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The Effects of Onion Extracts on Mercury-Induced Toxicity and Lipid Peroxidation in Rat Hepatocyte Primary Culture

랫드 간세포 일차배양에서 양파 추출물이 수은에 의해 유도된 독성 및 지질과산화에 미치는 영향

  • Rhim, Tae-Jin (Division of Environment and Biosystem, College of Life Science and Natural Resources, Sangji University) ;
  • Lim, Sang-Cheol (Division of Environment and Biosystem, College of Life Science and Natural Resources, Sangji University)
  • 임태진 (상지대학교 생명자원과학대학 환경바이오시스템학부) ;
  • 임상철 (상지대학교 생명자원과학대학 환경바이오시스템학부)
  • Published : 2005.06.30

Abstract

The objective of present study was to investigate the effect of onion extracts on mercuryinduced cytotoxicity, lipid peroxidation and antioxidant enzyme activities in primary monolayer cultures of rat hepatocytes. Primary cultures of rat hepatocytes were incubated for 6 hr in the presence of various concentrations (0, 1, 5, 10, 30 or 50 ppm) of $HgCl_2$. Cytotoxicity and cell viability were determined by measuring glutamic oxaloacetic transaminase (GOT) activity, lactate dehydrogenase (LDH) activity and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) value. Lipid peroxidation w as evaluated using thiobarbituric acid reactive substances (TBARS) assay. Effects of onion extract on antioxidant system were determined by measuring catalase, glutathione peroxidase (GSH-Px), glutathione reductase (GSH-Rd) activities as well as DPPH free radical scavenging activity. $HgCl_2$ at the concentration of 10 ppm increased GOT activity and TBARS concentration but decreased %MTT reduction, whereas $HgCl_2$ at the concentration of 30 ppm increased LDH activity, representing that $HgCl_2$ caused cytotoxicity and lipid peroxidation in dose-dependent manner, $HgCl_2$ at the concentration of 30 ppm significantly decreased catalase, GSH-Px and GSH-Rd activities. When primary cultures of rat hepatocytes were incubated with various concentrations (0, 0.01, 0.05, 0.1 or 0.3 mg/ml) of onion extract for 6 hr in the presence of 30 ppm of $HgCl_2$, onion extracts at the concentration of 0.05 mg/ml decreased GOT activity, but increased %MTT reduction by 30 ppm of $HgCl_2$. $HgCl_2-induced$ LDH activity and TBARS concentration were decreased by onion extract at the concentration of 0.01 mg/ml. Taken together, onion extract prevented H$HgCl_2-induced$ hepatocyte injury and lipid peroxidation. Onion extracts at the concentration of 0.1 mg/ml almost or completely inhibited $HgCl_2-induced$ catalase and GSB-Px activities. GSH-Rd activity, however, was not affected by onion extract. Free radical scavengjing activity was increased as concentration of onion extract increased. Onion extract at the concentrion of 5 mg/ml possesed mote than 93% scavenging activity comparing to 100% radical scavenging activity by pyrogallol solution as a reference. These results demonstrate that onion extracts suppressed mercury-induced cytoctoxicity and lipid peroxidation by scavenging free radical and increasing catalase and GSH-Px activities.

본 연구의 목적은 랫드 간세포 일차배양에서 양파추출물이 수은에 의해 유발된 세포독성, 지질과산화 및 항산화효소 활성에 미치는 효과를 조사하기 위함이다. 수은 농도별 효과를 조사하기 위해 0, 1, 5, 10, 30 및 50 ppm의 다양한 농도의 $HgCl_2$로 6시간 동안 간세포를 일차배양하였다. 간세포 독성과 생존율은 배양액의 GOT와 LDH 활성 및 MTT 값으로 결정하였고, 지질과산화는 TBARS 농도로 측정하였다. 항산화에 미치는 효과는 catalase, GSH-Px, GSH-Rd 활성 및 DPPH free radical 소거활성으로 결정하였다. 10 ppm 이상의 $HgCl_2$ 농도는 GOT 활성을 증가시켰고 %MTT 감소를 현저히 억제시켰으며 TBARS 농도를 증가시켰다. 또한 30 ppm 이상의 $HgCl_2$ 농도는 LDH 활성을 증가시켜 수은이 농도 의존적으로 간세포 손상과 지질과산화를 촉진시켰다. 6시간 동안 30 ppm 농도의 $HgCl_2$, 처리는 간세포의 catalase, GSH-Px 및 GSH-Rd 활성을 현저히 감소시켰다. 수은 독성에 대한 양파추출물의 효과를 조사하기 위해 30 ppm의 수은 존재하에 0, 0.01, 0.05, 0.1 및 0.3 mg/ml의 다양한 농도의 양파추출물로 6시간 동안 간세포를 일차배양하였다. 0.05 mg/ml이상 농도의 양파추출물 첨가는 30 ppm 농도의 수은에 의해 증가된 GOT 활성을 감소시켰으며 MTT 감소를 증가시켰다. 또한 0.01 mg/ml 이상 농도의 양파추출물은 수은에 의해 증가된 LDH 활성과 TBARS 농도를 감소시켜 양파추출물이 수은에 의해 유발된 간손상과 지질과산화를 억제시켰음을 알 수 있었다. 0.05 mg/ml와 0.01 mg/ml 이상 농도의 양파추출물 첨가는 수은에 의해 각각 억제된 catalase와 GSH-Px 활성을 증가시켰으나 GSH-Rd 활성에는 영향을 미치지 못하였다. 양파추출물의 농도가 증가할수록 free radical 소거활성은 증가하여 5 mg/ml 농도의 양파추출물은 pyrogallol 용액의 흡광도 감소를 100%로 기준하였을 때 93% 이상의 소거 활성을 나타내었다. 이상과 같이 간세포 일차배양에서 수은은 간독성 증가, 간세포 생존율 감소, 지질과산화 촉진 및 catalase, GSH-Px, GSH-Rd 등의 항산화효소 활성 감소를 유발시켰으며, 양파추출물은 catalase와 GSH-Px의 활성을 증가시키고 free radical을 소거시켜 수은에 의해 유발된 독성 및 지질과산화를 억제함으로써 항산화 및 간보호 효과를 나타내는 것으로 사료된다.

Keywords

References

  1. Stohs, S. J. and Bagchi, D. (1995) Oxidative mechanisms in the toxicity of metal ions, Free Radic. Biol. Med. 18, 321-336 https://doi.org/10.1016/0891-5849(94)00159-H
  2. Duncan-Achanzar, K. B., Jones, J. T., Burke, M. F., Carter, D. E. and Laird, H. E. (1996) Inorganic mercury chloride-induced apoptosis in the cultured porcine renal cell line LLCC-PK1, J. Pharmacol. Exp. Ther. 277, 1726-1732
  3. Homma-Takeda, S., Kugenuma, Y., Iwamuro, J., Kumagai, Y. and Shimojo, N. (2001) Impairment of speratogenesis in rats by methylmercury: involvement of stage- and cell-specific germ cell apoptosis, Toxicology, 169, 25-35 https://doi.org/10.1016/S0300-483X(01)00487-5
  4. Rao, M. V. (1989) Histophysiological changes of sex organs in methylmercury intoxicated mice, Endocrinol. Exper. 23, 55-62
  5. Yonaha, M., Itoh, E., Ohbayashi, Y. and Uchiyama, M. (1980) Induction of lipid peroxidation in rats by mercuric chloride, Res. Commun. Chem. Pathol. Pharmacol. 28, 105-112
  6. Sarafian, T. and Verity, M. A. (1991) Oxidative mechanisms underlying methyl mercury neurotoxicity, Int. J. Dev. Neurosci. 9, 147-153 https://doi.org/10.1016/0736-5748(91)90005-7
  7. Lund, B. O., Miller, D. M. and Woods, J. S. (1993) Studies on Hg(II)-induced $H_2O_2$ formation and oxidative stress in vivo and in vitro in rat kidney mitochondria, Biochem. Pharmacol. 45, 2017-2024 https://doi.org/10.1016/0006-2952(93)90012-L
  8. Stacey, N. H. and Kappus, H. (1982) Cellular toxicity and lipid peroxidation in response to mercury, Toxicol. Appl. Pharmacol. 63, 29-35 https://doi.org/10.1016/0041-008X(82)90023-0
  9. Kamiski, L. P. (1992) $Hg^{2+}$ and $Cu^+$ are ionophores, mediating Cl/OH exchange in liposomes and rabbit renal brush border membranes, J. Biol. Chem. 267, 19218-19225
  10. Lund, B. O., Miller, D. M. and Woods, J. S. (1991) Mercury-induced $H_O_2$ production and lipid peroxidation in vitro in rat kidney mitochondria, Biochem. Pharmacol. 42, 5181-187
  11. Nath, K. A., Croatt, A. J., Likely, S., Behrens, T. W. and Warden, D. (1996) Renal oxidant injury and oxidant response induced by mercury, Kidney Int. 50, 1032-1043 https://doi.org/10.1038/ki.1996.406
  12. Hussain, S., Rodgers, D. A., Duhart, H. M. and Ali, S. F. (1997) Mercuric chloride-induced reactive oxygen species and its effect on antioxidant eznymes in different regions of rat brain, J. Envion. Sci. Health B, 32, 395-409 https://doi.org/10.1080/03601239709373094
  13. Fridovich, I. (1983) Superoxide radical: an endogenous toxicant, Annu. Rev. Pharmacol. Toxicol. 23, 239-57 https://doi.org/10.1146/annurev.pa.23.040183.001323
  14. Harris, E. D. (1992) Regulation of antioxidant enzymes, FASEB J. 6, 2675-2683 https://doi.org/10.1096/fasebj.6.9.1612291
  15. Chung, A. S., Maines, M. D. and Reynolds, W. A. (1982) Inhibition of the enzymes of glutathione metabolism by mercuric chloride in the rat kidney: reversal by selenium, Biochem. Pharmacol. 31, 3093-3100 https://doi.org/10.1016/0006-2952(82)90085-5
  16. Gstraunthaler, G., Pfaller, W. and Kotanko, P. (1983) Glutathione depletion and in vitro lipid peroxidation in mercury or maleate induced acute renal failure, Biochem. Pharmacol. 32, 2969-2972 https://doi.org/10.1016/0006-2952(83)90404-5
  17. Girardi, G. and Elias, M. M. (1995) Mercuric chloride effects on rat renal redox enzymes activities: SOD protection, Free Radic. Biol. Med. 18, 61-66 https://doi.org/10.1016/0891-5849(94)00097-4
  18. Hussain, S., Atkinson, A, Thompson, S. J. and Khan, AI. (1999) Accumulation of mercury and its effect on antioxidant enzymes in brain, liver, and kidneys of mice, J. Environ. Sci. Health. B, 34, 645-660 https://doi.org/10.1080/03601239909373219
  19. Ashour, H., Abdel-Rahman, M. and Khodair, A. (1993) The mechanism of methyl mercury toxicity in isolated rat hepatocytes, Toxicol. Lett. 69, 87-96 https://doi.org/10.1016/0378-4274(93)90149-R
  20. Srivastava, K. C. (1986) Onion exerts antiaggregatory effects by altering arachidonic acid metabolism in platelets, Prostaglandins Leukot. Med. 24, 43-50 https://doi.org/10.1016/0262-1746(86)90205-2
  21. Kendler, B. S. (1987) Garlic (allium sativum) and onion (Allium cepa): a review of their relationship to cardiovascular disease, Prev. Med. 16, 670-685 https://doi.org/10.1016/0091-7435(87)90050-8
  22. Dorant, E., van den Brandt, P. A., Goldbohm, R. A. and Sturmans, F. (1996) Consumption of onions and a reduced risk of stomach carcinoma, Gstroenterology 110, 12-20 https://doi.org/10.1053/gast.1996.v110.pm8536847
  23. Price, K R and Rhodes, M. J. C (1997) Analysis of the major flavonol glycosides present in four varieties of onion (Allum cepa) and changes in composition resulting from autolysis, J. Sci. Food Agri. 74, 331-339 https://doi.org/10.1002/(SICI)1097-0010(199707)74:3<331::AID-JSFA806>3.0.CO;2-C
  24. Chu, Y.-H., Chang, C.-L. and Hsu, H.-F. (2000) Flavonoid content of several vegetables and their antioxidant activity, J. Agric. Food Chem. 44, 3426-3431 https://doi.org/10.1021/jf9602535
  25. Nuutila, A. M., Puupponen-Pimia, R., Aarni, M. and Oksman-Caldentey, K.-M. (2003) Comparison of antioxidant activities of onion and garlic extracts by inhibition of lipid peroxidation and radical scavenging activity, Food Chem. 81, 485-493 https://doi.org/10.1016/S0308-8146(02)00476-4
  26. Patil, B. S. and Pike, L. M. (1995) Distribution of quercetin content in different rings of various coloured onion (Allium cepa L.) cultivars, J. Horticul. Sci. 70, 643-650 https://doi.org/10.1080/14620316.1995.11515338
  27. Malterud, K. E., Farbrot, T. L., Huse, A. E. and Sund, R. B. (1993) Antioxidant and radical scavenging effects of anthraquinones and anthrones, Pharmacology 47, 77-85 https://doi.org/10.1159/000139846
  28. Seglen, P. O. (1976) Preparation of isolated rat liver cells, Methods Cell BioI. 13, 29-83 https://doi.org/10.1016/S0091-679X(08)61797-5
  29. Mosmann, T. (1983) Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays, J. Immunol. Methods 65, 55-63 https://doi.org/10.1016/0022-1759(83)90303-4
  30. Uchiyama, M. and Mihara, M. (1978) Determination of malonaldehyde precursor in tissues by thiobarbituric acid test, Anal. Biochem. 86, 271-278 https://doi.org/10.1016/0003-2697(78)90342-1
  31. Sunderman, F. W. Jr., Marzouk, A., Hopfer, S., Zaharia, O. and Reid, M. C. (1985) Increased lipid peroxidation in tissues of nickel chloride-treated rats, Ann. Clin. Lab. Sci. 15, 229-236
  32. Reitman, S. and Frankel, S. (1957) A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases, Am. J. Clin. Pathol. 28, 56-63 https://doi.org/10.1093/ajcp/28.1.56
  33. Vassault, A. (1983) Lactate dehydrogenase: UV-method with pyruvate and NADH. In: Bergmeyer, H. U., Bergmeyer, J. and Grassl, M.(eds), 'Methods of Enzymatic Analysis. III. Enzymes 1: Oxidoreductases, Transferases', Verlag-Chemie, Weinheim, p.118-126
  34. Aebi, H. (1984) Catalase in vitro, Methods Enzymol. 105, 121-126 https://doi.org/10.1016/S0076-6879(84)05016-3
  35. Flohe, L. and Gunzler, W. A. (1984) Assays of glutathione peroxidase, Methods Enzymol. 105, 114-121 https://doi.org/10.1016/S0076-6879(84)05015-1
  36. Carlberg, I. and Mannervik, B. (1955) Glutathione reductase, Methods Enzymol. 113, 484-490
  37. Bradford, M. M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding, Anal. Biochem. 72, 248-254 https://doi.org/10.1016/0003-2697(76)90527-3
  38. Steel, R. G. D. and Torre, J. H. (1980) Principles and Procedures of Statistics, 2nd ed, McGraw-Hill, New York, p.186-187
  39. Stacey, N. H. and Klaassen, C. D. (1981) Comparison of the effects of metals on cellular injury and lipid peroxidation in isolated rat hepatocytes, J. Toxicol. Environ. Health 7, 139-147 https://doi.org/10.1080/15287398109529965
  40. Fridovich, I. (1978) The biology of oxygen radicals, Science 201, 875-879 https://doi.org/10.1126/science.210504
  41. Fridovich, I. and Frreman, B. (1986) Antioxidant defenses in the lung, Ann. Rev. Physiol. 48, 693-702 https://doi.org/10.1146/annurev.ph.48.030186.003401
  42. Rall, T. W. and Lehninger, A. L. (1952) Glutathione reductase of animal tissues, J. Biol. Chem. 194, 119-130
  43. Guillemette, J., Marion, M., Denizeau, F., Fournier, M. and Brousseau, P. (1993) Characterization of the in vitro hepatocyte model for toxicological evaluation: repeated growth stimulation and glutathione response, Biochem. Cell Biol. 71, 7-13 https://doi.org/10.1139/o93-002
  44. Mahboob, M., Shireen, K. F., Atkinson, A. and Khan, A. T. (2001) Lipid peroxidation and antioxidant enzyme activity in different organs of mice exposed to low level of mercury, J. Environ. Sci. Health B. 36, 687-697 https://doi.org/10.1081/PFC-100106195

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