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孤独症儿童和青少年小脑和前额皮质中单胺氧化酶-A 和 B 的活性。

Monoamine oxidase-A and B activities in the cerebellum and frontal cortex of children and young adults with autism.

机构信息

NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York.

出版信息

J Neurosci Res. 2017 Oct;95(10):1965-1972. doi: 10.1002/jnr.24027. Epub 2017 Feb 2.

Abstract

Monoamine oxidases (MAOs) catalyze the metabolism of monoamine neurotransmitters, such as serotonin, dopamine, and norepinephrine, and are key regulators for brain function. In this study, we analyzed the activities of MAO-A and MAO-B in the cerebellum and frontal cortex from subjects with autism and age-matched control subjects. In the cerebellum, MAO-A activity in subjects with autism (aged 4-38 years) was significantly lower by 20.6% than in controls. When the subjects were divided into children (aged 4-12 years) and young adults (aged 13-38 years) subgroups, a significant decrease by 27.8% in the MAO-A activity was observed only in children with autism compared with controls. When the 95% confidence interval of the control group was taken as a reference range, reduced activity of MAO-A was observed in 70% of children with autism. In the frontal cortex, MAO-A activity in children with autism was also lower by 30% than in the control group, and impaired activity of MAO-A was observed in 55.6% of children with autism, although the difference between the autism and control groups was not significant when all subjects were considered. On the contrary, there was no significant difference in MAO-B activity in both the cerebellum and frontal cortex between children with autism and the control group as well as in adults. These results suggest impaired MAO-A activity in the brain of subjects with autism, especially in children with autism. Decreased activity of MAOs may lead to increased levels of monoaminergic neurotransmitters, such as serotonin, which have been suggested to have a critical role in autism. © 2017 Wiley Periodicals, Inc.

摘要

单胺氧化酶(MAO)催化单胺神经递质(如血清素、多巴胺和去甲肾上腺素)的代谢,是大脑功能的关键调节剂。在这项研究中,我们分析了自闭症患者和年龄匹配的对照组小脑和前额皮质中的 MAO-A 和 MAO-B 活性。在小脑中,自闭症患者(年龄 4-38 岁)的 MAO-A 活性比对照组低 20.6%。当将患者分为儿童(年龄 4-12 岁)和青年成年人(年龄 13-38 岁)亚组时,仅在自闭症儿童中观察到 MAO-A 活性显著下降 27.8%,与对照组相比。当将对照组的 95%置信区间作为参考范围时,观察到 70%的自闭症儿童 MAO-A 活性降低。在前额皮质中,自闭症儿童的 MAO-A 活性也比对照组低 30%,并且观察到 55.6%的自闭症儿童 MAO-A 活性受损,尽管当考虑所有患者时,自闭症组和对照组之间的差异无统计学意义。相反,自闭症儿童和对照组以及成年组小脑和前额皮质中的 MAO-B 活性均无显著差异。这些结果表明自闭症患者大脑中的 MAO-A 活性受损,尤其是自闭症儿童。MAO 活性的降低可能导致单胺能神经递质(如血清素)水平升高,血清素被认为在自闭症中具有关键作用。© 2017 Wiley Periodicals, Inc.

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