Leonurus cardiaca L. (Motherwort): A Review of its Phytochemistry and Pharmacology

被引:82
作者
Wojtyniak, Katarzyna [1 ]
Szymanski, Marcin [1 ]
Matlawska, Irena [1 ]
机构
[1] Poznan Univ Med Sci, Dept Pharmacognosy, 4 Swiecickiego St, PL-61771 Poznan, Poland
关键词
motherwort; Leonurus cardiaca L; pharmacology; phytochemistry; MEDICINAL-PLANTS; ANTIOXIDANT ACTIVITY; LABDANE DITERPENES; LAMIACEAE; EXTRACTS;
D O I
10.1002/ptr.4850
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Leonurus cardiaca is a perennial plant indigenous to central Europe and Scandinavia, but it is also found in the area spanning temperate Russia to central Asia. It has been introduced to North America and has become established locally in the wild. Motherwort (Leonuri cardiacae herba) consists of aerial parts of Leonurus cardiaca gathered during the flowering period, dried at 35 degrees C and, according to European Pharmacopoeia 7th edition, should contain a minimum of 0.2% flavonoids, expressed as hyperoside. Compounds belonging to the group of monoterpenes, diterpenes, triterpenes, nitrogen- containing compounds, phenylpropanoids, flavonoids and phenolic acids, as well as volatile oils, sterols and tannins, have been identified in motherwort. Traditionally, extracts of the herb have been used internally, mainly for nervous heart conditions and digestive disorders. However, they have also been used for bronchial asthma, climacteric symptoms and amenorrhoea, as well as externally in wounds and skin inflammations. Mild negative chronotropic, hypotonic and sedative effects can be attributed to the herb and preparations thereof. Pharmacological studies have confirmed its antibacterial, antioxidant, anti-inflammatory and analgesic activity, as well as its effects on the heart and the circulatory system. Sedative and hypotensive activity has been demonstrated in clinical trials. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:1115 / 1120
页数:6
相关论文
共 47 条
[1]   New labdane diterpenes from Leonurus cardiaca [J].
Agnihotri, Vijai K. ;
Elsohly, Hala N. ;
Smillie, Troy J. ;
Khan, Ikhlas A. ;
Walker, Larry A. .
PLANTA MEDICA, 2008, 74 (10) :1288-1290
[2]   Ursolic acid: A potent inhibitor of superoxides produced in the cellular system [J].
Ali, Muhammad S. ;
Ibrahim, Syed A. ;
Jalil, Saima ;
Choudhary, Muhammad I. .
PHYTOTHERAPY RESEARCH, 2007, 21 (06) :558-561
[3]  
Bernatoniene J, 2009, ACTA POL PHARM, V66, P415
[4]  
Blumenthal M, 2000, INTEGRATIVE MED COMM, P267
[5]  
Bradley PR, 1992, BRIT HERBAL COMPENDI, V1, P161
[6]  
Brand K., 1999, Arch. Pharm, V331, P6
[7]  
Brieskorn C.H., 1979, Tetrahedron. Lett, V20, P2511
[8]  
Chen Z. S., 2000, Biomedical Research (Aligarh), V11, P209
[9]  
FOKINA GI, 1991, VOP VIRUSOL+, V36, P18
[10]  
Gulubov A., 1970, Materialia Fizika Khimicheskaya Biologica, V8, P129