Publications by authors named "Chunjuan Fang"

Article Synopsis
  • Continuous hyperglycemia and poor blood flow in diabetes lead to chronic wounds, particularly ulcers on the feet, which may require amputation in extreme cases.
  • This study investigates the effects of geniposide, known for its anti-inflammatory and anti-apoptotic properties, on wound healing in diabetic rats.
  • Results showed that administering geniposide significantly improved wound healing and reduced inflammation and cell death in diabetic rats, indicating its potential as a treatment for diabetic wounds.
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Context: Huanglian Jiedu Decoction (HLJJD) has a variety of pharmacological activities, such as anti-inflammatory and neuroprotection against ischaemic brain injury.

Objectives: This study explores its antithrombosis activity and inhibition of platelet aggregation.

Material And Methods: To study the antithrombosis activity of HLJJD , saline, or HLJDD (100, 200, and 500 mg/kg) was treated prophylactically by gavage for 3 days in Wistar rats ( = 4).

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Tumor-specific targeted delivery is a major obstacle to clinical treatment of hepatocellular carcinoma (HCC). Here we have developed a novel multi-functional nanostructure GAL-GNR-siGPC-3, which consists of Galactose (GAL) as the HCC-targeting moiety, golden nanorods (GNR) as a framework to destroy tumor cells under laser irradiation, and siRNA of Glypican-3 (siGPC-3) which induce specifically gene silence of GPC-3 in HCC. Glypican-3 (GPC-3) gene is highly associated with HCC and is a new potential target for HCC therapy.

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The content of polysaccharides in was investigated by isolation and purification, followed with the further antioxidant studies in total reducing capacity and radical scavenging activities. The crude extract of polysaccharides was purified by dialysis, column chromatography, and High Performance Liquid Chromatography. The main components of monosaccharide (s) and molecular structure of single polysaccharide were studied by using methylation, GC-MS, and NMR analysis.

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While dendritic cell (DC)‑based immunotherapy has achieved satisfactory results in animal models, its effects were not satisfactory as initially expected in clinical applications, despite the safety and varying degrees of effectiveness in various types of cancer. Improving the efficacy of the DC‑based vaccine is essential for cancer immunotherapy. The present study aimed to investigate methods with which to amplify and enhance the antitumor immune response of a DC‑based tumor vaccine by silencing the expression of indoleamine 2,3‑dioxygenase 2 (IDO2), a tryptophan rate‑limiting metabolic enzyme in DCs.

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This study was designed to investigate the effect of salidroside (SAL) on bone marrow haematopoiesis in a mouse model of myelosuppressed anemia. After the mouse model was established by 60Co γ irradiation and cyclophosphamide, pancytopenia and a sharp reduction in bone marrow stromal cells and bone marrow haematopoietic stem cells (lineage-Sca1+c-kit+) were observed. This was greatly alleviated by SAL (25 mg/kg, 50 mg/kg, 100 mg/kg) in a dose-dependent manner (50% effective dose value of 35.

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The biocontrol function of the repressor of cellulase expression I (ACE1) in was verified through constructing Δ mutant strain by -mediated transformation. The activities of cell wall-degrading enzymes (cellulase, xylanase, chitinase, β-1,3-glucanase, and protease) in the supernatant of Δ mutant strain were distinctly higher than those of control strain, followed with the elevation of related genes transcript levels. Besides, the Δ mutant resulted in an elevating transcript level of , but no obvious change in the expression of , which suggested that ACE1 was negative regulator of the transcription, but not involved in transcription.

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