Biochemical pharmacology of biflavonoids: Implications for anti-inflammatory action

被引:106
作者
Kim, Hyun Pyo [1 ]
Park, Haeil [1 ]
Son, Kun Ho [2 ]
Chang, Hyeun Wook [3 ]
Kang, Sam Sik [4 ]
机构
[1] Kangwon Natl Univ, Coll Pharm, Chunchon 200701, South Korea
[2] Andong Natl Univ, Dept Food Nutr, Andong 760749, South Korea
[3] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
[4] Seoul Natl Univ, Inst Nat Prod Res, Seoul 110640, South Korea
关键词
biflavonoid; flavonoid; anti-inflammation; phospholipase; cyclooxygenase; proinflammatory gene;
D O I
10.1007/s12272-001-1151-3
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Biflavonoids belong to a subclass of the plant flavonoid family. Distribution of biflavonoids in the plant kingdom is limited to several species. Previously, some pharmacological activities of biflavonoids were described such as inhibition of histamine release from mast cells and inhibition of lymphocyte proliferation, suggesting the anti-inflammatory/antiallergic potential of the biflavonoids. Furthermore, several natural biflavonoids including ochnaflavone and ginkgetin inhibit phospholipase A(2). Most importantly, certain biflavonoids exhibit anti-inflammatory activity through the regulation of proinflammatory gene expression in vitro and in vivo. Recently, several synthetic approaches yielded new biflavonoid molecules with anti-inflammatory potential. These molecules also exhibit phospholipase A2 and cyclooxygenase-2 inhibitory activity. Although the bioavailability needs be improved, certain biflavonoids may have potential as new anti-inflammatory agents. This is the first review of biflavonoid pharmacology to date.
引用
收藏
页码:265 / 273
页数:9
相关论文
共 62 条
[1]   A weakly antimalarial biflavanone from Rhus retinorrhoea [J].
Ahmed, MS ;
Galal, AM ;
Ross, SA ;
Ferreira, D ;
ElSohly, MA ;
Ibrahim, ARS ;
Mossa, JS ;
El-Feraly, FS .
PHYTOCHEMISTRY, 2001, 58 (04) :599-602
[2]  
AMELLA M, 1985, PLANTA MED, V16
[3]  
ARENS H, 1986, PLANTA MED, P468, DOI 10.1055/s-2007-969256
[4]   The effects of two new antagonists of secretory PLA2 on TNF, iNOS, and COX-2 expression in activated macrophages [J].
Baek, SH ;
Yun, SS ;
Kwon, TK ;
Kim, JR ;
Chang, HW ;
Kwak, JY ;
Kim, JH ;
Kwun, KB .
SHOCK, 1999, 12 (06) :473-478
[5]   Inhibition of TNFα-induced cyclooxygenase-2 expression by amentoflavone through suppression of NF-κB activation in A549 cells [J].
Banerjee, T ;
Valacchi, G ;
Ziboh, VA ;
van der Vliet, A .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 238 (1-2) :105-110
[6]  
Bittar M, 2000, PLANTA MED, V66, P84, DOI 10.1055/s-0029-1243118
[7]   Amentoflavone from Biophytum sensitivum and its effect on COX-1/COX-2 catalysed prostaglandin biosynthesis [J].
Bucar, F ;
Jackak, SM ;
Noreen, Y ;
Kartnig, T ;
Perera, P ;
Bohlin, L ;
Schubert-Zsilavecz, M .
PLANTA MEDICA, 1998, 64 (04) :373-374
[8]  
Cechinel V, 2000, Z NATURFORSCH C, V55, P820
[9]   ISOLATION OF AMENTOFLAVONE FROM SELAGINELLA-RUPESTRIS AND ITS PHARMACOLOGICAL ACTIVITY ON CENTRAL NERVOUS-SYSTEM, SMOOTH MUSCLES AND ISOLATED FROG-HEART PREPARATIONS [J].
CHAKRAVARTHY, BK ;
RAO, YV ;
GAMBHIR, SS ;
GODE, KD .
PLANTA MEDICA, 1981, 43 (01) :64-70
[10]   INACTIVATION OF PHOSPHOLIPASE A(2) BY NATURALLY-OCCURRING BIFLAVONOID, OCHNAFLAVONE [J].
CHANG, HW ;
BAEK, SH ;
CHUNG, KW ;
SON, KH ;
KIM, HP ;
KANG, SS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (01) :843-849