Limonoids from the Fresh Young Leaves and Buds of Toona sinensis and Their Potential Neuroprotective Effects

被引:22
作者
Fu, Yan-Hui [1 ,2 ,3 ]
Xie, Yu-Tong [1 ,2 ]
Guo, Jia-Ming [1 ,2 ]
Wang, Xiao-Ping [3 ]
Jiang, Bo [1 ,2 ]
Zhang, Wei [1 ,2 ]
Qiang, Lei [3 ]
Kong, Ling-Ying [3 ]
Liu, Yan-Ping [1 ,2 ,3 ]
机构
[1] Hainan Normal Univ, Key Lab Trop Med Resource Chem, Minist Educ, Haikou 571158, Hainan, Peoples R China
[2] Hainan Normal Univ, Key Lab Res & Dev Trop Fruit & Vegetable Haikou C, Haikou 571158, Hainan, Peoples R China
[3] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Toona sinensis; limonoids; toonasinenoids A-E; neuroprotective effects; OXIDATIVE STRESS; ROOT BARK; ALKALOIDS; TRITERPENOIDS; HETEROPHYLLUS; GLYCOSIDES; TWIGS;
D O I
10.1021/acs.jafc.0c06352
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Toona sinensis, popularly known as Chinese toon or Chinese mahogany, is a perennial deciduous arbor belonging to the genus Toona in the Meliaceae family, which is widely distributed and cultivated in eastern and southeastern Asia. Its fresh young leaves and buds have been consumed as a very popular nutritious vegetable in China and confirmed to display a wide variety of biological activities. To investigate the chemical constituents and their potential health benefits from the fresh young leaves and buds of T. sinensis, a phytochemical study on its fresh young leaves and buds was therefore undertaken. In our current investigation, 16 limonoids (1-16), including four new limonoids, toonasinenoids A-D (1-4), and a new naturally occurring limonoid, toonasinenoid E (5), were isolated and characterized from the fresh young leaves and buds of T. sinensis. The chemical structures and absolute configurations of limonoids 1-5 were elucidated by comprehensive spectroscopic data analyses. All known limonoids (6-16) were identified via comparing their experimental spectral data containing mass spectrometry data, H-1 and C-13 nuclear magnetic resonance data, and optical rotation values to the data reported in the literature. All known limonoids (6-16) were isolated from T. sinensis for the first time. Furthermore, the neuroprotective effects of all isolated limonoids 1-16 against 6-hydroxydopamine-induced cell death in human neuroblastoma SH-SYSY cells were assessed in vitro. Limonoids 1-16 exhibited notable neuroprotective activities, with EC50 values in the range from 0.27 +/- 0.03 to 17.28 +/- 0.16 mu M. These results suggest that regular consumption of the fresh young leaves and buds of T. sinensis might prevent the occurrence and development of Parkinson's disease (PD). Moreover, the isolation and characterization of these limonoids that exhibit notable neuroprotective activities from the fresh young leaves and buds of T. sinensis could be very significant for researching and developing new neuroprotective drugs used for the prevention and treatment of PD.
引用
收藏
页码:12326 / 12335
页数:10
相关论文
共 43 条
[1]   Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson's disease [J].
Blum, D ;
Torch, S ;
Lambeng, N ;
Nissou, MF ;
Benabid, AL ;
Sadoul, R ;
Verna, JM .
PROGRESS IN NEUROBIOLOGY, 2001, 65 (02) :135-172
[2]   Neuroprotective Benzyl Benzoate Glycosides from Disporum viridescens Roots in HT22 Hippocampal Neuronal Cells [J].
Cho, Namki ;
Yang, Heejung ;
Lee, Mina ;
Huh, Jungmoo ;
Kim, Hyeon-Woo ;
Kim, Hong-Pyo ;
Sung, Sang-Hyun .
JOURNAL OF NATURAL PRODUCTS, 2013, 76 (12) :2291-2297
[3]   Quivisianthone, an evodulone limonoid from the Madagascan Meliaceae Quivisia papinae [J].
Coombes, PH ;
Mulholland, DA ;
Randrianarivelojosia, M .
PHYTOCHEMISTRY, 2004, 65 (04) :377-380
[4]   The Role of Oxidative Stress in Parkinson's Disease [J].
Dias, Vera ;
Junn, Eunsung ;
Mouradian, M. Maral .
JOURNAL OF PARKINSONS DISEASE, 2013, 3 (04) :461-491
[5]   New Limonoids and a Dihydrobenzofuran Norlignan from the Roots of Toona sinensis [J].
Dong, Xiao-Jie ;
Zhu, Yun-Fei ;
Bao, Guan-Hu ;
Hu, Feng-Lin ;
Qin, Guo-Wei .
MOLECULES, 2013, 18 (03) :2840-2850
[6]  
Editorial Committee of Flora of China Chinese Academy of Sciences, 1997, FLOR CHIN, V43, P36
[7]   Prenylated Chromones from the Fruits of Artocarpus heterophyllus and Their Potential Anti-HIV-1 Activities [J].
Fu, Yan-Hui ;
Guo, Jia-Ming ;
Xie, Yu-Tong ;
Yu, Xiao-Mei ;
Su, Qin-Ting ;
Qiang, Lei ;
Kong, Ling-Yi ;
Liu, Yan-Ping .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2020, 68 (07) :2024-2030
[8]   Angustifonines A and B, Cytotoxic Bisindole Alkaloids from Bousigonia angustifolia [J].
Fu, Yan-hui ;
Di, Ying-tong ;
He, Hong-ping ;
Li, Shun-lin ;
Zhang, Yu ;
Hao, Xiao-jiang .
JOURNAL OF NATURAL PRODUCTS, 2014, 77 (01) :57-62
[9]   Strynuxlines A and B, Alkaloids with an Unprecedented Carbon Skeleton from Strychnos nux-vomica [J].
Fu, Yanhui ;
Zhang, Yu ;
He, Hongping ;
Hou, Li ;
Di, Yingtong ;
Li, Shunlin ;
Luo, Xiaodong ;
Hao, Xiaojiang .
JOURNAL OF NATURAL PRODUCTS, 2012, 75 (11) :1987-1990
[10]   Isolation of a new tetranortriterpenoid from the uncrushed green leaves of Azadirachta indica [J].
Govindachari, TR ;
Malathi, R ;
Gopalakrishnan, G ;
Suresh, G ;
Rajan, SS .
PHYTOCHEMISTRY, 1999, 52 (06) :1117-1119