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1.
Biomed Res Int ; 2022: 4483009, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35647185

RESUMO

Recent studies indicate existence of beige adipocytes in adults. Upon activation, beige adipocytes burn energy for thermogenesis and contribute to regulation of energy balance. In this study, we have analyzed whether Jinlida granules (JLD) could activate beige adipocytes. JLD suspended in 0.5% carboxymethyl cellulose (CMC) was gavage fed to db/db mice at a daily dose of 3.8 g/kg. After 10 weeks, body weight, biochemical, and histological analyses were performed. In situ hybridization, immunofluorescence, and western blotting were conducted to test beige adipocyte activation in mice. X9 cells were induced with induction medium and maintenance medium containing 400 µg/mL of JLD. After completion of induction, cells were analyzed by Nile red staining, time polymerase chain reaction (PCR), western blotting, and immunofluorescence to understand the effect of JLD on the activation of beige adipocytes. A molecular docking method was used to preliminarily identify compounds in JLD, which hold the potential activation effect on uncoupling protein 1 (UCP1). JLD treatment significantly improved obesity in db/db mice. Biochemical results showed that JLD reduced blood glucose (GLU), triglyceride (TG), and low-density lipoprotein cholesterol (LDL) levels as well as liver aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels in mice. Hematoxylin and eosin staining (H&E) showed that JLD reduced hepatocyte ballooning changes in the liver. Immunofluorescence showed that JLD increased the expression of the thermogenic protein, UCP1, in the beige adipose tissue of mice. JLD also increased the expression of UCP1 and inhibited the expression of miR-27a in X9 cells. Molecular docking results showed that epmedin B, epmedin C, icariin, puerarin, and salvianolic acid B had potential activation effects on UCP1. The results suggest that JLD may activate beige adipocytes by inhibiting miR-27a expression, thereby promoting thermogenesis in beige adipocytes. This study provides a new pharmacological basis for the clinical use of JLD.


Assuntos
Adipócitos Bege , MicroRNAs , Adipócitos Bege/metabolismo , Animais , Medicamentos de Ervas Chinesas , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos , MicroRNAs/metabolismo , Simulação de Acoplamento Molecular , Obesidade/tratamento farmacológico , Obesidade/metabolismo , Proteína Desacopladora 1/genética , Proteína Desacopladora 1/metabolismo
2.
J Nanosci Nanotechnol ; 19(9): 5554-5561, 2019 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-30961709

RESUMO

In this study, a two-dimensional heterojunction consisting of bismuth trioxide nanoplates and layered reduced graphene oxide was synthesized using a facile In Situ growth route. A series of characterization tests indicated that the reduction of graphene oxide played a key role as an electron collector for enhancing photoinduced charge carrier separation efficiency. Thus, the as-prepared reduced graphene oxide/bismuth trioxide composite exhibited enhanced photocatalytic water oxidation, which was higher than that of pristine bismuth trioxide under simulated solar light irradiation. Furthermore, the photoelectrochemical properties of the prepared hybrid system were investigated to understand the transfer of photoinduced electrons and holes between layered reduced graphene oxide and bismuth trioxide nanoplates. Thus, this strategy provided an efficient approach for the fabrication of graphene composites containing hierarchical ternary oxides for photocatalysis.

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