(2020) Protective Effects of Citicoline and Benfotiamine Each Alone and in Combination on Streptozotocin-induced Memory Impairment in Mice. Clinical Psychopharmacology and Neuroscience. pp. 81-92. ISSN 1738-1088
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Abstract
Objective: Diabetes mellitus is associated with cognitive disorders such as Alzheimer's disease. Studies have shown that citicoline and benfotiamine can improve memory and learning through different mechanism of actions. The aim of this study was to compare the individual effects of benfotiamine (100, 200, 300 mg/kg) and citicoline (50, 100, 250, 500 mg/kg, gavage) and their co-administration on memory impairments in diabetic mice. Methods: Diabetes was induced by a single dose of streptozotocin (STZ, 140 mg/kg, intraperitoneal) and benfotiamine and/or citicoline were administered for three weeks. Memory was evaluated using the object recognition task (ORT) and passive avoidance test (PAT). Results: Results from ORT shows that citicoline at 50, 100, 250, and 500 mg/kg and benfotiamine at 100, 200, and 300 mg/kg and their combination (benfotiamine at 100 mg/kg added to citicoline at 50, 100, and 250 mg/kg) are equally effective in reversing the memory loss induced by STZ (p < 0.001). PAT results demonstrate that citicoline at 100, 250, and 500 mg/kg and benfotiamine at above doses did not improve the latency time when administered separately, but benfotiamine at a fixed dose of 100 mg/kg in the presence of citicoline at 50, 100, and 250 mg/kg increased the latency time and improved memory significantly. Conclusion: In conclusion, in PAT, co-administration of benfotiamine and citicoline was more effective than either alone in improving memory. Regarding ORT, although benfotiamine added to citicoline improved memory notably, the difference between combination therapy and single-drug therapy was not considerable.
Item Type: | Article |
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Keywords: | Citicoline Benfotiamine Memory Dementia Cognitive Streptozotocin GLYCATION END-PRODUCTS ALZHEIMERS-DISEASE ANIMAL-MODEL ACETYLCHOLINESTERASE ACTIVITY COGNITIVE IMPAIRMENT CEREBROSPINAL-FLUID RECOGNITION MEMORY PREFRONTAL CORTEX THIAMINE DEFICIENCY |
Subjects: | QV Pharmacology QV Pharmacology > QV 600-666 Toxicology |
Divisions: | Faculty of Pharmacy and Pharmaceutical Sciences > Department of Toxicology and Pharmacology Isfahan Pharmaceutical Sciences Research center |
Page Range: | pp. 81-92 |
Journal or Publication Title: | Clinical Psychopharmacology and Neuroscience |
Journal Index: | ISI |
Volume: | 18 |
Number: | 1 |
Identification Number: | https://doi.org/10.9758/cpn.2020.18.1.81 |
ISSN: | 1738-1088 |
Depositing User: | Zahra Otroj |
URI: | http://eprints.mui.ac.ir/id/eprint/13578 |
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