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1.
Nat Prod Res ; 35(24): 6147-6152, 2021 Dec.
Article in English | MEDLINE | ID: mdl-33025828

ABSTRACT

Roemerine is a naturally occurring aporphine alkaloid. In this study, we screened a conformer library of Food and Drug Administration (FDA)-approved drugs to identify similar drugs that can assist in identifying the biological targets of roemerine. To assess the neuroactivity in vitro, we measured the levels of cell metabolites, Brain-Derived Neurotrophic Factor (BDNF) and serotonin (5-HT) in SH-SY5Y cell line. By means of structure-based virtual screening, we identified five drugs that are similar to roemerine; mirtazapine, atomoxetine, epinastine, diphenhydramine and orphenadrine. GC-MS metabolomics study revealed that roemerine has a high impact on alanine-aspartate-glutamate pathway in cell lysate and cultured medium. Additionally, roemerine increased intercellular 5-HT level and intracellular BDNF protein expression at 10 µM. In conclusion, roemerine - a major alkaloid in antidepressant-like effect possessing plants (P. lacerum and P. syriacum) - has a neuronal activity through increasing BDNF protein expression and affecting serotonergic and glutamatergic systems in SH-SY5Y cell line.


Subject(s)
Alkaloids , Aporphines , Alkaloids/pharmacology , Aporphines/pharmacology , Brain-Derived Neurotrophic Factor , Cell Line, Tumor , Humans , Plant Extracts , Serotonin
2.
J Biochem Mol Toxicol ; 34(12): e22601, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32852096

ABSTRACT

Pronuciferine is a naturally occurring proaporphine alkaloid that belongs to isoquinoline alkaloids. The aim of this study is to investigate the neuroactivity of pronuciferine. We assessed the neuroprotective effect of pronuciferine against hydrogen peroxide (H2 O2 )-induced apoptosis in human neuronal SH-SY5Y cells. In addition, we measured the effect of pronuciferine on cell metabolites and brain-derived neurotrophic factor (BDNF) level in SH-SY5Y cells. In vitro result shows that pronuciferine at 10 µM significantly (P < .001) increased the proliferation of SH-SY5Y by 45%, and upon H2 O2 addition, pronuciferine significantly (P < .001) suppressed neuronal death caused by H2 O2 . Gas Chromatography-Mass Spectrometry (GC-MS) metabolomics study revealed that pronuciferine has a high impact on glycine-serine-threonine pathway by changing the intracellular level of serine dimethylglycine, sarcosine, and threonine. Also, pronuciferine increased the intercellular level of aspartic acid, glutamine, and tryptophan. Additionally, pronuciferine significantly (P < .05) increased the intracellular BDNF protein expression at 10 µM. Therefore, pronuciferine is a neuroactive molecule that might act as a neuroprotective agent to prevent apoptosis in neurodegenerative diseases.


Subject(s)
Alkaloids/pharmacology , Neuroprotective Agents/pharmacology , Spiro Compounds/pharmacology , Cell Line, Tumor , Cell Survival/drug effects , Humans , Hydrogen Peroxide/pharmacology , Oxidative Stress/drug effects
3.
J Ethnopharmacol ; 261: 113143, 2020 Oct 28.
Article in English | MEDLINE | ID: mdl-32687958

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Solanum melongena L. (eggplant) is used for treatment of rheumatism, beriberi, itching, toothache, bleeding, asthma, bronchitis, cholera, neuralgia and hemorrhoids in traditional medicine (Turkish, Chinese, and Indian). Hemorrhoids from these diseases, are common illness in all over the world, which are treated with various approaches including ethnobotanicals. AIM OF THE STUDY: This study aimed to evaluate the anti-hemorrhoidal activity of eggplant, an edible plant, which is commonly utilized around the world. MATERIALS & METHODS: In vivo anti-hemorrhoidal activity of the methanolic extract prepared from eggplant was evaluated by experimental hemorrhoid model, subsequently histological and biochemical analysis. Hemorrhoid, which was induced by applying croton oil to the anal area of the rats. Furthermore, the extract was screened for anti-inflammatory activity which is based on the inhibition of acetic acid-induced increase in capillary permeability. The healing potential was comparatively assessed with a reference Pilex® tablet and cream. Phytochemical analysis performed by HPLC. The amount of the major phenolic compound (chlorogenic acid) in extract was found by using HPLC method. RESULTS: Histological and biochemical analysis demonstrated that eggplant extract is highly effective against hemorrhoid in comparison to the controls and the commercial preparation. In addition, the methanolic extract demonstrated significant inhibitory effect on acetic acid-induced increase in capillary permeability. The phytochemical studies identified major compound as chlorogenic acid (2.86%) by liquid chromatography. CONCLUSION: The eggplant calyxes, not edible, are easy to reach, by products/vast from the food sources. This is the first scientific evidence revealing that the eggplant extract has significant anti-hemorrhoidal and anti-inflammatory activity.


Subject(s)
Anal Canal/blood supply , Anti-Inflammatory Agents/pharmacology , Hemorrhoids/drug therapy , Plant Extracts/pharmacology , Solanum melongena , Wound Healing/drug effects , Animals , Anti-Inflammatory Agents/isolation & purification , Capillary Permeability/drug effects , Croton Oil , Disease Models, Animal , Hemorrhoids/chemically induced , Hemorrhoids/pathology , Male , Mice, Inbred BALB C , Plant Extracts/isolation & purification , Rats, Wistar , Solanum melongena/chemistry
4.
Phytomedicine ; 74: 152920, 2020 Aug.
Article in English | MEDLINE | ID: mdl-30979692

ABSTRACT

BACKGROUND: Identification of the low abundance of phytochemicals in plant extracts is very difficult. Pharmacological activity observed in such plants is not due to a single compound. In most cases, plant extracts show activity based on synergistic or antagonistic effects. Therefore, the idea of a holistic approach is more rational. PURPOSE: This study was planned to compare the metabolomics and proteomics profiles of Valeriana officinalis L. (Valerianaceae), Melissa officinalis L. (Lamiaceae), Hypericum perforatum L. (Hypericaceae) and Passiflora incarnata L. (Passifloraceae) used in sedative anxiolytic and sleep disorders. Integrated omics analyses were used to provide a better understanding of the effect of plant extracts on the brain-derived neurotrophic factor (BDNF) expression levels on the SH-SY5Y cell line by a holistic approach. METHODS: Metabolomic profiling of the plants was performed using the GC-MS and LC-qTOF-MS systems, and the proteomics analysis using the LC-qTOF-MS system after trypsin digestion. The Human BDNF Quantikine ELISA kit was utilized to test BDNF expression activity on the SH-SY5Y cell line. RESULTS: The investigated plant extracts showed a significant increase in BDNF expression (p < 0.05). M. officinalis was found as the most active extract. According to the correlation analyses between BDNF activity and metabolomics or proteomics level, 94 metabolites had a positive correlation while 23 metabolites had a highly negative correlation; those for proteins are 24 and 6, respectively. CONCLUSION: The multivariate data analysis revealed a similar metabolomics profile of H. perforatum and P. incarnata, which also had a similar activity profile. Remarkably, all the primary metabolites belonging to the Krebs Cycle (citric acid, fumaric acid, succinic acid, pyruvic acid, malic acid and citramalic acid, an analog of malic acid) were positively correlated with BDNF activity. Secondary metabolites with a high BDNF expression belonged to flavonoids, xanthone, coumarines, tannin, naphtalenes, terpenoids and carotenoid skeleton. Two proteins from the cytochrome P450 family (P450 71B11 and P450 94B3) were positively correlated with BDNF activity. Employing omics technologies in the plant research area will offer a better understanding of the role of plant extracts and may lead to the discovery of new compounds with specific activity.


Subject(s)
Brain-Derived Neurotrophic Factor/metabolism , Drug Evaluation, Preclinical/methods , Plant Extracts/pharmacology , Plants, Medicinal/chemistry , Chromatography, Liquid , Flavonoids/analysis , Flavonoids/pharmacology , Gas Chromatography-Mass Spectrometry , Humans , Hypericum/chemistry , Mass Spectrometry , Metabolomics/methods , Passiflora/chemistry , Plant Extracts/chemistry , Plants, Medicinal/metabolism , Proteomics/methods , Secondary Metabolism , Terpenes/analysis , Terpenes/pharmacology , Valerian/chemistry
5.
J Med Food ; 21(6): 625-631, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29719159

ABSTRACT

Cuscuta arvensis Beyr. is a parasitic plant, and commonly known as "dodder" in Europe, in the United States, and "tu si zi shu" in China. It is one of the preferred spices used in sweet and savory dishes. Also, it is used as a folk medicine for the treatment particularly of liver problems, knee pains, and physiological hepatitis, which occur notably in newborns and their mothers in the southeastern part of Turkey. The purpose of this study was to investigate the hepatoprotective effects and antioxidant activities of aqueous and methanolic extracts of C. arvensis Beyr. on acetaminophen (APAP)-induced acute hepatotoxicity in rats. The results were supported by subsequent histopathological studies. The hepatoprotective activity of both the aqueous and methanolic extracts at an oral dose of 125 and 250 mg/kg was investigated by observing the reduction levels or the activity of alkaline phosphatase, alkaline transaminase, aspartate aminotransferase, blood urine nitrogen, and total bilirubin content. In vivo antioxidant activity was determined by analyzing the serum superoxide dismutase, malondialdehyde, glutathione, and catalase levels. Chromatographic methods were used to isolate biologically active compounds from the extract, and spectroscopic methods were used for structure elucidation. Both the methanolic and aqueous extracts exerted noticable hepatoprotective and antioxidant effects supporting the folkloric usage of dodder. One of the bioactive compounds was kaempferol-3-O-rhamnoside, isolated and identified from the methanolic extract.


Subject(s)
Acetaminophen/toxicity , Chemical and Drug Induced Liver Injury/drug therapy , Cuscuta/chemistry , Plant Extracts/administration & dosage , Alkaline Phosphatase/metabolism , Animals , Antioxidants/administration & dosage , Antioxidants/chemistry , Aspartate Aminotransferases/metabolism , Bilirubin/metabolism , Catalase/metabolism , Chemical and Drug Induced Liver Injury/etiology , Chemical and Drug Induced Liver Injury/metabolism , Female , Humans , Liver/drug effects , Liver/metabolism , Malondialdehyde/metabolism , Plant Extracts/chemistry , Rats , Rats, Sprague-Dawley , Superoxide Dismutase/metabolism
6.
Nat Prod Commun ; 9(4): 505-6, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24868869

ABSTRACT

Gentiana verna L. subsp. pontica (Soltok.) Hayek, G. pyrenaica L., and G. verna L. subsp. balcanica Pritchard from Turkey were tested for their MAO-A inhibitory effects. A photometric peroxidase linked MAO-A bioassay performed on the H20 extracts prepared from the methanolic extracts of the title plants revealed the potential effect of G. verna subsp. pontica and three benzophenone glucosides; 2,3'-dihydroxy-4-methoxy-benzophenone-6-O-beta-glucopyranoside (1), 2,4,3',4'-tetrahydroxy-benzophenone-6-O-beta-glucopyranoside (maclurin-6-O-f-glucopyranoside) (2) and 2,4,3'-trihydroxy-benzophenone-6-O-beta-glucopyranoside (3) isolated from G. verna subsp. pontica. Among the benzophenone glucosides 1 and 2 exhibited significant inhibition of MAO-A (IC50 = 31.3 +/- 4 microM and 41 +/- 4.7 microM resp.).


Subject(s)
Benzophenones/chemistry , Gentiana/chemistry , Glucosides/chemistry , Monoamine Oxidase Inhibitors/pharmacology , Monoamine Oxidase/metabolism , Monoamine Oxidase Inhibitors/chemistry
7.
J Ethnopharmacol ; 148(2): 423-32, 2013 Jul 09.
Article in English | MEDLINE | ID: mdl-23665056

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: Trifolium species are used in Turkish folk medicine as a wound healing agent, expectorant, antiseptic, sedative and to alleviate pain in rheumatism. In the present study, the aqueous methanolic extracts (80%) of 13 Trifolium species (Trifolium ambigum, Trifolium arvense var. arvense, Trifolium campestre, Trifolium canescens, Trifolium hybridum var. anatolicum, Trifolium hybridum var. hybridum, Trifolium pannonicum, Trifolium pratense var. pratense, Trifolium purpureum var. purpureum, Trifolium repens var. repens, Trifolium resupinatum var. microcephalum, Trifolium spadiceum and Trifolium trichocephalum) collected from different regions of Anatolia were evaluated for their in vivo wound healing effects. MATERIALS AND METHODS: In vivo wound healing activities of the plant aqueous methanolic extracts were evaluated by linear incision and circular excision wound models subsequent to histopathological analysis. Active constituents were determined by a validated high performance liquid chromatographic method. Precision of the method was performed by the evaluation of intra-day and inter-day variations of the each standard at limits of quantification (LOQ) levels. RESULTS: The aqueous methanolic extracts of Trifolium canescens and Trifolium pretense var. pratense possessed better wound healing activity compared to the other extracts and control groups. The animal groups treated with the Trifolium canescens extract demonstrated increased contraction (48.96%) on excision and a significant increase in wound tensile strength (35.6%) on incision models. The main compounds were detected as genistein and biochanin A for Trifolium canescens. CONCLUSION: The results of the present study revealed the wound healing potential of Trifolium canescens. This might be due to the combined effect of the isoflavones genistein, formononetin, daidzein, and biochanin A present in the extract.


Subject(s)
Isoflavones/pharmacology , Plant Extracts/pharmacology , Skin/drug effects , Trifolium/chemistry , Wound Healing/drug effects , Animals , Genistein/chemistry , Genistein/pharmacology , Isoflavones/chemistry , Male , Medicine, Traditional , Methanol/chemistry , Mice , Plant Extracts/chemistry , Rats , Rats, Sprague-Dawley , Turkey , Water/chemistry
8.
Z Naturforsch C J Biosci ; 57(7-8): 584-90, 2002.
Article in English | MEDLINE | ID: mdl-12240980

ABSTRACT

The chemical composition of the brown alga Cystoseira crinita Bory from the Eastern Mediterranean was investigated. Fourteen sterols have been identified, five of them for the first time in algae. The structure of one new sterol was established. The origin of seven sterols with short side chains was discussed. In the volatile fraction 19 compounds and in the polar fraction 15 compounds were identified. The main lipid classes were isolated and their fatty acid composition was established.


Subject(s)
Magnoliopsida/chemistry , Plant Extracts/chemistry , Alcohols/chemistry , Alcohols/isolation & purification , Carboxylic Acids/chemistry , Carboxylic Acids/isolation & purification , Gas Chromatography-Mass Spectrometry , Glycolipids/chemistry , Glycolipids/isolation & purification , Lipids/chemistry , Lipids/isolation & purification , Mediterranean Region , Phospholipids/chemistry , Phospholipids/isolation & purification , Terpenes/chemistry , Terpenes/isolation & purification , Triglycerides/chemistry , Triglycerides/isolation & purification , Volatilization
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