共 39 条
Chemical components and against alzheimer's disease effects of the calyxes of Physalis alkekengi L. var. franchetii (Mast.) Makino
被引:1
|作者:
Teng, Yang
[1
,2
]
Gao, Jia
[1
]
Tan, Tian
[2
]
Zhang, Xiangrong
[1
]
Wang, Yuliang
[1
]
Zhang, Jiaguang
[2
]
Ni, Lei
[3
]
机构:
[1] Jiamusi Univ, Dept Pharm, Jiamusi, Peoples R China
[2] Dept Vocat Educ Grp, Jiamusi, Peoples R China
[3] Jiamusi Univ, Dept Clin Med, Jiamusi, Peoples R China
关键词:
Physalis alkekengi L. var. franchetii (Mast.);
Makino;
UPLC-Q-TOF-MS;
Alzheimer's disease;
Oxidative stress;
Neuroinflammatory;
TOLL-LIKE RECEPTORS;
OXIDATIVE STRESS;
EXPRESSION;
NEUROINFLAMMATION;
MECHANISMS;
PATHWAY;
ACID;
D O I:
10.1016/j.jchemneu.2024.102390
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Physalis alkekengi L. var. franchetii (Mast.) Makino (PA), a traditional Chinese medicine, is utilised for treating dermatitis, sore throat, dysuria, and cough. This research aimed to identify the main constituents in the four extracted portions from the calyces of PA (PAC) utilising ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS). The Alzheimer's disease (AD) mice model was induced by D-galactose (D-gal) combined with aluminium chloride (AlCl3). Subsequent investigation into the underlying mechanisms involved behavioural and histopathological observations. The results demonstrated that four extracted portions of PAC (PACE) significantly enhanced memory and learning abilities in the Morris water maze. The concentrations of A beta, tau and p-tau in brain tissue exhibited a significant decrease relative to the model group. Moreover, the four PACE treatment groups increased the glutathione (GSH) and superoxide dismutase (SOD) levels, while concurrently reducing malondialdehyde (MDA), interleukin-1 beta (IL-1 beta) and interleukin-6 (IL-6), tumour necrosis factor-alpha (TNF-alpha) levels. In summary, the current study demonstrates that the four PACE formulations exhibit beneficial anti-AD properties, with the most pronounced efficacy observed in the EA group. Additionally, PAC shows potential in mitigating neuroinflammation and oxidative damage by inhibiting the TLR4/NF-kappa B signalling pathway. This research lays a theoretical groundwork for the future clinical development and utilisation of PAC in treating AD.
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