Subscribe to RSS
DOI: 10.1055/s-0031-1298172
© Georg Thieme Verlag KG Stuttgart · New York
Anti-inflammatory, Gastroprotective, and Cytotoxic Effects of Sideritis scardica Extracts
Publication History
received October 10, 2011
revised Dec. 12, 2011
accepted Dec. 19, 2011
Publication Date:
24 January 2012 (online)

Abstract
Sideritis scardica Griseb. (ironwort, mountain tea), an endemic plant of the Balkan Peninsula, has been used in traditional medicine in the treatment of gastrointestinal complaints, inflammation, and rheumatic disorders. This study aimed to evaluate its gastroprotective and anti-inflammatory activities. Besides, continuously increasing interest in assessing the role of the plant active constituents preventing the risk of cancer was a reason to make a detailed examination of the investigated ethanol, diethyl ether, ethyl acetate, and n-butanol extracts regarding cytotoxicity. Oral administration of the investigated extracts caused a dose-dependent anti-inflammatory effect in a model of carrageenan-induced rat paw edema. Gastroprotective activity of the extracts was investigated using an ethanol-induced acute stress ulcer in rats. The cytotoxic activity of plant extracts was assessed on PBMC, B16, and HL-60 cells and compared to the cytotoxicity of phenolic compounds identified in extracts. Apoptotic and necrotic cell death were analyzed by double staining with fluoresceinisothiocyanate (FITC)-conjugated annexin V and PI. The developed HPLC method enabled qualitative fingerprint analysis of phenolic compounds in the investigated extracts. Compared to the effect of the positive control, the anti-inflammatory drug indomethacine (4 mg/kg), which produced a 50 % decrease in inflammation, diethyl ether and n-butanol extracts exhibited about the same effect in doses of 200 and 100 mg/kg (53.6 and 48.7 %; 48.4 and 49.9 %, respectively). All investigated extracts produced dose-dependent gastroprotective activity with the efficacy comparable to that of the reference drug ranitidine. The diethyl ether extract showed significant dose-dependent cytotoxicity on B16 cells and HL-60 cells, decreasing cell growth to 51.3 % and 77.5 % of control, respectively, when used at 100 µg/mL. It seems that phenolic compounds (apigenin, luteolin, and their corresponding glycosides) are responsible for the diethyl ether extract cytotoxic effect. It also appears that induction of oxidative stress might be involved in its cytotoxicity, since B16 and HL-60 cells increased their ROS production in response to treatment with diethyl ether extract. Neither of the tested extracts nor any phenolic compounds showed significant cytotoxic effect to human PBMC. These results demonstrated the potent anti-inflammatory and gastroprotective activities, as well as the promising cytotoxicity.
Key words
Sideritis scardica Griseb. - Lamiaceae - anti-inflammatory - gastroprotective activity - cytotoxicity - polyphenols - flavonoids
References
- 1
Lui Z, Tao X, Zhang C, Lu Y, Wei D.
Protective effects of hyperoside (Quercetin-3-O-galactoside) to PC12 cells against
cytotoxicity induced by hydrogen peroxide and tert-butyl hydro-peroxide.
Biomed Pharmacother.
2005;
59
481-490
MissingFormLabel
- 2
Basile A, Senatore F, Gargano R, Sorbo S, Del Pezzo M, Lavitola A, Ritieni A, Bruno M, Spatuzzi D, Rigano D, Vuotto M L.
Antibacterial and antioxidant activities in Sideritis italica (Miller) Greuter et Burdet essential oils.
J Ethnopharmacol.
2006;
107
240-248
MissingFormLabel
- 3
Charami M, Lazari D, Karioti A, Skaltsa H, Hadjipavlou-Litina D, Souleles C.
Antioxidant and antiinflammatory activities of Sideritis perfoliata subsp. perfoliata (Lamiaceae).
Phytother Res.
2008;
22
450-454
MissingFormLabel
- 4
Küpeli E, Şahin F P, Çalış I, Yeşilada E, Ezer N.
Phenolic compounds of Sideritis ozturkii and their in vivo anti-inflammatory and antinociceptive activities.
J Ethnopharmacol.
2007;
118
356-360
MissingFormLabel
- 5
Aboutabl E A, Nassar M I, Elsakhawy F M, Maklad Y A, Osman A F, El-Khrisy E A M.
Phytochemical and pharmacological studies on Sideritis taurica Stephan ex Wild.
J Ethnopharmacol.
2002;
82
177-184
MissingFormLabel
- 6
Hernàndez-Pérez M, Rabanal R M.
Evaluation of the antinflammatory and analgesic activity of Sideritis canariensis var. pannosa in mice.
J Ethnopharmacol.
2002;
81
43-47
MissingFormLabel
- 7
Navarro A, de Las Heras B, Villar A.
Anti-inflammatory and immunomodulating properties of a sterol fraction from Sideitis foetens Clem.
Biol Pharm Bull.
2001;
24
470-473
MissingFormLabel
- 8
de las Heras B, Navarro A, Díaz-Guerra M J, Bermejo P, Castrillo A, Boscá L, Villar A.
Inhibition of NOS-2 expression in macrophages through the inactivation of NF-kB by
andalusol.
Br J Pharmacol.
1999;
28
605-612
MissingFormLabel
- 9
Güvenç A, Okada Y, Küpeli Akkol E, Duman H, Okuyama T, Çalıs I.
Investigations of anti-inflammatory, antinociceptive, antioxidant and aldose reductase
inhibitory activities of phenolic compounds from Sideritis brevibracteata.
Food Chem.
2010;
118
686-692
MissingFormLabel
- 10
Demirtas I, Sahin A, Ayhan B, Tekin S, Telci I.
Antiproliferative effects of the methanolic extracts of Sideritis libanotica Labill. subsp. linearis.
Rec Nat Prod.
2009;
3
104-109
MissingFormLabel
- 11
Ertaş A, Öztürk M, Boga B, Topçu G.
Antioxidant and anticholinesterase activity evaluation of ent-kaurane diterpenoids
from Sideritis arguta.
J Nat Prod.
2009;
72
500-502
MissingFormLabel
- 12
Kassi E, Papoutsi Z, Fokialakis N, Messari J, Mitakou S, Moutsatsou P.
Greek plant extracts exhibit selective estrogen receptor modulator (SERM)-like properties.
J Agric Food Chem.
2004;
52
6956-6961
MissingFormLabel
- 13
Plioukas M, Termentzi A, Gabrieli C, Zervou M, Kefalas P, Kokkalou E.
Novel acylflavones from Sideritis syriaca ssp. syriaca.
Food Chem.
2010;
123
1136-1141
MissingFormLabel
- 14
Petreska J, Stefova M, Ferreres F, Moreno D A, Thomas-Barberan F A, Stefkov G, Kulevanova S, Gil-Izquiredo A.
Potential bioactive phenolics of Macedonian Sideritis species used for medicinal “Mountain tea”.
Food Chem.
2011;
125
13-20
MissingFormLabel
- 15
Alipieva K I, Kostadinova E P, Evstatieva L N, Stefova M, Bankova V S.
An iridoid and a flavonoid from Sideritis lanata L.
Fitoterapia.
2009;
80
51-53
MissingFormLabel
- 16
Kilic T.
Isolation and biological activity of new and known diterpenoids from Sideritis stricta Boiss. & Heldr.
Molecules.
2006;
11
257-262
MissingFormLabel
- 17
Rios J L, Manez S, Paya M, Alcaraz M J.
Antioxidant activity of flavonoids from Sideritis javalabrensis.
Phytochemistry.
1992;
31
1047-1050
MissingFormLabel
- 18 Diklić N. Genus Sideritis L. In: Josifović M, editor Flora of Serbia, Volume IV. Serbia: Serbian Academy of Science and Art; 1974: 371-372
MissingFormLabel
- 19
Koleva I, Linssen J P H, van Beek T A, Evstatieva L N, Kortenska V, Handjieva N.
Antioxidant activity screening of extracts from Sideritis species (Labiatae) grown in Bulgaria.
J Sci Food Agric.
2003;
83
809-819
MissingFormLabel
- 20
Velioglu Y S, Mazza Gao L, Oomah B D.
Antioxidant activity and total phenolics in selected fruits, vegetables, and grain
products.
J Agric Food Chem.
1998;
46
4113-4117
MissingFormLabel
- 21 Council of Europe .Determinations of tannins in herbal drugs. European Pharmacopoeia 6.0, edition no. 6, Volume 1 Strasbourg: Council of Europe; 2004: 255
MissingFormLabel
- 22
Blois M S.
Antioxidant determinations by the use of a stable free radical.
Nature.
1958;
181
1199-1200
MissingFormLabel
- 23
Oyanagui Y, Sato S.
Inhibition by nilvadipine of ischemic and carrageenan paw oedema as well as of superoxide
radical production from neutrophils and xanthine oxidase.
Drug Res.
1991;
41
469-474
MissingFormLabel
- 24
Adami E, Marazzi-Uberti E, Turba C.
Pharmacological research on gefarnate, a new synthetic isoprenoid with an anti-ulcer
action.
Arch Int Pharmacodyn Ther.
1964;
58
1780-1783
MissingFormLabel
- 25 Touhey S, Heenan M. Cell culture. In: Davey J, Lord J M, editors Essential cell biology. Oxford: Oxford University Press; 2003
MissingFormLabel
- 26
Mijatovic S, Maksimovic-Ivanic D, Radovic J, Miljkovic D, Harhaji L, Vuckovic O, Stosic-Grujicic S, Mostarica Stojkovic M, Trajkovic V.
Anti-glioma action of aloe emodin: the role of ERK inhibition.
Cell Mol Life Sci.
2005;
62
589-598
MissingFormLabel
- 27
Badovinac V, Trajkovic V, Mostarica-Stojkovic M.
Nitric oxide promotes growth and major histocompatibility complex-unrestricted cytotoxicity
of interleukin-2-activated rat lymphocytes.
Scand J Immunol.
2000;
52
62-70
MissingFormLabel
- 28
Özkan G, Sagdiç O, Özcan M, Özçelik H, Ünver A.
Antioxidant and antibacterial activities of Turkish endemic Sideritis extracts.
Grasas Aceites.
2005;
56
16-20
MissingFormLabel
- 29
Tunalier Z, Kosar M, Ozturk N, Baser K H C, Duman H, Kirimer N.
Antioxidant properties and phenolic composition of Sideritis species.
Chem Nat Comp.
2004;
40
206-210
MissingFormLabel
- 30
Spencer J, Mohsen M, Rice-Evans C.
Cellular uptake and metabolism of flavonoids and their metabolites: implications for
their bioactivity.
Arch Biochem Biophys.
2004;
423
148-161
MissingFormLabel
- 31
Rice-Evans C A, Miller N J, Paganga G.
Structure-antioxidant activity relationships of flavonoids and phenolic acids.
Free Radic Biol Med.
1996;
20
933-956
MissingFormLabel
- 32
Maleki N, Garjani A, Nazemiyeh H, Nilfouroushan N, Eftekhar Sadat A T, Allameh Z, Hasannia N.
Potent anti-inflammatory activities of hydroalcoholic extract from aerial parts of
Stachys inflata in rats.
J Ethnopharmacol.
2001;
75
213-218
MissingFormLabel
- 33
Salim A S.
Removing oxygen-derived free radicals stimulates healing of ethanol-induced erosive
gastritis in the rat.
Digestion.
1990;
47
24-28
MissingFormLabel
- 34
Shukla S, Gupta S.
Apigenin: a promising molecule for cancer prevention.
Pharm Res.
2010;
27
962-978
MissingFormLabel
- 35
Caltagirone S, Rossi C, Poggi A, Ranelletti F O, Natali P G, Brunetti M, Aiello F B, Piantelli M.
Flavonoids apigenin and quercetin inhibit melanoma growth and metastatic potential.
Int J Cancer.
2000;
87
595-600
MissingFormLabel
- 36
Fiers W, Beyaert R, Declercq W, Vandenabeele P.
More than one way to die: apoptosis, necrosis and reactive oxygen damage.
Oncogene.
1999;
18
7719-7730
MissingFormLabel
- 37
Chen D, Chen M S, Cui Q C, Yang H, Dou Q P.
Structure-proteasome-inhibitory activity relationships of dietary flavonoids in human
cancer cells.
Front Biosci.
2007;
12
1935-1945
MissingFormLabel
- 38
Abaza L, Talorete T P, Yamada P, Kurita Y, Zarrouk M, Isoda H.
Induction of growth inhibition and differentiation of human leukemia HL-60 cells by
a Tunisian gerboui olive leaf extract.
Biosci Biotechnol Biochem.
2007;
71
1306-1312
MissingFormLabel
- 39
Hou D X, Kumamoto T.
Flavonoids as protein kinase inhibitors for cancer chemoprevention: direct binding
and molecular modeling.
Antioxid Redox Signal.
2010;
13
691-719
MissingFormLabel
- 40
Sauter B, Albert M L, Francisco L, Larsson M, Somersan S, Bhardwaj N.
Consequences of cell death: exposure to necrotic tumor cells, but not primary tissue
cells or apoptotic cells, induces the maturation of immunostimulatory dendritic cells.
J Exp Med.
2000;
191
423-434
MissingFormLabel
Dr Vanja Tadić, Science Advisor
Department of Pharmacy
Institute for Medicinal Plant Research “Dr Josif Pančić”
Tadeusa Koscuska 1
11000 Belgrade
Serbia
Phone: +38 11 13 03 16 58
Fax: +38 11 13 03 16 55
Email: vtadic@mocbilja.rs