
Saudi Pharmaceutical Journal, Год журнала: 2024, Номер 32(12), С. 102210 - 102210
Опубликована: Ноя. 26, 2024
Phenylacetylglycine (PAGly) is a small molecule derived from phenylalanine in the gut
Язык: Английский
Saudi Pharmaceutical Journal, Год журнала: 2024, Номер 32(12), С. 102210 - 102210
Опубликована: Ноя. 26, 2024
Phenylacetylglycine (PAGly) is a small molecule derived from phenylalanine in the gut
Язык: Английский
Advanced Science, Год журнала: 2025, Номер unknown
Опубликована: Фев. 14, 2025
Abstract Acute pancreatitis (AP) is a primary contributor to hospitalization and in‐hospital mortality worldwide. Targeted elimination of mitochondrial reactive oxygen species (mtROS) within pancreatic acinar cells (PACs) represents an ideal strategy for treating AP. However, existing drugs fail overcome the physiological barriers pancreas effectively reach PACs mitochondria due trade‐off between conventional positively charged mitochondrial‐targeting groups their inability penetrate blood‐pancreas barrier (BPB). Here, tungsten‐based heteropolyacid nano‐antioxidant (mTWNDs) introduced, co‐modified with tannic acid (TA) melanin, enabling site‐specific clearance mtROS in PACs, offering highly effective treatment TA exhibits strong affinity proline‐rich type III collagen outer membrane protein TOM20. This unique property allows mTWNDs traverse damaged BPB‐exposing subsequently targeted elimination. In cerulein‐induced AP mice, reversed at 1/50th dose N‐acetylcysteine, suppressing apoptosis inflammation by blocking stimulator interferon genes pathway activation macrophage. study establishes antioxidant nanomedicine treatment.
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 162106 - 162106
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Journal of Colloid and Interface Science, Год журнала: 2025, Номер unknown, С. 137596 - 137596
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Inflammation, Год журнала: 2025, Номер unknown
Опубликована: Апрель 21, 2025
Intestinal Ischemia-Reperfusion (IIR) injury is a common clinical pathophysiological condition, yet the complex molecular mechanisms underlying its pathology remain incompletely understood. This study aims to explore precise of IIR injury, with focus on role cGAS-STING signaling pathway. Using mouse model and hypoxia/reoxygenation (HR) in HT-29 cells small intestinal organoids, we observed that significantly induces oxidative stress activates pathway, which associated exacerbated tissue damage enhanced inflammatory responses. Further investigation revealed mitochondrial DNA (mtDNA) leakage critical trigger for activation The introduction exogenous mtDNA into activated STING pathway cellular damage. In contrast, depletion intracellular effectively suppressed HR-induced Mechanistically, found downregulates transcription factor A (TFAM), subsequently affects stability, promoting release cytoplasm triggering Overexpression TFAM stabilized mtDNA, reduced accumulation cytoplasmic inhibited activation, alleviated Moreover, STING-deficient mice exhibited inflammation, less damage, improved survival rates following IIR, highlighting IIR-induced injury. Our findings elucidate close association between stress, IIR. downregulation are key driving this activation. Importantly, plays crucial stabilizing reducing during These results not only deepen our understanding pathogenesis but also provide potential therapeutic strategies targeting treating IIR-related diseases.
Язык: Английский
Процитировано
0International Journal of Biological Macromolecules, Год журнала: 2025, Номер 311, С. 143645 - 143645
Опубликована: Апрель 29, 2025
Язык: Английский
Процитировано
0Frontiers in Pharmacology, Год журнала: 2025, Номер 16
Опубликована: Май 2, 2025
Background Cerebral ischemia-reperfusion injury (CIRI) is a secondary brain that occurs after thrombolysis and primary cause of death in ischemic stroke patients. Antioxidants effectively reduce oxidative stress are an efficient treatment approach for CIRI. Here, novel diimide compound was synthesized using the chemical structure previously designed anti-inflammatory skeletons. Methods results The antioxidant activities five compounds (Z1–Z5) were preliminarily evaluated hydrogen peroxide-induced PC12 cell damage model, which Z3 exhibited best effect, even exceeding positive control (tert-butylhydroquinone). Enrichment analysis network targeting pharmacology methods predicted seven candidate core target genes Of these targets, computer molecular docking has strongest binding affinity nuclear factor erythroid 2-related (Nrf2). MTT colony formation assays, reactive oxygen species analysis, immunofluorescence, immunoblotting experiments verified reduced to play protective role via Nrf2/hemoxygenase 1 (HO-1) pathway. effect vivo explored through TTC staining neurobehavioral scoring CIRI model mice. Conclusion This study provides new drug development strategy CIRI, offering ideas design antioxidants.
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 164322 - 164322
Опубликована: Май 1, 2025
Язык: Английский
Процитировано
0Saudi Pharmaceutical Journal, Год журнала: 2024, Номер 32(12), С. 102210 - 102210
Опубликована: Ноя. 26, 2024
Phenylacetylglycine (PAGly) is a small molecule derived from phenylalanine in the gut
Язык: Английский
Процитировано
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