Hypericins as Potential Leads for New Therapeutics

被引:225
作者
Karioti, Anastasia [1 ]
Bilia, Anna Rita [1 ]
机构
[1] Univ Florence, Dept Pharmaceut Sci, Ugo Schiff 6, I-50019 Florence, Italy
关键词
Hypericum perforatum; naphthodianthrones; hypericin; pseudohypericin; photodynamic therapy; antiviral; antidepressant; ST-JOHNS-WORT; MEDIATED PHOTODYNAMIC THERAPY; IN-VITRO; CELL-DEATH; MASS-SPECTROMETRY; PHOTOCHEMICAL PROPERTIES; EFFICIENT PURIFICATION; ACTIVE CONSTITUENTS; PERFORATUM EXTRACTS; MOLECULAR-STRUCTURE;
D O I
10.3390/ijms11020562
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
70 years have passed since the first isolation of the naphthodianthrones hypericin and pseudohypericin from Hypericum perforatum L. Today, they continue to be one of the most promising group of polyphenols, as they fascinate with their physical, chemical and important biological properties which derive from their unique chemical structure. Hypericins and their derivatives have been extensively studied mainly for their antitumor, antiviral and antidepressant properties. Notably, hypericin is one of the most potent naturally occurring photodynamic agents. It is able to generate the superoxide anion and a high quantum yield of singlet oxygen that are considered to be primarily responsible for its biological effects. The prooxidant photodynamic properties of hypericin have been exploited for the photodynamic therapy of cancer (PDT), as hypericin, in combination with light, very effectively induces apoptosis and/or necrosis of cancer cells. The mechanism by which these activities are expressed continues to be a main topic of discussion, but according to scientific data, different modes of action (generation of ROS & singlet oxygen species, antiangiogenesis, immune responces) and multiple molecular pathways (intrinsic/extrinsic apoptotic pathway, ERK inhibition) possibly interrelating are implicated. The aim of this review is to analyse the most recent advances (from 2005 and thereof) in the chemistry and biological activities (in vitro and in vivo) of the pure naphthodianthrones, hypericin and pseudohypericin from H. perforatum. Extracts from H. perforatum were not considered, nor pharmakokinetic or clinical data. Computerised literature searches were performed using the Medline (PubMed), ChemSciFinder and Scirus Library databases. No language restrictions were imposed.
引用
收藏
页码:562 / 594
页数:33
相关论文
共 158 条
[41]  
CURLE P, 1988, NEUROCHEMICAL STUDIE
[42]   Glutathione S-transferase P1-1 expression modulates sensitivity of human kidney 293 cells to photodynamic therapy with hypericin [J].
Dabrowski, Michael J. ;
Maeda, Dean ;
Zebala, John ;
Lu, Weiya Doug ;
Mahajan, Surnit ;
Kavanagh, Terrance J. ;
Atkins, William M. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2006, 449 (1-2) :94-103
[43]   Hypericin phototoxicity induces different modes of cell death in melanoma and human skin cells [J].
Davids, Lester M. ;
Kleemann, Britta ;
Kacerovska, Denisa ;
Pizinger, Karl ;
Kidson, Susan H. .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2008, 91 (2-3) :67-76
[44]   Melanomas display increased cytoprotection to hypericin-mediated cytotoxicity through the induction of autophagy [J].
Davids, Lester M. ;
Kleemann, Britta ;
Cooper, Susan ;
Kidson, Susan H. .
CELL BIOLOGY INTERNATIONAL, 2009, 33 (10) :1065-1072
[45]  
Denke A., 1999, DRUG RES, V49, P109
[46]  
Dewick PM., 2002, MED NATURAL PRODUCTS, P67
[47]   St John's wort: Prozac from the plant kingdom [J].
Di Carlo, G ;
Borrelli, F ;
Ernst, E ;
Izzo, AA .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (06) :292-297
[48]   Determination of hypericin and pseudohypericin in pharmaceutical preparations by liquid chromatography with fluorescence detection [J].
Draves, AH ;
Walker, SE .
JOURNAL OF CHROMATOGRAPHY B, 2000, 749 (01) :57-66
[49]   Hypericin photoactivation triggers down-regulation of matrix metalloproteinase-9 expression in well-differentiated human nasopharyngeal cancer cells [J].
Du, H. -Y. ;
Olivo, M. ;
Mahendran, R. ;
Huang, Q. ;
Shen, H. -M ;
Ong, C. -N ;
Bay, B. -H .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (7-8) :979-988
[50]  
Du HY, 2006, ONCOL REP, V16, P1397