Sharma Rajat, Singh Swati, Tewari Nisha, Dey Priyankar
Department of Biotechnology, Thapar Institute of Engineering and Technology, Patiala, Punjab, India.
Department of Zoology, University of North Bengal, Siliguri, West Bengal, India.
Toxicon. 2023 Mar 1;224:107047. doi: 10.1016/j.toxicon.2023.107047. Epub 2023 Jan 25.
Nerium oleander L. is a medicinal plant, used for the treatment of cancers and hyperglycemia across the world, especially in Indian sub-continent, Turkey, Morocco, and China. Although clinical studies supporting its pharmacological effects remain critically underexplored, accidental and intentional consumption of any part of the plant causes fatal toxicity in animals and humans. While the polyphenolic fraction of oleander leaves has been attributed to its pre-clinical pharmacological activities, the presence of diverse cardiac glycosides (especially oleandrin) causes apoptosis to cancer cells in vitro and results in clinical signs of oleander poisoning. Thus, the dual pharmacological and toxicological role of oleander is a perplexing dichotomy in phytotherapy. The current investigative review, therefore, intended to analyze the intrinsic and extrinsic factors that likely contribute to this conundrum. Especially by focusing on gut microbial diversity, abundance, and metabolic functions, oleander-associated pharmacological and toxicological studies have been critically analyzed to define the dual effects of oleander. Electronic databases were extensively screened for relevant research articles (including pre-clinical and clinical) related to oleander bioactivities and toxicity. Taxonomic preference was given to the plant N. oleander L. and synonymous plants as per 'The World Flora Online' database (WCSP record #135196). Discussion on yellow oleander (Cascabela thevetia (L.) Lippold) has intentionally been avoided since it is a different plant. The review indicates that the gut microbiota likely plays a key role in differentially modulating the pharmacological and toxicological effects of oleander. Other factors identified influencing the oleander bioactivities include dose and mode of treatment, cardiac glycoside pharmacokinetics, host-endogenous glycosides, plant material processing and phytochemical extraction methods, plant genotypic variations, environmental effects on the phytochemical quality and quantity, gene expression variations, host dietary patterns and co-morbidity, etc. The arguments proposed are also relevant to other medicinal plants containing toxic cardiac glycosides.
夹竹桃是一种药用植物,在世界各地,尤其是印度次大陆、土耳其、摩洛哥和中国,被用于治疗癌症和高血糖。尽管支持其药理作用的临床研究仍严重缺乏探索,但意外或故意食用该植物的任何部分都会对动物和人类造成致命毒性。虽然夹竹桃叶中的多酚部分被认为与其临床前药理活性有关,但多种强心苷(尤其是夹竹桃苷)的存在会在体外导致癌细胞凋亡,并导致夹竹桃中毒的临床症状。因此,夹竹桃在植物疗法中具有双重药理和毒理作用,这是一个令人困惑的二分法。因此,当前的调查性综述旨在分析可能导致这一难题的内在和外在因素。特别是通过关注肠道微生物多样性、丰度和代谢功能,对夹竹桃相关的药理和毒理学研究进行了批判性分析,以确定夹竹桃的双重作用。我们广泛筛选了电子数据库中与夹竹桃生物活性和毒性相关的研究文章(包括临床前和临床研究)。根据《世界植物区系在线》数据库(WCSP记录#135196),对夹竹桃属植物Nerium oleander L.及其同义词植物进行了分类学优先选择。由于黄花夹竹桃(Cascabela thevetia (L.) Lippold)是一种不同的植物,因此有意避免对其进行讨论。该综述表明,肠道微生物群可能在差异调节夹竹桃的药理和毒理作用中起关键作用。其他被确定影响夹竹桃生物活性的因素包括剂量和治疗方式、强心苷药代动力学、宿主内源性糖苷、植物材料加工和植物化学提取方法、植物基因型变异、环境对植物化学物质质量和数量的影响、基因表达变异、宿主饮食模式和共病等。所提出的观点也适用于其他含有毒性强心苷的药用植物。