Lambda Cyhalothrin Elicited Dose Response Toxicity on Haematological, Hepatic, Gonadal and Lipid Metabolic Biomarkers in Rat and Possible Modulatory Role of Taurine
DOI:
https://doi.org/10.17140/TFMOJ-1-107Keywords:
Lambda cyhalothrin, Taurine, Wistar rat, Hepatic and gonadal toxicity, Lipid metabolismAbstract
Extensive application of pesticides is usually accompanied with serious problems of pollution and health hazards. Lambda-cyhalothrin (LCT), a type II synthetic pyrethroid, is widely used in agriculture, home pest control and protection of foodstuff. This study designed to evaluate the dose dependent haematological, hepatic and gonadal toxicity of LCT at different dose levels in Wistar rat. Investigations were also done to find out the toxic effect of lambda cyhalothrin on lipid metabolism in female rat and its amelioration by taurine. Rats were exposed to different doses of lambda cyhalothrin over a period of 14 consecutive days. Exposure to LCT produced ataxia, agitation, rolling and also tremors which were considered as the signs of toxicity. Significant decrease in erythrocyte count, haemoglobin percentage, seminal fructose concentration, hepatic and testicular reduced glutathione (GSH) content was observed.
Increase in leukocyte count, serum aspartic and alanine transaminase, hepatic and testicular malondialdehyde (MDA), testicular and ovarian cholesterol after LCT treatment were seen in male rats at the dose level of 10.83 mg/kg body wt. (1/7th LD50). Elevated ovarian cholesterol and MDA and reduced 3β hydroxy steroid dehydrogenase (HSD) and GSH level were also observed in lambda cyhalothrin exposed female rat at the dose level of 6.29 mg/kg body wt. (1/9th LD50). LCT caused increase in serum triglyceride, cholesterol, low density lipoproteins (LDL), very low density lipoproteins (VLDL) and bilirubin and decrease in serum high density lipoproteins (HDL) in female rat. Taurine pretreatment ameliorated LCT induced altered lipid metabolic biomarkers in female rat.
References
Magar RS, Bias UE. Histopathological impact of malathion on the ovary of the fresh water fish channa punctatus. Int Res J Environment Sci. 2013; 2: 59-61. Web site. http://www.isca.in/ IJENS/Archive/v2/i3/12.ISCA-IRJEvS-2012-098.pdf. Accessed September 9, 2016.
Sharaf S, Khan A, Khan MZ, Aslam F, Saleemi MK, Mah-mood F. Clinico-hematological and micronuclear changes in-duced by cypermethrin in broiler chicks: Their attenuation with vitamin E and selenium. Exp Toxicol Pathol. 2010; 62(4): 333- 341. doi: 10.1016/j.etp.2009.05.002
Khan A, Ahmad L, Khan MZ. Hemato-biochemical changes induced by pyrethroid insecticides in avian, fish and mammalian species. Int J Agric Biol. 2012; 14: 834-842. Web site. https:// www.cabdirect.org/cabdirect/abstract/20123332347. Accessed September 9, 2016.
Khan A, Faridi HAM, Ali M, et al. Effects of cyper-methrin on some clinico-hemato biochemical and pathological parame-ters in male dwarf goats. Exp Toxicol Pathol. 2009; 61: 151-160. doi: 10.1016/j.etp.2008.07.001
Jaeschke H, Gores GJ, Cederbaum AI, Hinson JA, Pessayre D, Lemasters JJ. Mechanisms of hepatotoxicity. Toxicol Sci. 2002; 65: 166-176. doi: 10.1093/toxsci/65.2.166
Song L, Wang Y, Sun H, et al. Effects of fenvalerate and cy-permethrin on rat sperm motility patterns in vitro as measured by computer-assisted sperm analysis. J Toxicol and Environ Health, Part A. 2008; 71(5): 325-332. doi: 10.1080/15287390701738517
Lifeng T, Shoulin W, Junmin J, Xuezhao S, Yannan L, Qian-li W. Effects of fenvalerate exposure on semen quality among occupational workers. Contraception. 2006; 73: 92-96. doi: 10.1016/j.contraception.2005.06.067
Yousef M, El-Demerdash F, Al-Salhen K. Protective role of isoflavones against the toxic effect of cypermethrin on semen quality and testosterone levels of rabbits. J Environ sci. 2003; 38: 463-478. doi: 10.1081/PFC-120021666
Hu JY, Wang SL, Zhao RC, et al. Effects of fenvalerate on re-productive and endocrine systems of male rats. Zhonghua Nanke xue. 2002; 8: 18-21. Web site. http://europepmc.org/abstract/ med/12479040. Accessed September 9, 2016.
Solati J. Effects of Permethrin on sexual behaviour and plas-ma concentrations of pituitary-gonadal hormones in adult male NMRI mice. J Kurdistan Univ of Med Sci. 2008; 13: 42-49.
Zhang S, Ito Y, Yamanoshita O, et al. Permethrin may disrupt testosterone biosynthesis via mitochondrial membrane dam-age of Leydig cells in adult male mouse. Endocrinology. 2007; 14(8): 3941. doi: 10.1210/en.2006-1497
Anadon A, Martinez M, Martinez MA, Diaz MJ. Martinez-Larranaga MR. Toxicokinetics of lambda-cyhalothrin in rats. Toxicol Lett. 2006; 165: 47-56.
Ratnasooriya WD, Ratnayake SS, Jayatunga YN. Effects of Icon, a pyrethroid insecticide on early pregnancy of rats. Hum Exp Toxicol. 2003; 22: 523-533. doi: 10.1191/0960327103ht381oa
Barata C, Baird DJ, Nogueira AJ, Soares AM, Riva MC. Toxicity of binary mixtures of metals and pyrethroid insecticides to daphnia magna straus. Implications for multi-substance risks assessment. Aquat Toxicol. 2006; 78: 1-14.
Schroer AF, Belgers JD, Brock TC, Matser AM, Maund SJ, Van den Brink PJ. Comparison of laboratory single species and field population-level effects of the pyrethroid insecticide lambda cyhalothrin on freshwater invertebrates. Arch Environ Contam Toxicol. 2004; 46: 324-335.
Meister RT. Farm Chemicals Handbook. Willoughby, OH, USA: Meister Publishing Co. 92; 1992.
Wright CE, Tallan HH, Lin YY, Gaul GE. Taurine: Biologi-cal update. Annu Rev Biochem. 1986; 49: 141.
Droge W, Breitkreutz R. N acetyl-cysteine in the therapy of HIV positive patients. Curr Opin Nut Metab Care. 1999; 2: 493-498. Web site. http://journals.lww.com/co-clinicalnutrition/ Abstract/1999/11000/N_acetyl_cysteine_in_the_therapy_of_ HIV_positive.11.aspx. Accessed September 9, 2016.
Birdsall TC. Therapeutic application of taurine. Alt Med Rev. 1998; 3: 128-136. Web site. http://europepmc.org/abstract/ med/9577248. Accessed September 9, 2016.
Huxtable RJ. Physiological actions of taurine. Physiol Rev. 1992; 72: 101-163. Web site. http://physrev.physiology.org/ content/72/1/101.long. Accessed September 9, 2016.
Redmond HP, Wang JH, Bouchier-Hayes D. Taurine attenu-ates nitric oxide and reactive oxygen intermediate-dependent hepatocytes injury. Arch Surg. 1996; 131: 1280-1287. doi: 10.1001/archsurg.1996.01430240034004
Wright EC, Lin TT, Syurman JA, Gaul GE. Taurine scav-enges oxidized cholride in biological system. In: Oja SS, Ahtee Kontro L, Passonen MK, eds. Taurine: Biological Actions and Clinical Perspectives. New York, USA: Alan R. Liss, Inc.; 1985: 137-147.
Sharma CD, Saxena NP, Sharma R. Assessment of clastoge-nicity of lambda cyhalothrin, A synthetic pyrethroid in cultured lymphocytes of albino rats. World Appl Sci J. 2010; 8: 1093- 1099. Web site. http://www.idosi.org/wasj/wasj8(9)/9.pdf. Ac-cessed September 9, 2016.
Ecobichon DJ. The Basis of Toxicology Testing. New York, USA: RC Press; 1997: 43-86.
Ozden S, Catalgol B, Gezginci-Oktayoglu S, Arda-Pirincci P, Bolkent S, Alpertunga B. Methiocarb-induced oxidative dam-age following subacute exposure and the protective effects of vitamin E and taurine in rats. Food Chem Toxicol. 2009; 47: 1676-1684. doi: 10.1016/j.fct.2009.04.018
Cetiner M, Sener G, Sehirli AO, et al. Taurine protects against methotrexate-induced toxicity and inhibits leukocyte death. Toxicol Appl Pharmacol. 2005; 209: 39-50.
Wintrobe MM. Clinical Hematology. 6th ed. Philadelphia, USA: Lea and Febiger; 1967.
Dacie JV, Lewis SM. Practical Haematology. London, UK: Churchill Livingstone; 1975.
Goel BK. Routine biochemical tests. In: Mukherjee KL, eds. Medical Laboratory Technology. New Delhi, India: Tata Mc Graw-Hill Publishing Company Ltd.; 1988: 985-1079.
Ohkawa H, Onishi N, Yagi K. Assay for lipid per-oxidation in animal tissue by thiobarbituric acid reaction. Anal Biochem. 1979; 95: 351-358. doi: 10.1016/0003-2697(79)90738-3
Griffith OW. Glutathione turnover in human erythrocytes. J Biochem. 1981; 256: 4900-4904. Web site. http://www.jbc.org/ content/256/10/4900.full.pdf. Accessed September 9, 2016.
Karvonen MJ, Malm M. Colorimetric determination of fruc-tose with indole. Scand J Clin Lab Invest. 1955; 7: 305-307. doi: 10.3109/00365515509134669
Zlatkis A, Zak B, Bole AJ. A new method for the direct determination of serum cholesterol. J Lab Clin Med. 1953; 41: 486-492. Web site. http://www.translationalres.com/ar-ticle/0022-2143(53)90125-5/abstract. Accessed September 9, 2016.
Talalay P. Hydroxysteriod dehydrogenase. In: Colowick SP, Kaplan NO, eds. Methods in Enzymology. New York, USA: Aca-demic Press; 1962; 512-516.
Jendrassik L, Grof P. Colorimetric method of determination of bilirubin. Biochem. 1938; 297: 81-82.
Trinder P. Determination of triglycerides. Ann Clin Biochem. 1969; 6: 24-27.
Friedwalds WT, Levy RT, Friedickson DS. Estimation of concentration of low density lipoprotein cholesterol in plas-ma without use of the preparative ultracentrifuge. Clin Chem. 1972; 18: 499-502. Web site. http://clinchem.aaccjnls.org/ content/18/6/499. Accessed September 9, 2016.
Mandal A, Chakraborty S, Lahiri P. Hematological changes produced by lindane (-HCH) in six species of birds. Toxicol. 1986; 40: 103-111. doi: 10.1016/0300-483X(86)90050-8
Yousef MI, El-Deerdash FM, Kamel KI, Al-Salhen KS. Changes in some haematological and biochemical indices of rabbits induced by isoflavones and cypermethrin. Toxicol. 2003; 189: 223-234.
Banerjee BD, Seth V, Bhattacharya A, Pasha ST, Chakraborty AK. Biochemical effects of some pesticides on lipid peroxida-tion and free radical scavengers. Toxicol Lett. 1999; 107: 33-47.
Goel A, Dani V, Dhawan DK. Protective effects of zinc on lipid peroxidation, antioxidant enzymes and hepatic histoar-chitecture in chlorpyrifos induced toxicity. Chem Biol Interac. 2005; 156: 131-140.
Mansour SA, Mossa AH. Lipid peroxidation and oxidative stress in rat erythrocytes induced by chlorpyrifos and the protec-tive effect of zinc. Pest Biochem Physio. 2009; l93: 34-39.
Mossa AH, Heikal TM, Omara EA. Physiological and his-topathological changes in the liver of male rats exposed to paracetamol and diazinon. Asian Pacific J Trop Biomed. 2012; 12: S1683-S1690. doi: 10.1016/S2221-1691(12)60478-X
Mossa AT, Refaie AA, Ramadan A, Bouajila J. Ameliora-tion of prallethrininduced oxidative stress and hepatotoxicity in rat by the administration of Origanummajorana essential oil. Biomed Res Int. 2013; 2013: 1-11. doi: 10.1155/2013/859085
Hales DB, Diemer T, Hales KH. Role of cytokines in tes-ticular function. Endocrine. 1999; 10: 201-217. doi: 10.1007/ BF02738619
Thirunavukkarasu C, Princevijeyasingh J, Selvendiran K, Sakthisekaran D. Chemopreventive efficacy of selenium against DEN-induced hepatoma in albino rats. Cell Biochem Funct. 2001; 19: 265-271. doi: 10.1002/cbf.924
Agarwal A, Aponte-Mellado A, Premkumar BJ, Shaman A, Gupta S. The effects of oxidative stress on female repro-duction: A review. Reprod Biol Endocrinol. 2012; 10: 49. doi: 10.1186/1477-7827-10-49
Fujii J, Iuchi Y, Okada F. Fundamental roles of reactive oxygen species and protective mechanisms in the female re-productive system. Reprod Biol Endocrinol. 2005; 3: 43. doi: 10.1186/1477-7827-3-43
Aldana L, Tsutsumi V, Craigmill A, Silveira MI, Mejia EGD. α-Tocopherol modulates liver toxicity of the pyrethroid cyper-methrin. Toxicol Lett. 2001; 125: 107-116.
Ibrahim NA, El-Gamal BA. Effect of Diazinon, an organo-phosphate insecticide on plasma lipid constituents in experi-mental animals. J Biochem Mol Biol. 2003; 36: 499-504. Web site. http://www.koreascience.or.kr/article/ArticleFullRecord. jsp?cn=E1MBB7_2003_v36n5_499. Accessed September 9, 2016.
Pimple BP, Kadam PV, Badgujar NS, Bafna AR, Patil MJ. Protective effect of tamarindus indica linn against paracetamol-induced hepatotoxicity in rats. Indian J Pharm Sci. 2007; 69(6): 827-831. Web site. http://web.a.ebscohost.com/abstract?dire-ct=true&profile=ehost&scope=site&authtype=crawler&jrnl=0 250474X&AN=31407925&h=LR%2b4C1AiaW3zmcTQBVw oM6N%2b5CS1Mj5teSVjKpKikx3QlNnICyIZMLgPGhXOR NLSqvsB3hYyWbSK5lZ6g1XkaQ%3d%3d&crl=c&resultNs =AdminWebAuth&resultLocal=ErrCrlNotAuth&crlhashurl=lo gin.aspx%3fdirect%3dtrue%26profile%3dehost%26scope%3d site%26authtype%3dcrawler%26jrnl%3d0250474X%26AN% 3d31407925. Accessed September 9, 2016.
Fakurazi S, Hairuszah I, Nanthini U. Moringa oleifera Lam prevents acetaminophen induced liver injury through restoration of glutathione level. Food Chem Toxicol. 2008; 46: 2611-2615. doi: 10.1016/j.fct.2008.04.018
Yamanaka Y, Tsuji K, Ichikawa T. Stimulation of cheno-deoxycholic acid excretion in hypercholesterolemic mice by dietary taurine. J Nutr Sci Vitaminol. 1986; 32: 287-296. doi: 10.3177/jnsv.32.287
Ebihara K, Miyazato S, Ogawa H, Kishida T. Taurine in-creases cholesterol 7α-hydroxylase activity and fecal bile acids excretion but does not reduce the plasma cholesterol concentra-tion in ovariectomized rats fed with coconut oil. Nutr Res. 2006; 26: 167-172. doi: 10.1016/j.nutres.2006.04.003
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