Shukla Rajendra K, Dhuriya Yogesh K, Chandravanshi Lalit P, Gupta Richa, Srivastava Pranay, Pant Aditya B, Kumar Ajay, Pandey Chandra M, Siddiqui M Haris, Khanna Vinay K
Developmenatl Toxicology Laboratory, Systems Toxicology & Health Risk Assessment Group CSIR - Indian Institute of Toxicology Research, Post Box 80, 31 MG Marg Lucknow - 226 001, India; Department of Biochemistry, Integral Institute of Medical Sciences & Research Integral University Lucknow - 226 026, India.
Developmenatl Toxicology Laboratory, Systems Toxicology & Health Risk Assessment Group CSIR - Indian Institute of Toxicology Research, Post Box 80, 31 MG Marg Lucknow - 226 001, India.
Neurotoxicology. 2017 May;60:187-196. doi: 10.1016/j.neuro.2016.07.002. Epub 2016 Jul 7.
Experimental studies have been carried out on rats to understand the influence of immobilization stress (IMS), a psychological stressor and forced swim stress (FSS), a physical stressor in the neurotoxicity of lambda-cyhalothrin (LCT), a new generation type II synthetic pyrethroid with extensive applications. No significant change in plasma corticosterone levels and blood brain barrier (BBB) permeability was observed in rats subjected to IMS (one session of 15min/day), FSS (one session of 3min/day) for 28days or LCT treatment (3.0mg/kg body weight, p.o. suspended in groundnut oil) for 3days (26th, 27th and 28th day) as compared to controls. Marginal changes in the levels of biogenic amines and their metabolites (NE, EPN, DA, HVA, DOPAC, 5-HT) in hypothalamus, frontal cortex, hippocampus, and corpus striatum were observed in rats subjected to IMS or FSS or LCT alone as compared to controls. It was interesting to note that pre-exposure to IMS or FSS followed by LCT treatment for 3days caused a marked increase in plasma corticosterone levels associated with disruption in the BBB permeability as compared to rats exposed to IMS or FSS or LCT alone. Pre-exposure to IMS or FSS followed by LCT treatment for 3days resulted to alter the levels of biogenic amines and their metabolites in hypothalamus, frontal cortex, hippocampus, and corpus striatum as compared to rats exposed to IMS or FSS or LCT alone. Although neurochemical changes were more intense in rats pre-exposed to IMS as compared to those subjected to FSS on LCT treatment, the results indicate that both psychological and physical stress could be important influencing factors in the neurotoxicity of LCT.
已在大鼠身上开展实验研究,以了解作为心理应激源的制动应激(IMS)和作为身体应激源的强迫游泳应激(FSS)对氯氟氰菊酯(LCT,一种广泛应用的新一代II型合成拟除虫菊酯)神经毒性的影响。与对照组相比,接受28天的IMS(每天1次,每次15分钟)、FSS(每天1次,每次3分钟)或3天(第26、27和28天)LCT处理(3.0毫克/千克体重,口服,悬浮于花生油中)的大鼠,其血浆皮质酮水平和血脑屏障(BBB)通透性未观察到显著变化。与对照组相比,单独接受IMS、FSS或LCT处理的大鼠,其下丘脑、额叶皮质、海马体和纹状体中生物胺及其代谢物(去甲肾上腺素、肾上腺素、多巴胺、高香草酸、3,4-二羟基苯乙酸、5-羟色胺)水平有轻微变化。值得注意的是,与单独暴露于IMS、FSS或LCT的大鼠相比,预先暴露于IMS或FSS后再进行3天LCT处理,会导致血浆皮质酮水平显著升高,并伴有BBB通透性破坏。与单独暴露于IMS、FSS或LCT的大鼠相比,预先暴露于IMS或FSS后再进行3天LCT处理,会导致下丘脑、额叶皮质、海马体和纹状体中生物胺及其代谢物水平发生改变。尽管在LCT处理时,预先暴露于IMS的大鼠神经化学变化比接受FSS的大鼠更强烈,但结果表明,心理应激和身体应激都可能是LCT神经毒性的重要影响因素。