Mechanisms of Metal-Induced Hepatic Inflammation
- PMID: 39499483
- DOI: 10.1007/s40572-024-00463-6
Mechanisms of Metal-Induced Hepatic Inflammation
Abstract
Purpose of review: Worldwide, there is an increasing prevalence of hepatic diseases. The most common diseases include alcoholic-associated liver disease (ALD), metabolic dysfunction-associated fatty liver disease/ metabolic dysfunction-associated steatohepatitis (MAFLD/MASH) and viral hepatitis. While there are many important mediators of these diseases, there is increasing recognition of the importance of the inflammatory immune response in hepatic disease pathogenesis.
Recent findings: Hepatic inflammation triggers the onset and progression of liver diseases. Chronic and sustained inflammation can lead to fibrosis, then cirrhosis and eventually end-stage cancer, hepatocellular carcinoma. Importantly, growing evidence suggest that metal exposure plays a role in hepatic disease pathogenesis. While in recent years, studies have linked metal exposure and hepatic steatosis, studies emphasizing metal-induced hepatic inflammation are limited. Hepatic inflammation is an important hallmark of fatty liver disease. This review aims to summarize the mechanisms of arsenic (As), cadmium (Cd) and chromium (Cr)-induced hepatic inflammation as they contribute to hepatic toxicity and to identify data gaps for future investigation.
Keywords: Fibrosis; Hepatic inflammation; Hepatic stellate cells; Immune cell infiltration; Metals.
© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
Conflict of interest statement
Declarations. Competing Interests: The authors declare no competing interests. Human and Animal Rights and Informed Consent: This article does not contain any studies with human or animal subjects performed by any of the authors.
References
-
- Ramírez-Mejía MM, Méndez-Sánchez N. What is in a name: from NAFLD to MAFLD and MASLD—unraveling the complexities and implications. Curr Hepatol Rep. 2023;22(4):221–7. - DOI
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