Zhen Lu, Derui Wang, Xiaodong Li, Zhi Yan, Xiuli Yin, Youhou Xu, Song Wang, Ke Li
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引用次数: 0
摘要
最新研究表明,海星的次生代谢物具有防污和驱虫特性,并在生物相互作用和各种生态功能中发挥作用。以前的研究表明,海星的皂苷通过与细胞膜胆固醇相互作用而对鱼类产生毒性作用。本研究探讨了海星皂苷以外的次生代谢物可能对鱼卵(尤其是与海星共栖的海青鱼卵)有害的假设。我们采用多种色谱方法系统地分离了 A. amurensis 的次级代谢物。我们发现了两种与胚胎致畸性有关的低聚糖苷,包括一种以前未曾描述过的四糖(1)和一种已知的吡咯低聚糖苷(2)。它们的结构主要是根据对核磁共振光谱(NMR)和质谱数据的详细分析确定的。化合物 1 和 2 表现出很强的致死性,并显著降低了青鳉胚胎的自主运动能力,其中化合物 2 对致畸性和心率的影响更为明显。观察到的主要形态异常包括头部发育延迟(DHD)、脊柱细小(TS)、油球吸收不完全(OB)、心脏异常(CA)和卵黄囊萎缩(SYS)。
Chemical warfare in the Environment - Secondary Metabolites from Starfish (Asterias amurensis) Induce Teratogenicity in Medaka embryos (Oryzias melastigma).
Recent research suggests that starfish secondary metabolites possess antifouling and antifeedant properties and play a role in biological interactions and various ecological functions. Previous research demonstrated that saponins from starfish exert their toxic effects on fish by interacting with cell membrane cholesterol. This study investigated the hypothesis that secondary metabolites, other than saponins, from the starfish Asterias amurensis may be harmful to fish eggs, particularly marine medaka (Oryzias melastigma) eggs, which share starfish habitat. We systematically separated the secondary metabolites of A. amurensis by a variety of chromatographic methods. Two oligoglycosides related to embryonic teratogenicity were identified, including one previously undescribed tetrasaccharide (1) and one known pyrrole oligoglycoside (2). Their structures were established mainly based on detailed analysis of the nuclear magnetic resonance spectroscopy (NMR) and mass spectroscopic data. Compounds 1 and 2 exhibited strong lethality and significantly reduced voluntary movements in medaka embryos, with compound 2 showing more pronounced effects on teratogenicity and heart rates. The main morphological abnormalities observed included delayed head development (DHD), tiny spines (TS), incomplete absorption of oil balls (OB), cardiac abnormalities (CA), and shrunken yolk sacs (SYS).
期刊介绍:
Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level.
Since 2017, Chemistry & Biodiversity is published in an online-only format.