Publications by authors named "Weifan Huang"

Gasdermin D (GSDMD)-mediated pyroptosis in macrophages plays a clear role in promoting inflammation and mortality in sepsis. The liver is a commonly damaged organ during sepsis and also an important organ for releasing acute response proteins. However, whether pyroptosis occurs and the function of GSDMD in hepatocytes remains unclear.

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Background: Hepatic ischemia-reperfusion injury, an inevitable complication in hepatic surgery, significantly compromises patient outcomes. Hypoxia-induced hepatocyte death is a critical early event that triggers inflammatory cascades and leads to organ damage during ischemia-reperfusion injury. However, the underlying mechanisms remain poorly defined.

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Background And Aims: Metabolic dysfunction-associated fatty liver disease (MAFLD) is a common chronic condition that can lead to cancer due to its complex pathogenesis. Therapeutic agents targeting AMP-activated protein kinase (AMPK) activation have been suggested as potential treatments for metabolic disorders such as metabolic dysfunction-associated steatohepatitis (MASH). Rhizoma Atractylodis Macrocephalae (RAM) has been clinically used to treat obesity-related health problems, but its therapeutic effects on MAFLD and the underlying mechanism remain unclear.

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Sepsis is a life-threatening condition characterized by excessive inflammatory responses and oxidative stress, leading to organ dysfunction, high mortality, and morbidity. Quercetin, a natural flavonoid with anti-inflammatory and antioxidant properties, has limited clinical application due to its poor solubility and bioavailability. To address these limitations, we designed and synthesized a novel quercetin β-aminobutyrate derivative, Quercetin-3-β-aminobutyrate (HPS-β), using a prodrug strategy.

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Background: Hepatic Ischemia-Reperfusion Injury (IRI) is a critical complication in liver transplantation and resection, driven by oxidative stress and sterile inflammation mediated by damage-associated molecular patterns (DAMPs). Current therapeutic challenges arise from interconnected cell death pathways and redundant inflammatory mechanisms.

Objective: This review synthesizes mechanistic insights into DAMP signaling and regulated cell death modalities in IRI, aiming to identify translational gaps and propose precision-targeted therapies.

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The aim of this study was to evaluate the therapeutic effect of puerarin (PUE) on alcoholic liver disease (ALD) and elucidate the potential mechanism from the perspective of lipolysis and hepatic steatosis. Assessment of PUE efficacy against ALD was performed using serum biochemical parameters and the histological examination of liver and adipose tissue via Hematoxylin and eosin (H&E) staining. The potential mechanisms underlying the amelioration of ALD by PUE were investigated using Western blotting (WB) analysis and immunofluorescence (IHC) staining.

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Ethnopharmacological Relevance: Acute liver failure (ALF) is the result of progression from acute liver injury with high mortality, and novel treatments are needed. Yin-chen Wu-ling powder (YWP), a traditional herbal medicine in China, has been used for treating acute liver injury for thousands of years. However, the mechanism of YWP is unknown.

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Background And Aims: Kehuang (KH) capsule is an herbal medical product approved for the treatment of liver diseases, including liver injury, in China. However, the mechanism is still unclear. This study aimed to elucidate the protective effects of KH capsule against carbon tetrachloride (CCl)-induced acute liver injury (ALI) in a murine model.

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Ethnopharmacological Relevance: Epimedium Tourn. ex L. is a traditional Chinese medicine used for thousands of years in China to treat forgetfulness.

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Lack of liver regenerative capacity is the primary cause of hepatic failure and even mortality in patients undergoing hepatectomy, with no effective intervention strategies currently available. Therefore, identifying efficacious interventions to enhance liver regeneration is pivotal for optimizing clinical outcomes. Recent studies have demonstrated that vagotomy exerts an inhibitory effect on liver regeneration following partial hepatectomy, thereby substantiating the pivotal role played by the vagus nerve in the process of liver regeneration.

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Cholestasis is characterized by impaired bile secretion and flow, leading to the accumulation of toxic bile acids in the liver, further causing inflammatory reaction, fibrosis, and ultimately liver transplantation. Although first-line clinical agents such as Ursodeoxycholic acid (UDCA) and Obeticholic acid (OCA) are available, serious side effects still exist. Therefore, pharmacologic treatment of cholestatic liver disease remains challenging.

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Article Synopsis
  • Liver ischemia-reperfusion injury (IRI) is a critical issue, especially in patients with Nonalcoholic fatty liver disease (NAFLD), which is more vulnerable to such injuries.
  • The study investigated how different inhibitors of cell death — specifically apoptosis, necroptosis, pyroptosis, and ferroptosis — affect liver damage during IRI in a mouse model with steatotic liver.
  • Results indicated that while all inhibitors offered some protection, those targeting pyroptosis in macrophages and ferroptosis in hepatocytes were particularly effective in reducing liver injury and inflammation.
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