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普拉德-威利综合征或安吉尔曼综合征患者的血浆γ-氨基丁酸(GABA)水平升高。

Elevated plasma gamma-aminobutyric acid (GABA) levels in individuals with either Prader-Willi syndrome or Angelman syndrome.

作者信息

Ebert M H, Schmidt D E, Thompson T, Butler M G

机构信息

Department of Psychiatry, John F Kennedy Center, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2647, USA.

出版信息

J Neuropsychiatry Clin Neurosci. 1997 Winter;9(1):75-80. doi: 10.1176/jnp.9.1.75.

Abstract

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.

摘要

对14名普拉德-威利综合征患者、9名安吉尔曼综合征患者以及相匹配的对照受试者进行了血浆γ-氨基丁酸(GABA)水平检测。两个患者组的平均水平均比智力正常的中度肥胖对照受试者或智力发育迟缓的非肥胖对照受试者高出2至3倍。每个患者组的水平与两个对照组均有显著差异。两个患者组之间以及两个对照组之间均无差异。GABA水平似乎与遗传状态(15号染色体缺失或二体性)无关。这些血浆GABA水平升高的初步发现可能代表了突触前GABA释放的代偿性增加,以应对一部分GABA受体的低敏状态,并可能导致其他正常GABA受体亚型的突触后激活增加,从而引起全脑GABA能功能的复杂改变。

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