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Exenatide treatment exerts anxiolytic- and antidepressant-like effects and reverses neuropathy in a mouse model of type-2 diabetes.

Med Sci Monit Basic Res · 2014

Last updated 2026-05-28

In a mouse study of type-2 diabetes, twice-daily injections of exenatide at 0.1 µg/kg for two weeks reduced anxiety- and depression-like behaviors and improved neuropathy symptoms. The mice had diabetes induced by streptozocin (100 mg/kg) and nicotinamide (240 mg/kg). The findings suggest exenatide may help with these conditions in people with type-2 diabetes.

AI summary of the abstract below.

JournalMed Sci Monit Basic Res, 2014
Citations34
Relative citation ratio1.29
NIH percentile59
Molecules exenatide
Conditions studied Type 2 Diabetes, Anxiety, Depression

Abstract

BACKGROUND: Comorbid neurobehavioral disturbances and type-2 diabetes mellitus (T2DM) warrant immediate research attention. Exenatide, which is a potent and selective agonist for the glucagon-like peptide-1 (GLP-1), is used in the treatment of T2DM. Exenatide displays a multitude of effects in the central nervous system. The aim of this study was to investigate the anxiolytic- and antidepressant-like effects and analgesic effects of exenatide in a type-2 diabetic mouse model. MATERIAL/METHODS: Modified elevated plus-maze test for anxiolytic-like, forced swimming test for depression-like behavior and hotplate test for neuropathy were used as behavioral tasks. Behavioral parameters were investigated in a streptozocin--(100 mg/kg, i.p.) and nicotinamide--(240 mg/kg, i.p.) induced type-2 diabetic mouse model. Exenatide (0.1 µg/kg, s.c., twice daily) was administered for 2 weeks. Vehicle (control), diabetic, and exenatide-treated diabetic mice were tested. RESULTS: Our results confirm that exenatide exerts anxiolytic- and antidepressant-like effects and might be effective in diabetic neuropathy in a diabetic mouse model. CONCLUSIONS: Exenatide may be a good candidate as a treatment option for depression, anxiety, and neuropathy in patients with type-2 diabetes.

Verbatim abstract via PubMed 25076419 ↗

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