Cycloastragenol targets Fpr2 to inhibit the TLR4/NF-κB signaling pathway and alleviate neuroinflammation in Parkinson's disease.

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Tác giả: Zhi Chai, Zhenyu Li, Lianmei Liu, Xuemei Qin, Shengnan Xiao, Lei Xu

Ngôn ngữ: eng

Ký hiệu phân loại: 922.945 *Hindus

Thông tin xuất bản: Germany : Phytomedicine : international journal of phytotherapy and phytopharmacology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 690647

BACKGROUND: Parkinson's disease (PD) is a neurodegenerative disease, and neuroinflammation is an important factor in its pathogenesis. Therefore, improving neuroinflammation has become a key direction in PD research. Cycloastragenol (CAG) is one of the active ingredients in Astragalus membranaceus, which has pharmacological activities such as anti-inflammatory, antioxidant, and neuroprotective effects. However, there are few reports on its pharmacological effects on PD. Therefore, it is necessary to comprehensively evaluate the pharmacological effects of CAG on PD and elucidate the potential mechanisms of action, providing new ideas for drug development in PD. OBJECTIVE: To comprehensively and systematically evaluate the pharmacological effects of CAG on PD and reveal its potential mechanisms of action. RESEARCH DESIGN AND METHODS: Firstly, the pharmacological effects of CAG on cell viability, cytotoxicity, behavior, and pathology were evaluated using PD in vitro (MPP RESULT: CAG can significantly improve the behavioral indicators of PD mice, enhance neuronal vitality, and improve neuroinflammatory levels by inhibiting the expression of inflammatory factors. In addition, CAG can target and activate the expression of Fpr2, thereby regulating the TLR4/NF-κB signaling pathway and promoting the resolution of inflammation.
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