Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71622
Title: Not only metformin, but also D-allulose, alleviates metabolic disturbance and cognitive decline in prediabetic rats
Authors: Wasana Pratchayasakul
Kewarin Jinawong
Wanpitak Pongkan
Thidarat Jaiwongkam
Busarin Arunsak
Titikorn Chunchai
Masaaki Tokuda
Nipon Chattipakorn
Siriporn C. Chattipakorn
Authors: Wasana Pratchayasakul
Kewarin Jinawong
Wanpitak Pongkan
Thidarat Jaiwongkam
Busarin Arunsak
Titikorn Chunchai
Masaaki Tokuda
Nipon Chattipakorn
Siriporn C. Chattipakorn
Keywords: Medicine;Neuroscience;Nursing
Issue Date: 1-Jan-2020
Abstract: © 2020 Informa UK Limited, trading as Taylor & Francis Group. Background: Prediabetes can be characterized as obesity with metabolic disturbance, leading to cognitive decline and brain pathologies. D-allulose administration in obese animals decreased metabolic disturbance. However, the comparative effects of D-allulose and metformin on cognition and brain functions in the diet-induced prediabetic condition are unclear. We assume that both D-allulose and metformin equally restore cognition and brain functions in prediabetic rats to an equal extent. Materials and methods: Fifty-six rats were randomly divided into two groups: a control and diet-induced prediabetic group which had received a normal diet (ND) and a high-fat diet (HFD) for 24 weeks, respectively. After dietary protocol had been followed for 12 weeks, ND rats were given solely drinking water daily for 12 weeks. HFD-prediabetic rats randomly received drinking water with either D-allulose (1.9 g/kg/day of D-allulose) or metformin (300 mg/kg/day of metformin) for 12 weeks. Following this, cognition and brain parameters were determined. Results: Brain oxidative stress, mitochondrial dysfunction, microglial hyper-activation, apoptosis, brain insulin insensitivity, hippocampal synaptic dysfunction, and cognitive decline were observed in prediabetic rats. D-allulose and metformin equally attenuated brain oxidative stress, brain mitochondrial ROS production, hippocampal apoptosis, brain insulin insensitivity, hippocampal synaptic dysfunction, resulting in improved learning process in prediabetic rats. Metformin conferred greater advantage on the amelioration of brain mitochondrial dysfunction and brain microglial hyper-activation than D-allulose, resulting in improvement in both learning and memory processes in prediabetic rats. Conclusions: Not only metformin, but also D-allulose, has beneficial effects on the enhancement of brain function and cognition in prediabetic condition.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85095723810&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/71622
ISSN: 14768305
1028415X
Appears in Collections:CMUL: Journal Articles

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