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1.
Molecules ; 21(1): 78, 2016 Jan 12.
Artículo en Inglés | MEDLINE | ID: mdl-26771591

RESUMEN

The present research aimed to isolate the non-polar secondary metabolites that produce the vasodilator effects induced by the dichloromethane extract of Prunus serotina (P. serotina) fruits and to determine whether the NO/cGMP and the H2S/KATP channel pathways are involved in their mechanism of action. A bioactivity-directed fractionation of the dichloromethane extract of P. serotina fruits led to the isolation of ursolic acid and uvaol as the main non-polar vasodilator compounds. These compounds showed significant relaxant effect on rat aortic rings in an endothelium- and concentration-dependent manner, which was inhibited by NG-nitro-L-arginine methyl ester (L-NAME), DL-propargylglycine (PAG) and glibenclamide (Gli). Additionally, both triterpenes increased NO and H2S production in aortic tissue. Molecular docking studies showed that ursolic acid and uvaol are able to bind to endothelial NOS and CSE with high affinity for residues that form the oligomeric interface of both enzymes. These results suggest that the vasodilator effect produced by ursolic acid and uvaol contained in P. serotina fruits, involves activation of the NO/cGMP and H2S/KATP channel pathways, possibly through direct activation of NOS and CSE.


Asunto(s)
Sulfuro de Hidrógeno/agonistas , Óxido Nítrico/agonistas , Prunus avium/química , Triterpenos/farmacología , Vasodilatación/efectos de los fármacos , Vasodilatadores/farmacología , Alquinos/antagonistas & inhibidores , Alquinos/farmacología , Animales , Aorta/citología , Aorta/efectos de los fármacos , Aorta/metabolismo , GMP Cíclico/metabolismo , Cistationina gamma-Liasa/química , Cistationina gamma-Liasa/metabolismo , Endotelio Vascular/citología , Endotelio Vascular/efectos de los fármacos , Activación Enzimática/efectos de los fármacos , Frutas/química , Gliburida/antagonistas & inhibidores , Gliburida/farmacología , Glicina/análogos & derivados , Glicina/antagonistas & inhibidores , Glicina/farmacología , Sulfuro de Hidrógeno/metabolismo , Canales KATP/agonistas , Canales KATP/metabolismo , Masculino , Simulación del Acoplamiento Molecular , NG-Nitroarginina Metil Éster/antagonistas & inhibidores , NG-Nitroarginina Metil Éster/farmacología , Óxido Nítrico/biosíntesis , Óxido Nítrico Sintasa de Tipo III/química , Óxido Nítrico Sintasa de Tipo III/metabolismo , Extractos Vegetales/química , Unión Proteica , Ratas , Triterpenos/aislamiento & purificación , Vasodilatadores/aislamiento & purificación , Ácido Ursólico
2.
Molecules ; 20(2): 3479-95, 2015 Feb 17.
Artículo en Inglés | MEDLINE | ID: mdl-25690299

RESUMEN

Prunus serotina (black cherry), commonly known in Mexico as capulín, is used in Mexican traditional medicine for the treatment of cardiovascular, respiratory, and gastrointestinal diseases. Particularly, P. serotina seeds, consumed in Mexico as snacks, are used for treating cough. In the present study, nutritional and volatile analyses of black cherry seeds were carried out to determine their nutraceutical potential. Proximate analysis indicated that P. serotina raw and toasted seeds contain mostly fat, followed by protein, fiber, carbohydrates, and ash. The potassium content in black cherry raw and toasted seeds is high, and their protein digestibility-corrected amino acid scores suggest that they might represent a complementary source of proteins. Solid phase microextraction and gas chromatography/flame ionization detection/mass spectrometry analysis allowed identification of 59 and 99 volatile compounds in the raw and toasted seeds, respectively. The major volatile compounds identified in raw and toasted seeds were 2,3-butanediol and benzaldehyde, which contribute to the flavor and odor of the toasted seeds. Moreover, it has been previously demonstrated that benzaldehyde possesses a significant vasodilator effect, therefore, the presence of this compound along with oleic, linoleic, and α-eleostearic fatty acids indicate that black cherry seeds consumption might have beneficial effects on the cardiovascular system.


Asunto(s)
Carbohidratos de la Dieta/análisis , Grasas de la Dieta/análisis , Análisis de los Alimentos , Valor Nutritivo , Proteínas de Vegetales Comestibles/análisis , Prunus domestica/química , Semillas/química , Compuestos Orgánicos Volátiles/análisis
3.
Molecules ; 18(12): 14597-612, 2013 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-24287993

RESUMEN

In Mexico black cherry (Prunus serotina Ehrh.) fruits are consumed fresh, dried or prepared in jam. Considering the evidence that has linked intake of fruits and vegetables rich in polyphenols to cardiovascular risk reduction, the aim of this study was to characterize the phenolic profile of black cherry fruits and to determine their antioxidant, vasorelaxant and antihypertensive effects. The proximate composition and mineral contents of these fruits were also assessed. Black cherry fruits possess a high content of phenolic compounds and display a significant antioxidant capacity. High-performance liquid chromatography/mass spectrometric analysis indicated that hyperoside, anthocyanins and chlorogenic acid were the main phenolic compounds found in these fruits. The black cherry aqueous extract elicited a concentration-dependent relaxation of aortic rings and induced a significant reduction on systolic blood pressure in L-NAME induced hypertensive rats after four weeks of treatment. Proximate analysis showed that black cherry fruits have high sugar, protein, and potassium contents. The results derived from this study indicate that black cherry fruits contain phenolic compounds which elicit significant antioxidant and antihypertensive effects. These findings suggest that these fruits might be considered as functional foods useful for the prevention and treatment of cardiovascular diseases.


Asunto(s)
Antihipertensivos/química , Antioxidantes/química , Suplementos Dietéticos/análisis , Frutas/química , Extractos Vegetales/química , Prunus/química , Animales , Antihipertensivos/administración & dosificación , Antihipertensivos/farmacología , Antioxidantes/farmacología , Aorta/efectos de los fármacos , Presión Sanguínea/efectos de los fármacos , Cromatografía Líquida de Alta Presión , Relación Dosis-Respuesta a Droga , Endotelio Vascular/efectos de los fármacos , Flavonoides/química , Masculino , Espectrometría de Masas , Minerales/análisis , Minerales/química , Estructura Molecular , Fenoles/química , Extractos Vegetales/administración & dosificación , Extractos Vegetales/farmacología , Ratas
4.
Fitoterapia ; 153: 104985, 2021 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-34237389

RESUMEN

Affinin is mainly recognized by its antinociceptive effect. Recently, our research group demonstrated that this compound produces vasodilation via activation of the gasotransmitters signaling pathways. However, the molecular targets of affinin were not identified. Considering the structural similarity of this alkamide with anandamide, we hypothesized that affinin-induced vasodilation could involve participation of TRP channels and cannabinoid receptors. In this work, by using the isolated rat aorta assay, we assessed involvement of TRP channels, the cannabinoid system, and the HNO-CGRP-TRPA1 pathway on the mechanism of action of affinin. Additionally, we measured NO and H2S levels elicited by affinin on rat aorta homogenates and carried out computer simulations of molecular interactions between affinin and the TRPA1 and TRPV1 channels and the CB1 receptor. Our results indicated that affinin induces an increase in aortic NO and H2S levels. We found evidence that the vasodilator effect induced by affinin involves activation of TRPA1 and TRPV1 channels and the CB1 and eCB receptors. In silico analyses showed that affinin is able to bind with high affinity to these molecular targets. Moreover, we also proved that affinin-induced vasodilation is partly mediated via activation of the HNO-TRPA1-CGRP pathway. Based on these results we propose a novel mechanism of action to explain the vasodilatory effect of affinin, which could be developed as an alternative drug to treat cardiovascular diseases.


Asunto(s)
Alcamidas Poliinsaturadas/farmacología , Receptores de Cannabinoides/metabolismo , Canales Catiónicos TRPV/metabolismo , Vasodilatación/efectos de los fármacos , Animales , Aorta/efectos de los fármacos , Sulfuro de Hidrógeno , Técnicas In Vitro , Masculino , Simulación del Acoplamiento Molecular , Óxido Nítrico , Ratas , Ratas Wistar
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