{"title":"肉桂精油中反式肉桂醛驱虫靶点及作用机制的研究。","authors":"Guillermina Hernando, Ornella Turani, Noelia Rodriguez Araujo, Alcibeth Pulido Carrasquero, Cecilia Bouzat","doi":"10.1038/s41598-025-89883-4","DOIUrl":null,"url":null,"abstract":"<p><p>Parasitic nematodes pose a significant global socio-economic threat and contribute to neglected diseases. Current infection control relies on drug therapy, but increasing anthelmintic resistance highlights the urgent need for novel treatments. In this study, we investigate the molecular targets and mechanisms of action of trans-cinnamaldehyde (TCA), a principal component of Cinnamon Essential Oil (Cinnamomum verum EO), using Caenorhabditis elegans as a model organism. Our research offers new insights into the anthelmintic effects of TCA by identifying its specific interactions with key Cys-loop receptors and detailing its inhibitory mechanisms. The anthelmintic activity of C. verum EO and TCA manifests as rapid alterations in locomotor activity and inhibition of egg hatching. TCA screening of mutant worms lacking Cys-loop receptors reveal multiple receptor targets, including the levamisole-sensitive nicotinic ACh receptor (L-AChR), GABA-activated chloride channel (UNC-49) and glutamate-activated chloride channel. The mechanism behind the egg hatching inhibition by TCA remains unclear, as none of the mutants studied were found to be resistant to TCA. Furthermore, TCA increases the paralyzing effects of the anthelmintics levamisole and monepantel in a synergistic manner, offering a route for more effective polytherapy strategies. Electrophysiological studies on C. elegans Cys-loop receptors, in both native and heterologous systems, were used to elucidate the molecular mechanisms of TCA-induced paralysis. TCA reduces ACh- and GABA-elicited macroscopic currents and decreases single-channel activity and open durations of native muscle L-AChR channels, indicating an inhibitory action. Thus, by acting through a different mechanism to that of classical anthelmintics, TCA may be beneficial to counteract resistance in combined anthelmintic therapies. Our findings underscore the potential of the multitarget compound TCA as a valuable tool in integrated pharmacological strategies.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"5422"},"PeriodicalIF":3.9000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11825704/pdf/","citationCount":"0","resultStr":"{\"title\":\"Unraveling anthelmintic targets and mechanisms of action of trans-cinnamaldehyde from cinnamon essential oil.\",\"authors\":\"Guillermina Hernando, Ornella Turani, Noelia Rodriguez Araujo, Alcibeth Pulido Carrasquero, Cecilia Bouzat\",\"doi\":\"10.1038/s41598-025-89883-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Parasitic nematodes pose a significant global socio-economic threat and contribute to neglected diseases. 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The mechanism behind the egg hatching inhibition by TCA remains unclear, as none of the mutants studied were found to be resistant to TCA. Furthermore, TCA increases the paralyzing effects of the anthelmintics levamisole and monepantel in a synergistic manner, offering a route for more effective polytherapy strategies. Electrophysiological studies on C. elegans Cys-loop receptors, in both native and heterologous systems, were used to elucidate the molecular mechanisms of TCA-induced paralysis. TCA reduces ACh- and GABA-elicited macroscopic currents and decreases single-channel activity and open durations of native muscle L-AChR channels, indicating an inhibitory action. Thus, by acting through a different mechanism to that of classical anthelmintics, TCA may be beneficial to counteract resistance in combined anthelmintic therapies. 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引用次数: 0
摘要
寄生虫对全球社会经济构成重大威胁,并导致被忽视的疾病。目前的感染控制依赖于药物治疗,但越来越多的驱虫虫耐药性突出了迫切需要新的治疗方法。本研究以秀丽隐杆线虫为模型生物,研究了肉桂精油(Cinnamomum verum EO)主要成分反式肉桂醛(trans-cinnamaldehyde, TCA)的分子靶点和作用机制。我们的研究通过确定TCA与关键Cys-loop受体的特异性相互作用并详细描述其抑制机制,为TCA的驱虫作用提供了新的见解。C. verum EO和TCA的驱虫活性表现为运动活性的快速改变和卵孵化的抑制。对缺乏Cys-loop受体的突变虫进行TCA筛选,发现了多个受体靶点,包括左旋咪唑敏感的烟碱乙酰胆碱受体(L-AChR)、gaba激活的氯离子通道(UNC-49)和谷氨酸激活的氯离子通道。TCA抑制卵孵化的机制尚不清楚,因为所研究的突变体中没有发现对TCA具有抗性。此外,TCA以协同的方式增加了驱虫药左旋咪唑和莫奈潘特的麻痹作用,为更有效的综合治疗策略提供了途径。通过对秀丽隐杆线虫Cys-loop受体在原生和异种系统中的电生理研究,阐明了tca诱导瘫痪的分子机制。TCA降低了ACh-和gaba引发的宏观电流,降低了天然肌肉L-AChR通道的单通道活性和开放时间,表明其具有抑制作用。因此,通过与经典驱虫药不同的作用机制,TCA可能有利于对抗联合驱虫药治疗中的耐药性。我们的研究结果强调了多靶点化合物TCA作为综合药理策略的有价值工具的潜力。
Unraveling anthelmintic targets and mechanisms of action of trans-cinnamaldehyde from cinnamon essential oil.
Parasitic nematodes pose a significant global socio-economic threat and contribute to neglected diseases. Current infection control relies on drug therapy, but increasing anthelmintic resistance highlights the urgent need for novel treatments. In this study, we investigate the molecular targets and mechanisms of action of trans-cinnamaldehyde (TCA), a principal component of Cinnamon Essential Oil (Cinnamomum verum EO), using Caenorhabditis elegans as a model organism. Our research offers new insights into the anthelmintic effects of TCA by identifying its specific interactions with key Cys-loop receptors and detailing its inhibitory mechanisms. The anthelmintic activity of C. verum EO and TCA manifests as rapid alterations in locomotor activity and inhibition of egg hatching. TCA screening of mutant worms lacking Cys-loop receptors reveal multiple receptor targets, including the levamisole-sensitive nicotinic ACh receptor (L-AChR), GABA-activated chloride channel (UNC-49) and glutamate-activated chloride channel. The mechanism behind the egg hatching inhibition by TCA remains unclear, as none of the mutants studied were found to be resistant to TCA. Furthermore, TCA increases the paralyzing effects of the anthelmintics levamisole and monepantel in a synergistic manner, offering a route for more effective polytherapy strategies. Electrophysiological studies on C. elegans Cys-loop receptors, in both native and heterologous systems, were used to elucidate the molecular mechanisms of TCA-induced paralysis. TCA reduces ACh- and GABA-elicited macroscopic currents and decreases single-channel activity and open durations of native muscle L-AChR channels, indicating an inhibitory action. Thus, by acting through a different mechanism to that of classical anthelmintics, TCA may be beneficial to counteract resistance in combined anthelmintic therapies. Our findings underscore the potential of the multitarget compound TCA as a valuable tool in integrated pharmacological strategies.
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