Antiallergic Properties of Biflavonoids Isolated from the Flowers of Mesua ferrea Linn.

被引:6
作者
Manse, Yoshiaki [1 ]
Sakamoto, Yusuke [1 ]
Miyachi, Taiki [1 ]
Nire, Mitsuyo [1 ]
Hashimoto, Yoshinori [1 ]
Chaipech, Saowanee [1 ,2 ]
Pongpiriyadacha, Yutana [3 ]
Morikawa, Toshio [1 ]
机构
[1] Kindai Univ, Pharmaceut Res & Technol Inst, 3-4-1 Kowakae, Higashiosaka, Osaka 5778502, Japan
[2] Rajamangala Univ Technol Srivijaya, Fac Agroind, Thungyai 80240, Nakhon Si Thamm, Thailand
[3] Rajamangala Univ Technol Srivijaya, Fac Sci & Technol, Thungyai 80240, Nakhon Si Thamm, Thailand
关键词
Mesua ferrea; mesuaferrone; biflavonoid; hyaluronidase inhibitor; degranulation inhibitor; Calophyllaceae; CHINESE NATURAL MEDICINES; ANTIGEN-INDUCED DEGRANULATION; MELANOGENESIS INHIBITORY-ACTIVITY; BIOACTIVE CONSTITUENTS; RBL-2H3; CELLS; TNF-ALPHA; STRUCTURAL REQUIREMENTS; PHENOLIC-COMPOUNDS; ALPINIA-GALANGA; MAMMEASINS C;
D O I
10.3390/separations9050127
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The methanolic extract from the flowers of Mesua ferrea Linn. (Calophyllaceae) showed significant hyaluronidase inhibitory activity. Following a bioassay-guided separation of the extract, two biflavonoids, viz., mesuaferrone-A (1) and mesuaferrone-B (2), were isolated, along with ten flavonoids (3-12), two xanthones (13 and 14), three triterpenes (15-17), a phenylpropanoid (18), and five aromatics (19-24). Among the isolates, 1 and 2 (IC50 = 51.1 mu M and 54.7 mu M, respectively) exhibited hyaluronidase inhibitory activity equivalent to that of the commercially available antiallergic agents disodium cromoglycate (64.8 mu M) and ketotifen fumarate (76.5 mu M). These biflavonoids (1 and 2) are 8-8 '' linked dimers that are composed of naringenin (1a) or apigenin (3), with their corresponding monomers lacking inhibitory activity (IC50 > 300 mu M). In addition, 1 and 2 (IC50 = 49.4 mu M and 49.2 mu M, respectively) inhibited the release of beta-hexosaminidase, which is a marker of antigen-IgE-mediated degranulation, in rat basophilic leukemia (RBL-2H3) cells. These inhibitory activities were more potent than those of the antiallergic agents tranilast and ketotifen fumarate (IC50 = 282 mu M and 158 mu M, respectively), as well as one of the corresponding monomers (1a; IC50 > 100 mu M). Nonetheless, these effects were weaker than those of the other monomer (3; IC50 = 6.1 mu M).
引用
收藏
页数:12
相关论文
共 65 条
  • [1] Triterpenoid Saponins from Symplocos lancifolia
    Acebey-Castellon, Ivone Lucia
    Voutquenne-Nazabadioko, Laurence
    Huong Doan Thi Mai
    Roseau, Nathalie
    Bouthagane, Naima
    Muhammad, Dima
    Debar, Elisabeth Le Magrex
    Gangloff, Sophie C.
    Litaudon, Marc
    Sevenet, Thierry
    Nguyen Van Hung
    Lavaud, Catherine
    [J]. JOURNAL OF NATURAL PRODUCTS, 2011, 74 (02): : 163 - 168
  • [2] ALAM MS, 1987, CHEM IND-LONDON, P565
  • [3] Urease inhibitors from Hypericum oblongifolium WALL.
    Arfan, Mohammad
    Ali, Mumtaz
    Ahmad, Habib
    Anis, Itrat
    Khan, Ajmal
    Choudhary, M. Iqbal
    Shah, Muhammad Raza
    [J]. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2010, 25 (02) : 296 - 299
  • [4] Isoledene from Mesua ferrea oleo-gum resin induces apoptosis in HCT 116 cells through ROS-mediated modulation of multiple proteins in the apoptotic pathways: A mechanistic study
    Asif, Muhammad
    Shafaei, Armaghan
    Jafari, Seyedeh Fatemeh
    Mohamed, Shazmin Kithur
    Ezzat, Mohammed Oday
    Majid, Aman Shah Abdul
    Oon, Chern Ein
    Petersen, Sven H.
    Kono, Koji
    Majid, Amin Malik Shah Abdul
    [J]. TOXICOLOGY LETTERS, 2016, 257 : 84 - 96
  • [5] Chahar M. K., 2013, African Journal of Pharmacy and Pharmacology, V7, P211
  • [6] In-vivo antioxidant and immunomodulatory activity of mesuol isolated from Mesua ferrea L. seed oil
    Chahar, Manoj Kumar
    Kumar, D. S. Sanjaya
    Lokesh, T.
    Manohara, K. P.
    [J]. INTERNATIONAL IMMUNOPHARMACOLOGY, 2012, 13 (04) : 386 - 391
  • [7] Cytotoxic xanthones from the roots of Mesua ferrea L.
    Chukaew, Arnon
    Saithong, Saowanit
    Chusri, Sasitorn
    Limsuwan, Surasuk
    Watanapokasin, Ramida
    Voravuthikunchai, Supayang P.
    Chakthong, Suda
    [J]. PHYTOCHEMISTRY, 2019, 157 : 64 - 70
  • [8] A NEW CYCLO HEXADIONE FROM MESUA-FERREA
    DENNIS, TJ
    KUMAR, KA
    SRIMANNARAYANA, G
    [J]. PHYTOCHEMISTRY, 1988, 27 (07) : 2325 - 2327
  • [9] Natural and synthetic 2′-hydroxy-chalcones and aurones: Synthesis, characterization and evaluation of the antioxidant and soybean lipoxygenase inhibitory activity
    Detsi, Anastasia
    Majdalani, Maya
    Kontogiorgis, Christos A.
    Hadjipavlou-Litina, Dimitra
    Kefalas, Panagiotis
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (23) : 8073 - 8085
  • [10] FUKUNAGA T, 1988, CHEM PHARM BULL, V36, P1180