Fagbohun Oladapo F, Rollins Amanda, Mattern Lindsey, Cipollini Kendra, Rupasinghe Hp Vasantha
Department of Biology, Wilmington College, 1870 Quaker Way, Wilmington, OH 45177, United States.
Department of Plant, Food, and Environmental Sciences, Faculty of Agriculture, Dalhousie University, Truro, Nova Scotia, Canada.
J Pharm Pharmacol. 2025 Jan 6;77(1):32-42. doi: 10.1093/jpp/rgae059.
Cucumaria frondosa (Gennerus, 1767) or orange-footed sea cucumbers are traditional food and are used as natural sources of anti-diabetic, anti-inflammatory, antioxidant, anti-angiogenic, antimicrobial, and anticancer agents. Currently, the introduction of value-added sea cucumber products to the global market has inspired basic research on frondoside A and other saponins in sea cucumbers. These saponins serve as a means of their chemical defence. However, recent studies revealed that exposure to these saponins can lead to irritating symptoms from aerosolization of various holothurins. Moreover, extraction methods are critical to the bioavailability of various bioactive compounds found in sea cucumbers. Therefore, we have critically reviewed recent studies on the chemistry, biosynthesis, and pharmacological properties of frondoside A. Furthermore, the mechanism of actions of frondoside A was postulated and further studies are required for applications in functional foods, nutraceuticals, and pharmaceuticals. Frondoside A was first discovered from Cucumaria frondosa, and it is involved in protein kinase (PI3K/AKT/ERK1/2/p38 MAPK, RAC/CDC42 PAK1, NFκB/MAPK/JNK, and LXR-β) signalling pathways. It is also involved in the suppression of MYC oncogene transcriptional factors implicated and upregulated in over 70% of cancer types. Future research needs to be aimed at optimized green extraction techniques, efficient delivery methods, safety, and efficacy.
棕色拟刺参(属,1767年)或橙足海参是传统食物,并被用作抗糖尿病、抗炎、抗氧化、抗血管生成、抗菌和抗癌药物的天然来源。目前,将增值海参产品引入全球市场激发了对海参中Afrondoside A和其他皂苷的基础研究。这些皂苷是它们化学防御的一种手段。然而,最近的研究表明,接触这些皂苷会因各种海参毒素的雾化而导致刺激症状。此外,提取方法对海参中发现的各种生物活性化合物的生物利用度至关重要。因此,我们对最近关于Afrondoside A的化学、生物合成和药理特性的研究进行了批判性综述。此外,还推测了Afrondoside A的作用机制,在功能性食品、营养保健品和药物中的应用还需要进一步研究。Afrondoside A最初是从棕色拟刺参中发现的,它参与蛋白激酶(PI3K/AKT/ERK1/2/p38 MAPK、RAC/CDC42 PAK1、NFκB/MAPK/JNK和LXR-β)信号通路。它还参与抑制在70%以上的癌症类型中涉及并上调的MYC癌基因转录因子。未来的研究需要针对优化的绿色提取技术、有效的递送方法、安全性和有效性。