Neuroprotective Mechanisms of Salidroside in Alzheimer's Disease: A Systematic Review and Meta-analysis of Preclinical Studies

被引:12
作者
Zhang, Nan [1 ]
Nao, Jianfei [2 ]
Dong, Xiaoyu [2 ]
机构
[1] China Med Univ, Clin Coll 7, Dept Neurol, Fushun 113000, Liaoning, Peoples R China
[2] China Med Univ, Shengjing Hosp, Dept Neurol, Shenyang 110000, Liaoning, Peoples R China
关键词
salidroside; Alzheimer's disease; neuroprotection; animal models; systematic review; meta-analysis; INDUCED COGNITIVE IMPAIRMENT; INDUCED RAT MODEL; OXIDATIVE STRESS; AMYLOID-BETA; CELL-DEATH; NEUROINFLAMMATION; TAU; MICROGLIA; NEURONS; TARGET;
D O I
10.1021/acs.jafc.3c06672
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disease of the central nervous system that occurs in old age and pre-aging, characterized by progressive cognitive dysfunction and behavioral impairment. Salidroside (Sal) is a phenylpropanoid mainly isolated from Rhodiola species with various pharmacological effects. However, the exact anti-AD mechanism of Sal has not been clearly elucidated. This meta-analysis aims to investigate the possible mechanisms by which Sal exerts its anti-AD effects by evaluating behavioral indicators and biochemical characteristics. A total of 20 studies were included, and the results showed that the Sal treatment significantly improved behavior abnormalities in AD animal models. With regard to neurobiochemical indicators, Sal treatment could effectively increase the antioxidant enzyme superoxide dismutase, decrease the oxidative stress indicator malondialdehyde, and decrease the inflammatory indicators interleukin 1 beta, interleukin 6, and tumor necrosis factor alpha. Sal treatment was effective in reducing neuropathological indicators, such as amyloid-beta levels and the number of apoptotic cells. When the relevant literature on the treatment of rodent AD models is combined with Sal, the therapeutic potential of Sal through multiple mechanisms was confirmed. However, further confirmation by higher quality studies, larger sample sizes, and more comprehensive outcome evaluations in clinical trials is needed in the future.
引用
收藏
页码:17597 / 17614
页数:18
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