AI Article Synopsis

  • Cognitive dysfunction involves a gradual decline in learning and memory capabilities, and Jiao-tai-wan (JTW), a Chinese medicinal formula, has shown potential in treating this condition despite its primary use for insomnia.
  • In experiments with mice experiencing cognitive deficits induced by scopolamine, JTW administration significantly improved spatial recognition, learning, and memory abilities while also impacting important neurotransmitters involved in cognition.
  • Moreover, JTW reduced oxidative stress and enhanced neuroprotective factors, suggesting its effectiveness in alleviating cognitive dysfunction and highlighting its potential as a therapeutic option.

Article Abstract

Cognitive dysfunction is characterized as the gradual loss of learning ability and cognitive function, as well as memory impairment. Jiao-tai-wan (JTW), a Chinese medicine prescription including Coptis chinensis and cinnamon, is mainly used for the treatment of insomnia, while the effect of JTW in improving cognitive function has not been reported. In this study, we employed a scopolamine- (SCOP-) treated learning and memory deficit model to explore whether JTW could alleviate cognitive dysfunction. In behavioral experiments, Morris water maze, Y-maze, fearing condition test, and novel object discrimination test were conducted. Results showed that oral administration of JTW (2.1 g/kg, 4.2 g/kg, and 8.4 g/kg) can effectively promote the ability of spatial recognition, learning and memory, and the memory ability of fresh things of SCOP-treated mice. In addition, the activity of acetylcholinesterase (AChE) was effectively decreased; the activity of choline acetyltransferase (ChAT) and concentration of acetylcholine (Ach) were improved after JTW treatment in both hippocampus and cortex of SCOP-treated mice. JTW effectively ameliorated oxidative stress because of decreased the levels of malondialdehyde (MDA) and reactive oxygen species (ROS) and increased the activities of superoxide dismutase (SOD) and catalase (CAT) in hippocampus and cortex. Furthermore, JTW promotes the expressions of neurotrophic factors including postsynaptic density protein 95 (PSD95) and synaptophysin (SYN) and brain-derived neurotrophic factor (BDNF) in both hippocampus and cortex. Nissl's staining shows that the neuroprotective effect of JTW was very effective. To sum up, JTW might be a promising candidate for the treatment of cognitive dysfunction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6040267PMC
http://dx.doi.org/10.1155/2018/3538763DOI Listing

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