4.7 Article

Sophora alopecuroides Alleviates Neuroinflammation and Oxidative Damage of Parkinson's Disease In Vitro and In Vivo

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AMERICAN JOURNAL OF CHINESE MEDICINE
卷 51, 期 2, 页码 309-328

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WORLD SCIENTIFIC PUBL CO PTE LTD
DOI: 10.1142/S0192415X23500167

关键词

Parkinson's Disease; N-methylene-(5; 7; 4'-trihydroxy)-isoflavone; Oxidative Damage; Neuroinflammation; Sophora alopecuroides L

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Sophora alopecuroides L., a plant commonly used in northern China for food and herbal medicine, contains a new cytisine-type alkaloid called LY01, which has neuroprotective effects against Parkinson's disease (PD). PD is an irreversible neurodegenerative disease that seriously affects the elderly population. Current treatments have limited efficacy and numerous side effects, highlighting the need for new pharmacological options. This study evaluated the neuroprotective effects of LY01 and its underlying mechanisms using in vitro and in vivo models of PD.
For centuries, Sophora alopecuroides L. has been used both as a food and an herbal medicine in northern China. A new cytisine-type alkaloid, N-methylene-(5,7,4 & PRIME;-trihydroxy)-isoflavone (LY01), was found in the fruits of Sophora alopecuroides L. and shows neuroprotective effects against Parkinson's disease (PD). PD is a frequently occurring, irreversible neurodegenerative disease that seriously threatens the health of the elderly population. There is no cure for PD. The available treatments help manage the symptoms, but their use is limited by multiple side effects. Therefore, more pharmacological treatments addressing this pathology are urgently required. This study aimed to evaluate the neuroprotective effects of LY01 against PD, as well as their underlying mechanisms, using both in vitro and in vivo experimental models. A 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine hydrochloride (MPTP)-induced mouse model of PD was used to assess the effects of LY01 on the motor coordination deficit, progression of the pathology, and molecular characteristics. 1-Methyl-4-phenylpyridinium (MPP+)-activated SH-SY5Y cells and lipopolysaccharide (LPS)-activated BV-2 cells were used to evaluate LY01 effects on oxidative damage and neuroinflammation. In the rotarod test, LY01 alleviated the impaired motor coordination in PD mice. Furthermore, LY01 treatment prevented the loss of dopaminergic neurons in the substantia nigra and striatum of the PD mice, reduced neuroinflammation in the mice with MPTP-induced PD and the LPS-activated BV-2 cells, and diminished oxidative stress in the PD mice and the MPP +-induced SH-SY5Y cells. In conclusion, these results suggest the potential of LY01 as a therapeutic agent for treating PD.

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