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1.
Molecules ; 26(23)2021 Nov 25.
Article in English | MEDLINE | ID: mdl-34885703

ABSTRACT

Traditionally, arctic Finnish Angelica (Angelica archangelica L.), marsh Labrador tea (Rhododendron tomentosum, syn. Ledum palustre) and common tansy (Tanacetum vulgare) have been used as medicinal herbs in folklore medicine. However, these underutilised plants are a source of, e.g., oil-based compounds, which could benefit many modern applications implemented by the green chemistry extraction methods, as well. We extracted Angelica, marsh Labrador tea and common tansy by non-toxic and recyclable extraction methods, i.e., hydrodistillation and supercritical carbon dioxide (scCO2) extraction; characterised the essential oils (EOs) and scCO2 extracts by combination of gas chromatography and mass spectrometry (GC-MS), and in addition, analysed the antimicrobial properties. As expected for Angelica root and common tansy inflorescence, the scCO2 extraction method produced less amount of volatile compounds compared to hydrodistillation. On the other hand, more coumarins, alkanes, fatty alcohols and fatty acids were obtained. Additionally, sesquiterpenoids palustrol and ledol were predominant compounds in both marsh Labrador tea EO and scCO2 extract. According to our results, however, all the EOs and scCO2 extracts showed broad spectrum of antimicrobial activities against the selected microbes, but the effects were extract-specific. The strongest and broadest antimicrobial activities were performed by marsh Labrador tea scCO2 extract, which showed extremely strong effect on Staphylococcusaureus subsp. aureus and strong effect on Candida albicans.


Subject(s)
Angelica archangelica/chemistry , Oils, Volatile/chemistry , Rhododendron/chemistry , Tanacetum/chemistry , Bacterial Infections/drug therapy , Bacterial Infections/microbiology , Candida albicans/drug effects , Candida albicans/pathogenicity , Carbon Dioxide/chemistry , Gas Chromatography-Mass Spectrometry , Oils, Volatile/pharmacology , Plant Extracts/chemistry , Plant Extracts/pharmacology , Staphylococcus aureus/drug effects , Staphylococcus aureus/pathogenicity
2.
J Food Sci ; 85(11): 3700-3710, 2020 Nov.
Article in English | MEDLINE | ID: mdl-33047814

ABSTRACT

The plant Angelica archangelica, owing to its magnificent therapeutic effectiveness in folklore medicine system, has been regarded as an "angel plant." The current investigation was aimed to optimize extraction conditions of A. archangelica roots and to investigate in vivo role of optimized extract in fibromyalgia. Plant material (dried roots) was subjected to methanol extraction at variable temperature (40 to 60 °C) and time (12 to 36 hr) conditions as per two-factorial design strategy, and responses in terms of antioxidant activity were determined. The optimized extraction conditions were found to be temperature of 60 °C and time of 36 hr. HPLC fingerprinting indicated the presence of coumarins in extract. To induce fibromyalgia, the mice were administered reserpine at a dose of 0.5 mg/kg. Mice were orally treated with 100, 200, and 400 mg/kg extract, and magnitude of fibromyalgia was quantified. In comparison to reserpine group, the extract treatment attenuated pain as shown by significant increase in paw withdrawal threshold against mechanical stimuli (P < 0.05), improved motor ability indicated by increase in fall-off time in inclined plane test (P < 0.05), improved locomotion indicated by increased square crossings in open field test (P < 0.05), and improved cognition as shown by significant reduction in time to reach platform in Morris water maze test and passive avoidance task test (P < 0.05). Extract treatment significantly halted reserpine-induced rise in serum cytokine level (P < 0.05) and brain oxidative stress (P < 0.05). Angelica archangelica extract exerted its beneficial effects in fibromyalgia possibly through the attenuation of oxidative stress-mediated inflammatory cascade. PRACTICAL APPLICATION: Leads from natural products have become an integral part of drug designing processes and have high acceptability due to their better tolerance. The optimization of extraction conditions of plant yields better results and could reduce the processing time, thus increasing its industrial value.


Subject(s)
Angelica archangelica/chemistry , Chemical Fractionation/methods , Drugs, Chinese Herbal/administration & dosage , Drugs, Chinese Herbal/isolation & purification , Fibromyalgia/drug therapy , Plant Extracts/administration & dosage , Plant Extracts/isolation & purification , Animals , Antioxidants/administration & dosage , Antioxidants/isolation & purification , Chromatography, High Pressure Liquid , Coumarins/administration & dosage , Coumarins/isolation & purification , Female , Humans , Male , Mice , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Plant Roots/chemistry
3.
Psychogeriatrics ; 20(5): 726-736, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32767414

ABSTRACT

AIM: Many researchers argue that Alzheimer's disease is at least partly caused by deposition of amyloid beta (Aß) in the brain. Ferulic acid (FA) and Angelica archangelica (AA) are candidate agents for reducing Aß and improving cognitive function. Feru-guard 100M is a supplement containing FA and AA extract. Using this supplement, we planned to assess the effect of FA and AA on Aß deposition in the human brain. METHODS: This was an open-label, interventional multi-institutional joint study of Kobe University and the Institute of Biomedical Research and Innovation (Kobe, Japan). Seventeen subjects diagnosed with mild cognitive impairment were divided into two groups: the intervention group (n = 10) and the control group (n = 7). The subjects in the intervention group used Feru-guard 100M every day for 48 weeks, whereas the subjects in the control group did not use the supplement. We assessed the differences between the two groups by examining Aß deposition and brain atrophy at 48 weeks and cognitive function every 24 weeks. We used carbon-11-labelled Pittsburgh compound B (PiB) positron emission tomography to evaluate Aß deposition. RESULTS: There were no significant differences in Aß deposition, brain atrophy, and cognitive function between the two groups. Specifically, differences in Aß deposition change in seven regions of interest examined with PiB positron emission tomography, brain atrophy change in four indicators of voxel-based morphometry, and cognitive impairment measured by five psychological tests were not significantly between the two groups. CONCLUSION: Treatment with Feru-guard 100M, a supplement containing FA and AA extract, for 48 weeks did not reduce cortical PiB retention, which reflects Aß deposition. It also did not suppress the aggravation of brain atrophy or decline in cognitive function.


Subject(s)
Amyloid beta-Peptides/drug effects , Angelica archangelica/chemistry , Brain/pathology , Cognitive Dysfunction/diagnosis , Coumaric Acids/therapeutic use , Aged , Alzheimer Disease/etiology , Alzheimer Disease/psychology , Amyloid beta-Peptides/metabolism , Aniline Compounds , Atrophy , Brain/diagnostic imaging , Carbon Radioisotopes , Cognitive Dysfunction/diagnostic imaging , Disease Progression , Female , Humans , Japan , Male , Positron-Emission Tomography/methods , Radiopharmaceuticals , Thiazoles
4.
Molecules ; 25(9)2020 Apr 28.
Article in English | MEDLINE | ID: mdl-32353989

ABSTRACT

Naturally occurring coumarins are bioactive compounds widely used in Asian traditional medicine. They have been shown to inhibit proliferation, induce apoptosis, and/or enhance the cytotoxicity of currently used drugs against a variety of cancer cell types. The aim of our study was to examine the antiproliferative activity of different linear furanocoumarins on human rhabdomyosarcoma, lung, and larynx cancer cell lines, and dissolve their cellular mechanism of action. The coumarins were isolated from fruits of Angelica archangelica L. or Pastinaca sativa L., and separated using high-performance counter-current chromatography (HPCCC). The identity and purity of isolated compounds were confirmed by HPLC-DAD and NMR analyses. Cell viability and toxicity assessments were performed by means of methylthiazolyldiphenyl-tetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays, respectively. Induction of apoptosis and cell cycle progression were measured using flow cytometry analysis. qPCR method was applied to detect changes in gene expression. Linear furanocoumarins in a dose-dependent manner inhibited proliferation of cancer cells with diverse activity regarding compounds and cancer cell type specificity. Imperatorin (IMP) exhibited the most potent growth inhibitory effects against human rhabdomyosarcoma and larynx cancer cell lines owing to inhibition of the cell cycle progression connected with specific changes in gene expression, including CDKN1A. As there are no specific chemotherapy treatments dedicated to laryngeal squamous cell carcinoma and rhabdomyosarcoma, and IMP seems to be non-toxic for normal cells, our results could open a new direction in the search for effective anti-cancer agents.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Furocoumarins/pharmacology , Laryngeal Neoplasms/pathology , Rhabdomyosarcoma/pathology , Angelica archangelica/chemistry , Apoptosis , Cell Cycle , Cell Line, Tumor , Cell Proliferation , Cell Survival , Chromatography , Cyclin-Dependent Kinase Inhibitor p21/metabolism , Drug Screening Assays, Antitumor , Fibroblasts/drug effects , Flow Cytometry , Fruit/chemistry , Humans , L-Lactate Dehydrogenase/metabolism , Laryngeal Neoplasms/drug therapy , Pastinaca/chemistry , Rhabdomyosarcoma/drug therapy
5.
J Integr Med ; 17(2): 132-140, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30799248

ABSTRACT

OBJECTIVE: Although Angelica archangelica is a medicinal and aromatic plant with a long history of use for both medicinal and food purposes, there are no studies regarding the antineoplastic activity of its root. This study aimed to evaluate the cytotoxicity and antitumor effects of the crude extract of A. archangelica root (CEAA) on breast cancer. METHODS: The cytotoxicity of CEAA against breast adenocarcinoma cells (4T1 and MCF-7) was evaluated by a 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay. Morphological and biochemical changes were detected by Hoechst 33342/propidium iodide (PI) and annexin V/PI staining. Cytosolic calcium mobilization was evaluated in cells staining with FURA-4NW. Immunoblotting was used to determine the effect of CEAA on anti- and pro-apoptotic proteins (Bcl-2 and Bax, respectively). The 4T1 cell-challenged mice were used for in vivo assay. RESULTS: Using ultra-high-performance liquid chromatography-mass spectrometry analysis, angelicin, a constituent of the roots and leaves of A. archangelica, was found to be the major constituent of the CEAA evaluated in this study (73 µg/mL). The CEAA was cytotoxic for both breast cancer cell lines studied but not for human fibroblasts. Treatment of 4T1 cells with the CEAA increased Bax protein levels accompanied by decreased Bcl-2 expression, in the presence of cleaved caspase-3 and cytosolic calcium mobilization, suggesting mitochondrial involvement in breast cancer cell death induced by the CEAA in this cell line. No changes on the Bcl-2/Bax ratio were observed in CEAA-treated MCF7 cells. Gavage administration of the CEAA (500 mg/kg) to 4T1 cell-challenged mice significantly decreased tumor growth when compared with untreated animals. CONCLUSION: Altogether, our data show the antitumor potential of the CEAA against breast cancer cells in vitro and in vivo. Further research is necessary to better elucidate the pharmacological application of the CEAA in breast cancer therapy.


Subject(s)
Angelica archangelica/chemistry , Antineoplastic Agents, Phytogenic/administration & dosage , Breast Neoplasms/drug therapy , Plant Extracts/administration & dosage , Animals , Antineoplastic Agents, Phytogenic/chemistry , Apoptosis/drug effects , Breast Neoplasms/genetics , Breast Neoplasms/metabolism , Breast Neoplasms/physiopathology , Caspase 3/genetics , Caspase 3/metabolism , Cell Proliferation/drug effects , Female , Humans , MCF-7 Cells , Mice , Mice, Inbred BALB C , Plant Extracts/chemistry , Rhizome/chemistry , bcl-2-Associated X Protein/genetics , bcl-2-Associated X Protein/metabolism
6.
Food Chem Toxicol ; 109(Pt 2): 1026-1031, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28487231

ABSTRACT

The dichloromethane extract from fruits of Angelica archangelica L. was separated by the modern high-performance countercurrent chromatography (HPCCC). The extract and five pure compounds: xanthotoxin, bergapten, imperatorin, phellopterin and isoimperatorin, and the mixture of imperatorin and phellopterin, have been studied as the potential antiviral agents against Herpes simplex virus type l and Coxsackievirus B3. The cytotoxicity was measured using the MTT method. Compounds were tested for the in vitro antiviral activity using the cytopathic effect (CPE) inhibitory assay and by the virus titre reduction assay. Real-time PCR was used to quantify the relative inhibition of the HSV-1 replication. The results indicate that the highest activity was demonstrated by the extract, imperatorin, phellopterin and the mixture of imperatorin and phellopterin, reducing the HSV-1 replication by 5.61 log, 4.7 log, 3.01 log and 3.73 log, respectively. The influence of isolated compounds on the CVB3 replication was not significant. Only the extract caused the decrease in the titre of virus in relation to the virus control. Our results show that coumarins of A. archangelica L. might be a potential candidate for the development of the alternative natural anti- HSV-1 compound. Moreover, the presence of isopentenyloxy moiety at C-8 position significantly improves their activity.


Subject(s)
Angelica archangelica/chemistry , Antiviral Agents/chemistry , Antiviral Agents/pharmacology , Enterovirus B, Human/drug effects , Herpesvirus 1, Human/drug effects , Plant Extracts/chemistry , Plant Extracts/pharmacology , Antiviral Agents/isolation & purification , Countercurrent Distribution , Coxsackievirus Infections/virology , Enterovirus B, Human/physiology , Herpes Simplex/virology , Herpesvirus 1, Human/physiology , Humans , Plant Extracts/isolation & purification , Virus Replication/drug effects
7.
Nat Prod Commun ; 12(2): 205-206, 2017 Feb.
Article in English | MEDLINE | ID: mdl-30428212

ABSTRACT

Roots of wild growing Angelica archangelica L. from Mt. Ozren (Serbia) were subjected to hydrodistillation and GC-MS analysis. The roots contained 0.10% of essential oil with a-pinene (29.7%), 8-3-carene (14.2%), and a mixture of P-phellandrene and limonene (13.2%) as main compounds. The modified resazurin microtiter-plate assay was used to evaluate the antibacterial activity of the essential oil against Staphylococcus aureus and Escherichia coli. The minimum inhibitory concentration (MIC) values were 14.2 µL/mL for S. aureus and 28.4 µL/mL for E. coli, while the minimum bactericidal concentrations (MBC) were 56.8 µL/mL and 113.6 µL/mL, respectively. According to the obtained results, the angelica root essential oil can be applied as a natural preservative in food and as a natural antibiotic for the treatment of several infectious diseases caused by these two bacteria.


Subject(s)
Angelica archangelica/chemistry , Anti-Bacterial Agents/pharmacology , Oils, Volatile/pharmacology , Microbial Sensitivity Tests , Oils, Volatile/analysis , Plant Roots/chemistry
8.
Pharmazie ; 72(1): 3-4, 2017 Jan 10.
Article in English | MEDLINE | ID: mdl-29441889

ABSTRACT

Saga Pro is a food supplement product manufactured in Iceland and marketed internationally. It is claimed to have anti-nocturia effect and the flavonoid isoquercitrin has been suggested to play a role in this assumed activity. The purpose of this study was to identify and quantify the main flavonoids and furanocoumarins in the SagaPro tablets and to evaluate the importance of their presence. Isoquercitrin was identified as a constituent in an amount of 158 µg/tablet. This is a p.o. dosage highly unlikely to have an effect on nocturia or any other pharmacologically significant effect in humans. The main furanocoumarins, xanthotoxin and imperatorin, were also identified and quantified to 280 and 2 µg/tablet, respectively.


Subject(s)
Angelica archangelica/chemistry , Dietary Supplements/analysis , Nocturia/drug therapy , Flavonoids/analysis , Furocoumarins/analysis , Humans , Methoxsalen/analysis , Plant Extracts/analysis , Plant Leaves/chemistry , Quercetin/analogs & derivatives , Quercetin/analysis , Tablets
9.
PLoS One ; 11(6): e0157458, 2016.
Article in English | MEDLINE | ID: mdl-27322374

ABSTRACT

OBJECTIVE: In developed countries with westernized diets, the excessive consumption of added sugar in beverages and highly refined and processed foods is associated with increased risk for obesity, diabetes, and cardiovascular diseases. As a major constituent of added sugars, fructose has been shown to cause a variety of adverse metabolic effects, such as impaired insulin sensitivity, hypertriglyceridemia, and oxidative stress. Recent studies have shown that ketohexokinase isoform C is the key enzyme responsible in fructose metabolism that drive's fructose's adverse effects. The objective of this study was to identify botanical ingredients with potential for inhibitory activity against ketohexokinase-C and fructose-induced metabolic effects by using a series of in vitro model systems. METHODS: Extracts from 406 botanicals and 1200 purified phytochemicals were screened (initial concentration of 50 µg/mL and 50 µM, respectively) for their inhibitory activity using a cell free, recombinant human ketohexokinase-C assay. Dose response evaluations were conducted on botanical extracts and phytochemicals that inhibited ketohexokinase-C by > 30% and > 40%, respectively. Two different extract lots of the top botanical candidates were further evaluated in lysates of HepG2 cells overexpressing ketohexokinase-C for inhibition of fructose-induced ATP depletion. In addition, extracts were evaluated in intact Hep G2 cells for inhibition of fructose-induced elevation of triglyceride and uric acid production. RESULTS: Among the botanical extracts, phloretin (Malus domestica) extracts were the most potent (IC50: 8.9-9.2 µg/mL) followed by extracts of Angelica archangelica (IC50: 22.6 µg/mL-57.3 µg/mL). Among the purified phytochemicals, methoxy-isobavachalcone (Psoralea corylifolia, IC50 = 0.2 µM) exhibited the highest potency against ketohexokinase isoform C activity followed by osthole (Angelica archangelica, IC50 = 0.7 µM), cratoxyarborenone E (Cratoxylum prunifolium, IC50 = 1.0 µM), and α-/γ-mangostin (Cratoxylum prunifolium, IC50 = 1.5 µM). Extracts of Angelica archangelica, Garcinia mangostana, Petroselinum crispum, and Scutellaria baicalensis exhibited ketohexokinase inhibitory activity and blocked fructose-induced ATP depletion and fructose-induced elevation in triglyerides and uric acid. CONCLUSIONS: Angelica archangelica, Garcinia mangostana, Petroselinum crispum, and Scutellaria baicalensis were the top four botanical candidiates identified with inhibitory activity against ketohexokinase-C. Future studies are needed to show proof of mechanism and the efficacy of these botanical extracts in humans to blunt the negative metabolic effects of fructose-containing added sugars.


Subject(s)
Enzyme Inhibitors/chemistry , Fructokinases/chemistry , Fructose/metabolism , Hypertriglyceridemia/drug therapy , Phytochemicals/chemistry , Angelica archangelica/chemistry , Enzyme Inhibitors/administration & dosage , Fructokinases/antagonists & inhibitors , Fructose/chemistry , Garcinia mangostana/chemistry , Hep G2 Cells , Humans , Hypertriglyceridemia/metabolism , Insulin/metabolism , Oxidative Stress/drug effects , Petroselinum/chemistry , Phytochemicals/administration & dosage , Plant Extracts/administration & dosage , Plant Extracts/chemistry
10.
J Med Food ; 17(9): 1043-7, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24788027

ABSTRACT

In this paper, the chemical composition and the antimicrobial activity of the essential oil of Angelica archangelica L. (Apiaceae) roots from central Italy were analyzed. The major constituents of the oil were α-pinene (21.3%), δ-3-carene (16.5%), limonene (16.4%) and α-phellandrene (8.7%). The oil shows a good antimicrobial activity against Clostridium difficile, Clostridium perfringens, Enterococcus faecalis, Eubacterium limosum, Peptostreptococcus anaerobius, and Candida albicans with minimum inhibitory concentration (MIC) values of 0.25, 0.25, 0.13, 0.25, 2.25, and 0.50% v/v, respectively. A weaker antimicrobial activity against bifidobacteria and lactobacilli-very useful in the intestinal microflora-has also been shown with MIC values >4.0% v/v.


Subject(s)
Angelica archangelica/chemistry , Anti-Infective Agents/pharmacology , Bacteria/drug effects , Candida albicans/drug effects , Oils, Volatile/pharmacology , Plant Extracts/pharmacology , Terpenes/pharmacology , Anti-Bacterial Agents/analysis , Anti-Bacterial Agents/pharmacology , Anti-Infective Agents/analysis , Antifungal Agents/analysis , Antifungal Agents/pharmacology , Bicyclic Monoterpenes , Cyclohexenes/analysis , Cyclohexenes/pharmacology , Limonene , Microbial Sensitivity Tests , Monoterpenes/analysis , Monoterpenes/pharmacology , Oils, Volatile/chemistry , Plant Extracts/chemistry , Plant Roots/chemistry , Terpenes/analysis
11.
Biochem Biophys Res Commun ; 441(2): 318-20, 2013 Nov 15.
Article in English | MEDLINE | ID: mdl-24140410

ABSTRACT

The aim of this study was to explore the effect of the acetylcholinesterase inhibiting mixture of extracts of Angelica archangelica fruit and Geranium sylvaticum on memory. Furthermore the effect of the main compound, the furanocoumarin imperatorin, which has been shown to affect several neurotransmitters, was studied. Passive avoidance was measured by step-down latency and step-through latency of 10 months old mice receiving 0.79 mg/kg of imperatorin daily, pure or as part of the extracts, for 14 days or longer. Step-down latency was significantly higher in both groups receiving imperatorin than in the control group. In contrast, no difference was found between treatment groups regarding step-through latency. The results indicate that the imperatorin is the main active component of the extract mixture.


Subject(s)
Angelica archangelica/chemistry , Cholinesterase Inhibitors/pharmacology , Furocoumarins/pharmacology , Memory/drug effects , Animals , Cholinesterase Inhibitors/chemistry , Female , Furocoumarins/chemistry , Mice , Mice, Inbred ICR , Plant Extracts/chemistry , Plant Extracts/pharmacology
12.
Nat Prod Commun ; 8(7): 925-8, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23980425

ABSTRACT

Both enantiomers of 12-methyl-13-tridecanolide{(R)-(+)-1, (S)-(-)-1} and 14-methyl-15-pentadecanolide (muscolide) {(R)-(+)-2, (S)-(-)-2} were synthesized from either (S)-(+)- or (R)-(-)-3-bromo-2-methyl-1-propanol 8 as a chiral building block.


Subject(s)
Angelica archangelica/chemistry , Fatty Acids, Monounsaturated/chemical synthesis , Lactones/chemical synthesis , Odorants , Stereoisomerism
13.
Toxicol Ind Health ; 29(1): 14-22, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22294442

ABSTRACT

PURPOSE: The aim of this study was to study the effect of ionizing radiation on apoptosis-related protein concentrations as well as the radio-protective role of Ginkgo biloba and Angelica archangelica. The experiments were performed on 68 adult Wistar rats weighing 175 g (±10 g). Animals were subdivided into control group in which the animals received neither the protector nor the isotopes. The second group represents the animals that received 1 mCi of (99m)Tc only. The third group represents the animals that received A. archangelica for 7 days. The fourth group represents the animals that received G. biloba for 7 days. The fifth group represents the animals that received 1 mCi of (99m)Tc once after receiving A. archangelica for 7 days. The sixth group represents the animals that received mCi of (99m)Tc once after receiving G. biloba for 7 days. Radiation was administered as intravenous injection by 1 mCi of (99m)Tc with the legend methoxyisobutylisonitrile for 24 h. The concentration of p53, Bcl2 and malondialdehyde in liver as well as histopathological examination of liver cells were carried out. Results showed that apoptotic to anti-apoptotic protein ratio significantly (p < 0.05) returned to its normal ratio when radioisotopic injection was administered after the protection period for a week by both A. archangelica and G. biloba in a dose based on the animal body weight. Electron microscope photographing supported this finding. CONCLUSION: It was concluded that both antioxidants can be used as radio-protective agents in cases of ionizing radiation exposure.


Subject(s)
Liver/drug effects , Plant Extracts/pharmacology , Radiation Injuries, Experimental/drug therapy , Radiation-Protective Agents/pharmacology , Tumor Suppressor Protein p53/drug effects , bcl-X Protein/drug effects , Angelica archangelica/chemistry , Animals , Apoptosis/drug effects , Apoptosis/radiation effects , Ginkgo biloba/chemistry , Hepatocytes/drug effects , Hepatocytes/radiation effects , Hepatocytes/ultrastructure , Injections, Intravenous , Liver/metabolism , Liver/radiation effects , Malondialdehyde/metabolism , Radiation Injuries, Experimental/metabolism , Radiation Injuries, Experimental/pathology , Radiopharmaceuticals/toxicity , Rats , Rats, Wistar , Sodium Pertechnetate Tc 99m/toxicity , Tumor Suppressor Protein p53/metabolism , Tumor Suppressor Protein p53/radiation effects , bcl-X Protein/metabolism , bcl-X Protein/radiation effects
14.
Z Naturforsch C J Biosci ; 67(1-2): 1-7, 2012.
Article in English | MEDLINE | ID: mdl-22486035

ABSTRACT

Angelica archangelica fruits were collected from 64 locations around Iceland and analysed for furanocoumarins by high-performance liquid chromatography. The average furanocoumarin content was found to be 22.5 mg/g, ranging from 14.0 to 31.6 mg/g. Whereas imperatorin was the main compound in all samples, the order of other compounds was highly diverse. Considerable differences were observed between individuals from the same location and between neighbouring locations. However, strong geographical impact was observed on the composition, with isoimperatorin and bergapten being more pronounced in South Iceland, and oxypeucedanin and an unidentified compound being more pronounced in North Iceland and absent in many samples from South Iceland.


Subject(s)
Angelica archangelica/chemistry , Furocoumarins/chemistry , Geography , Chromatography, High Pressure Liquid , Iceland , Magnetic Resonance Spectroscopy
15.
J Tradit Chin Med ; 32(3): 423-9, 2012 Sep.
Article in English | MEDLINE | ID: mdl-23297567

ABSTRACT

OBJECTIVE: Angelica archangelica Linn. is widely used in food and liquor preparations and also in Kashmiri folk medicine to reduce anxiety. We evaluated the anxiolytic effect of successive extracts of A. archangelica linn. (SAE) on rats tested in the elevated T-maze test (an animal model of generalized anxiety) at doses that exhibit antidepressant-like activity in humans. METHODS: A. archangelica (1 kg) was subjected to successive extraction in a soxhlet apparatus with solvents [petroleum ether (40-60 degrees C), chloroform, ethyl acetate, methanol and decoction with water] in order of increasing polarity (yield: 6.9%, 7.3%, 5.1%, 11.88% and 8.2% w/w, respectively). SAE were evaluated for anxiolytic effects using the elevated T-maze and forced swimming tests in rats. RESULTS: Oral dosing of diazepam (1 mg/kg) and extracts (50, 100 and 200 mg/kg) clearly showed an anxiolytic-like profile in the elevated T-maze test: it increased one-way escape and decreased inhibitory avoidance on the first, third and seventh day. In the forced swimming test, imipramine and SAE showed antidepressant- and anxiolytic-like effects as reflected by increased climbing time, swimming time and decreased immobility time on the first, third and seventh day. Aqueous and methanol extracts showed the most, petroleum ether (40-60 degrees C) and chloroform intermediate, and ethyl acetate the least anxiolytic activity (*P<0.05, **P<0.01, ***P< 0.001) in both models. CONCLUSIONS: These results suggest the anti-anxiety activity of various extracts of A. archangelica and strongly justify its use in traditional Indian medicine for the treatment of anxiety.


Subject(s)
Angelica archangelica/chemistry , Anti-Anxiety Agents/administration & dosage , Anxiety/drug therapy , Plant Extracts/administration & dosage , Animals , Anxiety/physiopathology , Female , Humans , Male , Maze Learning/drug effects , Motor Activity/drug effects , Rats , Rats, Wistar , Swimming
16.
Epilepsy Res ; 85(2-3): 293-9, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19406619

ABSTRACT

The aim of this study was to determine and compare the anticonvulsant and acute adverse (neurotoxic) effects of imperatorin and osthole (two natural coumarin derivatives) with valproate (a classical antiepileptic drug) in the maximal electroshock seizure and chimney tests in mice. The anticonvulsant and acute adverse effects of imperatorin, osthole and valproate were determined at 15, 30, 60 and 120 min after their systemic (i.p.) administration. The evaluation of time-course and dose-response relationships for imperatorin, osthole and valproate in the maximal electroshock seizure test revealed that the compounds produced a clear-cut antielectroshock action in mice and the experimentally derived ED(50) values for imperatorin ranged between 167 and 290 mg/kg, those for osthole ranged from 253 to 639 mg/kg, whereas the ED(50) values for valproate ranged from 189 to 255 mg/kg. The evaluation of acute neurotoxic effects in the chimney test revealed that the TD(50) values for imperatorin ranged between 329 and 443 mg/kg, the TD(50) values for osthole ranged from 531 to 648 mg/kg, while the TD(50) values for valproate ranged from 363 to 512 mg/kg. The protective index (as a ratio of TD(50) and ED(50) values) for imperatorin ranged between 1.13 and 2.60, for osthole ranged from 0.83 to 2.44, and for valproate ranged between 1.72 and 2.00. In conclusion, both natural coumarin derivatives deserve more attention from a preclinical point of view as compounds possessing some potentially favorable activities in terms of suppression of seizures, quite similar to those reported for valproate.


Subject(s)
Anticonvulsants/pharmacology , Anticonvulsants/toxicity , Behavior, Animal/drug effects , Coumarins/pharmacology , Coumarins/toxicity , Furocoumarins/pharmacology , Furocoumarins/toxicity , Neurotoxicity Syndromes/psychology , Seizures/prevention & control , Seizures/physiopathology , Valproic Acid/pharmacology , Valproic Acid/toxicity , Angelica archangelica/chemistry , Animals , Cnidium/chemistry , Dogs , Dose-Response Relationship, Drug , Electroshock , Mice , Plant Roots/chemistry , Postural Balance/drug effects
17.
Z Naturforsch C J Biosci ; 62(9-10): 689-93, 2007.
Article in English | MEDLINE | ID: mdl-18069242

ABSTRACT

The aim of this study was to explore the acetylcholinesterase (AChE) inhibition of several Icelandic medicinal herbs. Ethanolic extracts of Angelica archangelica seeds and the aerial parts of Geranium sylvaticum proved effective, with IC50 values of 2.20 mg/ml and 3.56 mg/ml, respectively. The activity of imperatorin and xanthotoxin from A. archangelica was measured. Xanthotoxin proved much more potent than imperatorin, with an IC50 value of 155 microg/ml (0.72 mM) but that for imperatorin was above 274 microg/ml (1.01 mM). However, furanocoumarins seem to have a minor part in the total activity of this extract. Synergistic interaction was observed between the extracts of A. archangelica and G. sylvaticum. Several medicinal herbs (Achillea millefolium, Filipendula ulmaria, Thymus praecox and Matricaria maritima) did not show AChE inhibitory activity.


Subject(s)
Angelica archangelica/chemistry , Cholinesterase Inhibitors/pharmacology , Geranium/chemistry , Plant Extracts/pharmacology , Animals , Brain/enzymology , Ethanol , Flowers/chemistry , Furocoumarins/chemistry , Furocoumarins/isolation & purification , Furocoumarins/pharmacology , Kinetics , Methoxsalen/chemistry , Methoxsalen/isolation & purification , Methoxsalen/pharmacology , Mice , Plant Extracts/isolation & purification , Plant Leaves/chemistry
18.
Anticancer Res ; 25(3B): 1877-80, 2005.
Article in English | MEDLINE | ID: mdl-16158920

ABSTRACT

BACKGROUND: The aim of this work was to study the constituents and cytotoxicity of the essential oils from the fruits of Angelica archangelica growing in Iceland. MATERIALS AND METHODS: Three samples of essential oils were prepared by steam distillation. Their composition was established with GC/MS. The effects of the oils were examined in PANC-1 human pancreas cancer cells and Crl mouse breast cancer cells in concentrations ranging from 10-400 microg/ml, measuring the reduction of the tetrazolium salt 3-(4,5-dimethylthiazol-2-yl) -5- (3-carboxymethoxyphenyl)-2- (4-sulphophenyl) -2H-tetrazolium (MTS) by mitochondrial enzymes. RESULTS: Two types of essential oils were found, differing mainly in the absence or presence of beta-phellandrene. The ED50 of the oils ranged from 48.6 microg/ml to 108.3 microg/ml for PANC-1 and 48.0 microg/ml to 91.8 microg/ml for Crl cells. CONCLUSION: The cytotoxic activity of the essential oils was independent of the quantity of their main components.


Subject(s)
Angelica archangelica/chemistry , Fruit/chemistry , Oils, Volatile/analysis , Oils, Volatile/pharmacology , Animals , Antineoplastic Agents, Phytogenic/analysis , Antineoplastic Agents, Phytogenic/isolation & purification , Antineoplastic Agents, Phytogenic/pharmacology , Cell Line, Tumor , Cyclohexane Monoterpenes , Cyclohexenes , Drug Screening Assays, Antitumor , Humans , Mammary Neoplasms, Experimental/drug therapy , Mice , Monoterpenes/analysis , Monoterpenes/pharmacology , Oils, Volatile/isolation & purification , Pancreatic Neoplasms/drug therapy , Plant Extracts/analysis , Plant Extracts/isolation & purification , Plant Extracts/pharmacology
19.
Phytochem Anal ; 15(5): 313-9, 2004.
Article in English | MEDLINE | ID: mdl-15508836

ABSTRACT

Optimal conditions for the extraction and analysis of furanocoumarins from fruits of Archangelica officinalis Hoffm. have been determined. The following extraction methods were used: exhaustive extraction in a Soxhlet apparatus, ultrasonication at 25 and 60 degrees C, microwave-assisted solvent extraction in open and closed systems, and accelerated solvent extraction (ASE). In most cases the yields of furanocoumarins were highest using the ASE method. The effects of extracting solvent, temperature and time of extraction using this method were investigated. The highest yield of furanocoumarins by ASE was obtained with methanol at 100-130 degrees C for 10 min. The extraction yields of furanocoumarins from plant material by ultrasonication at 60 degrees C and microwave-assisted solvent extraction in an open system were comparable to the extraction yields obtained in the time- and solvent-consuming exhaustive process involving the Soxhlet apparatus.


Subject(s)
Angelica archangelica/chemistry , Coumarins/isolation & purification , Furans/isolation & purification , Chemistry Techniques, Analytical/methods , Fruit/chemistry , Solvents/chemistry
20.
Phytochem Anal ; 15(3): 167-74, 2004.
Article in English | MEDLINE | ID: mdl-15202601

ABSTRACT

A reversed-phase HPLC method with atmospheric pressure chemical ionisation MS detection has been developed for the separation and identification of coumarins in plants of Peucedanum palustre L. (Moench) and Angelica archangelica (L.) var. archangelica. The Turbo Method Development program was utilised to optimise the mobile phase with two organic solvents (acetonitrile and methanol) and two aqueous solutions (1.0% formic acid and 10 mM ammonium acetate). Optimisation of the solvent gradients for the method was performed with the aid of the DryLab program. Analyses were carried out using a Phenomenex Prodigy RP C18 column. Fifty-two peaks (14 of which were associated with coumarins) were separated in 30 min from extracts of P. palustre, and 48 peaks (15 associated with coumarins) from extracts of A. archangelica. A total of 21 different coumarin-type compounds were identified in the aerial and the underground parts of the title plants. Isopimpinellin and pimpinellin were found for the first time in P. palustre and were identified by comparison of retention times and MS data obtained following the analysis of pure standards. This is the first report of the coumarin composition of the umbels of P. palustre.


Subject(s)
Angelica archangelica/chemistry , Apiaceae/chemistry , Coumarins/analysis , Chromatography, High Pressure Liquid/methods , Mass Spectrometry/methods , Plant Extracts/analysis , Plant Leaves/chemistry , Plant Roots/chemistry
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