School of Medical Science and Laboratory Medicine and the Laboratory Animal Center, Jiangsu University, China.
Dose Response. 2013;11(1):49-59. doi: 10.2203/dose-response.11-030.Yuanqing. Epub 2011 Nov 17.
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 pre-treatment. 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.
丙烯腈(AN)对动物和人类都是神经毒素,但它对乙酰胆碱酯酶(AChE)活性的影响仍存在争议。本研究旨在确定 AN 对 AChE 活性的剂量反应效应,以及乙醇预处理的调节作用。将 144 只昆明小鼠随机分为 18 组:9 组饮用含 5%乙醇的水,其余 9 组饮用自来水。一周后,所有饮用乙醇和自来水的组均腹腔注射以下剂量的 AN:0(对照)、0.156、0.3125、0.625、1.25、2.5、5、10 或 20mg AN/kg 体重。24 小时后测定全血和脑组织中的 AChE 活性。与对照组相比,所有剂量下 AN 注射组的全血 AChE 活性均升高。全血 AChE 活性呈剂量依赖性增加,在 0.156mg/kg 时达到峰值,之后逐渐下降,呈 β 型剂量反应关系。相反,单次 AN 注射后,脑组织 AChE 活性始终低于对照组,且持续下降至 0.313mg/kg 剂量,此后随剂量增加逐渐升高。接受 20mg/kg AN 剂量的小鼠的脑组织 AChE 活性与对照组小鼠无明显差异,表现出典型的 U 型剂量反应关系。AN+乙醇处理组的血液和大脑中的 AChE 活性向右侧移动,与 AN 单处理组相比,AN 诱导的 AChE 活性下降幅度减弱。这些结果表明,AN 以一种激动剂的方式影响小鼠血液和大脑中的 AChE 活性。乙醇预处理改变了 AN 对 AChE 的作用,表明母体 AN 在调节酶活性方面比其代谢物更重要。