首页> 美国卫生研究院文献>other >Elevated Plasma Gamma-Aminobutyric Acid (GABA) Levels in Individuals With Either Prader-Wili Syndrome or Angelman Syndrome
【2h】

Elevated Plasma Gamma-Aminobutyric Acid (GABA) Levels in Individuals With Either Prader-Wili Syndrome or Angelman Syndrome

机译:普拉德-威利综合症或安格曼综合症患者的血浆γ-氨基丁酸(GABA)水平升高

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Plasma gamma-aminobutyric acid (GABA) levels were measured in 14 subjects with Prader-Willi syndrome, 9 subjects with Angelman syndrome, and matched control subjects. Mean levels in both patient groups were 2 to 3 times higher than in nonretarded moderately obese or retarded nonobese control subjects. Levels in each patient group differed significantly from both control groups. Neither the two patient groups nor the two control groups differed. GABA levels seemed unrelated to genetic status (chromosome 15 deletion or disomy). These preliminary findings of elevated plasma GABA levels possibly represent a compensatory increase in presynaptic GABA release in response to hyposensitivity of a subset of GABA receptors and could produce increased postsynaptic activation of other normal GABA receptor subtypes, resulting in complex alterations of GABAergic function throughout the brain.
机译:在14名Prader-Willi综合征,9名Angelman综合征以及相匹配的对照组中测量了血浆γ-氨基丁酸(GABA)水平。两组患者的平均水平均比未延迟的中度肥胖或迟钝的非肥胖对照组高2至3倍。每个患者组的水平与两个对照组都有显着差异。两个患者组和两个对照组都没有区别。 GABA水平似乎与遗传状态无关(染色体15缺​​失或二体化)。血浆GABA水平升高的这些初步发现可能代表突触前GABA释放的代偿性增加,以响应一部分GABA受体的敏感性降低,并可能导致其他正常GABA受体亚型的突触后激活增加,从而导致整个大脑复杂的GABA能功能改变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号