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1.
Mar Drugs ; 18(11)2020 Nov 19.
Article in English | MEDLINE | ID: mdl-33227946

ABSTRACT

The aim of the present work was to evaluate the effects of Thalassia testudinum hydroethanolic extract, its polyphenolic fraction and thalassiolin B on the activity of phase I metabolizing enzymes as well as their antimutagenic effects. Spectrofluorometric techniques were used to evaluate the effect of tested products on rat and human CYP1A and CYP2B activity. The antimutagenic effect of tested products was evaluated in benzo[a]pyrene (BP)-induced mutagenicity assay by an Ames test. Finally, the antimutagenic effect of Thalassia testudinum (100 mg/kg) was assessed in BP-induced mutagenesis in mice. The tested products significantly (p < 0.05) inhibit rat CYP1A1 activity, acting as mixed-type inhibitors of rat CYP1A1 (Ki = 54.16 ± 9.09 µg/mL, 5.96 ± 1.55 µg/mL and 3.05 ± 0.89 µg/mL, respectively). Inhibition of human CYP1A1 was also observed (Ki = 197.1 ± 63.40 µg/mL and 203.10 ± 17.29 µg/mL for the polyphenolic fraction and for thalassiolin B, respectively). In addition, the evaluated products significantly inhibit (p < 0.05) BP-induced mutagenicity in vitro. Furthermore, oral doses of Thalassia testudinum (100 mg/kg) significantly reduced (p < 0.05) the BP-induced micronuclei and oxidative damage, together with an increase of reduced glutathione, in mice. In summary, Thalassia testudinum metabolites exhibit antigenotoxic activity mediated, at least, by the inhibition of CYP1A1-mediated BP biotransformation, arresting the oxidative and mutagenic damage. Thus, the metabolites of T. testudinum may represent a potential source of chemopreventive compounds for the adjuvant therapy of cancer.


Subject(s)
Antimutagenic Agents/pharmacology , Benzo(a)pyrene/toxicity , Cytochrome P-450 CYP1A1/antagonists & inhibitors , Cytochrome P-450 Enzyme Inhibitors/pharmacology , Flavonoids/pharmacology , Hydrocharitaceae/metabolism , Polyphenols/pharmacology , Salmonella typhi/drug effects , Activation, Metabolic , Animals , Antimutagenic Agents/isolation & purification , Benzo(a)pyrene/metabolism , Cytochrome P-450 CYP1A1/metabolism , Cytochrome P-450 CYP1A2/metabolism , Cytochrome P-450 CYP1A2 Inhibitors/isolation & purification , Cytochrome P-450 CYP1A2 Inhibitors/pharmacology , Cytochrome P-450 Enzyme Inhibitors/isolation & purification , DNA Damage/drug effects , Flavonoids/isolation & purification , Humans , Isoenzymes , Kinetics , Micronuclei, Chromosome-Defective/chemically induced , Micronucleus Tests , Oxidative Stress/drug effects , Polyphenols/isolation & purification , Rats , Salmonella typhi/genetics
2.
Rev. neuro-psiquiatr. (Impr.) ; 77(2): 70-77, abr. 2014. tab
Article in Spanish | LILACS-Express | LILACS, LIPECS | ID: lil-722544

ABSTRACT

La infección por el Virus de la Inmunodeficiencia Humana (VIH) es una endemia que ha impactado severamente a la población mundial en tiempos recientes. A lo largo de los años se han descrito numerosas alteraciones psiquiátricas en los individuos que padecen la infección por este virus: deterioro cognitivo, depresión, delirium, psicosis, manía y ansiedad. El presente artículo es una breve revisión sobre aspectos generales de la infección con el Virus de la Inmunodeficiencia Humana y la repercusión a nivel psiquiátrico que se evidencia en sujetos que padecen tanto de la infección como del Síndrome de Inmunodeficiencia Adquirida (SIDA) y sus complicaciones.


Infection with Human Immunodeficiency Virus is an endemic disease that has severely impacted the world population in recent times. Over the years, numerous psychiatric syndromes have been reported in individuals who are infected by this virus: cognitive impairment, depression, delirium, psychosis, mania and anxiety. This article is a brief review of general aspects of the infection with the Human Immunodeficiency Virus and its psychiatric impact on the patients suffering from both infection and Acquired Immunodeficiency Syndrome (AIDS) and their complications.

3.
Nat Prod Commun ; 6(8): 1179-82, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21922930

ABSTRACT

The chemical composition of Tornabenea bischoffii J. A. Schmidt essential oil from Cape Verde was studied by GC and GC/MS. Sixty volatile compounds were identified of which myristicin was the major constituent (33.6%). Using the 2,2-diphenyl-2-picrylhydrazyl free-radical scavenging method and the in vitro assay for prevention of lipid peroxidation by thiobarbituric reactive species, significant antioxidant activities were evidenced.


Subject(s)
Antioxidants/chemistry , Apiaceae/chemistry , Oils, Volatile/chemistry , Plant Oils/chemistry , Lipid Peroxidation , Plant Components, Aerial/chemistry , Thiobarbituric Acid Reactive Substances
4.
Photochem Photobiol ; 87(5): 1058-66, 2011.
Article in English | MEDLINE | ID: mdl-21615743

ABSTRACT

The apolar fraction F1 of Thalassia testudinum was chemically characterized by gas chromatography-mass spectrometry, which led to the identification of 43 metabolites, all of them reported for the first time in the genus Thalassia. More than 80% of the F1 composition was constituted by aromatic metabolites including the major components 1,1-bis(p-tolyl)ethane (6.0%), 4,4'-diisopropylbiphenyl (4.8%) and a 1,1-bis(p-tolyl)ethane isomer (4.7%). This lipophilic fraction was assayed for its antioxidant effects and skin protective action. In vitro assays showed that F1 strongly scavenged DPPH* (IC(50) 312.0 ± 8.0 µg mL(-1)), hydroxyl (IC(50) 23.8 ± 0.5 µg mL(-1)) and peroxyl radical (IC(50) 6.6 ± 0.3 µg mL(-1) ), as well as superoxide anion (IC(50) 50.0 ± 0.7 µg mL(-1)). Also, F1 markedly inhibited the spontaneous lipid peroxidation (LPO) in brain homogenates (IC(50) 93.0 ± 6.0 µg mL(-1)) and the LPS-stimulated nitrite generation on RAW624.7 macrophages (58.6 ± 3.2%, 400 µg mL(-1)). In agreement with these findings, its topical application at 250 and 500 µg cm(-2) strikingly reduced skin damage on mice exposed to acute UVB radiation by 45% and 70%, respectively and significantly attenuated the LPO developed following the first 48 h after acute exposure to UVB irradiation, as manifested by the decreased malondialdehide level and by the increased of reduced gluthatione content. Our results suggest that F1 may contribute to skin repair by attenuating oxidative stress due to its antioxidant activity.


Subject(s)
Free Radical Scavengers/pharmacology , Free Radicals/antagonists & inhibitors , Hydrocharitaceae/chemistry , Plant Extracts/pharmacology , Plant Leaves/chemistry , Skin/drug effects , Sunscreening Agents/pharmacology , Animals , Brain/drug effects , Brain/metabolism , Cell Line , Free Radical Scavengers/chemistry , Free Radical Scavengers/metabolism , Free Radicals/metabolism , Gas Chromatography-Mass Spectrometry , Glutathione/analysis , Glutathione/biosynthesis , Hydrophobic and Hydrophilic Interactions , Lipid Peroxidation/drug effects , Lipid Peroxidation/radiation effects , Lipopolysaccharides/adverse effects , Macrophages/cytology , Macrophages/drug effects , Macrophages/metabolism , Male , Malondialdehyde/analysis , Mice , Plant Extracts/chemistry , Plant Extracts/metabolism , Skin/metabolism , Skin/radiation effects , Sunscreening Agents/chemistry , Sunscreening Agents/metabolism , Tissue Extracts/metabolism , Ultraviolet Rays/adverse effects
5.
Chem Biodivers ; 7(9): 2281-8, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20860029

ABSTRACT

The phytochemical profile of Melaleuca leucadendra L. leaf and fruit oils from Cuba was investigated by GC and GC/MS. Forty-one and sixty-four volatile compounds were identified and quantified, accounting for 99.2 and 99.5% of the leaf-oil and fruit-oil total composition, respectively. The main components were 1,8-cineol (43.0%), viridiflorol (24.2%), α-terpineol (7.0%), α-pinene (5.3%), and limonene (4.8%) in the leaf oil, and viridiflorol (47.6%), globulol (5.8%), guaiol (5.3%), and α-pinene (4.5%) in the fruit oil. The antioxidant capacity of these essential oils was determined by three different in vitro assays (2,2-diphenyl-1-picrylhydrazyl (DPPH) radical, thiobarbituric acid reactive species (TBARS), and 2,2'-Azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical cation), and significant activities were evidenced for all of them.


Subject(s)
Free Radical Scavengers/chemistry , Melaleuca/chemistry , Oils, Volatile/chemistry , Plant Oils/chemistry , Biphenyl Compounds/chemistry , Free Radical Scavengers/isolation & purification , Free Radical Scavengers/pharmacology , Free Radicals/chemistry , Fruit/chemistry , Gas Chromatography-Mass Spectrometry , Molecular Structure , Oils, Volatile/isolation & purification , Oils, Volatile/pharmacology , Picrates/chemistry , Plant Leaves/chemistry , Plant Oils/isolation & purification , Plant Oils/pharmacology , Structure-Activity Relationship , Thiobarbituric Acid Reactive Substances/chemistry
6.
Chem Biodivers ; 7(5): 1325-32, 2010 May.
Article in English | MEDLINE | ID: mdl-20491086

ABSTRACT

The chemical composition of Artemisia gorgonum Webb essential oil from Cape Verde was analyzed by GC and GC/MS. A total of 111 volatile compounds, accounting for 94.9% of the essential oil, were identified by GC and GC/MS. The major compounds were camphor (28.7%), chrysanthenone (10.8%), lavandulyl 2-methylbutanoate (9.5%), alpha-phellandrene (5.5%), lavandulyl propanoate (4.2%), camphene (4.0%), and p-cymene (3.4%). The volatile oil of this endemic plant, which is used in Cape Verdean folk medicine against several ailments, was tested for its antioxidant and antimalarial properties, and was found to exhibit free-radical scavenging on 1,1-diphenyl-2-picrylhydrazyl (DPPH), prevention of lipid peroxidation-in vitro by TBARS (thiobarbituric acid reactive species) assay, and antiplasmodial activity.


Subject(s)
Antimalarials/chemistry , Artemisia/chemistry , Free Radical Scavengers/chemistry , Oils, Volatile/chemistry , Plant Oils/chemistry , Antimalarials/isolation & purification , Antimalarials/pharmacology , Free Radical Scavengers/isolation & purification , Free Radical Scavengers/pharmacology , Gas Chromatography-Mass Spectrometry , Lipid Peroxidation/drug effects , Oils, Volatile/isolation & purification , Oils, Volatile/pharmacology , Plant Extracts/chemistry
7.
Nat Prod Commun ; 4(9): 1277-80, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19831044

ABSTRACT

The chemical composition of essential oil from the air-dried aerial parts of Satureja forbesii (Benth.) Briq. from Cape Verde was studied by GC and GC/MS. Thirty-nine volatile compounds were identified of which geranial (42.0%) and neral (31.2%) were the major constituents. Using the 2,2-diphenyl-2-picrylhydrazyl free-radical scavenging method and the in vitro assay for prevention of lipid peroxidation by thiobarbituric reactive species, significant activities were evidenced.


Subject(s)
Free Radical Scavengers/isolation & purification , Plant Oils/chemistry , Satureja/chemistry , Terpenes/isolation & purification , Antioxidants/chemistry , Antioxidants/isolation & purification , Biphenyl Compounds/chemistry , Cabo Verde , Free Radical Scavengers/chemistry , Picrates/chemistry , Plant Components, Aerial/chemistry , Terpenes/chemistry , Thiobarbituric Acid Reactive Substances/analysis
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