Anti-inflammatory properties of phenolic lactones isolated from Caesalpinia paraguariensis stem bark

被引:19
作者
Sgariglia, Melina A. [1 ,2 ]
Soberon, Jose R. [1 ,2 ]
Cabanes, Ana Poveda [3 ]
Sampietro, Diego A. [1 ,2 ]
Vattuone, Marta A. [1 ,2 ]
机构
[1] Univ Nacl Tucuman, Fac Bioquim Quim Farm, Inst Estudios Vegetales Dr AR Sampietro, Catedra Fitoquim, RA-4000 San Miguel De Tucuman, Tucuman, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Buenos Aires, DF, Argentina
[3] Univ Autonoma Madrid, Lab Resonancia Magnet Nucl Liquidos SIdI, E-28049 Madrid, Spain
关键词
Caesalpinia paraguariensis stem bark; Ellagic acid derivatives; Phenolic lactones; Anti-inflammatory; antioxidant; ELLAGIC ACID-DERIVATIVES; NITRIC-OXIDE SYNTHASE; MEDICINAL-PLANTS; STREPTOCOCCUS-PNEUMONIAE; VIRULENCE FACTORS; TAMARIX-NILOTICA; HYALURONIC-ACID; HUMAN SKIN; FLAVONOIDS; OXYGEN;
D O I
10.1016/j.jep.2012.12.030
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Caesalpinia paraguariensis (D. Parodi) Burkart stem bark infusion (CPBI) is traditionally used in Argentina because their "vulnerary" properties. Aim of the study: CPBI was studied throughout bio-guided purification procedures conducted by in vitro biological assays in order to isolate the main bioactive compounds. Material and methods: Anti-inflammatory activity was assessed by enzyme inhibition assays of Hyaluronidase (Hyal) and inducible Nitric Oxide Synthase (iNOS). The antioxidant properties were evaluated by DPPH free radical scavenging assay, lipid peroxidation inhibition assay on erythrocyte membranes, and a cell-based assay that included the fluorescent probe (DCFH-DA) for indicating reactive oxygen species (ROS) generation. Bioactive compounds were purified by chromatographic methods and their structures elucidated using spectroscopic methods (ESI-MS and 1D/2D-H-1/C-13-NMR). Results: Four main bioactive compounds were isolated from CPBI: ellagic acid (1), 3-O-methylellagic acid (2), 3,3'-di-O-methylellagic acid (3) and 3,3'-di-O-methylellagic-4-beta-D-xylopyranoside (4). These were bioactive at concentrations in which are present in CPBI, being compounds 2 and 3 the best enzyme inhibitors of Hyal and iNOS, reaching the 90% inhibitory concentration (IC90) values ranging from 2.8 to 16.4 mu M, that are better than that of the positive controls, aspirin (IC90: no reached) and aminoguanidine (IC90: 20.2 mu M) respectively. Compounds 2 and 3 were also better scavengers for lipoperoxides than butylated hydroxytoluene (BHT), reaching the 90% effective concentration (EC90) at 1.2-4.5 mu g/ml, and for DPPH radical (2.5-7.3 mu g/ml); moreover compounds were able to exert its scavenging action on intracellular ROS. Structural features relevant to the biological activities are discussed. Conclusions: This work provides scientific validity to the popular usage of CPBI. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:63 / 73
页数:11
相关论文
共 61 条
[1]   Active oxygen chemistry within the liposomal bilayer Part IV:: Locating 2′,7′-dichlorofluorescein (DCF), 2′,7′-dichlorodihydrofluorescein (DCFH) and 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) in the lipid bilayer [J].
Afri, M ;
Frimer, AA ;
Cohen, Y .
CHEMISTRY AND PHYSICS OF LIPIDS, 2004, 131 (01) :123-133
[2]   Reactive oxygen species contribute to epidermal hyaluronan catabolism in human skin organ culture [J].
Agren, UM ;
Tammi, RH ;
Tammi, MI .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 23 (07) :996-1001
[3]   CAESALPINIA-PARAGUARIENSIS (FABACEAE) - FORAGE TREE FOR ALL SEASONS [J].
ARONSON, J ;
TOLEDO, CS .
ECONOMIC BOTANY, 1992, 46 (02) :121-132
[4]   Differential regulation of hyaluronan metabolism in the epidermal and dermal compartments of human skin by UVB irradiation [J].
Averbeck, Marco ;
Gebhardt, Carl A. ;
Voigt, Susanne ;
Beilharz, Simone ;
Anderegg, Ulf ;
Termeer, Christian C. ;
Sleeman, Jonathan P. ;
Simon, Jan C. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 (03) :687-697
[5]   PRELIMINARY PHARMACOLOGY OF ELLAGIC ACID FROM JUGLANS NIGRA (BLACK WALNUT) [J].
BHARGAVA, UC ;
WESTFALL, BA ;
SIEHR, DJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1968, 57 (10) :1728-&
[6]   L-ascorbic acid 6-hexadecanoate, a potent hyaluronidase inhibitor - X-ray structure and molecular modeling of enzyme-inhibitor complexes [J].
Botzki, A ;
Rigden, DJ ;
Braun, S ;
Nukui, M ;
Salmen, S ;
Hoechstetter, J ;
Bernhardt, G ;
Dove, S ;
Jedrzejas, MJ ;
Buschauer, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :45990-45997
[7]   Pharmacopoeia in a shamanistic society: the Izoceno-Guarani (Bolivian Chaco) [J].
Bourdy, G ;
de Michel, LRC ;
Roca-Coulthard, A .
JOURNAL OF ETHNOPHARMACOLOGY, 2004, 91 (2-3) :189-208
[8]   Antioxidant dehydrotocopherols as a new chemical character of Stemona species [J].
Brem, B ;
Seger, C ;
Pacher, T ;
Hartl, M ;
Hadacek, F ;
Hofer, O ;
Vajrodaya, S ;
Greger, H .
PHYTOCHEMISTRY, 2004, 65 (19) :2719-2729
[9]   Structure-radical scavenging activity relationships of phenolic compounds from traditional Chinese medicinal plants [J].
Cai, Yi-Zhong ;
Sun, Mei ;
Xing, Jie ;
Luo, Qiong ;
Corke, Harold .
LIFE SCIENCES, 2006, 78 (25) :2872-2888
[10]  
Corbett John A., 1996, Methods (Orlando), V10, P21, DOI 10.1006/meth.1996.0074