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1.
J Chromatogr Sci ; 53(9): 1577-87, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26014965

ABSTRACT

A new ultra-performance liquid chromatography (UPLC) using conventional and chemometric calibrations was improved for the simultaneous estimation of chlorogenic acid (CA) and rutin (RUT) in leaves of Ribes L. species (R. rubrum, R. biebersteinii, R. nigrum, R. uva-crispa, R. alpinum, R. orientale, R. multiflorum and R. anatolica). The UPLC separation for CA and RUT in samples were performed on a Waters UPLC BEH phenyl column (100 mm × 1.0 mm i.d., 1.7 µm) and mobile phase consisting of acetonitrile and 0.1 M formic acid buffer, pH = 3.77 (15:85, v/v) containing 1.0 mL triethylamine in 1,000 mL mobile phase. Multi-wavelength UPLC chromatograms of CA and RUT in calibration and plant samples were obtained by the photodiode array (PDA) detection at the wavelength set from 290 to 360 nm with the interval of Δλ = 10 nm. Conventional UPLC-single and chemometric calibrations were subjected to the analysis of the related compounds. By using UPLC data, conventional and chemometric calibrations in the linear concentration range between 2.5 and 40.0 µg/mL for all compounds were applied for the simultaneous quantitative analysis of CA and RUT in plant samples of seven different Ribes species.


Subject(s)
Chlorogenic Acid/analysis , Chromatography, High Pressure Liquid/methods , Plant Leaves/chemistry , Ribes/chemistry , Rutin/analysis , Calibration , Chromatography, High Pressure Liquid/standards , Limit of Detection , Linear Models , Plant Extracts/chemistry , Reproducibility of Results
2.
Food Chem Toxicol ; 58: 22-9, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23603383

ABSTRACT

This work aimed to evaluate and compare the phenolic profile and some biological properties of the ripe "berries" methanol extracts of Juniperus oxycedrus L. subsp. oxycedrus (Joo) and Juniperus oxycedrus L. subsp. macrocarpa (Sibth. & Sm.) Ball. (Jom) from Turkey. The total phenolic content resulted about 3-fold higher in Jom (17.89±0.23 mg GAE/g extract) than in Joo (5.14±0.06 mg GAE/g extract). The HPLC-DAD-ESI-MS analysis revealed a similar flavonoid fingerprint in Joo and Jom, whereas a difference in their quantitative content was found (4632 µg/g extract and 12644 µg/g extract). In addition, three phenolic acids were detected in Jom only (5765 µg/g extract), and protocatechuic acid was the most abundant one. The antioxidant capacity of the extracts was evaluated by different in vitro assays: in the DPPH and in the TBA tests a stronger activity in Jom was highlighted, while Joo exhibited higher reducing power and metal chelating activity. Joo and Jom did not affect HepG2 cell viability and both extracts resulted virtually non-toxic against Artemia salina. The extracts were also studied for their antimicrobial potential, displaying efficacy against Gram-positive bacteria.


Subject(s)
Anti-Infective Agents/pharmacology , Antineoplastic Agents/pharmacology , Antioxidants/pharmacology , Juniperus/chemistry , Phenols/analysis , Plant Extracts/pharmacology , Animals , Hep G2 Cells , Humans , Juniperus/classification , Species Specificity
3.
J Ethnopharmacol ; 144(3): 726-34, 2012 Dec 18.
Article in English | MEDLINE | ID: mdl-23107822

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Pseudevernia furfuracea (L.) Zopf (Parmeliaceae) is a common epiphytic lichen in the conifer-hardwood forest of Anatolia. This species is used in traditional medicine in Turkey as a treatment for wounds, eczema and hemorrhoids. AIM OF THE STUDY: The present study was designed to investigate the active compounds from Pseudevernia. furfuracea, and the isolation studies yielded atraric acid (Aslan et al., 2006) as the major compound and a mixture of methyl hematommate (Baumann, 1960) and methyl chlorohematommate (Bayir et al., 2006). Furthermore, methanolic extract from thalli of Pseudevernia. furfuracea and its fractions and isolates (Aslan et al., 2006; Baumann, 1960; Bayir et al., 2006) were investigated for in vitro antimicrobial and antioxidant activities, and in vivo antinociceptive, anti-inflammatory and wound healing activities. MATERIAL AND METHODS: Antimicrobial activities of the samples were determined by using the disc diffusion technique. 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay was used as a rapid TLC screening method to evaluate the antioxidant activity of Pseudevernia. furfuracea. The thiobarbituric acid (TBA) test was used to assess the efficacy of the extracts in protecting liposomes from lipid peroxidation. In vivo inhibitory effect of the extracts on the carrageenan-induced hind paw edema model in mice was studied for the assessment of anti-inflammatory activity. p-Benzoquinone-induced abdominal constriction test was used to explore the antinociceptive effects of the extracts. Moreover, the wound healing potential of the plant extracts that were evaluated by using in vivo incision and excision wound models on rats and mice, were comparatively assessed with a reference ointment Madecassol(®). RESULTS: Significant antimicrobial activities were observed against Gram (+) microorganisms and Candida krusei and Candida. dubliniensis in dichloromethane (DCM) and ethyl acetate (EtOAc) extracts and isolates. The methanol (MeOH), DCM and EtOAc extracts of the lichen were found to possess moderate inhibitory activity on lipid peroxidation. Methanolic extract of the lichen was found to possess significant inhibitory activity on the carrageenan-induced hind paw edema model in mice whereas the other fractions did not show any activity. While DCM and EtOAc extracts and fractions showed notable anti-inflammatory activity on carrageenan-induced hind paw edema model without inducing any apparent acute toxicity or gastric damage. Moreover, topical application of the ointment prepared with MeOH extract and EtOAc fraction onto the incised wounds exerted remarkable wound healing activity. CONCLUSION: The results of these experimental studies exhibited that nonpolar fractions of Pseudevernia. furfuracea have significant antimicrobial activity against especially Candida species and polar fractions (especially MeOH) display antioxidant, anti-inflammatory, antinociceptive and wound healing activities.


Subject(s)
Ascomycota , Complex Mixtures/pharmacology , Lichens , Analgesics/pharmacology , Analgesics/therapeutic use , Animals , Anti-Infective Agents/pharmacology , Anti-Infective Agents/therapeutic use , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/therapeutic use , Antioxidants/pharmacology , Antioxidants/therapeutic use , Bacteria/drug effects , Behavior, Animal/drug effects , Benzoquinones , Biphenyl Compounds/metabolism , Candida/drug effects , Carrageenan , Complex Mixtures/therapeutic use , Edema/chemically induced , Edema/drug therapy , Male , Mice , Microbial Sensitivity Tests , Pain/chemically induced , Pain/drug therapy , Pain/physiopathology , Picrates/metabolism , Rats , Rats, Sprague-Dawley , Skin/injuries , Skin/pathology , Thiobarbituric Acid Reactive Substances/metabolism , Wound Healing/drug effects
4.
Nat Prod Commun ; 7(7): 919-22, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22908582

ABSTRACT

Fatty acid compositions of seeds of five taxa of the Juniperus section of the genus Juniperus L. (Cupressaceae), i. e. J. drupacea Lab., J. communis L. var. communis, J. communis var. saxatilis Pall., J. oxycedrus L. subsp. oxycedrus, and J. oxycedrus subsp. macrocarpa (Sibth. & Sm.) Ball, were investigated. Methyl ester derivatized fatty acids of the lipophylic extracts of the five species were comparatively analyzed by capillary gas chromatography-mass spectrometry (GC-MS). Juniperus taxa showed uniform fatty acid patterns, among which linoleic (25.8 - 32.5%), pinolenic (11.9 - 24.1%) and oleic acids (12.4 - 17.2%) were determined to be the main fractions in the seed oils. Juniperonic acid was found to be remarkably high in J. communis var. saxatilis (11.4%), J. oxycedrus subsp. oxycedrus (10.4%), and J. communis var. communis (10.1%). To the best of our knowledge, the present work discloses the first report on the fatty acid compositions of seeds of this Juniperus section grown in Turkey.


Subject(s)
Fatty Acids/analysis , Juniperus/chemistry , Seeds/chemistry , Cupressaceae/chemistry , Gas Chromatography-Mass Spectrometry , Plant Oils/analysis , Turkey
5.
J Ethnopharmacol ; 139(2): 401-8, 2012 Jan 31.
Article in English | MEDLINE | ID: mdl-22138348

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: The leaves of Michauxia species are used for the treatment of wounds in Turkish traditional medicine. In the present study, wound healing, anti-inflammatory and antioxidant activities of the extracts obtained from the root and herb of 5 species of Michauxia collected in different parts of Turkey were evaluated. MATERIAL AND METHODS: In vivo incision and excision wound models were used in order to assess the wound healing effects of the methanolic extracts of the plants. Skin samples were also evaluated histopathologically. In vivo inhibitory effect of the extracts on acetic acid-induced increase in capillary permeability was studied for the assessment of anti-inflammatory activity. TBA (thiobarbituric acid) test, qualitative and quantitative DPPH (2,2-diphenyl-1-picrylhydrazyl) tests were used to evaluate the antioxidant activity. RESULTS: Noteworthy wound healing activity was observed for the ointment formulation prepared with 1% Michauxia nuda (root) and Michauxia tchihatchewii (herb) extracts. The results of histopathological evaluation supported the outcome of incision and excision wound models. Moreover, the Michauxia nuda (root) exerted remarkable anti-inflammatory effect. The highest antioxidant activity was observed with the ethyl acetate extract of Michauxia tchihatchewii herb. CONCLUSION: The experimental study revealed that Michauxia displays remarkable wound healing and anti-inflammatory and antioxidant activities.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Antioxidants/pharmacology , Campanulaceae , Inflammation/prevention & control , Plant Extracts/pharmacology , Skin/drug effects , Wound Healing/drug effects , Acetic Acid , Animals , Anti-Inflammatory Agents/chemistry , Antioxidants/chemistry , Biphenyl Compounds/chemistry , Capillary Permeability/drug effects , Disease Models, Animal , Dose-Response Relationship, Drug , Inflammation/chemically induced , Inflammation/metabolism , Lipid Peroxidation/drug effects , Male , Mice , Picrates/chemistry , Plant Extracts/chemistry , Plant Leaves , Plant Roots , Plants, Medicinal , Rats , Rats, Sprague-Dawley , Skin/pathology , Thiobarbituric Acid Reactive Substances/chemistry , Turkey
6.
Acta Biochim Pol ; 58(4): 471-5, 2011.
Article in English | MEDLINE | ID: mdl-22146136

ABSTRACT

Glutathione reductase (GR, E.C 1.6.4.2) is a flavoprotein that catalyzes NADPH-dependent reduction of oxidized glutathione (GSSG) to reduced glutathione (GSH). The aim of this study was to investigate in vitro effects of phenolic compounds isolated from Sideritis brevibracteata on bovine kidney GR. The Sideritis species are widely found in nature and commonly used as medicinal plants. 7-O-glycosides of 8-OH-flavones (hypolaetin, isoscutellarein and 3'-hydroxy-4'-O-methylisoscutellarein) were isolated from aerial parts of Sideritis brevibracteata. These compounds inhibited bovine kidney cortex GR in a concentration-dependent manner. Kinetic characterization of the inhibition was also performed.


Subject(s)
Glutathione Reductase/chemistry , Kidney Cortex/enzymology , Sideritis/chemistry , Animals , Cattle , Dose-Response Relationship, Drug , Enzyme Assays , Enzyme Inhibitors/isolation & purification , Enzyme Inhibitors/pharmacology , Flavones/isolation & purification , Flavones/pharmacology , Glutathione Reductase/isolation & purification , Glycosides/isolation & purification , Glycosides/pharmacology , Kidney Cortex/drug effects , Kinetics , Phenols/chemistry , Phenols/pharmacology , Plant Components, Aerial/chemistry
7.
Pharm Biol ; 49(10): 1014-22, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21592011

ABSTRACT

CONTEXT: Several Juniperus species (Cupressaceae) are utilized in folk medicine in the treatment of infections and skin diseases. OBJECTIVE: This work was designed to evaluate the antioxidant and antimicrobial potential of methanol and water branches extracts of Juniperus species from Turkey: Juniperus communis L. var. communis (Jcc), Juniperus communis L. var. saxatilis Pall. (Jcs), Juniperus drupacea Labill. (Jd), Juniperus oxycedrus L. subsp. oxycedrus (Joo), Juniperus oxycedrus L. subsp. macrocarpa (Sibth. & Sm.) Ball. (Jom). MATERIALS AND METHODS: Total phenolics, total flavonoids and condensed tannins were spectrophotometrically determined. The antioxidant properties were examined using different in vitro systems. The toxicity was assayed by Artemia salina lethality test. The antimicrobial potential against bacteria and yeasts was evaluated using minimum inhibitory concentration and minimum bactericidal concentration (MIC/MBC) measurements. The effect on bacteria biofilms was tested by microtiter plate assay. RESULTS: Both in the DPPH (1,1-diphenyl-2-picrylhydrazyl) and TBA (thiobarbituric acid) test Jom resulted the most active (IC(50) = 0.034 ± 0.002 mg/mL and 0.287 ± 0.166 µg/mL). Joo exhibited the highest reducing power (1.78 ± 0.04 ASE/mL) and Fe(2+) chelating activity (IC(50) = 0.537 ± 0.006 mg/mL). A positive correlation between primary antioxidant activity and phenolic content was found. The extracts were potentially non-toxic against Artemia salina. They showed the best antimicrobial (MIC = 4.88-30.10 µg/mL) and anti-biofilm activity (60-84%) against S. aureus. DISCUSSION AND CONCLUSION: The results give a scientific basis to the traditional utilization of these Juniperus species, also demonstrating their potential as sources of natural antioxidant and antimicrobial compounds.


Subject(s)
Anti-Infective Agents/pharmacology , Antioxidants/pharmacology , Juniperus , Plant Extracts/pharmacology , Animals , Anti-Infective Agents/analysis , Anti-Infective Agents/chemistry , Antioxidants/analysis , Antioxidants/chemistry , Artemia/drug effects , Bacteria/drug effects , Biofilms/drug effects , Disease Models, Animal , Drug Evaluation, Preclinical , Flavonoids/analysis , Flavonoids/chemistry , Flavonoids/pharmacology , Free Radical Scavengers/analysis , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , Fruit , Humans , Iron Chelating Agents/analysis , Iron Chelating Agents/chemistry , Iron Chelating Agents/pharmacology , Lethal Dose 50 , Lipid Peroxidation/drug effects , Methanol/chemistry , Methanol/metabolism , Microbial Sensitivity Tests , Phenols/analysis , Phenols/chemistry , Phenols/pharmacology , Plant Extracts/analysis , Plant Extracts/chemistry , Plants, Medicinal , Tannins/analysis , Tannins/chemistry , Tannins/pharmacology , Thiobarbituric Acid Reactive Substances/analysis , Turkey , Water/chemistry , Water/metabolism
8.
J Sep Sci ; 33(17-18): 2558-67, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20806240

ABSTRACT

New HPLC-chemometric approaches were proposed for the simultaneous chromatographic quantification of daidzein, genistein, formononetin, and biochanin A in the samples consisting of the aerial parts of Trifolium lucanicum Gasp. (Leguminosae). Partial least squares and principal component regression algorithms were applied to the multiple chromatographic data set obtained by measuring at 240, 248, 256, and 264 nm to construct HPLC-partial least squares and HPLC-principal component regression calibrations. Chromatographic separation was carried out by using a mobile phase containing methanol, acetate buffer (pH=4.75) and acetonitrile (21:58:21, v/v/v) on the reversed phase column, Supelcosil™ LC-18 (15 cm×4.6 mm id). In addition, conventional HPLC based on the detection at a single wavelength was used for the determination of each compound in the extracts of T. lucanicum. The validity and applicability of the proposed HPLC-chemometric and conventional HPLC methods were performed by analyzing various synthetic plant samples. A good agreement was observed in the application of the proposed HPLC-chemometric tools to the synthetic and extracted samples of T. lucanicum.


Subject(s)
Chromatography, High Pressure Liquid/methods , Isoflavones/analysis , Trifolium/chemistry , Algorithms , Chromatography, High Pressure Liquid/instrumentation , Humans , Molecular Structure , Reproducibility of Results
9.
FEMS Immunol Med Microbiol ; 59(3): 470-6, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20584079

ABSTRACT

Methanol and aqueous branch extracts of five Juniperus species were examined for their effects on Staphylococcus aureus ATCC 6538P and S. aureus 810 biofilm. The Turkish plant material was Juniperus communis L. var. communis, J. communis L. var. saxatilis Pall., Juniperus drupacea Labill., Juniperus oxycedrus L. ssp. oxycedrus, J. oxycedrus L. ssp. macrocarpa (Sibth. & Sm.) Ball. The Juniperus extracts were subjected to preliminary phytochemical analysis by thin-layer chromatography. The antimicrobial activity was evaluated using the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC). The effects of the extracts on biofilm formation and preformed biofilm were quantified by both biomass OD and the CFU counting method. The phytochemical screening revealed the presence of polyphenols, coumarins, lignans, steroids, alkaloids and terpenes. For both strains, the MICs of all extracts were in the range of 4.88-78.12 microg mL(-1). On S. aureus ATCC 6538P, the effects of subinhibitory concentration (0.5 MIC) of the extracts were minimal on planktonic growth and on adhering cells, whereas they were greater on biofilm formation. Differently, on S. aureus 810, they showed only a rather low efficacy on biofilm formation. The extracts at 2 MIC demonstrated a good activity on a preformed biofilm of S. aureus ATCC 6538P.


Subject(s)
Anti-Bacterial Agents/pharmacology , Biofilms/drug effects , Juniperus/chemistry , Plant Extracts/pharmacology , Staphylococcus aureus/drug effects , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/isolation & purification , Biomass , Chromatography, Thin Layer , Colony Count, Microbial , Microbial Sensitivity Tests , Microbial Viability/drug effects , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Spectrophotometry , Staphylococcus aureus/physiology , Turkey
10.
J Agric Food Chem ; 57(15): 6570-7, 2009 Aug 12.
Article in English | MEDLINE | ID: mdl-19580284

ABSTRACT

The present study was designed to define and compare the flavonoid composition and the biological potential of berries methanol extracts of Juniperus communis L. var. communis (Jcc) and Juniperus communis L. var. saxatilis. Pall. (Jcs) from Turkey. Total polyphenols (Folin-Ciocalteau method) were 3-fold higher in Jcc (59.17 +/- 1.65 mg GAE/g extract) than in Jcs (17.64 +/- 0.09 mg GAE/g extract). Flavonoid and biflavonoid content, evaluated by HPLC-DAD-ESI-MS analysis, was higher in Jcc (25947 +/- 0.86 and 4346 +/- 3.95 microg/g extract) than in Jcs (5387 +/- 34.88 and 1944 +/- 26.88 microg/g extract). The HPLC analysis of Jcc allowed the separation of 16 flavonoids; hypolaetin-7-pentoside and quercetin-hexoside are the main compounds. Moreover, gossypetin-hexoside-pentoside and gossypetin-hexoside were identified for the first time in Jcc berries. In Jcs eight flavonoids were identified: quercetin-hexoside and isoscutellarein-8-O-hexoside are the most abundant compounds. The in vitro antioxidant activity was determined using different methods; Jcc was found to be more active than Jcs in the DPPH test (IC(50) of 0.63 +/- 0.09 mg/mL and 1.84 +/- 0.10 mg/mL) in reducing power assay (12.82 +/- 0.10 ASE/mL and 64.14 +/- 1.20 ASE/mL), and in TBA assay (IC(50) of 4.44 +/- 0.70 microg/mL and 120.07 +/- 3.60 microg/mL). By contrast, Jcs exhibited more elevated Fe(2+) chelating ability than Jcc. The extracts were also studied for their antimicrobial potential, displaying antimicrobial capacity only against Gram-positive bacteria.


Subject(s)
Antioxidants/analysis , Flavonoids/analysis , Flavonoids/pharmacology , Fruit/chemistry , Gram-Positive Bacteria/drug effects , Juniperus/chemistry , Antioxidants/pharmacology , Turkey
11.
J Ethnopharmacol ; 125(2): 330-6, 2009 Sep 07.
Article in English | MEDLINE | ID: mdl-19505566

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Juniperus L. (Cupressaceae) species have been used to various inflammatory and infectious diseases such as bronchitis, colds, cough, fungal infections, hemorrhoids, gynecological diseases, and wounds in Turkish folk medicine. AIM OF THE STUDY: To evaluate this traditional information, anti-inflammatory and antinociceptive activities of the methanolic and aqueous extracts prepared from different parts (stem, fruit and leaves) of the five Turkish taxa under Juniperus section of the gender; J. drupacea, J. communis var. communis, J. communis var. saxatilis, J. oxycedrus subsp. oxycedrus, and J. oxycedrus subsp. macrocarpa growing were investigated. METHODS: For the anti-inflammatory activity, carrageenan-induced and PGE(2)-induced hind paw edema models, and for the antinociceptive activity p-benzoquinone-induced writhing and hot plate tests in mice were employed. RESULTS: The methanolic extracts of fruit and leaves from J. oxycedrus subsp. oxycedrus and J. communis var. saxatilis exhibited notable inhibition in carrageenan-induced edema model at a dose of 100mg/kg. The same extracts also displayed significant activity against PGE(2)-induced edema model. While, the remaining extracts were found inactive against these edema models. A similar activity pattern was observed against p-benzoquinone-induced abdominal constriction test without inducing any gastric damage or apparent acute toxicity, whereas all extracts were inactive in hot plate test. CONCLUSION: The experimental data demonstrated that J. oxycedrus subsp. oxycedrus and J. communis var. saxatilis displayed remarkable anti-inflammatory and antinociceptive activities; however, further studies are warranted to define and isolate the active anti-inflammatory and antinociceptive components from these active species which may yield safe and effective agents to be used in the treatment of inflammatory disorders.


Subject(s)
Analgesics/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Edema/drug therapy , Juniperus , Pain/drug therapy , Phytotherapy , Plant Extracts/therapeutic use , Analgesics/pharmacology , Animals , Anti-Inflammatory Agents/pharmacology , Behavior, Animal/drug effects , Benzoquinones , Carrageenan , Dinoprostone , Edema/chemically induced , Inflammation/drug therapy , Male , Mice , Pain/chemically induced , Plant Extracts/pharmacology , Plant Structures
12.
J Ethnopharmacol ; 116(2): 251-7, 2008 Mar 05.
Article in English | MEDLINE | ID: mdl-18164152

ABSTRACT

Erica L. species (Ericaceae) have been popularly used as antirheumatic, diuretic, astringent and treatment of urinary infections. In order to evaluate this information, anti-inflammatory and antinociceptive activities of different extracts prepared with methanol, chloroform, ethyl acetate, n-butanol and water from the aerial parts of Erica arborea L., Erica manipuliflora Salisb., Erica bocquetii (Pesmen) P.F. Stevens and Erica sicula Guss. subsp. libanotica (C.&W. Barbey) P.F. Stevens (Ericaceae) of Turkish origin were investigated by using in vivo methods. For the anti-inflammatory activity, carrageenan-induced hind paw edema model, PGE(2)-induced hind paw edema model, and 12-O-tetradecanoyl-13-acetate (TPA)-induced mouse ear edema model and for the antinociceptive activity p-benzoquinone-induced writhing test in mice were employed. The ethyl acetate extracts of Erica arborea (EAE), Erica bocquetii (EBE) and Erica manipuliflora (EME) exhibited notable inhibition against carrageenan-induced (24.1-32.3%, 23.8-36.1%, 29.2-35.1%, respectively) and PGE(2)-induced (21.2-37.7%, 6.8-29.7%, and 6.2-34.1%, respectively) hind paw edema as well as TPA-induced mouse ear edema models in mice, while the ethyl acetate extract of Erica sicula subsp. libanotica (ESE) (10.7-29.7%) displayed potent anti-inflammatory activity only on the PGE(2)-induced hind paw edema model. However, the remaining extracts were found to be inactive against inflammatory models. Same extracts, i.e., EAE, EBE and EME were also found to exhibit remarkable antinociceptive activity in p-benzoquinone-induced abdominal constriction test at a dose of 100mg/kg (46.5%, 27.7% and 36.3%, respectively).


Subject(s)
Analgesics/pharmacology , Anti-Inflammatory Agents/pharmacology , Ericaceae/chemistry , Plant Extracts/pharmacology , Animals , Dinoprostone/administration & dosage , Male , Mice , Tetradecanoylphorbol Acetate/toxicity , Turkey
13.
Biol Pharm Bull ; 27(7): 1140-3, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15256757

ABSTRACT

The inhibitory effects of 40 extracts prepared from 38 traditional Turkish folk medicines on human aldose reductase (h-AR) and hematological activity were investigated. Seven plants containing 5 species of Cistus genus exhibited a potent inhibition of h-AR. Ferulago amani (root) inhibited the platelet aggregation induced by sodium arachidonate, while C. laurifolius (fruit) was found to possess strong inhibition in the blood coagulation assay. An AcOEt extract derived from the leaf of C. laurifolius was purified to isolate three known flavonoids. The activity of one, quercetin-3-O-methyl ether, was found to be as potent as that of eparlestat, which is known to be a remedy for treating complications associated with diabetes.


Subject(s)
Aldehyde Reductase/antagonists & inhibitors , Anticoagulants/pharmacology , Cistus , Medicine, Traditional , Platelet Aggregation Inhibitors/pharmacology , Quercetin/analogs & derivatives , Quercetin/pharmacology , Aldehyde Reductase/metabolism , Anticoagulants/isolation & purification , Blood Coagulation/drug effects , Blood Coagulation/physiology , Enzyme Inhibitors/isolation & purification , Enzyme Inhibitors/pharmacology , Humans , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Plant Structures , Platelet Aggregation/drug effects , Platelet Aggregation/physiology , Platelet Aggregation Inhibitors/isolation & purification , Quercetin/isolation & purification , Turkey
14.
Phytochem Anal ; 14(1): 48-53, 2003.
Article in English | MEDLINE | ID: mdl-12597255

ABSTRACT

The threo and erythro forms of guaiacylglycerol-7'-O-methyl 8'-vanillic acid ethers, threo and erythro guaiacylglycerol 8'-vanillin ethers, and threo guaiacylglycerol 8'-(4-hydroxymethyl-2-methoxyphenyl) ether have been isolated from fruits of Boreava orientalis. Structural determinations were made on the basis of UV, MS, 1H- and 13C-NMR spectral data, including two-dimensional shift correlation. The relative configurations were assigned on the basis of 1H-NMR chemical shifts.


Subject(s)
Brassicaceae/chemistry , Guaifenesin/analogs & derivatives , Guaifenesin/analysis , Guaifenesin/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure
15.
Chem Pharm Bull (Tokyo) ; 50(2): 185-92, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11848207

ABSTRACT

Investigation of the constituents of the fruits of Morus alba LINNE (Moraceae) afforded five new nortropane alkaloids (1-5) along with nor-psi-tropine (6) and six new amino acids, morusimic acids A-F (7-12). The structures of the new compounds were determined to be 2alpha,3beta-dihydroxynortropane (1), 2beta,3beta-dihydroxynortropane (2), 2alpha,3beta,6exo-trihydroxynortropane (3), 2alpha,3beta,4alpha-rihydroxynortropane (4), 3beta,6exo-dihydroxynortropane (5), (3R)-3-hydroxy-12-[(1S,4S)-4-[(1S)-1-hydroxyethyl]-pyrrolidin-1-yll-dodecanoic acid-3-O-beta-D-glucopyranoside (7), (3R)-3-hydroxy-12-[(1S,4S)-4-[(1S)-1-hydroxyethyl]-pyrrolidin-1-yll-dodecanoic acid (8), (3R)-3-hydroxy-12-1(1R,4R,5S)-4-hydroxy-5-methyl-piperidin-1-yll-dodecanoic acid-3-O-beta-D-glucopyranoside (9), (3R)-3-hydroxy-12-[(1R,4R,5S)-4-hydroxy-5-methyl-piperidin-1-yll-dodecanoic acid (10), (3R)-3-hydroxy-12-[(1R,4R,5S)-4-hydroxy-5-hydroxymethyl-piperidin-1-yl]-dodecanoic acid-3-O-beta-D-glucopyranoside (11), and (3R)-3-hydroxy-12-[(1R,4S,5S)-4-hydroxy-5-methyl-piperidin-1-yl]-dodecanoic acid (12) on the basis of spectral and chemical data.


Subject(s)
Alkaloids/isolation & purification , Amino Acids/isolation & purification , Moraceae/chemistry , Alkaloids/chemistry , Amino Acids/chemistry , Fruit , Magnetic Resonance Spectroscopy , Turkey
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