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Acrylamide Exposure Exacerbates Type 2 Diabetes-Induced Neurotoxicity: An Integrated Neurobehavioral and Molecular
Abdulaziz Arif A Alshammari1, Abdullah Saleh Alkhamiss2, Minhajul Arfeen3
1Department of Pharmacology and Toxicology, College of Pharmacy, Qassim University, Buraydah 51452, Saudi Arabia.
Type 2 Diabetes Mellitus (T2DM) and acrylamide (ACY) exposure worsen cognitive decline and neurodegeneration. This study in diabetic rats shows combined T2DM and ACY significantly increases oxidative stress, neuroinflammation, and neuroapoptosis, highlighting risks from diet and lifestyle.
Area of Science:
- Neuroscience
- Toxicology
- Metabolic Disorders
Background:
- Type 2 Diabetes Mellitus (T2DM) is linked to cognitive impairment due to hyperglycemia-induced oxidative stress, neuroinflammation, and neuroapoptosis.
- Acrylamide (ACY), a neurotoxicant in food and smoke, may exacerbate these neurological issues.
Purpose of the Study:
- To investigate the combined effects of T2DM and ACY exposure on cognitive function, neurodegeneration, oxidative stress, neuroinflammation, and neuroapoptosis in a rat model.
- To elucidate the neurotoxic amplification of T2DM and ACY.
Main Methods:
- T2DM induced using nicotinamide and streptozotocin in rats.
- Rats received daily oral ACY doses for one month.
- Cognitive function assessed via EPM, NOR, and Y-maze tests.
- Brain tissue analyzed for markers of neurodegeneration, oxidative stress, neuroinflammation, and neuroapoptosis.
- Immunohistochemistry used to assess structural brain changes.
Main Results:
- Combined T2DM and ACY exposure significantly worsened cognitive deficits.
- Elevated markers of neurodegeneration, oxidative stress (MDA), neuroinflammation (COX-2, PGE2), and neuroapoptosis (Bax, Caspase-3) were observed.
- Increased Bcl-6 expression indicated structural brain changes.
Conclusions:
- T2DM and ACY exposure synergistically amplify neurotoxic effects, leading to cognitive decline and neuronal damage.
- Public health strategies to reduce ACY exposure are crucial, especially for T2DM populations.
- Further research into neuroprotective interventions is warranted.
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