Publications by authors named "Hao-Lun Chen"

Previous studies have shown that scutellarin inhibits the excessive activation of microglia, reduces neuronal apoptosis, and exerts neuroprotective effects. However, whether scutellarin regulates activated microglia-mediated neuronal apoptosis and its mechanisms remains unclear. This study aimed to investigate whether scutellarin can attenuate PC12 cell apoptosis induced by activated microglia via the JAK2/STAT3 signalling pathway.

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Article Synopsis
  • Scutellarin is investigated for its potential to treat brain ischaemia, with researchers aiming to uncover its mechanism of action using network pharmacology and lab experiments.
  • The study identified and confirmed that the JAK2/STAT3 signaling pathway plays a crucial role in how scutellarin alleviates brain damage during ischaemia.
  • Experiments showed that scutellarin significantly increased the levels of JAK2 and STAT3 proteins in astrocytes, supporting its therapeutic effects and providing a foundation for clinical use.
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Scutellarin, an herbal agent, is known to possess anti-oxidant and anti-inflammatory properties. In activated microglia, it has been reported that this is achieved through acting on the MAPKs, a key pathway that regulates microglia activation. This study sought to determine if scutellarin would affect the commonly described microglia phenotypes, namely, M1 and M2, thought to contribute to pro- and anti-inflammatory roles, respectively.

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Background: Scutellarin, an herbal compound, can effectively suppress the inflammatory response in activated microglia/brain macrophage(AM/BM) in experimentally induced cerebral ischemia; however, the underlying mechanism for this has not been fully clarified. We sought to elucidate if scutellarin would exert its anti-inflammatory effects on AM/BM through the MAPKs pathway.

Materials And Methods: Western blot and immunofluorescence labeling were used to determine the expression of the MAPKs pathway in AM/BM in rats subjected to middle cerebral artery occlusion (MCAO) also in lipopolysaccharide (LPS)-activated BV-2 microglia in vitro.

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