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遗传性肌张力障碍仓鼠特定脑区氨基酸神经递质的异常

Abnormalities in amino acid neurotransmitters in discrete brain regions of genetically dystonic hamsters.

作者信息

Löscher W, Hörstermann D

机构信息

Department of Pharmacology, Toxicology and Pharmacy, School of Veterinary Medicine, Hannover, F.R.G.

出版信息

J Neurochem. 1992 Aug;59(2):689-94. doi: 10.1111/j.1471-4159.1992.tb09423.x.

Abstract

The concentrations of 11 amino acids, including the neurotransmitters gamma-aminobutyric acid, glutamate, aspartate, glycine, and taurine, were determined by HPLC in 12 brain regions of genetically dystonic (dtSZ) hamsters and age-matched nondystonic controls. Since dystonia in mutant dtSZ hamsters is transient and disappears after about 70 days of age, amino acids were determined at the age of maximum severity of dystonia (30-40 days) and after disappearance of the disease, to examine which neurochemical changes were related to dystonia. In dtSZ hamsters with the maximum severity of dystonia, significant changes in concentrations of the neurotransmitters gamma-aminobutyric acid, glutamate, aspartate, and taurine were found in several regions involved in motor functions, e.g., cerebellum, thalamus, and corpus striatum. Most of these changes were not permanent but disappeared in parallel with dystonia, implicating a causal relationship between altered aminoacidergic neurotransmission and dystonia in mutant dtSZ hamsters.

摘要

通过高效液相色谱法(HPLC)测定了遗传性肌张力障碍(dtSZ)仓鼠和年龄匹配的非肌张力障碍对照仓鼠12个脑区中11种氨基酸的浓度,其中包括神经递质γ-氨基丁酸、谷氨酸、天冬氨酸、甘氨酸和牛磺酸。由于突变型dtSZ仓鼠的肌张力障碍是短暂的,在约70日龄后消失,因此在肌张力障碍最严重时(30 - 40日龄)以及疾病消失后测定氨基酸,以检查哪些神经化学变化与肌张力障碍有关。在肌张力障碍最严重的dtSZ仓鼠中,在几个参与运动功能的脑区,如小脑、丘脑和纹状体,发现神经递质γ-氨基丁酸、谷氨酸、天冬氨酸和牛磺酸的浓度有显著变化。这些变化大多不是永久性的,而是与肌张力障碍同时消失,这意味着突变型dtSZ仓鼠中氨基酸能神经传递改变与肌张力障碍之间存在因果关系。

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