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    Study on the Neuroprotective Mechanism of Salidroside Modified with Polydopamine Nanoparticles in Regulating Notch Pathway by Inhibiting miR-155 in Stroke Rats

    activity of AQP4, TLR TLR4, Song Liu1, Xiaomeng Lv1, Dong Wang1 Corresponding author

    1. 1Department of Neurosurgery, Dongping People’s Hospital, Tai’an, Shandong, CHINA.

    CORRESPONDENCE

    Dong Wang

    Department of Neurosurgery, Dongping People’s Hospital, Tai’an, Shandong, CHINA.

    13853873429@163.com

    Received: 01-04-2024; Accepted: 31-07-2024.

    Volume 21, Issue 4 · pp. 1176–1186 · PUBLISHED 2025 · DOI: 10.1177/09731296241282387

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Background and Objectives: Stroke threatens neurological function. Salidroside is widely used to treat neurological diseases such as stroke. Previous studies have shown that miR-155 plays an important regulatory role in the pathogenesis of stroke and that the Notch pathway plays an important role in nervous system development and regeneration. Materials and Methods: PDA NPs-SAL complex was prepared, a stroke rat model was constructed, and the cerebral infarction area of rats was measured. Analyze the changes of PDA NPs-SAL on rat brain tissue and evaluate the neuroprotective effect. Detect the changes in miR-155 and Notch pathway-related proteins in stroke rat models to further understand the role of miR-155 and Notch pathway in the pathogenesis of stroke and their relationship. Results: Salidroside had certain protective effects on the nerves of stroke rats, and the effect of PDA NPs-SAL was more prominent. At the same time, PDA NPs-SAL promotes the Notch pathway by inhibiting miR-155, thereby exerting a neuroprotective effect on stroke rats. Conclusion: Under the intervention of PDA NPs-SAL, the neurological function scores of rats were reduced, and the effect of PDA NPs-SAL was more significant. In addition, PDA NPs-SAL inhibited miR-155 and activated the Notch pathway, thereby reducing the water content of rat brain tissue and cerebral infarction area, thereby exerting a neuroprotective effect on stroke rats.

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      AQP, A. O., TLR, T., Liu, S., Lv, X., & Wang, D. (2025). Study on the Neuroprotective Mechanism of Salidroside Modified with Polydopamine Nanoparticles in Regulating Notch Pathway by Inhibiting miR-155 in Stroke Rats. Pharmacognosy Magazine, 21(4), 1176–1186. https://doi.org/10.1177/09731296241282387