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Updated: Jun 22, 2025

An In Ovo Model for Testing Insulin-mimetic Compounds
Published on: April 23, 2018
Putative mechanism of a multivitamin treatment against insulin resistance
José Antonio Palma-Jacinto1, Edgar López-López2,3, José Luis Medina-Franco2
1Laboratory of Biochemistry and Neurotoxicology, Faculty of Bioanalysis-Xalapa, Universidad Veracruzana, Médicos y Odontólogos S/N Unidad del Bosque, Xalapa, Mexico.
Abstract:
Insulin resistance is caused by the abnormal secretion of proinflammatory cytokines in adipose tissue, which is induced by an increase in lipid accumulation in adipocytes, hepatocytes, and myocytes. The inflammatory pathway involves multiple targets such as nuclear factor kappa B, inhibitor of nuclear factor κ-B kinase, and mitogen-activated protein kinase. Vitamins are micronutrients with anti-inflammatory activities that have unclear mechanisms. The present study aimed to describe the putative mechanisms of vitamins involved in the inflammatory pathway of insulin resistance. The strategy to achieve this goal was to integrate data mining and analysis, target prediction, and molecular docking simulation calculations to support our hypotheses. Our results suggest that the multitarget activity of vitamins A, B1, B2, B3, B5, B6, B7, B12, C, D3, and E inhibits nuclear factor kappa B and mitogen-activated protein kinase, in addition to vitamins A and B12 against inhibitor of nuclear factor κ-B kinase. The findings of this study highlight the pharmacological potential of using an anti-inflammatory and multitarget treatment based on vitamins and open new perspectives to evaluate the inhibitory activity of vitamins against nuclear factor kappa B, mitogen-activated protein kinase, and inhibitor of nuclear factor κ-B kinase in an insulin-resistant context.
Insights
Vitamins A, B, C, D3, and E show anti-inflammatory effects by inhibiting key pathways in insulin resistance. This research explores vitamin mechanisms against nuclear factor kappa B and mitogen-activated protein kinase.
Area of Science:
- Biochemistry
- Molecular Biology
- Nutritional Science
Background:
- Insulin resistance stems from proinflammatory cytokines in adipose tissue, driven by lipid accumulation.
- The inflammatory pathway involves critical targets: nuclear factor kappa B (NF-κB), inhibitor of nuclear factor κ-B kinase (IKK), and mitogen-activated protein kinase (MAPK).
- Vitamins possess anti-inflammatory properties, but their precise mechanisms in insulin resistance are not fully understood.
Purpose of the Study:
- To elucidate the potential mechanisms of vitamins within the inflammatory pathway of insulin resistance.
- To investigate the inhibitory effects of various vitamins on key inflammatory targets.
Main Methods:
- Integrated data mining and analysis.
- Utilized target prediction algorithms.
- Performed molecular docking simulations to validate interactions.
Main Results:
- Vitamins A, B1, B2, B3, B5, B6, B7, B12, C, D3, and E were found to inhibit NF-κB and MAPK.
- Vitamins A and B12 specifically demonstrated inhibitory activity against IKK.
- These findings suggest a multitarget inhibitory action of vitamins on the inflammatory cascade.
Conclusions:
- Vitamins exhibit significant potential as anti-inflammatory agents in the context of insulin resistance.
- A multitarget therapeutic strategy utilizing vitamins could offer a novel approach to managing insulin resistance.
- Further research is warranted to confirm the inhibitory roles of vitamins against NF-κB, MAPK, and IKK in insulin-resistant models.
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