The Glucagon-Like Peptide 1 Analog Liraglutide Impairs the Migration of Rat Intestinal Cells in vitro

Abstract Liraglutide plays a crucial role in managing weight and regulating glucose levels, but it can have adverse effects, particularly on the gastrointestinal tract. Here, we assessed the impact of liraglutide on the viability, cell death, morphology, reorganization of the actin cytoskeleton, and migration of rat intestinal epithelial cells. There was no change in the viability of cells treated with liraglutide at concentrations of 0.25, 0.5, and 1 μM, however, high concentrations of the drug reduced IEC- 6 cell viability. Additionally, the treatment with low doses of liraglutide decreased the rate of apoptosis of IEC-6 cells relative to the control. Also, the treated cells showed a modified actin cytoskeleton, with prominent stress fibers. Regarding cell migration, there was a decrease in the percentage of closure of the cell-free area over 24 h, relative to the untreated cells. This study revealed the direct effects of liraglutide on intestinal cells, including reduced apoptosis rates, actin cytoskeleton alterations, and inhibited cell migration.

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Publication Details

Journal
Brazilian Archives of Biology and Technology
Published
2025-01-01
DOI
https://doi.org/10.1590/1678-4324-2025240485
Primary Topic
Diabetes Treatment and Management
Type
article
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article

The Glucagon-Like Peptide 1 Analog Liraglutide Impairs the Migration of Rat Intestinal Cells in vitro

E Silva, Luciana Aparecida Corá, Jhony Willams Gusmão do Nascimento, Maria Danielma dos Santos Reis et al.
Brazilian Archives of Biology and Technology
Diabetes Treatment and Management
article

The Glucagon-Like Peptide 1 Analog Liraglutide Impairs the Migration of Rat Intestinal Cells in vitro

E Silva, Luciana Aparecida Corá, Jhony Willams Gusmão do Nascimento, Maria Danielma dos Santos Reis, Aline Duarte
article en

Abstract

Abstract Liraglutide plays a crucial role in managing weight and regulating glucose levels, but it can have adverse effects, particularly on the gastrointestinal tract. Here, we assessed the impact of liraglutide on the viability, cell death, morphology, reorganization of the actin cytoskeleton, and migration of rat intestinal epithelial cells. There was no change in the viability of cells treated with liraglutide at concentrations of 0.25, 0.5, and 1 μM, however, high concentrations of the drug reduced IEC- 6 cell viability. Additionally, the treatment with low doses of liraglutide decreased the rate of apoptosis of IEC-6 cells relative to the control. Also, the treated cells showed a modified actin cytoskeleton, with prominent stress fibers. Regarding cell migration, there was a decrease in the percentage of closure of the cell-free area over 24 h, relative to the untreated cells. This study revealed the direct effects of liraglutide on intestinal cells, including reduced apoptosis rates, actin cytoskeleton alterations, and inhibited cell migration.

Brazilian Archives of Biology and TechnologyVol. 68
Universidade Estadual de Ciências da Saúde de Alagoas (BR), Instituto Federal de Educação, Ciência e Tecnologia de Alagoas (BR), Universidade Federal de Alagoas (BR)
Openalex Percentile: Top 56%
Diabetes Treatment and Management
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