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Acrylonitrile has Distinct Hormetic Effects on Acetylcholinesterase Activity in Mouse Brain and Blood that are Modulated by Ethanol

机译:丙烯腈对乙醇调节的小鼠大脑和血液中乙酰胆碱酯酶活性具有明显的抑制作用

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Acrylonitrile(AN) is a neurotoxin both in animals and humans, but its effects on acetylcholinesterase (AChE) activity remain controversial. This study aimed to determine the dose-response effects of AN on AChE activity and the modulatory role of ethanol pretreatment. A total of 144 Kunming mice were randomly divided into 18 groups: nine groups received 5% ethanol in their drinking water, and the remaining nine groups received regular tap water. One week later, both the ethanol and tap water only groups were given an intraperitoneal injection of AN at the following doses: 0 (control), 0.156, 0.3125, 0.625, 1.25, 2.5, 5, 10 or 20 mg AN/kg body weight. AChE activity was determined on whole blood and brain 24 h later. Blood AChE activity was higher in AN-injected mice than in controls at all doses. AChE activity in blood increased in a dose-dependent manner, peaking at 0.156 mg/kg, after which a gradual decrease ensued, displaying a β-typed dose-response relationship. In contrast, brain AChE activity, following a single AN injection, was consistently lower than in control mice, and continued to fall up to a dose of 0.313 mg/kg, and thereafter increased gradually with higher doses. Mice receiving a 20 mg/kg dose of AN exhibited AChE brain activity indistinguishable from that of control mice, demonstrating a typical U-typed dose-response relationship. The activity of AChE in the blood and brain of the AN + ethanol-treated groups displayed a shift to the right, and the magnitude of the decrease in AChE activity induced by AN was attenuated relative to the AN-only group. These results suggest that AN affects AChE activity in both mouse blood and brain in a hormetic manner. Pretreatment with ethanol modifies the effect of AN on AChE, indicating that parent AN has a more prominent role than its metabolites in modulating enzyme activity.
机译:丙烯腈(AN)在动物和人类中都是一种神经毒素,但其对乙酰胆碱酯酶(AChE)活性的影响仍存在争议。这项研究旨在确定AN对AChE活性的剂量反应效应以及乙醇预处理的调节作用。总共144只昆明小鼠随机分为18组:9组在饮用水中接受5%的乙醇,其余9组接受常规自来水。一周后,仅对乙醇和自来水组进行腹膜内注射AN,剂量如下:0(对照组),0.156、0.3125、0.625、1.25、2.5、5、10或20 mg AN / kg体重。 24小时后测定全血和大脑的AChE活性。在所有剂量下,注射AN的小鼠的血液AChE活性均高于对照组。血液中的AChE活性以剂量依赖性方式增加,达到0.156 mg / kg的峰值,此后逐渐下降,表现出β型剂量反应关系。相反,单次AN注射后,脑AChE活性始终低于对照组小鼠,并持续下降至0.313 mg / kg的剂量,此后随着剂量的增加而逐渐增加。接受20 mg / kg剂量的AN的小鼠表现出与对照组小鼠无法区分的AChE脑活性,表明了典型的U型剂量反应关系。 AN +乙醇处理组的血液和大脑中AChE的活性向右移动,相对于仅使用AN的组,由AN诱导的AChE活性下降的幅度有所减弱。这些结果表明AN会以一种讨厌的方式影响小鼠血液和大脑中的AChE活性。用乙醇预处理可改变AN对AChE的影响,表明亲本AN在调节酶活性方面比其代谢产物具有更突出的作用。

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