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Equisetum arvense (common horsetail) modulates the function of inflammatory immunocompetent cells
© Gründemann et al.; licensee BioMed Central Ltd. 2014
Received: 12 March 2014
Accepted: 22 July 2014
Published: 4 August 2014
In Europe, extracts of Equisetum arvense (common horsetail) have a long tradition in the treatment of inflammatory disorders. To understand the molecular basis for its use, we investigated the immunomodulatory capacity of a standardized commercially available common horsetail extract on human primary lymphocyte function in vitro.
The standardized extract of Equisetum arvense was phytochemically characterized. Effects on proliferation, viability and activity of mitogen-activated human lymphocytes were assessed in comparison to cyclosporine A using annexin V/propidium iodide staining assays and flow cytometry-based surface receptor characterization, respectively. Intracellular levels of effector molecules (IL-2, IFN-γ and TNF-α) were analyzed with cytokine assays.
T cell proliferation was inhibited dose dependently by the Equisetum extract without induction of apoptosis or necrosis. This effect was mediated through inhibition of lymphocyte activation, specifically by diminishing CD69 and IL-2 surface receptor expression and intracellular IL-2 production. Furthermore, treatment with Equisetum arvense inhibited effector functions, as indicated by reduced production of IFN-γ and TNF-α.
The data indicate that the used extract of Equisetum arvense interferes with the polyfunctionality of immunocompetent cells thereby providing an anti-inflammatory mode-of-action.
Equisetum arvense (common horsetail, field horsetail, or giant horsetail) belongs to the Equisetopsida family and is native to the Arctic and temperate regions of the northern hemisphere, particularly Europe . Its traditional use as an herbal remedy is documented in several handbooks of phytotherapy [2, 3] and continues to be popular in complementary medicine, especially Anthroposophical Medicine . Among the species of this genus, only Equisetum arvense “Equiseti herba”) is listed in the German commission E Monograph (phytotherapy and herbal substances) of the German Federal Institute for Drugs and Medical Devices  as well as in the European Pharmacopoeia . The putative medicinal properties are supported by a number of studies, which found (I) hepatoprotective , (II) diuretic , (III) anti-bacterial [9, 10] or (IV) antioxidant effects [11–14]. Furthermore, (V) anti-inflammatory properties for the treatment of wounds or inflammatory diseases such as arthritis have been described [15, 16]. However, to date, there are no studies on the impact of Equisetum arvense extracts on lymphocytes involved in inflammatory immune processes. Lymphocytes are the body’s second line of defence and T cells are actively recruited to sites of inflammation where they maintain and activate fibroblasts or bystander dendritic cells and macrophages, transforming them into tissue-destructive effector cells . T lymphocytes are the dominant cells in inflammatory immune diseases [18, 19], and their proliferation and mediator release (IFN-γ, TNF-α) are targets for modern therapies . Immunosuppressants such as glucocorticoids  or calcineurin inhibitors, e.g. cyclosporine A, which specifically down-regulate the immune system , are the established treatment of choice. Despite the availability of effective conventional medications, approximately 60-90% of patients with inflammatory immune disorders resort to alternative or complementary therapies to avoid side effects . One such therapy involves use of Equisetum arvense. Because we were interested in exploring the “active principle”, we phytochemically characterized a standardized, commercially available extract of Equisetum arvense and defined its immunosuppressive capacity on cell proliferation, activation status and effector functions using mitogen-activated human lymphocytes.
Equisetum arvense (Equisetopsida), ethanol. Decoctum (=Equisetum: D1; Weleda AG, Schwäbisch Gmünd, Germany) was used for the experiments. The extract is manufactured according to method no. 19f of the German Homeopathic Pharmacopoeia . The Equisetum arvense was of European origin and came from wild harvests. The fresh plant material was kept refrigerated and sent to Weleda Naturals GmbH, Schwäbisch Gmünd, Germany, where the identity of the plant material was analyzed by botanic specialists using macroscopic and microscopic methods as well as comparison with depositions of specified botanical reference stocks. The plant material was dried, homogenized and a decoct was produced by boiling one part dried plant material with nine parts ethanol for 4 h. The absolute ethanol concentration of the preparation used was 36 Vol.-%. We used the same concentration of ethanol for vehicle control experiments and clearly demonstrated that these amounts have no influence on the behaviour of the cells. After cooling down to room temperature, the decoct was squeezed out mechanically, filtered sterile and filled into 50 mL bottles. Bottles from sale stocks were sent to our laboratory in Freiburg, Germany, where the experiments were performed. For each experiment, a fresh frozen aliquot of the Equisetum arvense extract was used, and concentrations of 0.05, 0.1, 0.2, 0.4 and 0.8 μg/mL were tested.
Phytochemical analysis of the Equisetum arvense extract
LC-MS analyses were performed on an UltiMate 3000 RSLC-series system (Dionex, Germering, Germany) coupled to a 3D quadrupole ion trap mass spectrometer equipped with an orthogonal ESI source (HCT, Bruker Daltonics, Bremen, Germany). HPLC separation was carried out on an Acclaim 120 C18, 2.1 × 150 mm, 3 μm column (Dionex) at 30°C using 0.1% aqueous formic acid and acetonitrile as mobile phase A and B, respectively. The flow rate was 0.5 mL/min and the following gradient program was used: 5% B (0 min), 5% B (2 min), 11% B (20 min), and 24% B (33 min), followed by a column cleaning and re-equilibration step. The eluent flow was split at a 1:4 ratio before the ESI ion source, which was operated as follows: capillary voltage: +3.5 kV, nebulizer: 26 psi (N2), dry gas flow: 9 L/min (N2), and dry temperature: 340°C. MS2, MS3, and MS4 spectra were obtained in an automated data-dependent acquisition mode (collision gas: He, isolation window: 4 Th, fragmentation amplitude: 1.0 V). 2 μL of the undiluted, centrifuged Equisetum extract were injected. Finally, two of the tentatively identified components were confirmed by comparison of the retention times, UV- and MSn-spectra with the reference compounds isoquercitrin (Carl Roth, Karlsruhe, Germany) and kaempferol-3-O-glucoside (Extrasynthese, Genay Cedex, France).
Quantification of the main flavonoid isoquercitrin (quercetin-3-O-glucoside) in the Equisetum arvense extract was performed by HPLC-DAD with external standard calibration, and the total flavonoid content was determined by a spectrophotometric assay adapted from the European Pharmacopoeia (Ph. Eur.) Monograph on Equiseti herba  (for details see Additional file 1).
Patients gave their written consent for giving blood for scientific research.
All experiments conducted on human material were approved by the Ethics committee of the University of Freiburg (55/14).
Preparation and cultivation of human peripheral lymphocytes
Human peripheral lymphocytes (PBMC) were isolated from the blood of healthy adult donors obtained from the Blood Transfusion Centre (Medical Center, University of Freiburg, Germany). Venous blood was centrifuged on a LymphoPrep™ gradient (density: 1.077 g/cm3, 20 min, 500 × g, 20°C; Progen, Heidelberg, Germany). Cells were washed twice in medium, and cell viability as well as concentration was determined using the trypan blue exclusion test. Cells were cultured in RPMI 1640 medium supplemented with 10% heat-inactivated fetal calf serum (PAA, Pasching, Austria), 2 mM L-glutamine, 100 U/mL penicillin and 100 U/mL streptomycin (all from Life Technologies, Paisley, UK). The cells were cultured at 37°C in a humidified incubator with 5% CO2/95% air atmosphere.
Activation and treatment of lymphocytes and T-cells
PBMC (105) were stimulated with phytohemagglutinin-L (PHA-L; 10 μg/mL; Roche Diagnostics, Mannheim, Germany) or lipopolysaccharide (LPS; 1 μg/mL; Sigma-Aldrich, Taufkirchen, Germany) in the presence of control agents cyclosporine A (CsA; 10 μg/mL obtained by dilution of Sandimmun® 50 mg/mL, Novartis Pharma GmbH, Nürnberg, Germany), camptothecin (CPT; 30 μg/mL; Tocris, Eching, Germany) and Triton-X 100 (0.5%; Carl Roth, Karlsruhe, Germany), or different concentrations of Equisetum arvense extract. After cultivation, the cells were assessed in bioassays as described in the text.
Cell division tracking using CFSE
PBMC were harvested and washed twice in cold PBS before they were resuspended in PBS at a concentration of 5 × 106 cells/mL. CFSE (carboxyfluorescein diacetate succinimidyl ester, 5 mM; Sigma, Taufkirchen, Germany) was added in 1/1000 dilution and the PBMC were incubated for 10 min at 37°C. The staining reaction was stopped by washing twice with complete medium. Afterwards, the cell division progress was analyzed using flow cytometry.
Determination of apoptosis and necrosis using annexin V and propidium iodide staining
PBMC were cultured in the presence of Equisetum arvense extract for 24 or 48 h, respectively, and the levels of apoptosis and necrosis were determined using Annexin V-FITC apoptosis detection kit (eBioscience, Frankfurt, Germany or BD Bioscience, Heidelberg, Germany) according to the manufacturer’s instructions. After annexin V staining, propidium iodide solution (PI; eBioscience or BD Bioscience) was added and the cells were incubated in the dark, followed by a flow cytometric analysis to determine the amount of apoptosis and necrosis. We used CPT (100 μM) and Triton-X 100 (0.5%) as positive controls for apoptosis and necrosis, respectively.
CD69 activation marker and IL-2 surface receptor analysis
Cultured cells (24 or 48 h) were washed with PBS and stained with FITC-labeled anti-human CD69 and PE-labeled anti-human CD25 mAbs (both eBioscience, Frankfurt, Germany) for 15 min at 4°C. Next, the cells were washed twice with PBS, resuspended and transferred into FACS vials. The expression of CD69 and IL-2 surface receptor α-chain CD25 was measured by FACS analysis using a FACSCalibur instrument.
Determination of cytokine production
Cells were treated for 36 h and were restimulated with PMA (50 ng/mL) and ionomycin (500 ng/mL) (both from Sigma-Aldrich, Taufkirchen, Germany) for additional 6 h. Cytokines were measured using intracellular cytokine analysis. For this purpose, the cells were surface-stained with anti-human CD8 mAbs (eBioscience), fixed, and permeabilized using 4% paraformaldehyde (Sigma-Aldrich) and Perm/Wash solution (Becton Dickinson, Franklin Lakes, NJ), followed by staining with PE-conjugated anti-human IFN-γ mAb or anti-human TNF-α mAb (both from eBioscience), respectively. Samples were analyzed with a BD FACSCalibur flow cytometer using BD CellQuest Pro Software.
Analysis of data
For statistical analysis, data were processed with Microsoft Excel and IBM SPSS software 20.0. Values are presented as mean ± SD for the indicated number of independent experiments. Statistical significance was determined by one-way ANOVA followed by Dunnett’s post hoc pairwise comparisons. For estimation of the inhibitory concentration (IC50), a probit regression model for the dose-response curve was used and data were processed by ToxRat® software. The asterisks represent significant differences from controls (*P < 0.05, **P < 0.01, ***P < 0.001).
Phytochemical analysis of the Equisetum arvense extract
Equisetum arvense decreased proliferation of mitogen-activated human lymphocytes
Equisetum arvense-mediated inhibition of proliferation is not mediated through apoptosis or necrosis induction
Equisetum arvense influences cell proliferation capacity through partial inhibition of lymphocyte activation and IL-2 biology
Equisetum arvense slightly affects effector function of activated human lymphocytes
Extracts of Equisetum arvense (common horsetail) have a long tradition in the treatment of inflammatory disorders, for which reason we were interested in clarifying whether there is a rational basis for its use. To this end, we characterized a standardized common horsetail extract in cell-based assays using activated immunocompetent cells.
We found a concentration-dependent inhibition of mitogen-activated lymphocyte proliferation with an IC50 value of 1.09 μg/mL. Furthermore, our data indicate that the inhibition of proliferation induced by the Equisetum arvense extract was not mediated by apoptosis and necrosis. Immunosuppressive effects of Equisetum arvense have also been observed by other groups, however, their investigations were only done with human cancer cell lines [11, 25]. T-cell proliferation is a process initiated by ligation of the T-cell receptor to antigens that triggers a complex T-cell receptor signalling pathway. During this process, the human transmembrane C-Type lectin protein CD69 is expressed on the surface of activated T-cells . CD69 is an early activation marker that is expressed at high amounts immediately after activation, and gene as well protein expression of this marker rapidly decreases 24 h after stimulation. We found a decrease in the activation status of stimulated T-cells after stimulation, whereby the effects of Equisetum are smaller than that of CsA. T-lymphocyte proliferation is further initiated by activation and expression of the autocrine growth factor interleukin-2 (IL-2), which promotes interaction with the receptor CD25 that is up-regulated on the surface of activated T-cells  and by release of endogenous IL-2. The expression of the IL-2 receptor was indeed slightly affected in the presence of Equisetum. Over time, however, inhibition was smaller than that of CsA, which specifically reduces the early activation state of lymphocytes due to suppression of the IL-2 receptor [26, 27]. The data further demonstrate that Equisetum reduces IL-2 cytokine production. Because IL-2 is pivotal for lymphocyte proliferation, inhibition of its production may at least partially explain the immunosuppressive effects of Equisetum in these experiments. In addition, a slight inhibition of IFN-γ- and TNF-α-production of activated T cells could be shown. Thus, we can conclude that the horsetail extract interferes with T-cell polyfunctionality, which results in diminished proliferation of immunocompetent cells.
The stems of Equisetum arvense contain high amounts of minerals, in particular silicic acid and silicates (5-8%), potassium and calcium, various flavonoids (0.2-0.9%) and phenolic acids, the phenolic petrosins onitin and oniti-9-O-glucoside, equisetumpyrone (only in the very early developmental stages), triterpenoids and phytosterols. They also contain low amounts of essential oil, the main constituents being hexahydrofarnesyl acetone, cis-geranyl acetone, thymol, and trans-phytol as well as a few other compounds [28, 29]. Especially, the considerable amounts of polyphenols and several compounds of this diverse group of phytochemicals have attracted interest in the past due to their presumptive physiological activities. However, there is no clear correlation between the traditional use of this herbal drug and any constituents in particular. The Ph. Eur. requires a minimum of 0.3% of total flavonoids expressed as isoquercitrin in the dried drug . Consequently, we focused our phytochemical analysis of the investigated Equisetum arvense extract on flavonoids and other polar phenolics. The phenolic pattern is largely in agreement with a previous study on the variation of phenolics in different species of the genus Equisetum subgenus Equisetum, and is characteristic for the European chemotype of E. arvense[29, 30]. The main difference found in the qualitative composition to the study by Veit et al.  is that we did not detect significant amounts of malonylated flavonoid glycosides. Several of the numerous known components of the characterized Equisetum extract have been reported to possess anti-inflammatory activity [31–34]. We know from the literature, that given orally polyphenols (specifically flavanols, flavonols, flavanones, flavones) are absorbed by enterocytes and do not reach circulation . Systemic effects of orally applied polyphenols therefore cannot be expected. Rather, topical treatment of the skin or mucosa would be more realistic to reach concentrations of Equisetum comparable to our in vitro experiments.
The presented data indicate that the Equisetum arvense extract used interferes polyfunctionally with immunocompetent cells, thereby providing a potential mechanism that explains its traditional use in the treatment of inflammatory disorders. However, further studies should be conducted to prove its clinical potency.
Consumables and fees for writing the manuscript were supported by Weleda AG. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
- Hager H: Hagers Handbuch der Pharmazeutischen Praxis: Drogen E-O. [S.l.]. Hagers Handbuch der Pharmazeutischen Praxis. 2013, Heidelberg: SpringerGoogle Scholar
- Czygan F-C, Wichtl M: Teedrogen und Phytopharmaka: Ein Handbuch für die Praxis auf wissenschaftlicher Grundlage. 1997, Stuttgart: Wiss. Verl.-GesGoogle Scholar
- Madaus G: Lehrbuch der Biologischen Heilmittel 10, Volume 10. 1990, Mediamed: RavensburgGoogle Scholar
- Pelikan W: Heilpflanzenkunde: Der Mensch und die Heilpflanzen. 1999, Verlag am Goethanum: DornachGoogle Scholar
- Bundesanzeiger: Equiseti berba (Schachtelhalmkraut). Bundesanzeiger Verlag GmbH. 1986, Köln: BundesanzeigerGoogle Scholar
- EP: (EP) European Pharmacopoeia. European Pharmacopoeia (European Treaty Series) from the Council of Europe. 2010, Strasbourg: Stationary Office BooksGoogle Scholar
- Oh H, Kim D-H, Cho J-H, Kim Y-C: Hepatoprotective and free radical scavenging activities of phenolic petrosins and flavonoids isolated from Equisetum arvense. J Ethnopharmacol. 2004, 95: 421-424.View ArticlePubMedGoogle Scholar
- Wright CI, Van-Buren L, Kroner CI, Koning MMG: Herbal medicines as diuretics: a review of the scientific evidence. J Ethnopharmacol. 2007, 114: 1-31.View ArticlePubMedGoogle Scholar
- Bessa Pereira C, Gomes PS, Costa-Rodrigues J, Almeida Palmas R, Vieira L, Ferraz MP, Lopes MA, Fernandes MH: Equisetum arvense hydromethanolic extracts in bone tissue regeneration: in vitro osteoblastic modulation and antibacterial activity. Cell Prolif. 2012, 45: 386-396.View ArticlePubMedGoogle Scholar
- Milovanović V, Radulović N, Todorović Z, Stanković M, Stojanović G: Antioxidant, antimicrobial and genotoxicity screening of hydro-alcoholic extracts of five serbian Equisetum species. Plant Foods Hum Nutr Dordr Neth. 2007, 62: 113-119.View ArticleGoogle Scholar
- Cetojević-Simin DD, Canadanović-Brunet JM, Bogdanović GM, Djilas SM, Cetković GS, Tumbas VT, Stojiljković BT: Antioxidative and antiproliferative activities of different horsetail (Equisetum arvense L.) extracts. J Med Food. 2010, 13: 452-459.View ArticlePubMedGoogle Scholar
- Stajner D, Popović BM, Canadanović-Brunet J, Anackov G: Exploring Equisetum arvense L., Equisetum ramosissimum L. and Equisetum telmateia L. as sources of natural antioxidants. Phytother Res PTR. 2009, 23: 546-550.View ArticlePubMedGoogle Scholar
- Stajner D, Popović BM, Canadanović-Brunet J, Boza P: Free radical scavenging activity of three Equisetum species from Fruska gora mountain. Fitoterapia. 2006, 77: 601-604.View ArticlePubMedGoogle Scholar
- Wu L-C, Jou AF-J, Chen S-H, Tien C-Y, Cheng C-F, Fan N-C, Ho J-AA: Antioxidant, anti-inflammatory and anti-browning activities of hot water extracts of oriental herbal teas. Food Funct. 2010, 1: 200-208.View ArticlePubMedGoogle Scholar
- Costa-Rodrigues J, Carmo SC, Silva JC, Fernandes MHR: Inhibition of human in vitro osteoclastogenesis by Equisetum arvense. Cell Prolif. 2012, 45: 566-576.View ArticlePubMedGoogle Scholar
- Do Monte FHM, dos Santos JG, Jr RM, Lanziotti VMNB, Leal LKAM, de A Cunha GM: Antinociceptive and anti-inflammatory properties of the hydroalcoholic extract of stems from Equisetum arvense L. in mice. Pharmacol Res Off J Ital Pharmacol Soc. 2004, 49: 239-243.Google Scholar
- Choy EH, Panayi GS: Cytokine pathways and joint inflammation in rheumatoid arthritis. N Engl J Med. 2001, 344: 907-916.View ArticlePubMedGoogle Scholar
- Berner B, Wolf G, Hummel KM, Müller GA, Reuss-Borst MA: Increased expression of CD40 ligand (CD154) on CD4+ T cells as a marker of disease activity in rheumatoid arthritis. Ann Rheum Dis. 2000, 59: 190-195.View ArticlePubMedPubMed CentralGoogle Scholar
- Cai Y, Fleming C, Yan J: New insights of T cells in the pathogenesis of psoriasis. Cell Mol Immunol. 2012, 9: 302-309.View ArticlePubMedPubMed CentralGoogle Scholar
- Macian F: NFAT proteins: key regulators of T-cell development and function. Nat Rev Immunol. 2005, 5: 472-484.View ArticlePubMedGoogle Scholar
- Rhen T, Cidlowski JA: Antiinflammatory action of glucocorticoids–new mechanisms for old drugs. N Engl J Med. 2005, 353: 1711-1723.View ArticlePubMedGoogle Scholar
- Rao JK, Mihaliak K, Kroenke K, Bradley J, Tierney WM, Weinberger M: Use of complementary therapies for arthritis among patients of rheumatologists. Ann Intern Med. 1999, 131: 409-416.View ArticlePubMedGoogle Scholar
- GHP: (GHP) German Homeopathic Pharmacopoeia. 2003, Stuttgart, London: Medpharm Scientific; Stationery OfficeGoogle Scholar
- Malek TR: The biology of interleukin-2. Annu Rev Immunol. 2008, 26: 453-479.View ArticlePubMedGoogle Scholar
- Li H, Wang P, Liu Q, Cheng X, Zhou Y, Xiao Y: Cell cycle arrest and cell apoptosis induced by Equisetum hyemale extract in murine leukemia L1210 cells. J Ethnopharmacol. 2012, 144: 322-327.View ArticlePubMedGoogle Scholar
- Bettens F, Walker C, Bonnard GD, de Weck AL: Effect of cyclosporin A on the early activation of human T helper lymphocytes: inhibition of RNA-synthesis and modification of the expression of activation antigens. Immunobiology. 1985, 170: 434-447.View ArticlePubMedGoogle Scholar
- Solbach W, Heeg K, Von Steldern DU, Röllinghoff M, Wagner H: On the partial suppression of IL-2 receptor expression and the prevention of lectin-induced lymphoblast formation by cyclosporine A. Clin Exp Immunol. 1985, 60: 501-508.PubMedPubMed CentralGoogle Scholar
- Radulović N, Stojanović G, Palić R: Composition and antimicrobial activity of Equisetum arvense L. essential oil. Phytother Res PTR. 2006, 20: 85-88.View ArticlePubMedGoogle Scholar
- Veit M, Beckert C, Höhne C, Bauer K, Geiger H: Interspecific and intraspecific variation of phenolics in the genus Equisetum subgenus Equisetum. Phytochemistry. 1995, 38: 881-891.View ArticleGoogle Scholar
- Mimica-Dukic N, Simin N, Cvejic J, Jovin E, Orcic D, Bozin B: Phenolic compounds in field horsetail (Equisetum arvense L.) as natural antioxidants. Mol Basel Switz. 2008, 13: 1455-1464.Google Scholar
- Kawai M, Hirano T, Higa S, Arimitsu J, Maruta M, Kuwahara Y, Ohkawara T, Hagihara K, Yamadori T, Shima Y, Ogata A, Kawase I, Tanaka T: Flavonoids and related compounds as anti-allergic substances. Allergol Int Off J Jpn Soc Allergol. 2007, 56: 113-123.View ArticleGoogle Scholar
- Kempuraj D, Madhappan B, Christodoulou S, Boucher W, Cao J, Papadopoulou N, Cetrulo CL, Theoharides TC: Flavonols inhibit proinflammatory mediator release, intracellular calcium ion levels and protein kinase C theta phosphorylation in human mast cells. Br J Pharmacol. 2005, 145: 934-944.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim HP, Son KH, Chang HW, Kang SS: Anti-inflammatory plant flavonoids and cellular action mechanisms. J Pharmacol Sci. 2004, 96: 229-245.View ArticlePubMedGoogle Scholar
- Rathee P, Chaudhary H, Rathee S, Rathee D, Kumar V, Kohli K: Mechanism of action of flavonoids as anti-inflammatory agents: a review. Inflamm Allergy Drug Targets. 2009, 8: 229-235.View ArticlePubMedGoogle Scholar
- Scholz S, Williamson G: Interactions affecting the bioavailability of dietary polyphenols in vivo. Int J Vitam Nutr Res Int Z Für Vitam- Ernährungsforschung J Int Vitaminol Nutr. 2007, 77: 224-235.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6882/14/283/prepub
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