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1.
Can J Cardiol ; 39(5): 646-659, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-36641049

RESUMEN

BACKGROUND: Vascular remodelling during pulmonary hypertension (PH) is characterized by the phenotypic transformation of pulmonary arterial smooth muscle cells (PASMCs). Swietenine (Swi), extracted from the seeds of traditional medicine Swietenia mahagoni, has been used to treat cardiac remodelling, but the effect of Swi on PH is unknown. This study aims to evaluate the effect of Swi on hypoxia-induced phenotypic transformation of PASMCs in experimental PH. METHODS: In our research, C57BL/6 mice were treated with SU5416 and exposed to hypoxia for 4 weeks to establish HySu-PH model. Mice in the Swi treatment group were subjected to HySu with daily administration of Swi. Hemodynamic parameters, echocardiography, and degree of vascular muscularization were measured to evaluate the PH model. Proliferation of PASMC was assessed by Ki67 and EdU assay. Cell migration was detected by wound-healing assay. Mitophagy levels were evaluated by mito-tracker and lyso-tracker, autophagic flux, and protein expression of Pink1 and Lc3 II. The molecular docking was used to validate the interaction of Swi with Nrf2. Immunofluorescence and immunohistochemical staining were applied to determine the subcellular localization of Nrf2. RESULTS: The results showed that Swi attenuated hypoxia-induced increase of right ventricle systolic pressure, Fulton index, and vascular remodelling and decreased PASMC proliferation, migration, and enhanced mitophagy. Furthermore, the interaction of Swi with Nrf2 promoted the translocation of Nrf2 into the nucleus, resulting in the induction of Pink1. CONCLUSIONS: This study demonstrates that Swi prevents vascular remodelling in experimental PH through inhibition of phenotypic transformation and hyperproliferation of PASMCs caused by reversing hypoxia-induced inhibition of mitophagy.


Asunto(s)
Hipertensión Pulmonar , Ratones , Animales , Remodelación Vascular/fisiología , Mitofagia , Simulación del Acoplamiento Molecular , Factor 2 Relacionado con NF-E2/metabolismo , Factor 2 Relacionado con NF-E2/farmacología , Proliferación Celular/fisiología , Ratones Endogámicos C57BL , Arteria Pulmonar , Hipoxia/complicaciones , Miocitos del Músculo Liso/metabolismo , Proteínas Quinasas/metabolismo , Proteínas Quinasas/farmacología , Células Cultivadas
2.
Fitoterapia ; 165: 105421, 2023 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-36587748

RESUMEN

Two rare flavonoid-2-(2-phenylethyl)chromones and five new dimeric 2-(2-phenylethyl)chromones were isolated from ethanol extract of agarwood of Aquilaria walla by LC-MS-guided fractionation procedure. Their structures were established based on extensive spectroscopic methods including HRESIMS, 1D and 2D NMR, as well as by comparison with the literature. Compound 1 showed cytotoxic activity against five human cancer cell lines with IC50 values ranging from 13.40 to 28.96 µM with cisplatin as the positive control.


Asunto(s)
Cromonas , Thymelaeaceae , Humanos , Cromonas/farmacología , Thymelaeaceae/química , Estructura Molecular , Flavonoides/química , Espectrometría de Masas , Madera/química
3.
Environ Toxicol ; 35(12): 1343-1351, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-32686902

RESUMEN

As a traditional plant medicine in tropical areas, Swietenia macrophylla seeds are usually applied for some chronic diseases, including hypertension, diabetes, and so on. Few studies have been carried out to identify the effective elements in seed extract and their indications. In this study, we first investigated the functions of the swietenine, an extract from S. macrophylla seeds, using a model of myocardial hypertrophy induced by isoprenaline (ISO). At cellular level, H9c2 cell hypertrophy was also established through the treatment with ISO. The cardiac pathological remodeling was evaluated by echocardiography and histological analysis. Western blot and RT-qPCR were used to detect the expression of possible hypertrophy-promoting genes. Here, our results indicated that swietenine remarkably attenuated ISO-induced myocardial hypertrophy in vivo and in vitro. Moreover, Akt phosphorylation, ANP and BNP mRNA expression were efficiently decreased. Based on these findings, we concluded that swietenine might be a promising anti-hypertrophic agent against cardiac hypertrophy.


Asunto(s)
Cardiomegalia/prevención & control , Corazón/efectos de los fármacos , Limoninas/farmacología , Meliaceae/química , Extractos Vegetales/farmacología , Animales , Cardiomegalia/inducido químicamente , Aumento de la Célula/efectos de los fármacos , Línea Celular , Supervivencia Celular/efectos de los fármacos , Isoproterenol/efectos adversos , Limoninas/aislamiento & purificación , Masculino , Ratones , Miocardio/metabolismo , Miocardio/patología , Miocitos Cardíacos/efectos de los fármacos , Miocitos Cardíacos/patología , Tamaño de los Órganos/efectos de los fármacos , Extractos Vegetales/aislamiento & purificación , Ratas , Semillas/química
4.
Molecules ; 23(11)2018 Nov 20.
Artículo en Inglés | MEDLINE | ID: mdl-30463280

RESUMEN

Six new phragmalin limonoids, named moluccensin Z1 (1), moluccensin Z2 (2), carapanolide Y (3), tabulalin N (4), chukvelutilide A1 (5), and velutinasin J (6), as well as two known compounds, chukvelutilide A (7) and velutinasin D (8) were isolated from the stems of Chukrasia tabularis A. Juss. The structures of the new compounds 1⁻6 were confirmed by spectroscopic methods, including IR and HRESIMS, as well as 1D and 2D NMR, and by comparisons with the data of known analogues. All compounds were tested for α-glucosidase and acetylcholinesterase inhibitory activities. However, none of the compounds was active against α-glucosidase and acetylcholinesterase in vitro.


Asunto(s)
Limoninas/aislamiento & purificación , Meliaceae/química , Limoninas/química , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Extractos Vegetales/química , Tallos de la Planta/química
5.
Molecules ; 21(9)2016 Aug 30.
Artículo en Inglés | MEDLINE | ID: mdl-27589710

RESUMEN

Four new mexicanolide-type limonoids 1-4, along with two known limonoids 5-6, were isolated from the ethanolic extracts of roots of the Traditional Chinese Medicine Trichilia sinensis. Their structures were unambiguously determined by analysis of spectroscopic data, including 1D and 2D NMR as well as MS, and by comparison with literature data. In addition, the acetylcholinesterase (AChE) inhibitory activity of compounds 1-6 was evaluated by the Ellman method. All these compounds showed weak AChE inhibitory activity, with the inhibition percentages ranging from 18.5% to 27.8%.


Asunto(s)
Inhibidores de la Colinesterasa , Limoninas , Meliaceae/química , Raíces de Plantas/química , Inhibidores de la Colinesterasa/química , Inhibidores de la Colinesterasa/aislamiento & purificación , Limoninas/química , Limoninas/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Estructura Molecular
6.
Nat Prod Commun ; 9(1): 7-8, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24660448

RESUMEN

One new diterpenoid, 11alpha,12betaH-dolabella-4,8(17)-dien-3alpha,7beta,18-triol (1) and one new sesquilignan, 9-methoxy-7',8'-cis-7",8"-cis-buddlenol B (2), together with three known compounds, (+)-diasyringaresinol (3), N-methyl-5- hydroxy-delta3-pyrrolin-2-one (4) and marmin (5), have been isolated from Aglaia odorata var. microphyllina. Their structures were determined using 1D and 2D NMR spectroscopy. Compound 1 exhibited cytotoxic activity against the K562 cell line with an IC50 value of 12.5 microg/mL.


Asunto(s)
Aglaia/química , Diterpenos/aislamiento & purificación , Diterpenos/química , Ensayos de Selección de Medicamentos Antitumorales , Humanos , Células K562 , Estructura Molecular , Plantas Medicinales/química
7.
Fitoterapia ; 92: 93-9, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24188859

RESUMEN

One new norsesquiterpene (1), and four new sesquiterpenes (2 - 5), along with four known ones, were isolated from the twigs of Aglaia odorata var. microphyllina C. DC. Monogr. Their structures were established based on spectroscopic methods including HR-ESI-MS, 1D, and 2D NMR. Compounds 1, 3, and 6 showed cytotoxic activity against SGC-7901 tumor cell.


Asunto(s)
Aglaia/química , Antineoplásicos Fitogénicos/uso terapéutico , Fitoterapia , Extractos Vegetales/uso terapéutico , Sesquiterpenos/uso terapéutico , Neoplasias Gástricas/tratamiento farmacológico , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/aislamiento & purificación , Antineoplásicos Fitogénicos/farmacología , Línea Celular Tumoral , Humanos , Estructura Molecular , Extractos Vegetales/química , Extractos Vegetales/farmacología , Tallos de la Planta , Sesquiterpenos/química , Sesquiterpenos/aislamiento & purificación , Sesquiterpenos/farmacología
8.
J Asian Nat Prod Res ; 15(8): 899-904, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23796077

RESUMEN

Two new acridone alkaloids, 3-methoxy-1,4,5-trihydroxy-10-methylacridone (1) and 2,3-dimethoxy-1,4,5-trihydroxy-10-methylacridone (2), were isolated from the ethanol extract of the branch of Atalantia buxifolia. Their structures were elucidated by spectroscopic methods including 1D and 2D NMR. Compounds 1 and 2 exhibited significant antibacterial activity against Staphylococcus aureus and weak inhibitory effect on acetylcholinesterase.


Asunto(s)
Acridinas/aislamiento & purificación , Acridinas/farmacología , Alcaloides/aislamiento & purificación , Alcaloides/farmacología , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Inhibidores de la Colinesterasa/aislamiento & purificación , Inhibidores de la Colinesterasa/farmacología , Medicamentos Herbarios Chinos/aislamiento & purificación , Medicamentos Herbarios Chinos/farmacología , Rutaceae/química , Acetilcolinesterasa , Acridinas/química , Acridonas , Alcaloides/química , Antibacterianos/química , Inhibidores de la Colinesterasa/química , Medicamentos Herbarios Chinos/química , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Raíces de Plantas/química , Staphylococcus aureus/efectos de los fármacos
9.
J Ethnopharmacol ; 148(3): 964-74, 2013 Jul 30.
Artículo en Inglés | MEDLINE | ID: mdl-23751393

RESUMEN

AIM OF THE STUDY: The main objectives were to document traditional knowledge on the use of medicinal plants and compare medicinal plant traditions between Li and Hmong living around Limu Mountains of Hainan Island. MATERIAL AND METHODS: Information was obtained from semi-structured interviews, personal conversation and guided fieldtrips with herbalists. Quantitative methods, such as the coefficient of similarity (S), Chi-square analysis and the 'informant agreement ratio' were applied for the comparison of medicinal plant tradition between Li and Hmong. RESULTS: In all, 224 plant species grown in the study areas are still traditionally used for the treatment of various diseases. Euphorbiaceae (17 species), Rubiaceae (16 species), Papilionaceae and Poaceae (11 species, respectively), Verbenaceae (10 species) and Compositae (7 species) are predominant families used by herbalists. The most species were reported to be used for injuries (25.1% of all the medicinal use-reports), digestive system disorders (24.8%), infections/infestations (14.7%) and muscular-skeletal system disorders (12.3%). The coefficient of similarity (29.0%) shows a relatively high overlap of medicinal plants used by Li and Hmong. Using Chi-square analysis, it was found that habit mentions were dependent upon the culture. Infections/infestations, injuries and muscular-skeletal system disorders scored high IAR value and mention in both Li and Hmong communities. CONCLUSIONS: Medicinal plants are of importance to indigenous people around Limu Mountains who still rely on medicinal plants to treat a wide range of illnesses. There is a close relationship of medicinal plant tradition between Li and Hmong who are culturally distinct.


Asunto(s)
Plantas Medicinales , China , Recolección de Datos , Etnobotánica , Humanos , Islas , Magnoliopsida , Medicina Tradicional China , Fitoterapia , Preparaciones de Plantas/uso terapéutico , Estructuras de las Plantas
10.
J Asian Nat Prod Res ; 15(3): 315-8, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23418880

RESUMEN

A new denitroaristolochic acid, demethylaristofolin C (1), together with six known alkaloids, crebanine N-oxide (2), (-)-sukhodianine-ß-N-oxide (3), palmatine (4), corydalmine (5), dehydrocorydalmine (6), and corynoxidine (7), was isolated from the tubers of Stephania succifera. The structure of demethylaristofolin C was elucidated by spectroscopic techniques (UV, IR, 1D, and 2D NMR) and HR-ESI-MS analyses. These compounds exhibited antibacterial activities against Staphylococcus aureus and methicillin-resistant S. aureus strains in different degrees.


Asunto(s)
Alcaloides/aislamiento & purificación , Alcaloides/farmacología , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Medicamentos Herbarios Chinos/aislamiento & purificación , Medicamentos Herbarios Chinos/farmacología , Fenantrenos/aislamiento & purificación , Fenantrenos/farmacología , Stephania/química , Alcaloides/química , Antibacterianos/química , Berberina/análogos & derivados , Alcaloides de Berberina , Medicamentos Herbarios Chinos/química , Resistencia a la Meticilina/efectos de los fármacos , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , Pruebas de Sensibilidad Microbiana , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Fenantrenos/química , Tubérculos de la Planta/química , Staphylococcus aureus/efectos de los fármacos
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