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吡啶甲酸及结构相关的吡啶羧酸对喹啉酸诱导的皮质胆碱能损伤的作用。

Action of picolinic acid and structurally related pyridine carboxylic acids on quinolinic acid-induced cortical cholinergic damage.

作者信息

Cockhill J, Jhamandas K, Boegman R J, Beninger R J

机构信息

Department of Pharmacology, Queen's University, Kingston, Ont., Canada.

出版信息

Brain Res. 1992 Dec 18;599(1):57-63. doi: 10.1016/0006-8993(92)90852-z.

Abstract

Picolinic acid, a pyridine monocarboxylic acid derived from tryptophan metabolism by the kynurenine pathway, was shown to block cortical cholinergic neurotoxicity induced by quinolinic acid (QUIN), a pyridine dicarboxylic acid yielded by the same pathway. This study examined the specificity of the anti-toxic effect of picolinic acid by comparing its effect with several structurally related mono- and dicarboxylic acids, and by evaluating its potential to influence cholinergic neurotoxicity produced by kainic, ibotenic and quisqualic acid. Picolinic acid or related agents were injected alone or in combination with a fixed dose of QUIN into the right nucleus basalis magnocellularis (nbM) of rats anesthetized with halothane. Cholinergic neurotoxicity was assessed 7 days post injection by measuring choline acetyltransferase (ChAT) activity in the frontoparietal cortex on the injected and uninjected side. In picolinate experiments, the staining of nbM neurons by acetylcholinesterase (AChE) histochemistry was also examined. Focal injections of QUIN depleted cortical ChAT activity and staining of AChE in the nbM. Co-injection of picolinic acid with QUIN attenuated the decline in these two cholinergic neuron markers. Isonicotinate (4-pyridine monocarboxylate), but not nicotinate (3-pyridine monocarboxylate), significantly attenuated QUIN's effect on cortical ChAT activity. Among several dicarboxylic acids examined, only dipicolinate (2,6-pyridine dicarboxylate) showed activity. It produced a modest QUIN-like effect, but in co-injection experiments it attenuated the QUIN-induced decrease in cortical ChAT. When co-injected into the nbM with a neurotoxic dose of kainic, ibotenic or quisqualic acid which produced a neurotoxic response comparable to that of QUIN, picolinic acid attenuated kainic acid-induced neurotoxicity, but not ibotenate or quisqualate neurotoxicity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

吡啶甲酸是一种通过犬尿氨酸途径由色氨酸代谢产生的吡啶单羧酸,已被证明可阻断喹啉酸(QUIN)诱导的皮质胆碱能神经毒性,喹啉酸是由同一途径产生的吡啶二羧酸。本研究通过将吡啶甲酸的作用与几种结构相关的单羧酸和二羧酸进行比较,并评估其影响由 kainic 酸、鹅膏蕈氨酸和 quisqualic 酸产生的胆碱能神经毒性的潜力,来检验吡啶甲酸抗毒性作用的特异性。将吡啶甲酸或相关试剂单独或与固定剂量的 QUIN 联合注射到用氟烷麻醉的大鼠右侧大细胞基底核(nbM)中。注射后 7 天,通过测量注射侧和未注射侧额顶叶皮质中的胆碱乙酰转移酶(ChAT)活性来评估胆碱能神经毒性。在吡啶甲酸盐实验中,还通过乙酰胆碱酯酶(AChE)组织化学检查了 nbM神经元的染色情况。局部注射 QUIN 可降低皮质 ChAT 活性并减少 nbM 中 AChE 的染色。将吡啶甲酸与 QUIN 共同注射可减弱这两种胆碱能神经元标志物的下降。异烟酸酯(4 - 吡啶单羧酸酯)而非烟酸酯(3 - 吡啶单羧酸酯)可显著减弱 QUIN 对皮质 ChAT 活性的影响。在所检测的几种二羧酸中,只有联吡啶甲酸盐(2,6 - 吡啶二羧酸酯)表现出活性。它产生了适度的类似 QUIN 的作用,但在共同注射实验中,它减弱了 QUIN 诱导的皮质 ChAT 的下降。当与产生与 QUIN 相当的神经毒性反应的神经毒性剂量的 kainic 酸、鹅膏蕈氨酸或 quisqualic 酸共同注射到 nbM 中时,吡啶甲酸减弱了 kainic 酸诱导的神经毒性,但未减弱鹅膏蕈氨酸或 quisqualate 的神经毒性。(摘要截断于 250 字)

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