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磷酸吡哆醛-γ-谷氨酰腙对发育中大鼠的惊厥作用及谷氨酸脱羧酶的抑制作用

Convulsions and inhibition of glutamate decarboxylase by pyridoxal phosphate-gamma-glutamyl hydrazone in the developing rat.

作者信息

Massieu L, Rivera A, Tapia R

机构信息

Departamento de Neurociencias, Universidad Nacional Autónoma de México, México, D.F.

出版信息

Neurochem Res. 1994 Feb;19(2):183-7. doi: 10.1007/BF00966814.

Abstract

We have previously shown that in the adult rat the inhibition of brain glutamate decarboxylase (GAD) activity by pyridoxal phosphate-gamma-glutamyl hydrazone (PLPGH) administration does not result in convulsions, whereas in the adult mouse intense convulsions invariably occur. In the present study we report that, surprisingly, immature rats from 2 to 20 days of age treated with PLPGH (80 mg/kg) showed generalized tonic-clonic convulsions, whereas no convulsions at all were present in 30 days-old or older rats. GAD activity, measured by enzymic determination of GABA formed in forebrain homogenates, was inhibited by about 60% at the time of convulsions in 15 days-old and younger rats, whereas the inhibition was between 40 and 50% in older animals. The addition of the coenzyme pyridoxal 5'-phosphate to the incubation medium completely reversed this inhibition. In all treated animals GABA levels were lower compared to controls. The results indicate that the susceptibility of GAD in vivo to a diminished cofactor concentration decreases with age. It seems possible that changes in the expression of enzyme forms are reflected in developmental variations in the susceptibility to seizures induced by vitamin B6 depletion, but alterations of other B6-dependent biochemical pathways cannot be discarded.

摘要

我们之前已经表明,在成年大鼠中,通过给予磷酸吡哆醛-γ-谷氨酰腙(PLPGH)抑制脑谷氨酸脱羧酶(GAD)活性并不会导致惊厥,而在成年小鼠中则总会发生强烈惊厥。在本研究中,我们报告了一个令人惊讶的发现:用PLPGH(80毫克/千克)处理的2至20日龄未成熟大鼠出现全身性强直阵挛性惊厥,而30日龄及以上的大鼠根本没有惊厥。通过酶法测定前脑匀浆中生成的GABA来测量GAD活性,在15日龄及更小的大鼠惊厥发作时,GAD活性被抑制了约60%,而在年龄较大的动物中抑制率在40%至50%之间。向孵育培养基中添加辅酶磷酸吡哆醛5'-磷酸可完全逆转这种抑制作用。与对照组相比,所有处理过的动物体内GABA水平都较低。结果表明,体内GAD对辅因子浓度降低的敏感性会随着年龄增长而降低。酶形式表达的变化似乎反映在维生素B6缺乏诱导的癫痫易感性的发育变化中,但其他B6依赖的生化途径的改变也不能排除。

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