GLPwatch

Exendin-4 Pretreatment Attenuates Kainic Acid-Induced Hippocampal Neuronal Death.

Cells · 2021

Last updated 2026-05-28

In a mouse study, researchers tested whether a GLP-1 drug called Exendin-4 (Ex-4) could protect the brain from damage caused by seizures. Mice given Ex-4 injections three days before seizures showed reduced brain cell death, less severe seizures, and lower brain inflammation compared to mice not given Ex-4. Ex-4 also helped maintain normal levels of a brain protein and reduced damage to the blood-brain barrier.

AI summary of the abstract below.

JournalCells, 2021
Citations8
Relative citation ratio0.59
NIH percentile33
Molecules
Conditions studied Alzheimers

Abstract

Exendin-4 (Ex-4) is a glucagon-like peptide-1 receptor (GLP-1R) agonist that protects against brain injury. However, little is known about the effect of Ex-4 on kainic acid (KA)-induced seizures and hippocampal cell death. Therefore, this study evaluated the neuroprotective effects of Ex-4 pretreatment in a mouse model of KA-induced seizures. Three days before KA treatment, mice were intraperitoneally injected with Ex-4. We found that Ex-4 pretreatment reversed KA-induced reduction of GLP-1R expression in the hippocampus and attenuated KA-induced seizure score, hippocampal neuronal death, and neuroinflammation. Ex-4 pretreatment also dramatically reduced hippocampal lipocalin-2 protein in KA-treated mice. Furthermore, immunohistochemical studies showed that Ex-4 pretreatment significantly alleviated blood-brain barrier leakage. Finally, Ex-4 pretreatment stimulated hippocampal expression of phosphorylated cyclic adenosine monophosphate (cAMP) response element-binding protein (p-CREB), a known target of GLP-1/GLP-1R signaling. These findings indicate that Ex-4 pretreatment may protect against KA-induced neuronal damage by regulating GLP-1R/CREB-mediated signaling pathways.

Verbatim abstract via PubMed 34685508 ↗