Ginsenoside Rb1 Improves Cognitive Impairment Induced by Insulin Resistance through Cdk5/p35-NMDAR-IDE Pathway

Author:

Yang Ranyao123,Jiang Xue4,He Xiqian5,Liang Donglou1,Sun Shusen6,Zhou Guangyan7ORCID

Affiliation:

1. Department of Clinical Pharmacy, Jining No. 1 People’s Hospital, Jining Medical University, Jining, Shandong, China

2. The State Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China

3. Department of Medicine, The University of Hong Kong, Hong Kong, China

4. Joint Laboratory of Guangdong and Hong Kong on Metabolic Diseases, Guangdong Pharmaceutical University, Guangzhou, Guangdong, China

5. Department of Rehabilitation Medicine, Jining No. 1 People’s Hospital, Jining Medical University, Jining, Shandong, China

6. Department of Pharmacy Practice, Western New England University, Springfield, USA

7. Department of Emergency, Jining No. 1 People’s Hospital, Jining Medical University, Jining, Shandong, China

Abstract

The relationship between diabetes mellitus (DM) and Alzheimer’s disease (AD) has attracted wide attention. Studies have reported that ginsenoside Rb1 can improve human cognitive ability and glucose tolerance during the development of diabetes. The mechanism behind the improvement in cognitive ability and glucose tolerance still remains unclear. In this study, streptozotocin- (STZ-) injected mice were used as models to explore the mechanisms behind the cognitive improvement of ginsenoside Rb1. According to the results of behavioral tests, ginsenoside Rb1 improved memory and cognitive ability of STZ-lesioned mice. In addition to that, ginsenoside Rb1 also relieved glucose intolerance induced by STZ injection by enhancing insulin sensitivity. These beneficial effects of ginsenoside Rb1 is most likely mediated by upregulating the expression of NMDAR1 and IDE in the hippocampus through inhibiting the activity of Cdk5/p35. This work will be of great importance in illustrating the mechanisms of ginsenoside Rb1 for improving cognitive ability, as well as revealing the relationship between diabetes and AD.

Funder

Natural Science Foundation of Shandong Province

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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