Ruscus Genus: A Rich Source of Bioactive Steroidal Saponins

被引:28
作者
Masullo, Milena [1 ]
Pizza, Cosimo [1 ]
Piacente, Sonia [1 ]
机构
[1] Univ Salerno, Dipartimento Farm, Via Giovanni Paolo 2 132, I-84084 Fisciano, SA, Italy
关键词
Ruscus genus; Asparagaceae; spirostanol saponins; furostanol saponins; chronic venous insufficiency; CYCLO; 3; FORT; TANDEM MASS-SPECTROMETRY; H-1-NMR CHEMICAL-SHIFTS; HAMSTER-CHEEK POUCH; UNDERGROUND PARTS; LIQUID-CHROMATOGRAPHY; CYTOSTATIC ACTIVITY; ENDOTHELIAL-CELLS; HL-60; CELLS; ACULEATUS L;
D O I
10.1055/s-0042-119728
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The genus Ruscus (Asparagaceae family) is native to the Mediterranean, Southern and Western Europe and is represented by perennial, rhizomatous, and evergreen shrubs. Among the approximately seven species spread throughout Europe up to Iran, Ruscus aculeatus L. (butcher's broom) is the most widely distributed and appreciated. This review provides an overview of the traditional use of Ruscus spp., the current knowledge of the chemistry of this genus, and the pharmacological studies carried out on Ruscus spp. extracts. The underground parts of Ruscus plants are a source of steroidal saponins that can be classified into two structural classes: the hexacyclic spiro-stanol saponins and the pentacyclic furostanol saponins. The main aglycones are ruscogenin and neoruscogenin. From the pharmacological point of view, the most studied Ruscus species is undoubtedly R. aculeatus, a very ancient phlebotherapeutic agent. Pharmacological investigations since the discovery of the vasoconstrictive and venotonic properties of ruscogenin and neoruscogenin in the underground parts of R. aculeatus are discussed. Preparations based on Ruscus species are currently used for the treatment of chronic venous insufficiency, varicose veins, haemorrhoids, and orthostatic hypotension. Finally, analytical techniques for the quality control of R. aculeatus extracts are reported.
引用
收藏
页码:1513 / 1524
页数:12
相关论文
共 80 条
[1]   Assigning stereodiversity of the 27-Me group of furostane-type steroidal saponins via NMR chemical shifts [J].
Agrawal, PK .
STEROIDS, 2005, 70 (10) :715-724
[2]   Dependence of 1H NMR chemical shifts of geminal protons of glycosyloxy methylene (H2-26) on the orientation of the 27-methyl group of furostane-type steroidal saponins [J].
Agrawal, PK .
MAGNETIC RESONANCE IN CHEMISTRY, 2004, 42 (11) :990-993
[3]   25R/25S stereochemistry of spirostane-type steroidal sapogenins and steroidal saponins via chemical shift of geminal protons of ring-F [J].
Agrawal, PK .
MAGNETIC RESONANCE IN CHEMISTRY, 2003, 41 (11) :965-968
[4]   Dependence of the 1H NMR chemical shifts of ring F resonances on the orientation of the 27-methyl group of spirostane-type steroidal sapogenins [J].
Agrawal, PK ;
Bunsawansong, P ;
Morris, GA .
PHYTOCHEMISTRY, 1998, 47 (02) :255-257
[5]   Antimicrobial activity of 20 plants used in folkloric medicine in the Palestinian area [J].
Ali-Shtayeh, MS ;
Yaghmour, RMR ;
Faidi, YR ;
Salem, K ;
Al-Nuri, MA .
JOURNAL OF ETHNOPHARMACOLOGY, 1998, 60 (03) :265-271
[6]  
Allaert FA, 2011, INT ANGIOL, V30, P272
[7]  
Balica G, 2013, J FOOD AGRIC ENVIRON, V11, P106
[8]   Spirostanol saponins and esculin from Rusci rhizoma reduce the thrombin-induced hyperpermeability of endothelial cells [J].
Barbic, M. ;
Willer, E. A. ;
Rothenhoefer, M. ;
Heilmann, J. ;
Fuerst, R. ;
Juergenliemk, G. .
PHYTOCHEMISTRY, 2013, 90 :106-113
[9]   Novel Phenyl-1-benzoxepinols from Butcher's Broom (Rusci rhizoma) [J].
Barbic, Matej ;
Schmidt, Thomas J. ;
Juergenliemk, Guido .
CHEMISTRY & BIODIVERSITY, 2012, 9 (06) :1077-1083
[10]   An open-label, randomized multicenter study comparing the efficacy and safety of Cyclo 3 Fort® versus hydroxyethyl rutoside in chronic venous lymphatic insufficiency [J].
Beltramino, R ;
Penenory, A ;
Buceta, AM .
ANGIOLOGY, 2000, 51 (07) :535-544