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阿尔茨海默病型及其他痴呆症患者死后大脑中与pH值和乳酸相关的酶活性

Enzyme activities in relation to pH and lactate in postmortem brain in Alzheimer-type and other dementias.

作者信息

Yates C M, Butterworth J, Tennant M C, Gordon A

机构信息

Department of Pharmacology, University of Edinburgh, Scotland.

出版信息

J Neurochem. 1990 Nov;55(5):1624-30. doi: 10.1111/j.1471-4159.1990.tb04948.x.

Abstract

Phosphate-activated glutaminase, glutamic acid decarboxylase, pyruvate dehydrogenase, succinic dehydrogenase, pH, and lactate were measured in frontal cortex and caudate nucleus of postmortem brains from cases of Alzheimer-type dementia (ATD), Down's syndrome, Huntington's disease, and one case of Pick's disease, as well as from sudden death and agonal controls. Lactate levels were higher and pH, phosphate-activated glutaminase, and glutamic acid decarboxylase levels were lower in the agonal controls than in the sudden death controls. Phosphate-activated glutaminase and glutamic acid decarboxylase were correlated with tissue pH and lactate, and also were reduced by in vitro acidification, suggesting that the low activities of these enzymes in agonal controls were related to decreased pH consequent upon lactate accumulation. Compared with control tissues at the same pH, phosphate-activated glutaminase and glutamic acid decarboxylase were unaltered in ATD and Down's frontal cortex and reduced in Huntington's caudate nucleus, and glutamic acid decarboxylase was reduced in Huntington's frontal cortex. These data suggest that GABAergic neurons are not affected in ATD and confirm the GABAergic defect in Huntington's disease. Pyruvate dehydrogenase and succinic dehydrogenase activities were the same in agonal controls and sudden death controls and were unaffected by acid pH and lactate in vitro, and pyruvate dehydrogenase was not correlated with pH or lactate. Reduced pyruvate dehydrogenase in frontal cortex of individual ATD, Down's, and Pick's cases, and in the caudate nucleus of Huntington's and Down's cases, was accompanied by gliosis/neuron loss. We conclude that decreased pyruvate dehydrogenase reflects neuronal loss.

摘要

在阿尔茨海默型痴呆(ATD)、唐氏综合征、亨廷顿舞蹈病以及一例匹克氏病患者的尸检大脑额叶皮质和尾状核中,测量了磷酸激活谷氨酰胺酶、谷氨酸脱羧酶、丙酮酸脱氢酶、琥珀酸脱氢酶、pH值和乳酸水平,同时也测量了猝死和濒死对照样本。濒死对照样本中的乳酸水平高于猝死对照样本,而pH值、磷酸激活谷氨酰胺酶和谷氨酸脱羧酶水平则低于猝死对照样本。磷酸激活谷氨酰胺酶和谷氨酸脱羧酶与组织pH值和乳酸相关,并且在体外酸化时活性降低,这表明濒死对照样本中这些酶的低活性与乳酸积累导致的pH值降低有关。与相同pH值的对照组织相比,ATD和唐氏综合征额叶皮质中的磷酸激活谷氨酰胺酶和谷氨酸脱羧酶未发生改变,而亨廷顿舞蹈病尾状核中的这两种酶活性降低,亨廷顿舞蹈病额叶皮质中的谷氨酸脱羧酶活性也降低。这些数据表明,GABA能神经元在ATD中未受影响,并证实了亨廷顿舞蹈病中的GABA能缺陷。濒死对照样本和猝死对照样本中的丙酮酸脱氢酶和琥珀酸脱氢酶活性相同,并且在体外不受酸性pH值和乳酸的影响,丙酮酸脱氢酶与pH值或乳酸无关。个别ATD、唐氏综合征和匹克氏病病例额叶皮质以及亨廷顿舞蹈病和唐氏综合征病例尾状核中的丙酮酸脱氢酶活性降低,同时伴有胶质增生/神经元丢失。我们得出结论,丙酮酸脱氢酶活性降低反映了神经元丢失。

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