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Mehraban, Reza, Babaei, Parvin, Rohampour, Kambiz, Jafari, Adele, Golipoor, Zoleikha. (1402). Metformin improves memory via AMPK/mTOR-dependent route in a rat model of Alzheimer’s disease. , 27(3), 360-365. doi: 10.22038/ijbms.2023.73075.15879
Reza Ale Mahmoud Mehraban; Parvin Babaei; Kambiz Rohampour; Adele Jafari; Zoleikha Golipoor. "Metformin improves memory via AMPK/mTOR-dependent route in a rat model of Alzheimer’s disease". , 27, 3, 1402, 360-365. doi: 10.22038/ijbms.2023.73075.15879
Mehraban, Reza, Babaei, Parvin, Rohampour, Kambiz, Jafari, Adele, Golipoor, Zoleikha. (1402). 'Metformin improves memory via AMPK/mTOR-dependent route in a rat model of Alzheimer’s disease', , 27(3), pp. 360-365. doi: 10.22038/ijbms.2023.73075.15879
Mehraban, Reza, Babaei, Parvin, Rohampour, Kambiz, Jafari, Adele, Golipoor, Zoleikha. Metformin improves memory via AMPK/mTOR-dependent route in a rat model of Alzheimer’s disease. , 1402; 27(3): 360-365. doi: 10.22038/ijbms.2023.73075.15879

Metformin improves memory via AMPK/mTOR-dependent route in a rat model of Alzheimer’s disease

Iranian Journal of Basic Medical Sciences
مقاله 13، دوره 27، شماره 3، خرداد 2024، صفحه 360-365    اصل مقاله (434.72 K)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22038/ijbms.2023.73075.15879
نویسندگان
Reza Ale Mahmoud Mehraban1، 2؛ Parvin Babaei1، 2، 3؛ Kambiz Rohampour3، 2؛ Adele Jafari* 2؛ Zoleikha Golipoor3
1Cellular and Molecular Research Center, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
2Department of Physiology, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
3Neuroscience Research Center, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
چکیده
Objective(s): Metformin, as an insulin sensitizer, is a familiar antidiabetic drug. Increasing evidence points to metformin’s protective effects against Alzheimer’s disease (AD). However, the mechanism is not well understood. The present study evaluated whether inhibiting AMPK and activating mTOR could stop metformin from improving memory in rats with streptozotocin (STZ) -induced Alzheimer’s disease.
Materials and Methods: Twelve-week-old Wistar rats, were injected 3 mg/kg STZ intracerebroventricularly on days 1 and 3 to develop the animal model. Metformin was applied orally at 100 mg/kg (17 days). Forty-five min before the retrieval phase, dorsomorphin (DM; AMPK inhibitor, 2 M) and MHY (mTOR activator, 0.1 M) were administered. Morris Water Maze (MWM) and shuttle box were utilized to measure spatial and passive avoidance memory, respectively. Congo red staining was used to identify cortical amyloid deposition.
Results: The findings exhibited a considerable enhancement in spatial learning and memory in the metformin treatment group (P≤0.05). Injection of DM and MHY alone could not significantly change MWM and passive avoidance. Additionally, co-administration of DM and MHY increased escape latency (P≤0.001) and reduced the total time spent in the target quadrant (TTS) (P≤0.05) compared to the STZ+MET group during retrieval of MWM. Also, co-injection of DM and MHY increased step-through latency (STL) and decreased time spent in the dark compartment (TDC) compared to the STZ+MET group (P≤0.001).
Conclusion: Metformin appears to have a therapeutic impact by activating AMPK and inactivating mTOR. As a result, it could be used as an Alzheimer’s treatment strategy.
کلیدواژه‌ها
Alzheimer disease؛ AMP-activated protein - kinase؛ Memory؛ Metformin؛ mTOR
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