期刊论文详细信息
BMC Complementary and Alternative Medicine
Antioxidant effects of Dendropanax morbifera Léveille extract in the hippocampus of mercury-exposed rats
In Koo Hwang2  Yeo Sung Yoon2  Seung Myung Moon3  Jung Hoon Choi1  Dong-Woo Kim4  Jong Whi Kim2  Hyo Young Jung2  Dae Young Yoo2  Dae Won Kim5  Woosuk Kim2 
[1] Department of Anatomy, College of Veterinary Medicine, Kangwon National University, Chuncheon 200-701, South Korea;Department of Anatomy and Cell Biology, College of Veterinary Medicine, and Research Institute for Veterinary Science, Seoul National University, Seoul 151-742, South Korea;Department of Neurosurgery, Dongtan Sacred Heart Hospital, College of Medicine, Hallym University, Hwaseong 445-170, South Korea;Central Research Center, Egreen Co. Ltd, Seongnam 463-862, South Korea;Department of Biochemistry and Molecular Biology, Research Institute of Oral Sciences, College of Dentistry, Kangneung-Wonju National University, Gangneung 210-702, South Korea
关键词: Protein modification;    Reactive oxygen species;    Hippocampus;    Mercury;    Dendropanax morbifera extract;   
Others  :  1221181
DOI  :  10.1186/s12906-015-0786-1
 received in 2015-03-19, accepted in 2015-07-17,  发布年份 2015
PDF
【 摘 要 】

Background

Dendropanax morbifera Léveille has been employed for the treatment of infectious diseases using folk medicine. In this study, we evaluated the antioxidant effects of a leaf extract of Dendropanax morbifera Léveille in the hippocampus of mercury-exposed rats.

Methods

Seven-week-old Sprague–Dawley rats received a daily intraperitoneal injection of 5 μg/kg dimethylmercury and/or oral Dendropanax morbifera Léveille leaf extract (100 mg/kg) for 4 weeks. Animals were sacrificed 2 h after the last dimethylmercury and/or leaf extract treatment. Mercury levels were measured in homogenates of hippocampal tissue, a brain region that is vulnerable to mercury toxicity. In addition, we measured reactive oxygen species production, lipid peroxidation levels, and antioxidant levels in these hippocampal homogenates.

Results

Treatment with Dendropanax morbifera Léveille leaf extract significantly reduced mercury levels in hippocampal homogenates and attenuated the dimethylmercury-induced increase in the production of reactive oxygen species and formation of malondialdehyde. In addition, this leaf extract treatment significantly reversed the dimethylmercury-induced reduction in the hippocampal activities of Cu, Zn-superoxide dismutase, catalase, glutathione peroxidase, and glutathione-S-transferase.

Conclusion

These results suggest that a leaf extract of Dendropanax morbifera Léveille had strong antioxidant effects in the hippocampus of mercury-exposed rats.

【 授权许可】

   
2015 Kim et al.

【 预 览 】
附件列表
Files Size Format View
20150728010523441.pdf 841KB PDF download
Fig. 3. 60KB Image download
Fig. 2. 69KB Image download
Fig. 1. 55KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

Fig. 3.

【 参考文献 】
  • [1]Yang H, Xu Z, Liu W, Wei Y, Deng Y, Xu B. Effect of grape seed proanthocyanidin extracts on methylmercury-induced neurotoxicity in rats. Biol Trace Elem Res. 2012; 147:156-64.
  • [2]Sumathi T, Shobana C, Christinal J, Anusha C. Protective effect of Bacopa monniera on methyl mercury-induced oxidative stress in cerebellum of rats. Cell Mol Neurobiol. 2012; 32:979-87.
  • [3]Lucena GM, Prediger RD, Silva MV, Santos SN, Silva JF, Santos AR, Azevedo MS, Ferreira VM. Ethanolic extract from bulbs of Cipura paludosa reduced long-lasting learning and memory deficits induced by prenatal methylmercury exposure in rats. Dev Cogn Neurosci. 2013; 3:1-10.
  • [4]Christinal J, Sumathi T. Effect of Bacopa monniera extract on methylmercury-induced behavioral and histopathological changes in rats. Biol Trace Elem Res. 2013; 155:56-64.
  • [5]Sharma B, Singh S, Siddiqi NJ. Biomedical implications of heavy metals induced imbalances in redox systems. Biomed Res Int. 2014; 2014:640754.
  • [6]Risher JF, Amler SN. Mercury exposure: evaluation and intervention the inappropriate use of chelating agents in the diagnosis and treatment of putative mercury poisoning. Neurotoxicology. 2005; 26:691-9.
  • [7]Clarkson TW, Magos L, Myers GJ. The toxicology of mercury - current exposures and clinical manifestations. N Engl J Med. 2003; 349:1731-7.
  • [8]Kim NY, Ahn SJ, Ryu DY, Choi BS, Kim H, Yu IJ, Park JD. Effect of lifestyles on the blood mercury level in Korean adults. Hum Exp Toxicol. 2013; 32:591-9.
  • [9]Lapham LW, Cernichiari E, Cox C, Myers GJ, Baggs RB, Brewer R, Shamlaye CF, Davidson PW, Clarkson TW. An analysis of autopsy brain tissue from infants prenatally exposed to methymercury. Neurotoxicology. 1995; 16:689-704.
  • [10]Sokolowski K, Falluel-Morel A, Zhou X, DiCicco-Bloom E. Methylmercury (MeHg) elicits mitochondrial-dependent apoptosis in developing hippocampus and acts at low exposures. Neurotoxicology. 2011; 32:535-44.
  • [11]Kim DK, Park JD, Choi BS. Mercury-induced amyloid-beta (Aβ) accumulation in the brain is mediated by disruption of Aβ transport. J Toxicol Sci. 2014; 39:625-35.
  • [12]Rai DK, Sharma RK, Rai PK, Watal G, Sharma B. Role of aqueous extract of Cynodon dactylon in prevention of carbofuran- induced oxidative stress and acetylcholinesterase inhibition in rat brain. Cell Mol Biol (Noisy-le-rand). 2011; 57:135-42.
  • [13]Kumar Rai P, Kumar Rai D, Mehta S, Gupta R, Sharma B, Watal G. Effect of Trichosanthes dioica on oxidative stress and CYP450 gene expression levels in experimentally induced diabetic rats. Cell Mol Biol (Noisy-le-grand). 2011; 57:31-9.
  • [14]Srivastava N, Chauhan AS, Sharma B. Isolation and characterization of some phytochemicals from Indian traditional plants. Biotechnol Res Int. 2012; 2012:549850.
  • [15]Singh RK, Sharma B. Certain traditional Indian plants and their therapeutic applications: A review. VRI Phytomedicine. 2013; 1:1-11.
  • [16]Jaiswal D, Rai PK, Mehta S, Chatterji S, Shukla S, Rai DK, Sharma G, Sharma B, Khair S, Watal G. Role of Moringa oleifera in regulation of diabetes-induced oxidative stress. Asian Pac J Trop Med. 2013; 6:426-32.
  • [17]Kim W, Kim DW, Yoo DY, Jung HY, Nam SM, Kim JW, Hong SM, Kim DW, Choi JH, Moon SM, Yoon YS, Hwang IK. Dendropanax morbifera Léveille extract facilitates cadmium excretion and prevents oxidative damage in the hippocampus by increasing antioxidant levels in cadmium-exposed rats. BMC Complement Altern Med. 2014; 14:428. BioMed Central Full Text
  • [18]Park BY, Min BS, Oh SR, Kim JH, Kim TJ, Kim DH, Bae KH, Lee HK. Isolation and anticomplement activity of compounds from Dendropanax morbifera. J Ethnopharmacol. 2004; 90:403-8.
  • [19]Chung IM, Kim MY, Park SD, Park WH, Moon HI. In vitro evaluation of the antiplasmodial activity of Dendropanax morbifera against chloroquine-sensitive strains of Plasmodium falciparum. Phytother Res. 2009; 23:1634-7.
  • [20]Hyun TK, Kim MO, Lee H, Kim Y, Kim E, Kim JS. Evaluation of anti-oxidant and anti-cancer properties of Dendropanax morbifera Léveille. Food Chem. 2013; 141:1947-55.
  • [21]Moon HI. Antidiabetic effects of dendropanoxide from leaves of Dendropanax morbifera Leveille in normal and streptozotocin-induced diabetic rats. Hum Exp Toxicol. 2011; 30:870-5.
  • [22]Lebel CP, Ali SF, McKee M, Bondy SC. Organometal-induced increases in oxygen reactive species: the potential of 2′,7’-dichlorofluorescin diacetate as an index of neurotoxic damage. Toxicol Appl Pharmacol. 1990; 104:17-24.
  • [23]Hwang IK, Yoo KY, Kim DW, Lee CH, Choi JH, Kwon YG, Kim YM, Choi SY, Won MH. Changes in the expression of mitochondrial peroxiredoxin and thioredoxin in neurons and glia and their protective effects in experimental cerebral ischemic damage. Free Radic Biol Med. 2010; 48:1242-51.
  • [24]Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976; 72:248-54.
  • [25]McCord JM, Fridovich I. Superoxide dismutase: an enzymic function for erythrocuprein (hemocuprein). J Biol Chem. 1969; 244:6049-55.
  • [26]Beauchamp C, Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem. 1971; 44:276-87.
  • [27]Aebi H. Catalase in vitro. Methods Enzymol. 1984; 105:121-6.
  • [28]Maral J, Puget K, Michelson AM. Comparative study of superoxide dismutase, catalase and glutathione peroxidase levels in erythrocytes of different animals. Biochem Biophys Res Commun. 1977; 77:1525-35.
  • [29]Riddles PW, Blakeley RL, Zerner B. Reassessment of Ellman’s reagent. Methods Enzymol. 1983; 91:49-60.
  • [30]Habig WH, Jakoby WB, Guthenberg C, Mannervik B, Vander Jagt DL. 2-Propylthiouracil does not replace glutathione for the glutathione transferases. J Biol Chem. 1984; 259:7409-10.
  • [31]Horn HD, Burns FH. Methods of enzymatic analysis. (ed. Bergmeyer HV). Academic, New York; 1978.
  • [32]Allen JW, Shanker G, Tan KH, Aschner M. The consequences of methylmercury exposure on interactive functions between astrocytes and neurons. Neurotoxicology. 2002; 23:755-9.
  • [33]Shanker G, Aschner JL, Syversen T, Aschner M. Free radical formation in cerebral cortical astrocytes in culture induced by methylmercury. Brain Res Mol Brain Res. 2004; 128:48-57.
  • [34]Faro LR, do Nascimento JL, Campos F, Vidal L, Alfonso M, Durán R. Protective effects of glutathione and cysteine on the methylmercury-induced striatal dopamine release in vivo. Life Sci. 2005; 77:444-51.
  • [35]Falluel-Morel A, Sokolowski K, Sisti HM, Zhou X, Shors TJ, Dicicco-Bloom E. Developmental mercury exposure elicits acute hippocampal cell death, reductions in neurogenesis, and severe learning deficits during puberty. J Neurochem. 2007; 103:1968-81.
  • [36]Onishchenko N, Tamm C, Vahter M, Hökfelt T, Johnson JA, Johnson DA, Ceccatelli S. Developmental exposure to methylmercury alters learning and induces depression-like behavior in male mice. Toxicol Sci. 2007; 97:428-37.
  • [37]Sokolowski K, Obiorah M, Robinson K, McCandlish E, Buckley B, DiCicco-Bloom E. Neural stem cell apoptosis after low-methylmercury exposures in postnatal hippocampus produce persistent cell loss and adolescent memory deficits. Dev Neurobiol. 2013; 73:936-49.
  • [38]Ali SF, LeBel CP, Bondy SC. Reactive oxygen species formation as a biomarker of methylmercury and trimethyltin neurotoxicity. Neurotoxicology. 1992; 13:637-48.
  • [39]Yee S, Choi BH. Oxidative stress in neurotoxic effects of methylmercury poisoning. Neurotoxicology. 1996; 17:17-26.
  • [40]Myhre O, Fonnum F. The effect of aliphatic, naphthenic, and aromatic hydrocarbons on production of reactive oxygen species and reactive nitrogen species in rat brain synaptosome fraction: the involvement of calcium, nitric oxide synthase, mitochondria, and phospholipase A. Biochem Pharmacol. 2001; 62:119-28.
  • [41]Franco JL, Braga HC, Stringari J, Missau FC, Posser T, Mendes BG, Leal RB, Santos AR, Dafre AL, Pizzolatti MG, Farina M. Mercurial-induced hydrogen peroxide generation in mouse brain mitochondria: protective effects of quercetin. Chem Res Toxicol. 2007; 20:1919-26.
  • [42]Lucena GM, Franco JL, Ribas CM, Azevedo MS, Meotti FC, Gadotti VM, Dafre AL, Santos AR, Farina M. Cipura paludosa extract prevents methyl mercury-induced neurotoxicity in mice. Basic Clin Pharmacol Toxicol. 2007; 101:127-31.
  • [43]Chang JY, Tsai PF. Prevention of methylmercury-induced mitochondrial depolarization, glutathione depletion and cell death by 15-deoxy-delta-12,14-prostaglandin J 2. Neurotoxicology. 2008; 29:1054-61.
  • [44]Farina M, Campos F, Vendrell I, Berenguer J, Barzi M, Pons S, Suñol C. Probucol increases glutathione peroxidase-1 activity and displays long-lasting protection against methylmercury toxicity in cerebellar granule cells. Toxicol Sci. 2009; 112:416-26.
  • [45]Farina M, Aschner M, Rocha JB. Oxidative stress in MeHg-induced neurotoxicity. Toxicol Appl Pharmacol. 2011; 256:405-17.
  • [46]Farina M, Rocha JB, Aschner M. Mechanisms of methylmercury-induced neurotoxicity: evidence from experimental studies. Life Sci. 2011; 89:555-63.
  • [47]Kaur P, Aschner M, Syversen T. Glutathione modulation influences methyl mercury induced neurotoxicity in primary cell cultures of neurons and astrocytes. Neurotoxicology. 2006; 27:492-500.
  • [48]Zimmermann LT, dos Santos DB, Colle D, dos Santos AA, Hort MA, Garcia SC, Bressan LP, Bohrer D, Farina M. Methionine stimulates motor impairment and cerebellar mercury deposition in methylmercury-exposed mice. J Toxicol Environ Health A. 2014; 77:46-56.
  • [49]Kim ES, Lee JS, Akram M, Kim KA, Shin YJ, Yu JH, Bae ON. Protective activity of Dendropanax morbifera against Cisplatin-induced acute kidney injury. Kidney Blood Press Res. 2015; 40:1-12.
  • [50]Lu SC. Glutathione synthesis. Biochim Biophys Acta. 1830; 2013:3143-53.
  文献评价指标  
  下载次数:7次 浏览次数:8次