Studies of the Anti-amnesic Effects and Mechanisms of Single and Combined Use of Donepezil and Ginkgo Ketoester Tablet on Scopolamine-Induced Memory Impairment in Mice.
Jing ZhangJun WangGui-Sheng ZhouYa-Jie TanHui-Juan TaoJia-Qian ChenZong-Jin PuJia-Yan MaWen SheAn KangYue ZhuPei LiuZhen-Hua ZhuXu-Qin ShiYu-Ping TangJin-Ao DuanPublished in: Oxidative medicine and cellular longevity (2019)
Ginkgo ketoester tablets (GT) and donepezil were a clinically used combination for the treatment of Alzheimer's disease (AD). The aim of the study was undertaken to investigate the antiamnesic effects of the two drugs alone and in combination through in vivo models of the Morris water maze along with in vitro antioxidants, acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). The potential mechanisms were speculated by the activities of acetylcholine (ACh), AChE, superoxide dismutase (SOD), and malondialdehyde (MDA) and the protein expression of brain-derived neurotrophic factor (BDNF) and tyrosine protein kinase B (TrkB). The combination group showed a concentration-dependent inhibition of cholinesterase and antioxidation. As far as its mechanism was concerned, the combination of two drugs exerted excellent effects on oxidative stress, cholinergic pathway damage, and inactivation of the BDNF-TrkB signaling pathway. Additionally, to elucidate the binding mechanism of GT active ingredients into the structure of AChE, the results of molecular docking studies indicated that hydrogen and/or hydrophobic bonds might play an important role in their binding process. Thus, the combination of drugs could treat AD perfectly and further verify the scientific rationality of clinical medication.
Keyphrases
- molecular docking
- oxidative stress
- signaling pathway
- protein kinase
- dna damage
- molecular dynamics simulations
- emergency department
- diabetic rats
- drug induced
- hydrogen peroxide
- epithelial mesenchymal transition
- working memory
- risk assessment
- ischemia reperfusion injury
- cell proliferation
- binding protein
- human health
- amyotrophic lateral sclerosis
- insulin resistance
- endoplasmic reticulum stress
- electronic health record
- adverse drug