Oridonin loaded peptide nanovesicles alleviate nonalcoholic fatty liver disease in mice DOI
Lifen Zhang, Yu Yao, Qi Wang

и другие.

Pharmaceutical Development and Technology, Год журнала: 2024, Номер 29(2), С. 123 - 130

Опубликована: Фев. 7, 2024

This study was to construct a nanovesicle delivery system improve the loading efficiency and stability of ORI for treatment nonalcoholic fatty liver disease (NAFLD). nanovesicles (NVs) exerted narrow size distribution (195.6 ± 11.49 nm) high entrapment (84.46 1.34%). In vitro cell studies demonstrated that NVs enhanced cellular uptake reduced lipid over-accumulation total cholesterol levels in NAFLD model. At same time, vivo proved that, compared with normal group, model group mice showed decrease body weight, significant increase index (6.71 0.62, p < 0.01), symptoms accumulation, vesicles, tissue fibrosis. Compared after high-dose intervention, gained decreased (4.69 0.55, hepatic droplet vacuoles, accumulation (reduced oil red area, 0.001), alleviated degree fibrosis blue collagen 0.001). conclusion, ORI/HP-β-CD/H9-HePC specific improved therapeutic effects, nano drug provides promising strategy encapsulation effectively alleviate process NAFLD.

Язык: Английский

Oridonin alleviates hyperbilirubinemia through activating LXRα-UGT1A1 axis DOI
Zhikun Zhan,

Fahong Dai,

Tao Zhang

и другие.

Pharmacological Research, Год журнала: 2022, Номер 178, С. 106188 - 106188

Опубликована: Март 22, 2022

Язык: Английский

Процитировано

5

Changes in physiological activities are responsible for homoyessotoxin-induced toxicity in abalone Haliotis discus hannai DOI
Ye Liang,

NI Zi-yin,

Tian Zhu

и другие.

Toxicology, Год журнала: 2022, Номер 477, С. 153270 - 153270

Опубликована: Июль 1, 2022

Язык: Английский

Процитировано

5

Oridonin ameliorates acetaminophen‐induced acute liver injury through ATF4/PGC‐1α pathway DOI
Dongsheng Yu,

Jiye Li,

Yu Wang

и другие.

Drug Development Research, Год журнала: 2022, Номер 84(2), С. 211 - 225

Опубликована: Дек. 26, 2022

Abstract Acetaminophen (APAP) overdose‐induced acute liver injury (ALI) causes hepatocyte cell death, oxidative stress, and inflammation. Oridonin (Ori), a covalent NLRP3‐inflammasome inhibitor, ameliorates APAP‐induced ALI through an unclear molecular mechanism. This study found that Ori decreased hepatic cytochrome P450 2E1 level increased glutathione content to prevent APAP metabolism, then reduced the necrotic area, improved function, inhibited proinflammatory cytokines stress. also activating transcription factor 4 (ATF4) protein levels peroxisome proliferator‐activated receptor‐γ coactivator‐1α (PGC‐1α) reduce endoplasmic reticulum stress activation mitochondrial dysfunction. Furthermore, western blot luciferase assay ATF4 in PGC‐1α promoter −507 −495 region levels, while knockdown neutralized hepatoprotective effect of Ori. Molecular docking showed bound ATF4's amino acid residue glutamate 302 6, 7, 18 hydroxyl bands. Our findings demonstrated prevented metabolic further ATF4/PGC‐1α pathway alleviate toxicity, which illuminated its potential therapeutic effects on ALI.

Язык: Английский

Процитировано

4

Research Progress and Future Development Potential of Oridonin in Pharmacological Activities DOI
Jinhuan Jiang,

Shiying Ye,

Shaowei Sun

и другие.

Current Molecular Pharmacology, Год журнала: 2022, Номер 16(7)

Опубликована: Дек. 2, 2022

In recent years, attention has increasingly focused on herbal medicines and their bioactive components attributed to multi-target pharmacological activity low side effects. Oridonin is a natural diterpenoid extracted from the traditional Chinese herb one of main active Rabdosia rubescens. Modern studies have shown that oridonin anti-tumor, anti-bacterial, anti-inflammatory, anti-oxidant, cardiovascular protective, immunomodulatory, other Based published literature in we outline activities oridonin, aiming provide theoretical basis for design development new oridonin-based drugs, as well facilitate process clinical use.

Язык: Английский

Процитировано

3

Oridonin loaded peptide nanovesicles alleviate nonalcoholic fatty liver disease in mice DOI
Lifen Zhang, Yu Yao, Qi Wang

и другие.

Pharmaceutical Development and Technology, Год журнала: 2024, Номер 29(2), С. 123 - 130

Опубликована: Фев. 7, 2024

This study was to construct a nanovesicle delivery system improve the loading efficiency and stability of ORI for treatment nonalcoholic fatty liver disease (NAFLD). nanovesicles (NVs) exerted narrow size distribution (195.6 ± 11.49 nm) high entrapment (84.46 1.34%). In vitro cell studies demonstrated that NVs enhanced cellular uptake reduced lipid over-accumulation total cholesterol levels in NAFLD model. At same time, vivo proved that, compared with normal group, model group mice showed decrease body weight, significant increase index (6.71 0.62, p < 0.01), symptoms accumulation, vesicles, tissue fibrosis. Compared after high-dose intervention, gained decreased (4.69 0.55, hepatic droplet vacuoles, accumulation (reduced oil red area, 0.001), alleviated degree fibrosis blue collagen 0.001). conclusion, ORI/HP-β-CD/H9-HePC specific improved therapeutic effects, nano drug provides promising strategy encapsulation effectively alleviate process NAFLD.

Язык: Английский

Процитировано

0