# Dexamethasone and Insulin Modulate Alanine Aminotransferase (ALT) Activity and Alanine Oxidation in C2C12 Cells in a Dose-Dependent Manner

**Authors:** Saed Woraikat, Defei Chen, Fuyu Yang, Chenglin Tang, Fan He, Kun Qian

PMC · DOI: 10.7759/cureus.59331 · Cureus · 2024-04-30

## TL;DR

This study shows how insulin and dexamethasone affect ALT activity and alanine metabolism in muscle cells, depending on the drug doses.

## Contribution

The study reveals a dose-dependent modulation of ALT activity and alanine oxidation by insulin and dexamethasone in C2C12 cells.

## Key findings

- ALT activity in C2C12 cells is influenced by differentiation and drug treatments.
- Dexamethasone and insulin treatments modulate alanine oxidation in a dose-dependent manner.
- The study highlights the dynamic interplay between ALT activity and cellular states like differentiation and stress.

## Abstract

Background: The muscle cells myocytes are differentiated for the purpose of contraction function, which plays a major role in body metabolism and energy haemostasis, through different metabolic pathways, such as glucose and protein metabolic pathways. Alanine aminotransferase (ALT) plays a crucial role by reversibly catalysing transamination between alanine and a-ketoglutarate to form pyruvate and glutamate and by mediating the conversion of these four major intermediate metabolites. ALT plays important roles for energy homeostasis during fasting and prolonged exercise anaerobically, when muscle protein must first be broken down into its constituent amino acids.

Methods: Mouse skeletal myoblast cell line C2C12 was cultured in Dulbecco's modified eagle medium (DMEM) growth medium, supplied with 2% horse serum supplemented with 1 uM insulin, 2 mM glutamine and penicillin and streptomycin antibiotics for seven days. The differentiation medium is refreshed every 24 hours. Then, C2C12 cells were treated with insulin and dexamethasone to examine their effects on myocytes' ALT activity.

Results: In our study, we found an impact on ALT activity under different influences, including C2C12 differentiation, dexamethasone and insulin treatments, which shed light on the dynamic interplay between ALT activity, alanine metabolism, and cellular states, like differentiation and stress responses.

Conclusion: The study provides valuable insights into the dynamic regulation of ALT activity and alanine metabolism in C2C12 cells across differentiation and drug treatments. Further research is encouraged to explore the underlying mechanisms and their implications for muscle function, differentiation and potential therapeutic interventions in metabolic disorders.

## Linked entities

- **Proteins:** GPT (glutamic--pyruvic transaminase)
- **Chemicals:** dexamethasone (PubChem CID 5743), insulin (PubChem CID 70678557), glutamine (PubChem CID 738), penicillin (PubChem CID 2349), streptomycin (PubChem CID 5297)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}
- **Diseases:** metabolic disorders (MESH:D008659)
- **Chemicals:** penicillin (MESH:D010406), streptomycin (MESH:D013307), pyruvate (MESH:D019289), glutamate (MESH:D018698), DMEM (-), amino acids (MESH:D000596), glucose (MESH:D005947), glutamine (MESH:D005973), Dexamethasone (MESH:D003907), Alanine (MESH:D000409)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C2C12 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0188)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11137606/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC11137606/full.md

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Source: https://tomesphere.com/paper/PMC11137606