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真菌震颤素:含单一氮毒素的作用机制——一种假说

Fungal tremorgens: the mechanism of action of single nitrogen containing toxins--a hypothesis.

作者信息

Selala M I, Daelemans F, Schepens P J

机构信息

Toxicology Unit, University of Antwerp (UIA), Wilrijk, Belgium.

出版信息

Drug Chem Toxicol. 1989 Sep-Dec;12(3-4):237-57. doi: 10.3109/01480548908999156.

Abstract

Tremorgenic mycotoxins are fungal secondary metabolites with a specific effect on the central nervous system (CNS). Except for a few toxins that are produced by Claviceps paspali, a plant parasitic fungus, most tremorgenic mycotoxins are synthesized by common saprophytic moulds of the genera Penicillium and Aspergillus. Since these compounds produce sustained tremor in the abscence of other neurotoxic effects, several authors have suggested that they are the causative agents of a number of naturally occurring incoordination syndromes in ruminants. The nature of the tremor produced by these compounds in laboratory animals is clinically indistinguishable from that occurring naturally. In particular, the most implicated tremorgenic mycotoxins are those that contain a single nitrogen atom in their molecules. Although individual compounds within this group are produced by unrelated fungal species, they all contain a similar biologically active chemical moiety. To date, their mechanism of action is unknown, and their role in neuropharmacology has not yet been defined. However, the presence of a GABA-like conformation within their active nucleus and the limited torsional flexibility of this moiety suggest that they are partial agonists of GABA (gamma-aminobutyric acid). A hypothetical mode of action of these toxins at the GABA receptor sites is presented and discussed.

摘要

震颤性霉菌毒素是一类对中枢神经系统(CNS)有特定作用的真菌次级代谢产物。除了少数由植物寄生真菌黍坚轴黑粉菌产生的毒素外,大多数震颤性霉菌毒素是由青霉属和曲霉属常见的腐生霉菌合成的。由于这些化合物在没有其他神经毒性作用的情况下会产生持续性震颤,一些作者认为它们是反刍动物许多自然发生的共济失调综合征的致病因子。这些化合物在实验动物中产生的震颤性质在临床上与自然发生的震颤无法区分。特别是,最常涉及的震颤性霉菌毒素是那些分子中含有单个氮原子的毒素。虽然该组内的个别化合物由不相关的真菌物种产生,但它们都含有类似的生物活性化学部分。迄今为止,它们的作用机制尚不清楚,其在神经药理学中的作用也尚未明确。然而,它们活性核内存在类似γ-氨基丁酸(GABA)的构象以及该部分有限的扭转灵活性表明它们是GABA(γ-氨基丁酸)的部分激动剂。本文提出并讨论了这些毒素在GABA受体位点的一种假设作用模式。

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