|Year : 2015 | Volume
| Issue : 17 | Page : 63-72
Echinacea purpurea: Pharmacology, phytochemistry and analysis methods
Azadeh Manayi1, Mahdi Vazirian2, Soodabeh Saeidnia3
1 Medicinal Plants Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
2 Department of Pharmacognosy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
3 Medicinal Plants Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran; Division of Pharmacy, College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, Saskatchewan, Canada
|Date of Submission||21-Apr-2014|
|Date of Acceptance||02-Oct-2014|
|Date of Web Publication||05-May-2015|
Medicinal Plants Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran 1417614411, Iran
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Echinacea purpurea (Asteraceae) is a perennial medicinal herb with important immunostimulatory and anti-inflammatory properties, especially the alleviation of cold symptoms. The plant also attracted scientists' attention to assess other aspects of its beneficial effects. For instance, antianxiety, antidepression, cytotoxicity, and antimutagenicity as induced by the plant have been revealed in various studies. The findings of the clinical trials are controversial in terms of side effects. While some studies revealed the beneficial effects of the plant on the patients and no severe adverse effects, some others have reported serious side effects including abdominal pain, angioedema, dyspnea, nausea, pruritus, rash, erythema, and urticaria. Other biological activities of the plant such as antioxidant, antibacterial, antiviral, and larvicidal activities have been reported in previous experimental studies. Different classes of secondary metabolites of the plant such as alkamides, caffeic acid derivatives, polysaccharides, and glycoproteins are believed to be biologically and pharmacologically active. Actually, concurrent determination and single analysis of cichoric acid and alkamides have been successfully developed mainly by using high-performance liquid chromatography (HPLC) coupled with different detectors including UV spectrophotometric, coulometric electrochemical, and electrospray ionization mass spectrometric detectors. The results of the studies which were controversial revealed that in spite of major experiments successfully accomplished using E. purpurea, many questions remain unanswered and future investigations may aim for complete recognition of the plant's mechanism of action using new, complementary methods.
Keywords: Analysis methods, anti-inflammatory, clinical trial, cytotoxic, Echinacea purpurea, immunomodulatory, psychotic
|How to cite this article:|
Manayi A, Vazirian M, Saeidnia S. Echinacea purpurea: Pharmacology, phytochemistry and analysis methods. Phcog Rev 2015;9:63-72
| Introduction|| |
Echinacea purpurea (L.) Moench is one of the most important and well-known medicinal plants in the world, belonging to the Asteraceae (Compositae) family. The plant is the most widely cultivated medicinal plant in this species,  which has been mainly used in chemo-preventive and chemotherapy for infectious diseases in both upper and lower respiratory systems. , This species has been traditionally employed for the treatment of toothache, bowel pain, snake bite, skin disorders, seizure, chronic arthritis, and cancer.  Although the isolation and structural elucidation of its main compounds have been noticed by investigators, there is no affirmation about its mechanism of action. Alkamides, caffeic acid derivatives, and polysaccharides have been considered important constituents of the plant. A number of studies revealed that alkamides are involved in the immunomodulatory properties of Echinacea extracts in vitro and in vivo., Additionally, caffeic acid is found in some species of Echinacea and could be applied toward authentication and quality control of the plant extracts. The polysaccharides play an important role in the anti-inflammatory effect of Echinacea preparations.  Taxonomic, chemical, pharmacological, and clinical characteristics of some species of the Echinacea genus including E. angustifolia, E. pallida, and E. purpurea were reviewed in previous papers. , Medicinal properties of the plant were also considered in a review paper, which suggested that more research is required for more definitive medicinal recommendations.  This paper is a review about E. purpurea: Its phytochemical contents and its pharmacological and biological activities, along with common methods of plant extract analysis. In addition, the psychoactive and mosquitocidal effects of the plant are mentioned in this paper.
| Pharmacological activity|| |
The immunostimulant activity of the plant or its preparations is caused by three mechanisms: Phagocytosis activation, fibroblast stimulation, and the enhancement of respiratory activity that results in augmentation of leukocyte mobility.  There are numerous in vivo studies on the immunomodulatory and anti-inflammatory effects of E. purpurea that suggest that innate immunity is enhanced by administration of the plant and that the immune system is strengthened against pathogenic infections through activation of the neutrophils, macrophages, polymorphonuclear leukocytes (PMN), and natural killer (NK) cells.  For this reason, it can be suitable for prevention against and treatment of various infectious diseases such as infections of the upper and lower respiratory systems, wound infections, and chronic pelvic infections. , The complex chemical composition of the roots and herbs of Echinacea involves alkamides [Figure 1], ketoalkenes, caffeic acid derivatives, polysaccharides, and glycoproteins, which are believed to be responsible for noted immunostimulatory and anti-inflammatory activities.  Moreover, alkamides are demonstrated to be effective on cannabinoid receptor type 2 (CB2), and this is considered as a possible mechanism of their immunomodulatory properties. ,, Their possible molecular mechanism could be the increase of cyclic adenosine monophosphate (cAMP), p38 mitogen-activated protein kinases (p38/MAPK), and c-Jun N-terminal kinases (JNK) signaling, as well as nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), activating transcription factor 2/cAMP responsive element binding protein 1 (ATF-2/CREB-1) in primary human monocytes and macrophages.  Another study showed that N-alkamides from a root and herb tincture induce synergistic activity on CB2 and ultimately lead to immunomodulatory effects along with the superstimulation of interleukin-10 (IL-10) and the inhibition of tumor necrosis factor (TNF-α) in vitro.  They are also able to inhibit both cyclooxygenase enzymes (COX-1 and COX-2) and 5-lipoxygenase (F-LO), causing the inhibition of NK cells and anti-inflammatory activity.  The administration of the alkamide fraction of the plant in healthy rats, stimulated with bacterial lipopolysaccharide (LPS), caused a dose-dependent enhancement in nitric oxide (NO) and TNF-α release from alveolar macrophages as well as phagocytic activity. The mentioned effects may contribute to produce the first immune response mediators and to antiviral activity. However, different doses of alkamides, cichoric acid, and polysaccharides did not impact the release of TNF-α, interferon gamma (IFNg), or IL-2 by splenocytes.  Additionally, E. purpurea is reported to stimulate the NO response of peritoneal exudate cells (PEC) to LPS 2-4 times higher compared to the control in Swiss mice.  Moreover, alkamides diffuse through Caco-2 monolayers and their diffusion is not affected by the presence of other constituents.  They are also characterized after oral administration of the plant using liquid chromatography-tandem mass spectrometry (LC-MS/MS) in the blood stream. , Alkamides in lozenges made from E. purpurea have been rapidly absorbed through the buccal and esophageal membranes in six healthy volunteers. All the doses significantly decreased proinflammatory cytokines including IL-12p70, IL-8, IL-6, and TNF-α. It seems that this effect is independent of the alkamide doses, suggesting synergistic effects of the plant compounds.  Some pharmacological activities of alkamides are summarized in [Figure 2].
|Figure 1: Chemical structure of some secondary metabolites of E. purpurea|
Click here to view
|Figure 2: Schematic profile of some biological and pharmacological activities of alkamides isolated from E. purpurea. BM = Bone marrow, CB = Cannabinoid receptor, CNS = Central nervous system, COX = Cyclooxygenase enzyme, IL-10 = Interleukin-10, MP = Macrophage, NK = Natural killer cells, NO = Nitric oxide, TNF-α = Tumor necrosis Factor-α|
Click here to view
Another important type of bioactive compound of this plant is polysaccharides, which have been reported to increase production of interleukin-1 (IL-1), interleukin-6 (IL-6), and TNF-α by macrophage, along with the enhancement of their phagocytosis, microbicidal activity (both in vitro and in vivo), and the production and secretion of cerebrospinal fluids (CSFs). ,,, The results of some studies revealed that polysaccharides from E. purpurea cell culture are able to provide protection against Listeria monocytogenes and Candida albicans, mainly through macrophages and PMN) in normal mice.  Moreover, a polysaccharide treatment of immune-deficient mice by cyclophosphamide or cyclosporin A made them resistant toward L. monocytogenes and C. albicans, which are macrophage- and granulocyte-dependent infections, respectively. They also enhanced cytotoxicity against WEHI 164 tumor cells in macrophages in vitro, along with increasing the number of leukocytes and neutrophil granulocytes in immune-deficient mice.  It has been demonstrated that the oral administration of the root extract of E. purpurea increases the NK cells in normal, leukemic, and aging mice as well as neutrophils and eosinophils in rabbits. , The effects of both a polysaccharide-rich aqueous extract (of root) and an alkamide-rich ethanolic extract (of leaf) were assessed on dendritic cells (DCs). Investigation of the effects of the plant on DCs is important, since these cells play a role in both innate and adaptive immunity. The results of this investigation revealed that alkamides may suppress the function of DCs of murines; however, polysaccharides in the aqueous extract may activate DCs.  It is revealed that the expression of CD83 marker a marker of DC maturation, is significantly enhanced by flower and root extracts of the plant, while stem and leaf extracts can greatly decrease CD83 levels. Moreover, the extracts from root and aerial parts of the plant are reported to play a role in up- and down-regulation of insulin-like growth factor 1 receptor (IGF1R), respectively. In addition, the root extract can up-regulate some genes involved in immune cell activation or function including: Chemokine (C-C motif) ligand 4 (CCL4); interleukin-7 receptor (IL7R); nuclear factor of activated T-cells, cytoplasmic 2 (NFATC2); T-box transcription factor (TBX21); cytohesin-interacting protein (PSCDBP); integrin, alpha E (ITGAE); and intercellular adhesion molecule-1 (ICAM1), while CD34 and integrin beta-1 (ITGB1) were down-regulated by aerial part extract in DCs. It is implied that aerial parts of the plant except flowers decrease the adhesion, chemotaxis, and activation function of specific immune cell types such as DCs. Down-regulation of other immunomodulatory genes such as: Signal transducers and activators of transcription (STAT); tumor necrosis factor ligand superfamily, member 6 (FASLG); β2-microglobulin; elongation factor; proto-oncogene protein Wnt-1 (WNT1); and transcription factor ETV5 was observed with the root extract. The augmentation of gene expression by root extract can be attributed to the higher content of alkamides in it compared to extract of the aerial parts. 
When the plant root powder was administered to the male rats (in two doses: 30 and 100 mg/kg, for 3 and 15 days, respectively, to prolactin secretion), regulation of the immune system was observed. The low dose for 3 days did not affect prolactin secretion, while the higher dose for 15 days significantly inhibited prolactin secretion. A possible mechanism for this activity may be attributed to dopaminergic activity of the plant and/or structural similarity between chlorogenic acid and dopamine.  The activity of the combined preparation of E. purpurea and Glycyrrhiza glabra has been examined both in vitro and in vivo, and the results suggested that this mixture has a potential of synergic effects on immunostimulation, unlike the single plant therapy. 
Arabinogalactan-proteins from the suspension culture of E. purpurea did not influence the proliferation of mouse lymphocytes and only showed low activity on nitrite- and IL6 production in alveolar mouse macrophage culture and in the immunoglobulin M (IgM) production of mouse lymphocytes.  The root extract of the plant enhances NK cell numbers by increasing their production at the site of bone generation, causing an increase in their numbers in the spleen and also an increase in their antitumor and cytolytic functions in the aged mice.  Treatment with E. purpurea caused a significant increase in monocytes, neutrophils, and white blood cells (WBC) as well as in total protein and gamma globulin in rats. Besides, the plant extract and levamisole showed synergistic effects on phagocytic activity, and on monocyte and gamma globulin levels. 
The Echinacea preparation, interestingly, has reversed the inflammation caused by some bacteria in a culture of epithelial cells by reducing cytokines.  Carrageenan-induced paw edema in experimental animals is a test for the evaluation of anti-inflammatory effects of plants extracts.  Dried root powder of the plant, administered to the mice (30-100 mg/kg), inhibited carrageenan-induced paw edema similar to indomethacin.  This effect may be attributed to the inhibition of COX-1 and to a lesser extent COX-2 by alkamides.  Also, it is reported that the ethanol extracts of both aerial parts and roots of the plant have inhibited fibroblast-induced collagen concentration.  The effects of Echinacea and some of its compounds on NF-κB expression by Jurkat cells (a human T-cell line) were assessed in the presence and absence of stimulation by LPS and phorbol 12-myristate 13-acetate (PMA). NF-κB is a nuclear transcription factor stimulating the expression of some genes such as key factors of inflammation, e.g., TNF-α, IL-1, chemokines, adhesion molecules, and COX-2. In the absence of stimulants, all root extracts and compounds did not show a significant effect on NF-κB expression. In fact, LPS decreased NF-κB expression, while this effect was significantly reversed in the presence of root extracts, cichoric acid, and the alkamides fractions. Cichoric acid and a 2,4-diene alkamide are demonstrated to significantly increase NF-κB levels, while a 2-ene alkamide caused a significant inhibition, indicating considerable diversity in the bioactivity of this plant. 
The anxiolytic activity of Echinacea drugs was determined in experimental animals with lower doses than those used in traditional indications.  Alkamides of Echinacea have been reported to have cannabinomimetic properties on both cannabinoid CB1 and CB2 receptors, which may be attributed to their structural similarity to the endogenous cannabinoid receptor ligand anandamide.  Anandamide's effects are mediated in the brain and periphery by CB1 and CB2 receptors. The activation of the former with endogenous ligands plays a considerable role in controlling anxiety and the latter is mainly involved in immune system activities.  Plants rich in alkamides induce paresthesia and were applied by Native Americans traditionally and also by physicians in the early 20 th century as a sialogogue, an antitussive, and a remedy for toothache. , The slight differences in the structures of the alkamides revealed significant differences in CB receptor activity, for instance the replacement of isobutylamide moiety of the dodeca-2E,4E,8Z,10Z/E-tetraenoic acid isobutylamide for 2-methylbutylamide moiety turned the G-protein stimulation property from inverse agonist to partial agonist.  However, the extracts of E.purpurea were not active in the antiacetylcholinesterase (antiAChE) assay.  The plant tincture increased the stimulation effect of L-3,4-dihydroxyphenylalanine (L-DOPA) and showed antidepressant activity in the clofelin-induced depression test in white rats. 
The extract of the flowers and cichoric acid inhibited both the human colon cancer cell lines Caco-2 and HCT-116 in a dose dependent manner after 48 h. Cichoric acid has decreased telomerase activity in HCT-116 cell line, which could be assumed as the molecular mechanism of apoptosis indication.  Moreover, an n-hexane extract of the plant root obtained from three Echinacea species showed potential anticancer activity. 
The extract of E. purpurea flower did not exhibit mutagenicity against Salmonella typhimurium TA98 and TA100 with or without the S9 fraction. It also showed a dose-dependent inhibition against the mutagenicity of 2-aminoantheracene, therefore it could be a good antimutagenic agent.  High concentrations of the plant (8 mg/ml) reduced sperm motility and sperm penetration of hamster oocytes attributed to sperm DNA denaturation, while these effects were not observed by administrating low concentrations. ,
Generally, animal studies of various preparations of Echinacea species have shown low toxicity.  In a study of acute toxicity, LD50 value was calculated as 2500 mg/kg in an intraperitoneal injection of the polysaccharide fraction of the plant in female mice.  In other studies, the LD50 values of oral and intravenous administration of the plant juice evaluated more than 30 g/kg and 10 g/kg in mice, and 15 g/kg and 5 g/kg in rats, respectively. ,
The findings of clinical trials of the plant preparation are controversial. The results of a randomized blinded trial revealed no significant difference in the incidence and severity of colds and respiratory infection between Echinacea and placebo groups in 108 patients during 8 weeks of administration of the plant juice. Only a small decrease for the total lymphocyte counts was found, which may have occurred by chance rather than because of a true effect of the plant juice or placebo.  On the other hand, the results of a study showed that preparations of E. purpurea had a beneficial effect on adults with cold symptoms in clinical trials, especially in comparison to placebo, if the treatment is begun early. ,
In several clinical studies, the frequency of adverse effects in the Echinacea group and control group were similar and not statistically significant, while in some studies, rash and gastrointestinal symptoms were reported from the Echinacea group. Some adverse effects were also reported by the UK Committee on Safety of Medicines and the Medicines and Healthcare Products Regulatory Agency's spontaneous reporting scheme (the "yellow card" scheme), commonly including abdominal pain, angioedema, dyspnea, nausea, pruritus, rash, erythema, and urticaria. 
The Echinacea preparations are contraindicated in some patients including those with progressive systemic diseases such as tuberculosis, leukemia and leukemia-like diseases, collagen disorders, multiple sclerosis, and other autoimmune diseases.  Some Echinacea products are also contraindicated in AIDS and HIV infections. These statements are based on the theory of immunumodulatory activity of Echinacea, although there is an opposing idea that these products are not harmful in patients with autoimmune diseases.  There are no clinical data available supporting the mentioned views, but it is recommended to avoid these preparations in immune-related diseases.  The preparations of Echinacea should be administered with caution concomitantly with immunosuppressant drugs.  Effects of some preparations made from the root and herb of E. purpurea along with cichoric acid were tested on the human drug-metabolizing enzyme cytochrome P450 3A4 (CYP3A4). The results indicated that the preparations moderately inhibited the enzyme, while cichoric acid showed low inhibition activity.  The findings of a study of healthy nonsmoking volunteers showed that the plant root remedy inhibited cytochrome P450 1A2 (CYP1A2) and intestinal CYP3A4 but not cytochrome P450 2C9 (CYP2C9) or cytochrome P450 2D6 (CYP2D6), whereas induced hepatic CYP3A4 activity. The selective effects of the plant on CYP3A4 activity may be explained by several mechanisms: The constituents of the plant, that are responsible for CYP3A4 inhibition are not systematically available; the constituents that are responsible for CYP3A4 induction may rapidly be absorbed, leading to a lack of intestinal CYP3A4 induction; hepatic CYP3A4 induction may occur by the metabolites of the plant, or the CYP3A4 induction may involve tissue activators that are influenced by constituents of the plant.  Additionally, the plant inhibited metabolism of testosterone by CYP3A4 via nicotinamide adenine dinucleotide phosphate (NADPH)-dependent reaction. 
| Biological activity|| |
In some studies, radical-scavenging activities of the plant extracts were tested. , For this plant, antioxidant activity compared with the alkamides and cichoric acid that are the characteristic compounds of Echinacea. The free radical-scavenging activity of the extracts was related to their cichoric acid contents, while alkamides were inactive against free radicals. , Although in some studies it was revealed that the extract of the plant did not show any antioxidant property,  other investigations of the root extract of the plant revealed antioxidant activity,  which may be attributed to the phenolic contents and cichoric acid in the plant.  Cichoric acid shows an efficient radical-scavenging activity toward 2,2-diphenyl-1-picrylhydrazyl (DPPH), comparable to flavonoids and rosmarinic acid. Although alkamides have not exhibited antioxidant activity, they are able to increase the activity of cichoric acid through two mechanisms: First, surface activity that enables cichoric acid to have better access to inhibit lipid oxidation in the lipophilic droplets of emulsion, and second, regeneration of cichoric acid by donating allylic hydrogen to the one-electron oxidized cichoric acid. ,
Antibacterial and antifungal activity
The extract of E. purpurea considerably inhibited growth of Candida albicans and Saccharomyces cerevisiae, but no inhibition zone was observed for Aspergillus niger. The extract obtained by classical method showed higher antimicrobial activity in comparison with those obtained by ultrasound-assisted extraction.  In another study, three pathogens Streptococcus pyogenes, Haemophilus influenzae, and Legionella pneumophila were sensitive to the preparation of the plant, although Acinetobacter baumannii, Bacillus cereus, Bacillus subtilis, Enterococcus faecalis (vancomycin-resistant), Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa were relatively resistant to the drug, while two fungi organisms, C. albicans and Trichoderma viride, were essentially resistant to the preparation.  The hexane extract of the root inhibited both yeasts S. cerevisiae and C. albicans. Additionally, 1-Tridecene-3, 5, 7, 9, 11-pentayne, a polyacetylenic compound from root of the plant has showed light-mediated inhibition toward S. cerevisiae. 
The aqueous extract of E. purpurea were active against acyclovir-susceptible and acyclovir-resistant strains of both herpes simplex virus 1 (HSV-1) and herpes simplex virus 2 (HSV-2) in vitro,  whereas the hexane extract of the plant root and cichoric acid inhibited HSV-1.  In addition, cichoric acid inhibited human immunodeficiency virus type 1 (HIV-1) integrase. , Mouse embryonic fibroblasts incubating with the plant juice and alcoholic root extract were resistant to influenza A2, herpes, and vesicular stomatitis virus infection for 24 h.  The standard preparation of the plant showed strong inhibition against the influenza viruses A/Victoria/75 (H3N2) and A/Puerto Rico/8/1934 (H1N1), avian strains A/Thailand/1(KAN-1)/2004 (H5N1) and A/FPV/Dutch/1927 (H7N7), and the pandemic novel swine-origin influenza A (S-OIV) (H1N1) in direct contact. Moreover, the results of hemagglutination (HA) assays indicated that the preparation inhibited HA activity and could therefore block entry of a virus into treated cells.  The administration of a polysaccharide extract of the plant to infected mice with influenza A H1N1 (A/WSN/33) caused weight loss, but similar pulmonary viral titers were observed in comparison with untreated mice. Lower systemic and pulmonary keratinocyte chemoattract (KC) and interleukin 10 (IL-10) levels, and systemic levels of IFNg were observed in treated mice, indicating that E. purpurea could modulate the clinical symptoms of influenza by altering cytokines.  Based on the results of the two latter studies, it seems that different components of the plant have beneficial effects on influenza patients through different mechanisms.
Purified alkamides from E. purpurea show mosquitocidal activity against Aedes aegypti larvae. The alkamides with isobutylamide moiety show stronger mosquitocidal activity compared to those with 2-methylbutylamide moiety, suggesting that isobutyl plays a role in the mosquitocidal property of alkamides. ,
Various compounds belonging to different classes of secondary metabolites have been isolated and identified in E. purpurea extract. Alkamides, caffeic acid derivatives, and polysaccharides are the three major groups of secondary metabolites in the plant, which have been considered mostly in manuscripts [Figure 1]. In one study, 10 alkamides, mostly with isobutylamide and 2-methylbutylamide moieties, have been successfully purified from the n-hexane extract of the plant root.  Purification of the chloroform extract of the plant root also has resulted in the purification of some alkamides with isobutylamide and 2-methylbutylamide moieties and nitidanin-diisovalerianate as well as a sequesterpene, 1β-hydroxy-4 (15),5E,10 (14)-germacratriene, using chromatographic methods.  Isolated alkamides (with isobutylamides) mostly contained 2,4-dienoic units in their structures.  The results of a high-performance liquid chromatography-diode array detector-mass spectrometry (HPLC-DAD-MS) analysis of the roots and aerial parts of the plant showed that the storage conditions and methods of the extraction can significantly influence the contents of cichoric acid and alkamide derivatives.  Contents of alkamides and cichoric acid in E. purpurea (root and aerial parts) have been analyzed in different samples, and the results showed that high-quality root contains more than 6 mg/g alkamides, while cichoric acid content for root and aerial parts was evaluated as more than 15 mg/g. The aerial parts of the plant usually cannot be considered as a source of alkamides. For marketing, a minimum standard level could be assumed as > 3 mg/g for alkamides and > 5 mg/g for cichoric acid.  Polysaccharides and polyacetylenes along with glycoproteins were also purified from the aerial parts of the plant as well.  The juice of the plant contains heterogeneous polysaccharides (MW < 10 kDa), inulin-type fractions (MW = 6 kDa) and acidic highly branched arabinogalactan polysaccharide (MW = 70 kDa). Arabinogalactan-protein isolated from the aerial parts of the plant is composed of 83% polysaccharide (galactose/arabinose), 4-5% uronic acids, and 7% protein, with high concentrations of serine and hydroxyproline. , Other compounds including alkaloids, amides, and flavonoids (quercetin, kaempferol, isorhamnetin and their free phenolic acids including p-coumaric, p-hydroxybenzoic, and protocatechuic acids) have also been isolated and identified from the plant. ,
| Analysis methods of the echinacea extract|| |
Alkamides have been analyzed with reverse-phase HPLC coupled with different detectors including UV spectrophotometric, coulometric electrochemical, and electrospray ionization mass spectrometric. , Furthermore, caffeic acid derivatives have been determined using reverse-phase HPLC or capillary electrophoresis (CE) with photodiode array (FDA) UV spectrophotometric detection. ,, Phenolic acids were analyzed by micellar benzoic acid electrokinetic chromatography (MEKC), both charged and uncharged analytes, based on the use of sodium deoxycholate (SDC), a surfactant in borate buffer (pH 9.2), as well as in the E. purpurea extract.  However, determination methods for both caffeic acid derivatives and alkamides have been developed in single analysis. Although it is a difficult process to separate these diverse constituents in one analysis, methods for the concurrent determination of caffeic acid derivatives and alkamides have the advantages of reduced time and sample size needed for the analysis.  Gradient elution on reverse-phase HPLC has been employed for concurrent analysis of caffeic acid derivatives and alkamides from E. purpurea using various detectors such as FDA UV spectrophotometric and electrospray ionization mass spectrometry (EIMS). , Simultaneous analysis of both mentioned derivatives has also been performed by electrophoresis with FDA UV spectrophotometric detector, together with sodium dodecyl sulfate and hydroxypropyl-β-cyclodextrin in Britton Robinson buffer (10 mM, pH 8.0). 
| Discussion|| |
Echinacea purpurea has a worldwide reputation for its immunomodulatory and anti-inflammatory properties, capable of modulating of various immune system pathways. There are different classes of secondary metabolites of the plant showing immunostimulatory activity, such as alkamides, caffeic acid derivatives, polysaccharides, and glycoproteins.  Among the above, alkamides have been noticed in many studies, since they are absorbed through intestinal, buccal, and esophageal membranes. ,,, Alkamides' binding with CB1 and CB2 has been considered the possible mechanisms for their immunomodulatory and psychoactive activities, respectively. ,,,, They increase NF-κB, which regulates the expression of critical genes in innate immune responses and is strongly linked with apoptosis regulation. ,, It seems that in the absence of a stimulant (e.g. injury, stress, LPS, viral and microbial pathogens, cytokines and growth factors), the root extract and its compounds have no effect on NF-κB expression. ,, Based on the results of various experiments, the plant extract and its compounds activate the main players of innate immunity like macrophages, neutrophils, and DCs. ,,,
The plant and its compounds have shown different effects in various studies. For instance, alkamides could enhance TNF-α release from alveolar macrophages but have showed no effect on TNF-α in splenocytes,  while lozenges of E. purpurea decreased TNF-α and IL-6 in six healthy volunteers.  However, polysaccharides of the plant could increase production of IL-1, IL-6, and TNF-α by macrophage.  The plant extract (in high concentration; 8 mg/ml) also showed potential anticancer activity and antimutagenicity but caused reduction in sperm motility and sperm penetration, in vitro. ,,,, The beneficial effect of the plant preparations for patients with cold symptoms remains debatable, as the results of different studies are not entirely in agreement. ,, Preparations of E. purpurea are contraindicated in autoimmune diseases like HIV infection, and AIDS, but these overviews have not been supported by clinical data. ,, Cichoric acid has been considered a major antioxidant agent in the plant, whose activity is strengthened with the presence of alkamides. , Antibacterial and antiviral activities of the plant, especially against influenza viruses, and its larvicidal activity have been reported, too. ,,,
Alkamides of E. purpurea are mostly purified from nonpolar extracts and they are mainly concentrated in the root of the plant. Aerial parts of the plant are usually not considered a source of alkamides. As can be seen in [Figure 1], their structures contain some ethylenic and/or acetylenic bonds with an amide part, which has anisobutylamide or a 2-methylbutylamide moiety. , The polar extracts of the plant usually contain more polar metabolites, including polysaccharides and glycoproteins. , Other compounds like cichoric acid, alkaloids, flavonoids, phenolic acids, and amides have also been isolated from the plant ., As alkamides and caffeic acid derivatives have been considered the main and particular secondary metabolites of the plant, different methods have been employed for concurrent or separate analysis of them, such as HPLC. ,,
The results of the studies.which were controversial suggested that in spite of many successfully completed experiments on E. purpurea, many questions remain unanswered regarding beneficial effects of the plant in relieving cold symptoms and how the plant and its compounds stimulate the immune system. The results of a review paper, which focused on common cold treatment with Echinacea to assess essential factors of experimental design, indicated that most of the studies reporting positive effects of the plant preparation for use in cases of common cold failed to meet the criteria of experimental design.  In particular, there are some more important questions, such as "How does the plant differentially affect NF-κB, TNF-α, and IL-6 in the various functional cells?" and "When are these effects helpful in the body during treatment?"  Prominent concerns for future investigations should be the complete recognition of the plant's mechanisms of action, using new complementary methods, which could be essential for promoting the rational use of the plant as well as providing leads for new drugs.
| References|| |
McKeown KA. A review of the taxonomy of the genus Echinacea
. In: Janick J, editor Perspectives on new crops and new uses. Alexandria, VA: ASHS Press; 1999. p. 482-98.
Grimm W, Muller HH. A randomized controlled trial of the effect of fluid extract of Echinacea purpurea
on the incidence and severity of colds and respiratory infections. Am J Med 1999;106:138-43.
Patel T, Crouch A, Dowless K, Freier D. 122. Acute effects of oral administration of a glycerol extract of Echinacea purpurea
on peritoneal exudate cells in female swiss mice. Brain Behav Immun 2008;22:39.
Goel V, Chang C, Slama JV, Barton R, Bauer R, Gahler R, et al
. Alkylamides of Echinacea purpurea
stimulate alveolar macrophage function in normal rats. Int Immunopharmacol 2002;2:381-7.
Gertsch J, Schoop R, Kuenzle U, Suter A. Echinacea
alkylamides modulate TNF-alpha gene expression via cannabinoid receptor CB2 and multiple signal transduction pathways. FEBS Lett 2004;577:563-9.
Laasonen M, Wennberg T, Harmia-Pulkkinen T, Vuorela H. Simultaneous analysis of alkamides and caffeic acid derivatives for the identification of Echinacea purpurea
, Echinacea angustifolia
, Echinacea pallida
and Parthenium integrifolium
roots. Planta Med 2002;68:572-4.
Barnes J, Anderson LA, Gibbons S, Phillipson JD. Echinacea
species (Echinacea angustifolia
(DC.) Hell., Echinacea pallida
(Nutt.) Nutt., Echinacea purpurea
(L.) Moench): A review of their chemistry, pharmacology and clinical properties. J Pharm Pharmacol 2005;57:929-54.
Barrett B. Medicinal properties of Echinacea
: A critical review. Phytomedicine 2003;10:66-86.
WHO monographs on selected medicinal plants. Geneva: World Health Organization; 1999. p. 136-45.
Raduner S, Majewska A, Chen JZ, Xie XQ, Hamon J, Faller B, et al
. Alkylamides from Echinacea
are a new class of cannabinomimetics. Cannabinoid type 2 receptor-dependent and -independent immunomodulatory effects. J Biol Chem 2006;281:14192-206.
Woelkart K, Bauer R. The role of alkamides as an active principle of Echinacea
. Planta Med 2007;73:615-23.
Chicca A, Raduner S, Pellati F, Strompen T, Altmann KH, Schoop R, et al
. Synergistic immunomopharmacological effects of N-alkylamides in Echinacea purpurea
herbal extracts. Int Immunopharmacol 2009;9:850-8.
Muller-Jakic B, Breu W, Pröbstle A, Redl K, Greger H, Bauer R. In vitro
inhibition of cyclooxygenase and 5-lipoxygenase by alkamides from Echinacea
species. Planta Med 1994;60:37-40.
Matthias A, Blanchfield JT, Penman KG, Toth I, Lang CS, De Voss JJ, et al
. Permeability studies of alkylamides and caffeic acid conjugates from Echinacea
using a Caco-2 cell monolayer model. J Clin Pharm Ther 2004;29:7-13.
Dietz B, Heilmann J, Bauer R. Absorption of dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides after oral application of Echinacea purpurea
tincture. Planta Med 2001;67:863-4.
Goey AK, Rosing H, Meijerman I, Sparidans RW, Schellens JH, Beijnen JH. The bioanalysis of the major Echinacea purpurea
constituents dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamides in human plasma using LC-MS/MS. J Chromatogr B Analyt Technol Biomed Life Sci 2012;902:151-6.
Guiotto P, Woelkart K, Grabnar I, Voinovich D, Perissutti B, Invernizzi S, et al
. Pharmacokinetics and immunomodulatory effects of phytotherapeutic lozenges (bonbons) with Echinacea purpurea
extract. Phytomedicine 2008;15:547-54.
Luettig B, Steinmüller C, Gifford GE, Wagner H, Lohmann-Matthes ML. Macrophage activation by the polysaccharide arabinogalactan isolated from plant cell cultures of Echinacea purpurea
. J Natl Cancer Inst 1989;81:669-75.
Burger RA, Torres AR, Warren RP, Caldwell VD, Hughes BG. Echinacea
-induced cytokine production by human macrophages. Int J Immunopharmacol 1997;19:371-9.
Wagner H, Stuppner H, Schäfer W, Zenk M. Immunologically active polysaccharides of Echinacea purpurea
cell cultures. Phytochemistry 1988;27:119-26.
Proksch A, Wagner H. Structural analysis of a 4-O-methyl-glucuronoarabinoxylan with immuno-stimulating activity from Echinacea purpurea
. Phytochemistry 1987;26:1989-93.
Roesler J, Steinmüller C, Kiderlen A, Emmendörffer A, Wagner H, Lohmann-Matthes ML. Application of purified polysaccharides from cell cultures of the plant Echinacea purpurea
to mice mediates protection against systemic infections with Listeria monocytogenes and Candida albicans. Int J Immunopharmacol 1991;13:27-37.
Steinmuller C, Roesler J, Gröttrup E, Franke G, Wagner H, Lohmann-Matthes ML. Polysaccharides isolated from plant cell cultures of Echinacea purpurea
enhance the resistance of immunosuppressed mice against systemic infections with Candida albicans
and Listeria monocytogenes. Int J Immunopharmacol 1993;15:605-14.
Dussault I, Miller SC. Stimulation of natural killer cell numbers but not function in leukemic infant mice: A system primed in infancy allows survival in adulthood. Nat Immun 1993;12:66-78.
Benson JM, Pokorny AJ, Rhule A, Wenner CA, Kandhi V, Cech NB, et al
. Echinacea purpurea
extracts modulate murine dendritic cell fate and function. Food Chem Toxicol 2010;48:1170-7.
Wang CY, Chiao MT, Yen PJ, Huang WC, Hou CC, Chien SC, et al
. Modulatory effects of Echinacea purpurea
extracts on human dendritic cells: A cell- and gene-based study. Genomics 2006;88:801-8.
Di Carlo G, Pacilio M, Capasso R, Di Carlo R. Effect on prolactin secretion of Echinacea purpurea
, hypericum perforatum and Eleutherococcus senticosus. Phytomedicine 2005;12:644-7.
Wagner H, Jurcic K. Immunological studies of Revitonil, a phytopharmaceutical containing Echinacea purpurea
and Glycyrrhiza glabra root extract. Phytomedicine 2002;9:390-7.
Classen B, Thude S, Blaschek W, Wack M, Bodinet C. Immunomodulatory effects of arabinogalactan-proteins from Baptisia and Echinacea
. Phytomedicine 2006;13:688-94.
Currier NL, Miller SC. Natural killer cells from aging mice treated with extracts from Echinacea purpurea
are quantitatively and functionally rejuvenated. Exp Gerontol 2000;35:627-39.
Sadigh-Eteghad S, Khayat-Nuri H, Abadi N, Ghavami S, Golabi M, Shanebandi D. Synergetic effects of oral administration of levamisole and Echinacea purpurea
on immune response in Wistar rat. Res Vet Sci 2011;91:82-5.
Sharma SM, Anderson M, Schoop SR, Hudson JB. Bactericidal and anti-inflammatory properties of a standardized Echinacea
extract (Echinaforce): Dual actions against respiratory bacteria. Phytomedicine 2010;17:563-8.
Vazirian M, Dianat S, Manayi A, Ziari R, Mousazadeh A, Habibi E, et al
. Anti-inflammatory effect, total polysaccharide, total phenolics content and antioxidant activity of the aqueous extract of three basidiomycetes. Res J Pharmacogn 2014;1:15-21.
Raso GM, Pacilio M, Di Carlo G, Esposito E, Pinto L, Meli R. In-vivo and in-vitro anti-inflammatory effect of Echinacea purpurea
and Hypericum perforatum. J Pharm Pharmacol 2002;54:1379-83.
Clifford LJ, Nair MG, Rana J, Dewitt DL. Bioactivity of alkamides isolated from Echinacea purpurea
(L.) Moench. Phytomedicine 2002;9:249-53.
Zoutewelle G, van Wijk R. Effects of Echinacea purpurea
extracts on fibroblast populated collagen lattice contraction. Phytother Res 1990;4:77-81.
Matthias A, Banbury L, Bone KM, Leach DN, Lehmann RP. Echinacea
alkylamides modulate induced immune responses in T-cells. Fitoterapia 2008;79:53-8.
Haller J, Hohmann J, Freund TF. The effect of Echinacea
preparations in three laboratory tests of anxiety: Comparison with chlordiazepoxide. Phytother Res 2010;24:1605-13.
Woelkart K, Xu W, Pei Y, Makriyannis A, Picone RP, Bauer R. The endocannabinoid system as a target for alkamides from Echinacea angustifolia
roots. Planta Med 2005;71:701-5.
Pacher P, Bátkai S, Kunos G. The endocannabinoid system as an emerging target of pharmacotherapy. Pharmacol Rev 2006;58:389-462.
Greger H. Alkamides: Structural relationships, distribution and biological activity. Planta Med 1984;50:366-75.
Moerman DE. Native American ethnobotany. Portland: Timber Press; 1998. p. 205-6.
Hohmann J, Rédei D, Forgo P, Szabó P, Freund TF, Haller J, et al
. Alkamides and a neolignan from purpurea
roots and the interaction of alkamides with G-protein-coupled cannabinoid receptors. Phytochemistry 2011;72:1848-53.
Orhan I, Senol FS, Gülpinar AR, Kartal M, Sekeroglu N, Deveci M, et al
. Acetylcholinesterase inhibitory and antioxidant properties of Cyclotrichium niveum
, Thymus praecox
subsp. caucasicus var
, Echinacea purpurea
and E. pallida. Food Chem Toxicol 2009;47:1304-10.
Kurkin VA, Dubishchev AV, Ezhkov VN, Titova IN, Avdeeva EV. Antidepressant activity of some phytopharmaceuticals and phenylpropanoids. Pharm Chem J 2006;40:614-9.
Tsai YL, Chiu CC, Yi-Fu Chen J, Chan KC, Lin SD. Cytotoxic effects of Echinacea purpurea
flower extracts and cichoric acid on human colon cancer cells through induction of apoptosis. J Ethnopharmacol 2012;143:914-9.
Chicca A, Adinolfi B, Martinotti E, Fogli S, Breschi MC, Pellati F, et al
. Cytotoxic effects of Echinacea
root hexanic extracts on human cancer cell lines. J Ethnopharmacol 2007;110:148-53.
Tsai YL, Chiou SY, Chan KC, Sung JM, Lin SD. Caffeic acid derivatives, total phenols, antioxidant and antimutagenic activities of Echinacea purpurea
flower extracts. LWT-Food Sci Technol 2012;46:169-76.
Ondrizek RR, Chan PJ, Patton WC, King A. Inhibition of human sperm motility by specific herbs used in alternative medicine. J Assist Reprod Genet 1999;16:87-91.
Ondrizek RR, Chan PJ, Patton WC, King A. An alternative medicine study of herbal effects on the penetration of zona-free hamster oocytes and the integrity of sperm deoxyribonucleic acid. Fertil Steril 1999;71:517-22.
Lenk W. Acute toxicity of various polysaccharides from Echinacea purpurea
in the mouse. Z Phytother 1989;10:49-51.
Mengs U, Clare CB, Poiley JA. Toxicity of Echinacea purpurea
. Acute, subacute and genotoxicity studies. Arzneimittelforschung 1991;41:1076-81.
Mengs U, Leuschner J, Marshall RR. Toxicity studies with Echinacin-Third international conference on phytomedicine. Munich, Germany, October 11-13. Phytomedicine [Suppl] 2000;2:32.
Schwarz E, Parlesak A, Henneicke-von Zepelin HH, Bode JC, Bode C. Effect of oral administration of freshly pressed juice of Echinacea purpurea
on the number of various subpopulations of B- and T-lymphocytes in healthy volunteers: Results of a double-blind, placebo-controlled cross-over study. Phytomedicine 2005;12:625-31.
Woelkart K, Linde K, Bauer R. Echinacea
for preventing and treating the common cold. Planta Med 2008;74:633-7.
Brinkeborn RM, Shah DV, Degenring FH. Echinaforce and other Echinacea
fresh plant preparations in the treatment of the common cold. A randomized, placebo controlled, double-blind clinical trial. Phytomedicine 1999;6:1-6.
Schulz V, Hansel R, Tyler VE. Rational phytotherapy: A Physicians' Guide to Herbal Medicin. Berlin, Germany: Springer-Verlag; 2000. p. 182.
Mills S, Bone K. Principles and practice of phytotherapy. Edinburgh: Churchill Livingstone; 2000. p. 22-79.
Budzinski JW, Foster BC, Vandenhoek S, Arnason JT. An in vitro
evaluation of human cytochrome P450 3A4 inhibition by selected commercial herbal extracts and tinctures. Phytomedicine 2000;7:273-82.
Gorski JC, Huang SM, Pinto A, Hamman MA, Hilligoss JK, Zaheer NA, et al
. The effect of Echinacea
root) on cytochrome P450 activity in vivo. Clin Pharmacol Ther 2004;75:89-100.
Schroder-Aasen T, Nilsen OG. Inhibitory mechanisms on CYP3A4 by the herbal medicine Echinacea purpurea
. Toxicol Lett 2011;205:S176.
Manayi A, Khanavi M, Saiednia S, Azizi E, Mahmoodpour MR, Vafi F, et al
. Biological activity and microscopic characterization of Lythrum salicaria L. Daru 2013;21:61.
Manayi A, Mirnezami T, Saeidnia S, Ajani Y. Pharmacognostical evaluation, phytochemical analysis and antioxidant activity of the roots of Achillea
tenuifolia LAM. Pharmacogn J 2012;4:14-9.
Thygesen L, Thulin J, Mortensen A, Skibsted LH, Molgaard P. Antioxidant activity of cichoric acid and alkamides from Echinacea purpurea
, alone and in combination. Food Chem 2007;101:74-81.
Pietta P, Simonetti P, Mauri P. Antioxidant activity of selected medicinal plants. J Agric Food Chem 1998;46:4487-90.
Hu C, Kitts DD. Studies on the antioxidant activity of Echinacea
root extract. J Agric Food Chem 2000;48:1466-72.
Becker EM, Nissen L, Skibsted LH. Antioxidant evaluation protocols: Food quality or health effects. Europ Food Res Technol 2004;219:561-71.
Stojicevic S, Stanisavljevic A, Velickovic D, Veljkovic V, Lazic M. Antioxidant and antimicrobial activities of Echinacea
L.) extracts obtained by classical and ulterasound extraction. Chin J Chem Eng 2009;17:478-83.
Binns SE, Purgina B, Bergeron C, Smith ML, Ball L, Baum BR, et al
. Light-mediated antifungal activity of Echinacea
extracts. Planta Med 2000;66:241-4.
Thompson KD. Antiviral activity of viracea against acyclovir susceptible and acyclovir resistant strains of herpes simplex
virus. Antiviral Res 1998;39:55-61.
Binns SE, Hudson J, Merali S, Arnason JT. Antiviral activity of characterized extracts from Echinacea
spp. (Heliantheae: Asteraceae) against Herpes simplex
virus (HSV-I). Planta Med 2002;68:780-3.
McDougall B, King PJ, Wu BW, Hostomsky Z, Reinecke MG, Robinson WE Jr. Dicaffeoylquinic and dicaffeoyltartaric acids are selective inhibitors of human immunodeficiency virus type 1 integrase. Antimicrob Agents Chemother 1998;42:140-6.
Robinson WE Jr. L-chicoric acid, an inhibitor of human immunodeficiency virus type 1 (HIV-1) integrase, improves on the in vitro
anti-HIV-1 effect of Zidovudine plus a protease inhibitor (AG1350). Antiviral Res 1998;39:101-11.
Wacker A, Hilbig W. Virus-inhibition by Echinacea purpurea
(author's transl). Planta Med 1978;33:89-102.
Pleschka S, Stein M, Schoop R, Hudson JB. Anti-viral properties and mode of action of standardized Echinacea purpurea
extract against highly pathogenic avian influenza virus (H5N1, H7N7) and swine-origin H1N1 (S-OIV). Virol J 2009;6:197.
Fusco D, Liu X, Savage C, Taur Y, Xiao W, Kennelly E, et al
. Echinacea purpurea
aerial extract alters course of influenza infection in mice. Vaccine 2010;28:3956-62.
Saeidnia S, Gohari A, Mokhber-Dezfuli N, Kiuchi F. A review on phytochemistry and medicinal properties of the genus Achillea
. Daru 2011;19:173-86.
Bauer R, Remiger P, Wagner H. Alkamides from the roots of Echinacea purpurea
. Phytochemistry 1988;27:2339-42.
Luo XB, Chen B, Yao SZ, Zeng JG. Simultaneous analysis of caffeic acid derivatives and alkamides in roots and extracts of Echinacea purpurea
by high-performance liquid chromatography-photodiode array detection-electrospray mass spectrometry. J Chromatogr A 2003;986:73-81.
Wills RB, Stuart DL. Alkylamide and cichoric acid levels in Echinacea purpurea
grown in Australia. Food Chem 1999;67:385-8.
Classen B, Witthohn K, Blaschek W. Characterization of an arabinogalactan-protein isolated from pressed juice of Echinacea purpurea
by precipitation with the beta-glucosyl Yariv reagent. Carbohydr Res 2000;327:497-504.
Bohlmann F, Hoffmann H. Further amides from Echinacea purpurea
. Phytochemistry 1983;22:1173-5.
Spelman K, Wetschler MH, Cech NB. Comparison of alkylamide yield in ethanolic extracts prepared from fresh versus dry Echinacea purpurea
utilizing HPLC-ESI-MS. J Pharm Biomed Anal 2009;49:1141-9.
He X, Lin L, Bernart MW, Lian L. Analysis of alkamides in roots and achenes of Echinacea purpurea
by liquidmass spectrometry. J Chromatogr A 1998;815:205-11.
Cech NB, Eleazer MS, Shoffner LT, Crosswhite MR, Davis AC, Mortenson AM. High performance liquid chromatography/electrospray ionization mass spectrometry for simultaneous analysis of alkamides and caffeic acid derivatives from Echinacea purpurea
extracts. J Chromatogr A 2006;1103:219-28.
Mancek B, Kreft S. Determination of cichoric acid content in dried press juice of purple coneflower (Echinacea purpurea
) with capillary electrophoresis. Talanta 2005;66:1094-7.
Brown PN, Chan M, Paley L, Betz JM. Determination of major phenolic compounds in Echinacea
spp. raw materials and finished products by high-performance liquid chromatography with ultraviolet detection: Single-laboratory validation matrix extension. J AOAC Int 2011;94:1400-10.
Pomponio R, Gotti R, Hudaib M, Cavrini V. Analysis of phenolic acids by micellar electrokinetic chromatography: Application to Echinacea purpurea
plant extracts. J Chromatogr A 2002;945:239-47.
Gotti R, Pomponio R, Bertucci C, Cavrini V. Simultaneous analysis of the lipophilic and hydrophilic markers of Echinacea
plant extracts by capillary electrophoresis. J Sep Sci 2002;25:1079-86.
Liang Y, Zhou Y, Shen P. NF-kappaB and its regulation on the immune system. Cell Mol Immunol 2004;1:343-50.
Baeuerle PA, Baltimore D. NF-kappa B: Ten years after. Cell 1996;87:13-20.
Pahl HL. Activators and target genes of Rel/NF-kappa B transcription factors. Oncogene 1999;18:6853-66.
Akira S. Toll-like receptor signaling. J Biol Chem 2003;278:38105-8.
Caruso TJ, Gwaltney JM Jr. Treatment of the common cold with Echinacea
: A structured review. Clin Infect Dis 2005;40:807-10.
Paul AT, Gohil VM, Bhutani KK. Modulating TNF-alpha signaling with natural products. Drug Discov Today 2006;11:725-32.
[Figure 1], [Figure 2]
|This article has been cited by|
||High Altitude Medicinal Plants Against Multidrug Resistant Microorganisms: Screening and Chemical Profiling of the Most Active Nepeta longibracteata
| ||Anupama Sharma Avasthi,Manisha Bhatnagar,Sabari Ghosal |
| ||International Journal of Pharmacology. 2017; 13(6): 552 |
|[Pubmed] | [DOI]|
||Echinacea purpurea -derived alkylamides exhibit potent anti-inflammatory effects and alleviate clinical symptoms of atopic eczema
| ||Attila Oláh,Judit Szabó-Papp,Michael Soeberdt,Ulrich Knie,Stephan Dähnhardt-Pfeiffer,Christoph Abels,Tamás Bíró |
| ||Journal of Dermatological Science. 2017; |
|[Pubmed] | [DOI]|
||Pre-sowing seed treatment with cold plasma and electromagnetic field increases secondary metabolite content in purple coneflower (Echinacea purpurea
| ||Vida Mildaziene,Giedre Pauzaite,Zita Nauciene,Asta Malakauskiene,Rasa Zukiene,Irena Januskaitiene,Valdas Jakstas,Liudas Ivanauskas,Irina Filatova,Veronika Lyushkevich |
| ||Plasma Processes and Polymers. 2017; : e1700059 |
|[Pubmed] | [DOI]|
||Effects of extracts from Echinacea purpurea (L) MOENCH on mice infected with different strains of Toxoplasma gondii
| ||Arquimedes Gasparotto Junior,Maria Luiza Antonio Cosmo,Michelle de Paula Reis,Pamela Secundo dos Santos,Daniela Dib Gonçalves,Francielly Mourão Gasparotto,Italmar Teodorico Navarro,Emerson Luiz Botelho Lourenço |
| ||Parasitology Research. 2016; |
|[Pubmed] | [DOI]|