Glucosinolate Profiles of Capparis spp. and Maerua baillonii (Capparaceae) and Cytotoxicity of Methyl Isothiocyanate-Rich Isolates from Capparis spinosa subsp. rupestris.

IF 2.3 3区 化学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemistry & Biodiversity Pub Date : 2024-11-21 DOI:10.1002/cbdv.202402573
Azra Đulović, Mahenina Jaovita Manase, Vedrana Čikeš Čulić, Franko Burčul, Patrick Rollin, Ivica Blažević
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Abstract

This study investigates the glucosinolate profiles of various Capparis spp. and Maerua baillonii, from the Capparaceae family, and evaluates the cytotoxic potential of volatile isolates from Capparis spinosa subsp. rupestris. Using UHPLC-DAD-MS/MS, GSLs were identified and quantified across different plant tissues. Glucocapparin, predominant glucosinolate in C. spinosa subsp. spinosa, C. spinosa subsp. rupestris, and M. baillonii, was isolated and analyzed by NMR in its desulfo-form. Notably, glucosinolates were absent in C. richardii and specific tissues of M. baillonii (e.g., leaves and stems), underscoring species and/or tissue-specific variability within Capparaceae. Less common glucosinolates for Capparaceae plants, such as glucocochlearin, glucohirsutin, and glucoarabin were also detected. Methyl isothiocyanate was found to be the main volatile in all isolates obtained through various isolation methods, comprising ca. 80-90% of the total volatiles. Methyl isothiocyanate-rich volatile isolates were tested for cytotoxicity against human breast cancer (MDA-MB-231) and bladder cancer (T24) cell lines using the MTT assay, showing significant activity with IC50 values of 3.81 µg/mL and 5.95 µg/mL, respectively. These findings underscore the anticancer potential of glucocapparin-bearing plants from Capparaceae family.

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Capparis spp.和 Maerua baillonii(Capparaceae)的葡萄糖苷酸谱以及 Capparis spinosa subsp.
本研究调查了 Capparaceae 植物中各种 Capparis spp.和 Maerua baillonii 的葡萄糖苷酸谱,并评估了 Capparis spinosa subsp.利用 UHPLC-DAD-MS/MS 对不同植物组织中的 GSL 进行了鉴定和定量。在 C. spinosa subsp.spinosa、C. spinosa subsp.rupestris 和 M. baillonii 中最主要的葡糖苷酸是 Glucocapparin,它以去硫形式被分离出来并通过核磁共振进行了分析。值得注意的是,在 C. richardii 和 M. baillonii 的特定组织(如叶和茎)中不存在葡萄糖苷酸盐,这突显了 Capparaceae 中物种和/或组织的特异性。此外,还检测到了 Capparaceae 植物中较少见的葡萄糖苷酸盐,如糖桔梗苷、葡萄糖苷和葡萄糖苷。异硫氰酸甲酯是通过各种分离方法获得的所有分离物中的主要挥发物,约占总挥发物的 80-90%。使用 MTT 法测试了富含异硫氰酸甲酯的挥发性分离物对人类乳腺癌(MDA-MB-231)和膀胱癌(T24)细胞系的细胞毒性,结果显示其具有显著的活性,IC50 值分别为 3.81 微克/毫升和 5.95 微克/毫升。这些发现凸显了卡帕科含糖苷的植物的抗癌潜力。
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来源期刊
Chemistry & Biodiversity
Chemistry & Biodiversity 环境科学-化学综合
CiteScore
3.40
自引率
10.30%
发文量
475
审稿时长
2.6 months
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.
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