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Modulation of NLRP3 Inflammasome Activation by Qyht Decoction

Implications for the Treatment of Erectile Dysfunction in Hyperuricemia

Datos Bibliográficos

ID21748729
AutoresPingyu Ge (0000-0001-5146-0582, Guizhou University), Yinxue Guo (Guizhou University), Bangwei Che (Guizhou University), Hang Jin (0000-0002-6810-2527, Guizhou University), Lan Chen (0000-0002-8121-657X, Guizhou University), Zhichao Chen (0000-0002-9884-0002, Guizhou University), Kaifa Tang (0009-0000-5985-7824, Guizhou University, autor de correspondencia)
Año2025
Volumen19
Número1
Páginas15579883251318307-15579883251318307
Fecha de publicación2025-01-01
Peer ReviewedSí
Open AccessSí
TipoARTICLE
RevistaAmerican Journal of Men s Health (JOURNAL)
Identificadores de la revistaISSN: 1557-9883 • E-ISSN: 1557-9891
EditorialSAGE Publications (PUBLISHER • US)
DOI10.1177/15579883251318307
PMID40007058
OpenAlexW4407985207
IdiomaEN
Referencias citadas44

Hyperuricemia (HUA) causes vascular endothelial dysfunction and oxidative stress, and simultaneously activates the NLRP3 inflammasome, leading to inflammatory reactions and erectile dysfunction (ED). This study aimed to investigate the effects of QYHT (Quyuhuatanerxian decoction) decoction on the NLRP3 inflammasome and explore its potential in treating HUA-induced ED. This study employed four treatment methods: (a) treating HUA-induced ED patients with QYHT and analyzing changes in gut microbiota abundance and fecal metabolites through 16S sequencing; (b) establishing an HUA-induced ED rat model, treating with different doses of QYHT, and examining changes in serum metabolites; (c) conducting fecal microbiota transplantation (FMT) therapy; evaluating erectile function, oxidative stress, inflammatory response, and NLRP3 inflammasome activation levels; and (d) exploring key monomeric compounds and potential targets in QYHT through network pharmacology and molecular docking. The treatment with QYHT and FMT increased testosterone levels, reduced oxidative stress and inflammatory marker levels, and inhibited the expressions of NLRP3-related factors. QYHT affected the gut microbiota structure and metabolite levels. The key components were linoleoyl acetate and mandanol, and the target was JAK2. QYHT decoction regulates the distribution of gut microbiota, improves amino acid metabolism, and effectively inhibits the activation of NLRP3 inflammasomes. This, in turn, enhances erectile function and reduces oxidative stress and inflammatory response levels, leading to successful treatment of HUA-induced ED

Decoction · Endothelial Dysfunction · Erectile dysfunction · Gut flora · Hyperuricemia · Inflammasome · Inflammation · Oxidative stress · Uric acid · Gout, Hyperuricemia, Uric Acid · Inflammasome and immune disorders · Medicine · Sexual function and dysfunction studies · Immunology · Internal Medicine · Pharmacology

  • Simiao San alleviates hyperuricemia and kidney inflammation by inhibiting NLRP3 inflammasome and JAK2/STAT3 signaling in hyperuricemia mice

    Open Access•Yueyi Zhang, Shan Wang et al.•Journal of Ethnopharmacology•2023

  • A network pharmacology approach to investigate the blood enriching mechanism of Danggui buxue Decoction

    Open Access•Xu-Qin Shi, Shi-Jun Yue et al.•Journal of Ethnopharmacology•2019

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