Wild Mushrooms as a Source of Cholinesterase and Glutathione S-Transferase Inhibitors.

Tomaž Trobec, Ema Kurešepi, Larisa Lara Popošek, Luka Šparl, Robert Frangež, Matej Skočaj, Kristina Sepčić
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Abstract

Several fungal species, including mushrooms, produce bioactive and toxic compounds that exert many activities, such as direct action on DNA, inhibition of protein synthesis, damage to cell membranes, or direct suppression of certain enzymatic activities. This is particularly important as mushrooms can play an important role in human nutrition and/or are used as dietary supplements. In this context, we screened ethanolic extracts of 64 wild mushrooms for their potential to inhibit cholinesterases and glutathione S-transferase. Seven of the 64 extracts showed an inhibitory effect on cholinesterases, while 24 inhibited glutathione S-transferase. These results suggest that the toxic effects of some mushrooms may be directly linked to a specific class of compounds that act as inhibitors of physiologically relevant enzymes. Most of the identified activities are described for the first time and call for caution, especially when the human diet is rich in mushrooms. Conversely, these bioactive molecules may serve as inspiration for chemical synthesis and the development of potential drugs to combat neurodegenerative diseases or cancer.

野生蘑菇作为胆碱酯酶和谷胱甘肽s转移酶抑制剂的来源。
几种真菌,包括蘑菇,产生具有生物活性和毒性的化合物,这些化合物发挥许多活性,例如直接作用于DNA,抑制蛋白质合成,破坏细胞膜,或直接抑制某些酶的活性。这一点尤其重要,因为蘑菇可以在人体营养和/或用作膳食补充剂中发挥重要作用。在此背景下,我们筛选了64种野生蘑菇的乙醇提取物,以研究其抑制胆碱酯酶和谷胱甘肽s -转移酶的潜力。64个提取物中有7个对胆碱酯酶有抑制作用,24个对谷胱甘肽s -转移酶有抑制作用。这些结果表明,一些蘑菇的毒性作用可能与一类特定的化合物直接相关,这些化合物作为生理相关酶的抑制剂。大多数已确定的活动是第一次描述,并呼吁谨慎,特别是当人类饮食中富含蘑菇时。相反,这些生物活性分子可能为化学合成和潜在药物的开发提供灵感,以对抗神经退行性疾病或癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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