Cucumaria frondosa(Gennerus,1767 年)的伏龙芝苷 A:化学、生物合成、药用和作用机理。

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Oladapo F Fagbohun, Amanda Rollins, Lindsey Mattern, Kendra Cipollini, Hp Vasantha Rupasinghe
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引用次数: 0

摘要

Cucumaria frondosa(Gennerus,1767 年)或橙脚海参是传统食品,被用作抗糖尿病、抗炎、抗氧化、抗血管生成、抗菌和抗癌剂的天然来源。目前,高附加值海参产品进入全球市场,激发了对海参中的海参皂苷 A 和其他皂苷的基础研究。这些皂甙是海参化学防御的一种手段。然而,最近的研究表明,接触这些皂苷可能会因各种全皂甙的气溶胶作用而导致刺激症状。此外,提取方法对海参中各种生物活性化合物的生物利用率至关重要。因此,我们对近期有关海参皂苷 A 的化学、生物合成和药理特性的研究进行了批判性回顾。此外,我们还推测了海参皂苷 A 的作用机制,并对其在功能食品、营养保健品和药品中的应用进行了进一步研究。蛇床子甙 A 最早是从葫芦科植物中发现的,它参与蛋白激酶(PI3K/AKT/ERK1/2/p38 MAPK、RAC/CDC42 PAK1、NFκB/MAPK/JNK 和 LXR-β)信号传导途径。它还参与抑制 MYC 癌基因转录因子,70% 以上的癌症类型都与 MYC 癌基因转录因子有牵连并导致其上调。未来的研究需要以优化绿色提取技术、高效给药方法、安全性和有效性为目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Frondoside A of Cucumaria frondosa (Gennerus, 1767): Chemistry, biosynthesis, medicinal applications, and mechanism of actions.

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.

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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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