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δ-氨基乙酰丙酸的摄取、毒性及其对培养的神经元和神经胶质细胞摄取[14C]γ-氨基丁酸的影响。

delta-Aminolaevulinic acid uptake, toxicity, and effect on [14C]gamma-aminobutyric acid uptake into neurons and glia in culture.

作者信息

Percy V A, Lamm M C, Taljaard J J

出版信息

J Neurochem. 1981 Jan;36(1):69-76. doi: 10.1111/j.1471-4159.1981.tb02378.x.

Abstract

delta-Aminolaevulinic acid (ALA) uptake into neurons and glia in primary culture as well as ALA toxicity and its effects on gamma-aminobutyric acid (GABA) uptake were examined. [4-14C]ALA uptake into neurons and glia was nonsaturable, partially Na+- and temperature-dependent, and appeared to comprise mainly diffusion into the cell. 2,4-Dinitrophenol caused some inhibition of [4-14C]ALA uptake whereas ouabain, KCN, or amino acids at 1 mM concentration were without effect. ALA (1 mM) caused a slight inhibition of [U-14C]GABA uptake into neurons (14%) and glia (9%), but was without effect at lower concentrations. It is unlikely that, in acute porphyria, ALA reaches sufficiently high levels in nervous tissue to interfere with the reuptake of GABA into neurons or glia. ALA was shown to be toxic, judged by the loss of cells, to both neurons and glia at concentrations as low as 10 microM. Such a concentration of ALA may be expected to occur in the CSF of porphyric patients in the acute attack. However, results obtained with dispersed cells in culture may not necessarily reflect the situation in vivo where the cell may have a far greater resistance to the effects of toxic agents.

摘要

研究了原代培养的神经元和神经胶质细胞对δ-氨基乙酰丙酸(ALA)的摄取情况,以及ALA的毒性及其对γ-氨基丁酸(GABA)摄取的影响。[4-¹⁴C]ALA进入神经元和神经胶质细胞的过程是不饱和的,部分依赖于Na⁺和温度,且似乎主要是通过扩散进入细胞。2,4-二硝基苯酚对[4-¹⁴C]ALA的摄取有一定抑制作用,而1 mM浓度的哇巴因、KCN或氨基酸则没有影响。1 mM的ALA对神经元(14%)和神经胶质细胞(9%)摄取[U-¹⁴C]GABA有轻微抑制作用,但在较低浓度时没有影响。在急性卟啉症中,ALA在神经组织中不太可能达到足够高的水平来干扰GABA重新摄取进入神经元或神经胶质细胞。结果表明,低至10 μM的ALA对神经元和神经胶质细胞均有毒性,可通过细胞损失来判断。在急性发作期,卟啉症患者的脑脊液中可能会出现这样的ALA浓度。然而,在培养中分散细胞所获得的结果不一定能反映体内的情况,在体内细胞可能对有毒物质的影响具有更大的抵抗力。

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