mercury in Wistar rats: Biochemical and morphological alterations. Vet World. 2013;6(8):563–567, doi:10.5455/vetworld.2013.563-567.
   Google Scholar
• Stevens A, Lowe J. Pathology (2nd ed). Edinburgh, Scotland: Mosby, 2000.
   Google Scholar
• Tamashiro KLK, Wakayama T, Blanchard RJ, Blanchard C, Yanagimachi R. Postnatal growth and behavioral development of mice cloned from adult cumulus cells. Biol Reprod. 2000;63:328–334.
   Google Scholar
• Tranel D. Higher brain functions. In: PM Conn (Ed), Neuroscience in medicine. Philadelphia, PA: JB Lippincott Company, 1995.
   Google Scholar
• Uma C, Poornima K, Surya S, Ravikumar G, Gopalakrishnan VK. Nephroprotective effect of ethanolic extract of Tabernaemontana coronaria in mercuric chloride induced renal damage in Wistar albino rats. J Environ Pub Health. 2012;2012. Article ID 460508, doi:10.1155/2012/460508.
   Google Scholar
• Xu F, Farkas S, Kortbeek S, Zhang FX, Chen L, Zamponi GW, et al. Mercury-induced toxicity of rat cortical neurons is mediated through N-methyl-D-Aspartate receptors. Mol Brain. 2012;5:30, http://www.molecularbrain.com/content/5/1/30.
   Google Scholar
• Wang ZJ, Luo DH. Antioxidant activities of different fractions of polysaccharide purified from Gynostemma pentaphyllum Makino. Carbohyd Polym. 2007;68:54–58.
   Google Scholar