Hyperuricemia suppresses lumican, exacerbating adverse remodeling after myocardial infarction by promoting fibroblast phenotype transition DOI Creative Commons
Ze Zhuang, Ao Liu, Jinghong Zhang

et al.

Journal of Translational Medicine, Journal Year: 2024, Volume and Issue: 22(1)

Published: Oct. 31, 2024

Hyperuricemia is independently associated with a poor prognosis in patients myocardial infarction (MI). Furthermore, MI induces activation of the repair response local fibroblasts, resulting extracellular matrix accumulation that generates stable fibrotic scar infarcted area. However, researchers have not determined whether hyperuricemia affects fibroblast and its involvement postinfarction cardiac remodeling.

Language: Английский

Metabolomics Reveal the Anti‐Hyperuricemia Effects and Mechanisms of Sunflower Head Extract in Hyperuricemia Mice Model DOI Open Access
Gang Li, Ying Zhang, Yu Cheng

et al.

Molecular Nutrition & Food Research, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 9, 2025

Hyperuricemia (HUA) is a globally prevalent metabolic disease characterized by excessive production or insufficient excretion of uric acid in the serum. Although several drugs are available for treatment HUA, they have been associated with undesirable side effects. Therefore, this study aims to evaluate therapeutic effects sunflower head extract (KHE) on HUA mouse model and explore its potential mechanisms. All mice were randomly divided into three groups: Normal control (NC, 0.5% CMC-Na), (MD, yeast paste 20 g/kg), KHE group (KHE, 1 g/kg). Biochemical indicators, oxidative stress state, metabolomics analyzed. reduced levels 5-aminoimidazole ribonucleotide, xanthine, hypoxanthine, serum but increased adenine taurine. decreased activities superoxide dismutase (SOD) enzymes, hepatic hydrogen peroxide (H2O2) malondialdehyde (MDA) levels, betaine aldehyde beta-D-glucosamine. improved mitigated damage kidneys joints caused urate deposition. These findings provide comprehensive evidence supporting anti-HUA underlying mechanisms mice.

Language: Английский

Citations

0

Drug delivery for platinum therapeutics DOI
Hui Liu, Jiahui Zou, Xiaotong Li

et al.

Journal of Controlled Release, Journal Year: 2025, Volume and Issue: 380, P. 503 - 523

Published: Feb. 11, 2025

Language: Английский

Citations

0

A novel zinc ferrite nanoparticle protects against MSU-induced gout arthritis via Nrf2/NF-κB/NLRP3 pathway DOI
Feng Zhang,

Yuehao Gan,

Wenteng Xie

et al.

Life Sciences, Journal Year: 2025, Volume and Issue: unknown, P. 123475 - 123475

Published: Feb. 1, 2025

Language: Английский

Citations

0

Advancements in Uricase formulations: overcoming therapeutic challenges in enzyme replacement therapy DOI Creative Commons

Woo Ho Cho,

HyeSoon Kim,

So‐Yeol Yoo

et al.

Journal of Pharmaceutical Investigation, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 26, 2025

Language: Английский

Citations

0

Clinical significance of microRNA-328-3p and bone metabolism biomarkers in gout patients with different musculoskeletal ultrasonography imaging DOI Creative Commons
Qingqing Song,

Lifang Xue,

Jie Ren

et al.

Journal of Orthopaedic Surgery and Research, Journal Year: 2025, Volume and Issue: 20(1)

Published: April 1, 2025

MicroRNA (miRNA) participates in the pathophysiological processes of multiple metabolic diseases, including gout. In gout patients, there is concomitant derangement bone metabolism. The study aimed to explore correlation different ultrasonic manifestations and miR-328-3p levels with markers patients. A total 320 patients were grouped according musculoskeletal ultrasound (MSUS) imaging. Serum osteocalcin (BGP), C-terminal telopeptide type I collagen (CTX-I) osteopotin (OPN) detected evaluate via qRT-PCR. Pearson's analysis was performed relationships between variables. Patients tophi accompanied by erosion demonstrated significantly elevated BGP OPN compared those or aggregate MSU crystals absence erosions. Cases long course disease exhibited more severe destruction. without specific clinical presented highest serum miR-328-3p, whereas erosions lowest values. Significantly negative correlations also for values all associated diverse MSUS imaging are capable reflecting joint impairment

Language: Английский

Citations

0

Terminalia chebula Retz. extract relieves gout arthritis by inhibiting xanthine oxidase, the uric acid transporter, and NLRP3 inflammasome activation DOI

Anshun He,

Jialiang Wang,

Yulin Feng

et al.

Journal of Ethnopharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 119848 - 119848

Published: April 1, 2025

Language: Английский

Citations

0

Pure drug nanomedicines - where we are? DOI

Yaoyao Lai,

Bing Xie, Wanting Zhang

et al.

Chinese Journal of Natural Medicines, Journal Year: 2025, Volume and Issue: 23(4), P. 385 - 409

Published: April 1, 2025

Language: Английский

Citations

0

Estimation of the spatial pattern of gout prevalence across China by wastewater-based epidemiology DOI
Xinxin Zhou, Kexin Liu,

Shi Chen

et al.

The Science of The Total Environment, Journal Year: 2024, Volume and Issue: 924, P. 171565 - 171565

Published: March 8, 2024

Language: Английский

Citations

3

Gout Management Using Nanocarrier Systems: A Review DOI

Chia Wen Qi,

Ummu Umaimah Mohd Nordin, Syed Mahmood

et al.

ACS Applied Nano Materials, Journal Year: 2024, Volume and Issue: 7(9), P. 9816 - 9846

Published: April 22, 2024

Gout is an inflammatory arthropathy resulting from the deposition of monosodium urate crystals in and around joints, triggering release pro-inflammatory cytokines. Some key principles for managing gout are encompassing comorbidity screening, flare treatment, urate-lowering therapy, anti-inflammatory prophylaxis. One major concerns with treatment side effects drug due to uncontrolled biodistribution. Nanocarrier systems utilized surmount limitations current drugs, including not only biodistribution issues but also stability bioavailability drugs. Nanocarriers as promising delivery can effectively deliver drugs by specifically targeting inflamed tissues through enhanced permeability retention effect mediated delivery. Notable examples include liposomes, niosomes, ethosomes, transfersomes, solid lipid nanoparticles, polymeric nanoemulsions, liquid crystalline namely, cubosomes, hexosomes, spongosomes. These nanocarriers hold great promise vehicles transporting poorly therapeutic agents precise target sites, associated controlled capabilities bolster bioavailability. Preclinical studies have demonstrated efficacy nanocarrier-based therapies reducing inflammation tissues, inhibiting crystal formation, improving joint function animal models gout. In this review, we explore main nanocarrier systems, their respective advantages drawbacks, emphasize role nanoformulations advancing treatment. The encapsulation active within therapy represents a significant advancement pharmaceutical area nanomedicine application succeed overall context near future.

Language: Английский

Citations

3

Recent Progress and Future Perspectives on Anti-Hyperuricemic Agents DOI

Zhiqiang Sun,

Xuewen Zhang, Zean Zhao

et al.

Journal of Medicinal Chemistry, Journal Year: 2024, Volume and Issue: 67(22), P. 19966 - 19987

Published: Nov. 8, 2024

Increased biosynthesis or underexcretion of uric acid (UA urate) in the body ultimately leads to development hyperuricemia. Epidemiological studies indicate that hyperuricemia is closely associated with occurrence various diseases such as gout and cardiovascular diseases. Currently, first-line therapeutic medications used reduce UA levels primarily include xanthine oxidase (XO) inhibitors, which limit production, urate transporter 1 (URAT1) decrease reabsorption enhance excretion. Despite significant progress urate-lowering therapies, long-term use these drugs can cause hepatorenal toxicity well complications. Therefore, there an urgent need for novel anti-hyperuricemic agents better efficacy lower toxicity. This perspective mainly focuses on current research design strategy agents, particularly those targeting XO URAT1. It our hope this will provide insights into challenges opportunities drug discovery.

Language: Английский

Citations

3