Grifola frondosa polysaccharides alleviate Alzheimer's disease in rats

被引:0
|
作者
Behrad, Samira [1 ]
Pourranjbar, Sina [2 ]
Pourranjbar, Mohammad [3 ]
Abbasi-Maleki, Saeid [4 ]
Mehr, Samira Rostami [4 ]
Salmani, Reza Hossein Gholizadeh [5 ]
Moradikor, Nasrollah [6 ]
机构
[1] Semnan Univ Med Sci, Dent Sch, Dept Oral & Maxillofacial Pathol, Semnan, Iran
[2] Kerman Univ Med Sci, Fac Med, Kerman, Iran
[3] Kerman Univ Med Sci, Dept & Neurosci Res Ctr, Kerman, Iran
[4] Kermanshah Univ Med Sci, Hlth Inst, Pharmaceut Sci Res Ctr, Kermanshah, Iran
[5] Urmia Univ, Fac Vet Med, Dept Basic Sci, Orumiyeh, Iran
[6] Inst Intelligent Res, Int Ctr Neurosci Res, Tbilisi, Georgia
关键词
Grifola frondosa; Polysaccharides; Dementia; Behavioral responses; Inflammation; Alzheimer's disease; OXIDATIVE STRESS; DEMENTIA TYPE; AMYLOID-BETA; INFLAMMATION; NEUROINFLAMMATION; PATHOGENESIS; SYMPTOMS; ANXIETY;
D O I
10.4103/apjtb.apjtb_294_24
中图分类号
R188.11 [热带医学];
学科分类号
摘要
Objective: To evaluate the effect of Grifola frondosa polysaccharides (GFP) in a rat model of Alzheimer's disease (AD). Methods: Seventy-five rats were divided into five groups: the normal control group and the AD group treated with or without GFP (100, 200, and 400 mg/kg). Behavioral responses in the open field test and elevated plus maze test were assessed. Additionally, the levels of malondialdehyde and ferric-reducing ability of plasma, and the mRNA expressions of TNF-alpha, IL-6, and IL-1 beta in the hippocampus were measured. Results: Treatment with GFP significantly improved AD-induced behavioral changes in the open field test and elevated plus maze test (P < 0.05). In addition, the level of malondialdehyde and the mRNA expressions of TNF-alpha, IL-6, and IL-1 beta were decreased by GFP treatment in a dose-dependent manner in AD rats (P < 0.05), while the level of ferric-reducing ability of plasma was significantly increased (P < 0.05). Conclusions: Oral administration of GFP can reduce inflammation and oxidative stress, as well as improve behavioral responses associated with AD, suggesting its potential use in AD treatment. However, additional studies are needed to elucidate its underlying mechanisms and efficacy.
引用
收藏
页码:500 / 506
页数:7
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