Emerging Links between Cadmium Exposure and Insulin Resistance : Human, Animal, and Cell Study Data

Recent research has helped clarify the role of cadmium (Cd) in various pathological states. We have demonstrated Cd involvement in pancreatic cancer, as well as the bioaccumulation of Cd in the pancreas. Bioaccumulation and increased toxicity suggest that Cd may also be involved in other pancreas-mediated diseases, like diabetes. Cd falls into the category of "hyperglycemic" metals, i.e., metals that increase blood glucose levels, which could be due to increased gluconeogenesis, damage to β-cells leading to reduced insulin production, or insulin resistance at target tissue resulting in a lack of glucose uptake. This review addresses the current evidence for the role of Cd, leading to insulin resistance from human, animal, and in vitro studies. Available data have shown that Cd may affect normal insulin function through multiple pathways. There is evidence that Cd exposure results in the perturbation of the enzymes and modulatory proteins involved in insulin signal transduction at the target tissue and mutations of the insulin receptor. Cd, through well-described mechanisms of oxidative stress, inflammation, and mitochondrial damage, may also alter insulin production in β-cells. More work is necessary to elucidate the mechanisms associated with Cd-mediated insulin resistance.

Medienart:

E-Artikel

Erscheinungsjahr:

2020

Erschienen:

2020

Enthalten in:

Zur Gesamtaufnahme - volume:8

Enthalten in:

Toxics - 8(2020), 3 vom: 27. Aug.

Sprache:

Englisch

Beteiligte Personen:

Buha, Aleksandra [VerfasserIn]
Đukić-Ćosić, Danijela [VerfasserIn]
Ćurčić, Marijana [VerfasserIn]
Bulat, Zorica [VerfasserIn]
Antonijević, Biljana [VerfasserIn]
Moulis, Jean-Marc [VerfasserIn]
Goumenou, Marina [VerfasserIn]
Wallace, David [VerfasserIn]

Links:

Volltext

Themen:

β-cell toxicity
Cadmium
Diabetes
Hyperglycemia
Hyperinsulinemia
Insulin
Journal Article
Lipogenic
Review

Anmerkungen:

Date Revised 29.03.2024

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.3390/toxics8030063

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM314401318