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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Uptake and metabolism of Δ1-piperidine-2-carboxylic acid by synaptosomes from rat cerebral cortex
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Uptake and metabolism of Δ1-piperidine-2-carboxylic acid by synaptosomes from rat cerebral cortex

机译:大鼠大脑皮层突触小体对Δ1-哌啶-2-羧酸的吸收和代谢

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摘要

Δ1-Piperidine-2-carboxylic acid (P2C), an intermediate of the -lysine metabolic pathway in the brain, was studied for its uptake metabolism in the synaptosome of the rat cerebral cortex. The results of this study showed that the uptake of P2C into the synaptosome was NA+-and temperature-dependent with a two-tier transport kinetic (Km = 2.6 and 0.7 μM; Vmax = 1.6 and 0.73 pmol/min/mg). P2C uptake was only moderately inhibited (≈20%) by -lysine and its metabolites, -α-aminoadipic acid at up to 100 μM, and the putative amino acid neurotransmitters, γ-aminobutyric acid, -glutamic acid and -spartic acid (25–31%) at 5–500 μM. The synaptosomal preparation only has a very low activity for metabolizing P2C to its product -pipecolic acid. The metabolic activity for P2C was mainly contained in the 27 000 × g supernatant S2 fraction. Since P2C is the precursor of the putative neuromodulator -pipecolic acid, the understanding of its uptake and metabolic characteristics in the brain should be of significance.
机译:研究了Δ1-哌啶-2-羧酸(P2C)是大脑中-赖氨酸代谢途径的中间产物,它在大鼠大脑皮层的突触小体中吸收了代谢。这项研究的结果表明,P2C对突触体的摄取是NA +和温度依赖性的,具有两层传输动力学(Km = 2.6和0.7μM; Vmax = 1.6和0.73 pmol / min / mg)。 -赖氨酸及其代谢产物,高达100μM的-α-氨基己二酸以及假定的氨基酸神经递质,γ-氨基丁酸,-谷氨酸和-天冬氨酸仅适度抑制(约20%)P2C摄取(25 –31%)在5–500μM下。突触体制剂仅具有非常低的将P2C代谢为其产物-哌酸的活性。 P2C的代谢活性主要包含在27 000×g的上清液S2馏分中。由于P2C是假定的神经调节剂-哌酸的前体,因此了解其在大脑中的摄取和代谢特征应具有重要意义。

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