Mohammad-Reza Delnavazi
1, Parisa Saiyarsarai
1, Saeedeh Jafari-Nodooshan
2, Mahnaz Khanavi
1, Saeed Tavakoli
1, Hormoz Hadavinia
1, Narguess Yassa
1*1 Department of Pharmacognosy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
2 Department of Medicinal Biotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Abstract
Background: Stachys lavandulifolia Vahl is a herbaceous plant distributed in the west
and south western Asia. Despite of the wide medicinal uses, there are some
reports on toxicity potential of this plant. In present study we attempted to
evaluate the toxicity and to characterize the cytotoxic principles of S.
lavandulifolia.
Methods: Brine shrimp lethality test (BSLT)
was used to evaluate the general toxicity of the extracts and essential oil
obtained from the aerial parts of S. lavandulifolia. Phytochemical
constituents of the active extract were investigated using various
chromatographic and spectroscopic methods. GC and GC-MS were also used to
analyze the plant essential oil. GC and GC-MS were used to analyze the plant
essential oil. Cytotoxic activities of the isolated compounds were also evaluated
using MTT assay method.
Results:
In brine shrimp
lethality test (BSLT), chloroform extract and the plant
essential oil exhibited the most toxicity against Artemia salina larvae (LD50: 121.8±5.6 and
127.6±14.7 µg ml-1, respectively). GC and GC-MS analyses of essential oil
led to the characterization of forty compounds of which α-bisabolol (23.85%)
and thymol (17.88%) were identified as the main constituents. Nine flavonoids,
Pachypodol (1), chrysosplenetin (2), kumatakenin (3),
velutin (4), penduletin (5), viscosine (6), chrysoeriol (7),
hydroxygenkwanin (8) and apigenin (9) were isolated from the
chloroform extract of S.
lavandulifolia. Among the isolated compounds,
chrysosplenetin (2), a polymethoxylated flavonoid, was found as the most
toxic compound toward MDA-MB-23 and HT-29 cells, with IC50 values of
88.23 and 116.50 µg ml-1, respectively. Furthermore, chrysosplenetin
(2), kumatakenin (3) and viscosine (6) with selectivity
indices of 2.70, 2.59 and 3.33, respectively, showed higher preferential
toxicity against MDA-MB-23 cells in comparison with tamoxifen (SI:2.45).
Conclusion:
This study reports methoxylated flavonoids as compounds which could be involved
in toxicity of S.
lavandulifolia. The results of MTT assay also suggest
some of these compounds as appropriate candidates for anti-cancer drug
development research.