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/pharmacologyABSTRACT
OBJECTIVE: This study aimed to investigate the effect of SagaPro, a product derived from Angelica archangelica leaf, on nocturia. MATERIAL AND METHODS: Sixty-nine male patients 45 years or older with at least two nocturnal voids were randomized to receive SagaPro or placebo in a double-blind design for 8 weeks. Voiding diaries were assessed before and after the treatment. RESULTS: The results indicate that SagaPro is safe. The actual number of nocturnal voids (ANV), nocturnal polyuria index (NPi) and nocturnal bladder capacity index (NBC index) decreased in the test population, but there was no significant difference between the treatment groups. Subsequent subgroup analysis showed that SagaPro significantly reduced the NBC index and nocturnal voids per sleeping hour in comparison to the placebo in participants with baseline NBC index above 1.3. When participants with sleep disorders were excluded from this group, ANV was also significantly reduced for the SagaPro group in comparison to the placebo group. CONCLUSION: SagaPro, made from an extract of the medicinal herb Angelica archangelica, is safe. This study did not show that SagaPro improved nocturia overall compared to placebo. Subgroup analysis suggested a beneficial effect in individuals with decreased nocturnal bladder capacity, which warrants further study.
Subject(s)
Angelica archangelica , Nocturia/drug therapy , Phytotherapy/methods , Plant Extracts/therapeutic use , Plant Leaves , Aged , Aged, 80 and over , Double-Blind Method , Humans , Incidence , Male , Middle Aged , Nocturia/epidemiology , Patient Safety , Plant Extracts/adverse effects , Prevalence , Sleep Deprivation/epidemiology , Treatment OutcomeABSTRACT
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 SpectroscopyABSTRACT
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/chemistryABSTRACT
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/pharmacologyABSTRACT
BACKGROUND: The purpose of this study was to examine the effect of a leaf extract from A. archangelica on the growth of Crl mouse breast cancer cells in vitro and in vivo. MATERIALS AND METHODS: The antiproliferative activity of the extract was measured by 3H-thymidine uptake in the Crl cells in vitro. Twenty mice were injected with the Crl cells, and 11 of them were fed A. archangelica leaf extract, and the progress of the tumours was followed. RESULTS: The leaf extract was mildly antiproliferative on the Crl cells with an EC50 of 87.6 microg/ml The antitumour activity of the extract was expressed in the mice by marked reduction in tumour growth. In the experimental animals, 9 out of 11 mice developed no or very small tumours, whereas control animals, not receiving the extract, developed significantly larger tumours (p<0.01), as estimated by Mann-Whitney U-test. The antitumour activity of the leaf extract could not be explained by the antiproliferative activity of furanocoumarins present in the extract. CONCLUSION: The results demonstrate the antiproliferative activity in vitro and antitumour activity in vivo of a leaf extract from A. archangelica
Subject(s)
Angelica archangelica , Antineoplastic Agents/pharmacology , Breast Neoplasms/drug therapy , Cell Division/drug effects , Phytotherapy , Plant Extracts/pharmacology , Administration, Oral , Animals , Antineoplastic Agents/administration & dosage , Female , Mice , Mice, Inbred BALB C , Neoplasm Transplantation , Plant Leaves/chemistry , Thymidine/metabolism , Transplantation, Isogeneic , Tritium/metabolism , Tumor Cells, CulturedABSTRACT
The aim of this work was to study the antiproliferative effect of a tincture from fruits of Angelica archangelica and the active components using the human pancreas cancer cell line PANC-1 as a model. Significant dose-dependent antiproliferative activity was observed in the tincture with an EC50 value of 28.6 microg/ml. Strong antiproliferative activity resulted from the two most abundant furanocoumarins in the tincture, imperatorin and xanthotoxin. The contribution of terpenes to this activity was insignificant. Imperatorin and xanthotoxin proved to be highly antiproliferative, with EC50 values of 2.7 microg/ml and 3.7 microg/ml, respectively, equivalent to 10 and 17 microM. The results indicate that furanocoumarins account for most of the antiproliferative activity of the tincture.
