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SHR Neuro Cancer Cardio Lipid Metab Microb

Pandey, S; Mangmool, S; Madreiter-Sokolowski, CT; Wichaiyo, S; Luangmonkong, T; Parichatikanond, W.
Exendin-4 protects against high glucose-induced mitochondrial dysfunction and oxidative stress in SH-SY5Y neuroblastoma cells through GLP-1 receptor/Epac/Akt signaling
EUR J PHARMACOL. 2023; 954: 175896 Doi: 10.1016/j.ejphar.2023.175896
Web of Science PubMed FullText FullText_MUG

 

Leading authors Med Uni Graz

Parichatikanond Warisara

Co-authors Med Uni Graz

Madreiter-Sokolowski Corina

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Abstract:

Mitochondrial dysfunction under diabetic condition leads to the development and progression of neurodegen-erative complications. Recently, the beneficial effects of glucagon-like peptide-1 (GLP-1) receptor agonists on diabetic neuropathies have been widely recognized. However, molecular mechanisms underlying the neuro-protective effects of GLP-1 receptor agonists against high glucose (HG)-induced neuronal damages is not completely elucidated. Here, we investigated the underlying mechanisms of GLP-1 receptor agonist treatment against oxidative stress, mitochondrial dysfunction, and neuronal damages under HG conditions mimicking a diabetic hyperglycemic state in SH-SY5Y neuroblastoma cells. We revealed that treatment with exendin-4, a GLP-1 receptor agonist, not only increased the expression of survival markers, phospho-Akt/Akt and Bcl-2, but also decreased the expression of pro-apoptotic marker, Bax, and reduced the levels of reactive oxygen species (ROS) defense markers (catalase, SOD-2, and HO-1) under HG conditions. The expressions of mitochondrial function associated genes, MCU and UCP3, and mitochondrial fission genes, DRP1 and FIS1, were decreased by exendin-4 compared to non-treated levels, while the protein expression levels of mitochondrial homeostasis regulators, Parkin and PINK1, were enhanced. In addition, blockade of Epac and Akt activities was able to antagonize these neuroprotective effects of exendin-4. Collectively, we demonstrated that stimulation of GLP-1 receptor propa-gates a neuroprotective cascade against the oxidative stress and mitochondrial dysfunction as well as augments survival through the Epac/Akt-dependent pathway. Therefore, the revealed mechanisms underlying GLP-1 re-ceptor pathway by preserving mitochondrial homeostasis would be a therapeutic candidate to alleviate neuronal dysfunctions and delay the progression of diabetic neuropathies.

Find related publications in this database (Keywords)

Exendin-4

GLP-1 receptor

Epac

Akt

High glucose

Mitochondrial dysfunction

Neuroprotective effect

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