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Métodos Terapéuticos y Terapias MTCI
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1.
Transplantation ; 107(4): 878-889, 2023 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-36413144

RESUMEN

BACKGROUND: Liver ischemia/reperfusion injury (I/RI) is characterized by inflammatory actions. Understanding the mechanistic insights underpinning inflammation is critical to developing treatment strategies. In this study, we illustrated the mechanistic insights of transcription factor Yin-Yang 1 (YY1)-mediated microRNA (miR)-181a-5p/estrogen receptor alpha (ESR1)/epidermal growth factor receptor 2 (ERBB2) axis in liver I/RI. METHODS: First, we established liver I/RI models in mice and hypoxia-reperfusion (H/R) cell models in mouse hepatocytes (AML12). Subsequently, the expression of YY1, miR-181a-5p, and ESR1 was determined in the 2 models. I/RI mouse models were further injected with lentivirus carrying oe-YY1' and H/R-exposed AML12 cells were subjected to a series of inhibitors, mimics, and shRNAs to validate the mechanisms of YY1 in controlling miR-181a-5p and ESR1 in liver I/RI. RESULTS: Upregulated expression of miR-181a-5p and downregulated expression of YY1 were identified in the liver tissues of liver I/RI mice and H/R-exposed hepatocytes. Moreover, overexpression of YY1 inhibited the miR-181a-5p expression and thus repressed the H/R-induced hepatocyte apoptosis and inflammation. ESR1 was further validated as a target gene of miR-181a-5p and could be negatively regulated by miR-181a-5p. miR-181a-5p inhibition elevated ESR1 expression, which consequently enhanced the ERBB2 expression and reduced H/R-induced hepatocyte apoptosis and inflammation. CONCLUSIONS: Overall, these findings highlighted that YY1 repressed the miR-181a-5p expression and stimulated ESR1-mediated activation of ERBB2, thereby ameliorating liver I/RI. This study provides insight into the development of novel targets for liver I/RI.


Asunto(s)
MicroARNs , Daño por Reperfusión , Animales , Ratones , Apoptosis , Inflamación/metabolismo , Hígado/metabolismo , MicroARNs/genética , MicroARNs/metabolismo , Daño por Reperfusión/genética , Daño por Reperfusión/prevención & control , Daño por Reperfusión/metabolismo , Factores de Transcripción/metabolismo
2.
Drug Dev Ind Pharm ; 42(3): 456-63, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26422447

RESUMEN

Oxymatrine (OM) can be metabolized to matrine in gastrointestinal ileocecal valve after oral administration, which affects pharmacological activity and reduce bioavailability of OM. A type of multiple-unit alginate-chitosan (Alg-Cs) floating beads was prepared by the ionotropic gelation method for gastroretention delivery of OM. A solid dispersion technique was applied and incorporated into beads to enhance the OM encapsulation efficiency (EE) and sustain the drug release. The surface morphology and internal hollow structure of beads were evaluated using optical microscopy and scanning electron microscopy (SEM). The developed Alg-Cs beads were spherical in shape with hollow internal structure and had particle size of 3.49 ± 0.09 mm and 1.33 ± 0.09 mm for wet and dried beads. Over 84% of the optimized OM solid dispersion-loaded Alg-Cs beads were able to continuously float over the simulated gastric fluid for 12 h in vitro. The OM solid dispersion-loaded Alg-Cs beads showed drug EE of 67.07%, which was much higher than that of beads loading with pure OM. Compared with the immediate release of OM capsules and pure OM-loaded beads, the release of OM from solid dispersion-loaded Alg-Cs beads was in a sustained-release manner for 12 h. Prolonged gastric retention time of over 8.5 h was achieved for OM solid dispersion-loaded Alg-Cs floating beads in healthy rabbit in in vivo floating ability evaluated by X-ray imaging. The developed Alg-Cs beads loading with OM solid dispersion displayed excellent performance features characterized by excellent gastric floating ability, high drug EE and sustained-release pattern. The study illustrated the potential use of Alg-Cs floating beads combined with the solid dispersion technique for prolonging gastric retention and sustaining release of OM, which could provide a promising drug delivery system for gastric-specific delivery of OM for bioavailability enhancement.


Asunto(s)
Alginatos/farmacocinética , Alcaloides/farmacocinética , Quitosano/farmacocinética , Portadores de Fármacos/farmacocinética , Mucosa Gástrica/metabolismo , Quinolizinas/farmacocinética , Alginatos/síntesis química , Alcaloides/síntesis química , Animales , Quitosano/síntesis química , Preparaciones de Acción Retardada/síntesis química , Preparaciones de Acción Retardada/farmacocinética , Portadores de Fármacos/síntesis química , Sistemas de Liberación de Medicamentos/métodos , Evaluación Preclínica de Medicamentos , Ácido Glucurónico/síntesis química , Ácido Glucurónico/farmacocinética , Ácidos Hexurónicos/síntesis química , Ácidos Hexurónicos/farmacocinética , Quinolizinas/síntesis química , Conejos , Radiografía , Estómago/diagnóstico por imagen , Estómago/efectos de los fármacos
3.
Zhongguo Zhong Yao Za Zhi ; 31(20): 1674-7, 2006 Oct.
Artículo en Chino | MEDLINE | ID: mdl-17225531

RESUMEN

OBJECTIVE: To study the effects of HKL-4 on physiological changes during growth of leaves. METHOD: Using licorice (Glycyrrhiza uralensis) as material, the effects of HKL-4 on active oxygen metabolism and photochemical efficiency in licorice leaf were determined under field condition. RESULT AND CONCLUSION: The contents of chlorophyll, activity of SOD and CAT increased, while the MDA contents in leaves decreased. The senescence was delayed, so that the photochemical efficiency (Fv/Fm) was increasing comparing to the control.


Asunto(s)
Glycyrrhiza/crecimiento & desarrollo , Fotosíntesis , Reguladores del Crecimiento de las Plantas/farmacología , Plantas Medicinales/crecimiento & desarrollo , Catalasa/metabolismo , Clorofila/metabolismo , Glycyrrhiza/metabolismo , Malondialdehído/metabolismo , Peroxidasa/metabolismo , Hojas de la Planta/crecimiento & desarrollo , Hojas de la Planta/metabolismo , Plantas Medicinales/metabolismo , Superóxido Dismutasa/metabolismo
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