Refine your search
Collections
Co-Authors
Year
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Haris Siddiqui, M.
- Effect of Repeated Exposure to Lambda-Cyhalothrin and Immobilization or Forced Swim Stress on Oxidative Stress in Rat Brain
Abstract Views :407 |
PDF Views:0
Authors
Affiliations
1 Developmental Toxicology Laboratory, Systems Toxicology & Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research, IN
2 Department of Criminology and Forensic Science, Dr. Harisingh Gour Central University, Sagar, IN
3 Department of Biochemistry, Integral Institute of Medical Sciences & Research, Integral University, IN
4 Department of Bioengineering, Integral University, Lucknow, IN
1 Developmental Toxicology Laboratory, Systems Toxicology & Health Risk Assessment Group, CSIR-Indian Institute of Toxicology Research, IN
2 Department of Criminology and Forensic Science, Dr. Harisingh Gour Central University, Sagar, IN
3 Department of Biochemistry, Integral Institute of Medical Sciences & Research, Integral University, IN
4 Department of Bioengineering, Integral University, Lucknow, IN
Source
Toxicology International (Formerly Indian Journal of Toxicology), Vol 23, No 1 (2016), Pagination: 18-26Abstract
The present study has been undertaken to investigate role of immobilization stress (IMS), a psychological stressor and forced swim stress (FSS), a physical stressor on the neurobehavioral toxicity of lambda-cyhalothrin (LCT), a new generation, type-II synthetic pyrethroid with extensive uses to control insects and ectoparasites. Rats subjected to IMS (placed in plastic restrainer for 6 hour/day) or FSS (one session of 15 min/day) for 28 days exhibited a significant increase in lipid peroxidation and protein carbonyl levels in frontal cortex, corpus striatum, hippocampus and hypothalamus as compared to controls. Further, decrease in the levels of reduced glutathione and activity of superoxide dismutase, catalase and glutathione peroxidase was also observed in these brain regions of rats subjected either IMS or FSS as compared to rats in the control groups. No significant change in any of the parameters was observed in any of the brain regions of rats treated with LCT (0.5 mg/kg body weight, p.o., 28 days) as compared to controls. Simultaneous exposure of rats to LCT and IMS or FSS resulted to cause marked increase in protein carbonyl levels and lipid peroxidation as compared to controls. Further, decrease in the activity of superoxide dismutase, catalase and glutathione peroxidase, enzymes involved in antioxidant defense in these brain regions was also observed in rats simultaneously exposed to IMS or FSS and LCT as compared to controls. The data of the present study exhibit that both psychological and physical stress enhances the neurotoxicity of lambda-cyhalothrin by enhancing oxidative stress in rat brain.Keywords
Immobilization Stress, Forced Swim Stress, Lambda-Cyhalothrin, Oxidative Stress.
References
- Cohen S, Janicki-Deverts D and Miller GE. Psychological stress and disease. Jama. 2007; 298: 1685-7.
- Herman JP and Seroogy K. Hypothalamic-pituitary-adrenal axis, glucocorticoids, and neurologic disease. Neurologic clinics. 2006; 24: 461-81.
- Sapolsky RM. Glucocorticoids and hippocampal atrophy in neuropsychiatric disorders. Archives of general psychiatry. 2000; 57: 925-35.
- Cory-Slechta DA, Stern S, Weston D, Allen JL and Liu S. Enhanced learning deficits in female rats following lifetime Pb exposure combined with prenatal stress. Toxicological Sciences. 2010; 117: 427-38.
- Fink G. Stress: definition and history. Stress Science: Neuroendocrinology. 2010: 3-9.
- Friedman A, Kaufer D, Shemer J, Hendler I, Soreq H and Tur-Kaspa I. Pyridostigmine brain penetration under stress enhances neuronal excitability and induces early immediate transcriptional response. Nature medicine. 1996; 2: 1382-5.
- Hanin I. The Gulf War, stress and a leaky blood—brain barrier. Nature medicine. 1996; 2: 1307-8.
- Ansari RW, Shukla RK, Yadav RS, et al. Cholinergic dysfunctions and enhanced oxidative stress in the neurobehavioral toxicity of lambda-cyhalothrin in developing rats. Neurotoxicity research. 2012; 22: 292-309.
- Gandhi S and Abramov AY. Mechanism of oxidative stress in neurodegeneration. Oxidative medicine and cellular longevity. 2012; 2012.
- Madrigal JL, Olivenza R, Moro MA, et al. Glutathione depletion, lipid peroxidation and mitochondrial dysfunction are induced by chronic stress in rat brain. Neuropsychopharmacology. 2001; 24: 420-9.
- Zafir A and Banu N. Modulation of in vivo oxidative status by exogenous corticosterone and restraint stress in rats. Stress. 2009; 12: 167-77.
- Bhatia N, Maiti PP, Choudhary A, et al. Animal models in the study of stress: A review. J Pharm and Healthc Manag. 2011; 2: 42-50.
- Jaggi AS, Bhatia N, Kumar N, Singh N, Anand P and Dhawan R. A review on animal models for screening potential anti-stress agents. Neurological Sciences. 2011; 32: 993-1005.
- Abdel-Rahman A, Abou-Donia SM, El-Masry EM, Shetty AK and Abou-Donia MB. Stress and combined exposure to low doses of pyridostigmine bromide, DEET, and permethrin produce neurochemical and neuropathological alterations in cerebral cortex, hippocampus, and cerebellum. Journal of Toxicology and Environmental Health, Part A. 2004; 67: 163-92.
- Hancock S, Ehrich M, Hinckley J, Pung T and Jortner BS. The effect of stress on the acute neurotoxicity of the organophosphate insecticide chlorpyrifos. Toxicology and applied pharmacology. 2007; 219: 136-41.
- Pung T, Klein B, Blodgett D, Jortner B and Ehrich M. Examination of concurrent exposure to repeated stress and chlorpyrifos on cholinergic, glutamatergic, and monoamine neurotransmitter systems in rat forebrain regions. International journal of toxicology. 2006; 25: 65-80.
- Fetoui H, Garoui EM, Makni-ayadi F and Zeghal N. Oxidative stress induced by lambda-cyhalothrin (LTC) in rat erythrocytes and brain: attenuation by vitamin C. Environmental Toxicology and Pharmacology. 2008; 26: 225-31.
- Fetoui H, Feki A, Salah GB, Kamoun H, Fakhfakh F and Gdoura R. Exposure to lambda-cyhalothrin, a synthetic pyrethroid, increases reactive oxygen species production and induces genotoxicity in rat peripheral blood. Toxicology and industrial health. 2015; 31: 433-41.
- He L-M, Troiano J, Wang A and Goh K. Environmental chemistry, ecotoxicity, and fate of lambda-cyhalothrin. Reviews of environmental contamination and toxicology. Springer, 2008, p. 71-91.
- Fetoui H, Garoui EM and Zeghal N. Lambda-cyhalothrininduced biochemical and histopathological changes in the liver of rats: ameliorative effect of ascorbic acid. Experimental and Toxicologic Pathology. 2009; 61: 189-96.
- Barr DB, Olsson AO, Wong L-Y, et al. Urinary Concentrations of Metabolites of Pyrethroid Insecticides in the General U. S. Population: National Health and Nutrition Examination Survey 1999-2002. Environmental health perspectives. 2010; 118: 742-8.
- Muhammad F, Akhtar M, Rahman Z, Farooq H, Khaliq T and Anwar M. Multi-residue determination of pesticides in the meat of cattle in Faisalabad-Pakistan. Egypt Acad J Biol Sci. 2010; 2: 19-28.
- Rao BS, Madhavi R, Sunanda and Raju T. Complete reversal of dendritic atrophy in CA3 neurons of the hippocampus by rehabilitation in restraint stressed rats. Current science. 2001; 80: 653-9.
- Badowska-Szalewska E, Klejbor I, Cecot T, Spodnik JH and Moryś J. Changes in NGF/c-Fos double staining in the structures of the limbic system in juvenile and aged rats exposed to forced swim test. Acta neurobiologiae experimentalis. 2009; 69: 448-58.
- GItiwinski J and Iversen L. Regional studies of catecholamines in the rat brain. The disposition of 3H-norepinephrine, 3H-dopamine and3H-DOPA in various regions of the brain. J Neurochem. 1966; 13: 655-69.
- Ohkawa H, Ohishi N and Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical biochemistry. 1979; 95: 351-8.
- Levine RL, Garland D, Oliver CN, et al. Determination of carbonyl content in oxidatively modified proteins. Methods in enzymology. 1990: 464-78.
- Hasan M and Haider S. Acetyl-homocysteine thiolactone protects against some neurotoxic effects of thallium. Neurotoxicology. 1988; 10: 257-61.
- Kakkar P, Das B and Viswanathan P. A modified spectrophotometric assay of superoxide dismutase. Indian J Biochem Biophys. 1984; 21: 130-2.
- Aebi H. [13] Catalase in vitro. Methods in enzymology. 1984; 105: 121-6.
- Flohé L and Günzler WA. Assays of glutathione peroxidase. Methods in enzymology. 1984; 105: 114.
- Lowry OH, Rosebrough NJ, Farr AL and Randall RJ. Protein measurement with the Folin phenol reagent. J biol Chem. 1951; 193: 265-75.
- Ray DE and Fry JR. A reassessment of the neurotoxicity of pyrethroid insecticides. Pharmacology & therapeutics. 2006; 111: 174-93.
- Prasanthi K and Rajini P. Fenvalerate-induced oxidative damage in rat tissues and its attenuation by dietary sesame oil. Food and chemical toxicology. 2005; 43: 299-306.
- Kilian E, Delport R, Bornman M and Jager Cd. Simultaneous exposure to low concentrations of dichlorodiphenyltrichloroethane, deltamethrin, nonylphenol and phytoestrogens has negative effects on the reproductive parameters in male Spraque‐Dawley rats. Andrologia. 2007; 39: 128-35.
- Abdollahi M, Ranjbar A, Shadnia S, Nikfar S and Rezaiee A. Pesticides and oxidative stress: a review. Medical Science Review. 2004; 10: RA141-RA7.
- Mancuso C, Scapagini G, Curro D, et al. Mitochondrial dysfunction, free radical generation and cellular stress response in neurodegenerative disorders. Front Biosci. 2007; 12: 1107-23.
- Abidin I, Yargicoglu P, Agar A, et al. The effect of chronic restraint stress on spatial learning and memory: relation to oxidant stress. International journal of neuroscience. 2004; 114: 683-99.
- Olivenza R, Moro MA, Lizasoain I, et al. Chronic stress induces the expression of inducible nitric oxide synthase in rat brain cortex. Journal of neurochemistry. 2000; 74: 78591.
- Esch T, Fricchione GL and Stefano GB. The therapeutic use of the relaxation response in stress-related diseases. Medical Science Monitor. 2003; 9: RA23-RA34.
- de Pablos RM, Herrera AJ, Espinosa-Oliva AM, et al. Chronic stress enhances microglia activation and exacerbates death of nigral dopaminergic neurons under conditions of inflammation. J Neuroinflammation. 2014; 11: 34.
- Abdel-Rahman A, Shetty AK and Abou-Donia MB. Disruption of the blood–brain barrier and neuronal cell death in cingulate cortex, dentate gyrus, thalamus, and hypothalamus in a rat model of Gulf-War syndrome. Neurobiology of Disease. 2002; 10: 306-26.
- Habr SF, Macrini DJ, Spinosa HdS, Florio JC and Bernardi MM. Repeated forced swim stress has additive effects in anxiety behavior and in cathecolamine levels of adult rats exposed to deltamethrin. Neurotoxicology and teratology. 2014; 46: 57-61.
- Terçariol SG, Almeida AA and Godinho AF. Cadmium and exposure to stress increase aggressive behavior. environmental toxicology and pharmacology. 2011; 32: 40-5.
- Organization WH. Cyhalothrin. 1990.
- Reiter RJ, Tan D-x, Osuna C and Gitto E. Actions of melatonin in the reduction of oxidative stress. Journal of biomedical science. 2000; 7: 444-58.
- Mates J. Effects of antioxidant enzymes in the molecular control of reactive oxygen species toxicology. Toxicology. 2000; 153: 83-104.
- Škultétyová I, Tokarev D and Ježová D. Stress-induced increase in blood–brain barrier permeability in control and monosodium glutamate-treated rats. Brain research bulletin. 1998; 45: 175-8.