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Immune Response to Sub Acute Toxicity of Thiacloprid Insecticide in Gallus domesticus


Affiliations
1 Department of Veterinary Pharmacology and Toxicology, Guru Angad Dev Veterinary and Animal Science University, Ludhiana, India
     

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Thiacloprid is fairly a new chemical, but it has established itself as key component in insecticides because of its selectivity and low toxicity. It is effective on contact and via stomach action and bind agonistically to the nicotinic acetylcholine receptors in the CNS of insects, affecting synaptic transmission and leading to disruption of the nervous system. The immune system is a host defense system comprising many biological structures and processes within an organism that protects against disease. It can be the target of many chemicals, with potentially severe adverse effects on the host’s health. The health implications of these immune dysfunctions are increased risk of infectious diseases; development of neoplasia; autoimmune disorders and allergies. Estimation of total immunoglobulins and enumeration of B and T lymphocytes in blood after repeated oral administration of thiacloprid at the dose rate of 10 mg/kg/day revealed no significant alterations in Gallus domesticus. The observed findings in the present study indicated that repeated thiacloprid exposure in poultry birds did not adversely affect the immune status of Gallus domesticus and thus is immunologically safer insecticide.

Keywords

Toxicity, Gallus domesticus, Thiacloprid, Insecticide, Immune System.
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  • Uok K. Neonicotinoid Insecticides. Microbiology and Molecular Genetics. 2006; 2: 46-52.
  • National Registration Authority for Agricultural and Veterinary Chemicals. ISSN 1443-1335, Evaluation of the new active Thiacloprid in the new product Calypos 480 SC Insecticide. 2001.
  • Tomizawa M and Casida JE. Neonicotinoid insecticide toxicology: mechanisms of selective action. Annu. Rev. Pharmacol. Toxicol. 2005; 45: 247-268.
  • Felsot AS and Ruppert JR. Imidacloprid Residues in Willapa Bay (Washington State) Water and Sediment Following Application for Control of Burrowing Shrimp J. Agric. Food Chem. 2002; 50(15): 4417-23.
  • Ware GW and Whitacre DM. An Introduction to Insecticides fourth ed., MeisterPro Information Resources, A division of Meister Media Worldwide, Willoughby, Ohio, USA. 2004.
  • Anatra-M. and Durkin P. Imidacloprid. Human health assessment and ecological risk assessment Final report. Syracuse Environmental Research Associates, Inc., New York, SERA TR 2005; 5- 43-24-03.
  • Karabaym NUand Oguz, MG. Cytogenetic and genotoxic effects of the insecticides, imidacloprid and methamidophos Genet. Mol. Res. 2005; 4: 653-62.
  • Demsia G, Vlastos D, Goumenou M, Mathopoulos DP. Assesment of the genotoxicity of imidacloprid and metalaxyl in cultured human lymphocytes and rat bone marrow Mutat. Res. 2007; 634: 32-39.
  • Abou-Donia MB, Goldstein LB, Bulman S, Tu T, Khan WA, Dechkovskaia.AM and Abdel-Rahman AA. Imidacloprid induces neurobehavioral deficits an increase expression of glial fibrillary acidic protein in the motor cortex and hippocampus in offspring rats following in utero exposure. J.Toxicol. Environ. Health. 2008;. 71: 119–130.
  • Holsapple MP. Developmental immunotoxicity testing: a review.Toxicolology. 2003; 185: 193-203.
  • Meguire TC, Pfeiffer NE, Weikel JM, Bartsch, RC. Failure of cloistral immunoglobulin transfer in calves dying from infectious disease. JAVMA 1976; 169: 713-71.
  • Mcewan AD, Fisher EW, Selman IE Penhale WJ. A turbidity test for the estimation of immunoglobulin levels in neonatal calf serum. Clin. Chim. Acta, 1970; 27: 155-63.
  • Pfeiffer NE, Mcguire TC, Bendel RB. Quantitation of bovine immunoglobulins: comparison of single radial immunodiffusion, zinc sulfate turbidity, serum electrophoresis, and refractometer methods. Am J Vet Res, 1977; 38:693-698.
  • Boyum A. Separation of leukocytes from blood and bone marrow with special reference to factors which influence and modify redimentation properties of hematopoietic cells. Scandinavian Journal of Clinical and Laboratory Investigation 1968; 21: 1.
  • Julius MH, Simpson E, Herzenberg LA. A rapid method for the isolation of functional thymus-derived murine lymphocytes European Journal of Immunology. 1973; 3: 645-49.
  • Street JC. and Sharma RP. Alteration of induced cellular and humoral responses by pesticide and chemicals of environmental concern: Quantitative studies of immunosuppression by DDT, Aroclor 1254, carbaryl, carbofuran and Methylparathion. Toxicology and Applied Pharmacology 1995; 32: 58.
  • Goyal S and Sandhu HS. Immunological effects of sub chronic exposure to Thiacloprid insecticide in Gallus domesticus. The Veterinary Practitioner 2012; 13(2) 226-28.
  • Saha S. and Banerjee D. Effect of sub-chronic lindane exposure on humoral and cell-mediated immune responses in albino rats. Bulletin of Environmental Contamination and Toxicology.1993; 51: 795.
  • Khurana R and Chauhan RS. Immunopathological effects of lindane on humoral immune response in sheep. Journal of Immunology and Immunopathology1999; 1: 67-70.
  • Kumar S. Immunotoxic effects of endosulfan and cypermethrin in chickens. M.V.Sc. Thesis, CCS Haryana Agricultural University, Hisar. 1994.
  • Burns LA, Meade BJ and Murson AE. Toxic responses of the immune system. In: Klaassen C D.(ed) Casarett and Doull’s Toxicology: The Basic Science of Poisons. 5th edn. 1996; p 355-402. McGraw Hill, New York.
  • Ringer RK. PBB fed to immature chickens: Its effects on organ weights and function and on the cardiovascular system. Environmental Health Perspectives. 1978; 23: 247-55.
  • Sharma RP. Immunotoxicity. In: Gupta R C (ed) Veterinary Toxicology Basic and Clinical Principles. 2007; p 289-301. Academic Press Inc. San Diego.
  • Tamang RK, Gupta G and Chauhan H. In vivo immunosuppression by synthetic pyrethroid (cypermethrin) pesticide in mice and goats. Veterinary Immunology and Immunopathology. 1988; 19: 299-305.
  • Blaylock RL. Suppression of cellular immune responses in BALB/c mice following oral exposure to permethrin. Bulletin of Environmental Contamination and Toxicology. 1995; 54: 768-74.
  • Casale GP, Cohen SD and DiCapua RA. The effects of organophosphate-induced cholinergic stimulation on the antibody response to sheep erythrocytes in inbred mice. Toxicology and Applied Pharmacology.1983; 68: 198-205.
  • Chauhan RS and Tripathi BN. In: Veterinary Immunology Pathology Theory and Practice. International Book Distributing Co. Lucknow. 2002.
  • Parham P. The Immune System, Garland Science Publishing, New York. 2005.
  • Holtmeier W and Kabelitz D. Gamma delta T cells link innate and adaptive immune responses. Chemistry of Immunology Allergy 1990; 86: 151–83.
  • Katsenovich LA, Ruzybakiev, RM and Fedorin LA. T-and B-immunity in patients with pesticide poisoning. Gig. Tr. Prof Zabo. 1981; 4: 17.

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  • Immune Response to Sub Acute Toxicity of Thiacloprid Insecticide in Gallus domesticus

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Authors

Saloni Singla
Department of Veterinary Pharmacology and Toxicology, Guru Angad Dev Veterinary and Animal Science University, Ludhiana, India
V. K. Dumka
Department of Veterinary Pharmacology and Toxicology, Guru Angad Dev Veterinary and Animal Science University, Ludhiana, India

Abstract


Thiacloprid is fairly a new chemical, but it has established itself as key component in insecticides because of its selectivity and low toxicity. It is effective on contact and via stomach action and bind agonistically to the nicotinic acetylcholine receptors in the CNS of insects, affecting synaptic transmission and leading to disruption of the nervous system. The immune system is a host defense system comprising many biological structures and processes within an organism that protects against disease. It can be the target of many chemicals, with potentially severe adverse effects on the host’s health. The health implications of these immune dysfunctions are increased risk of infectious diseases; development of neoplasia; autoimmune disorders and allergies. Estimation of total immunoglobulins and enumeration of B and T lymphocytes in blood after repeated oral administration of thiacloprid at the dose rate of 10 mg/kg/day revealed no significant alterations in Gallus domesticus. The observed findings in the present study indicated that repeated thiacloprid exposure in poultry birds did not adversely affect the immune status of Gallus domesticus and thus is immunologically safer insecticide.

Keywords


Toxicity, Gallus domesticus, Thiacloprid, Insecticide, Immune System.

References





DOI: https://doi.org/10.22506/ti%2F2017%2Fv24%2Fi3%2F166503