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Pesticides Drive Liver Diseases Through Non-Apoptotic Regulated Cell Death Pathways
Zamza Khairullina1, Saulesh Kurmangaliyeva1, Rustam Yussupov2
1Department of Microbiology, Virology and Immunology, West Kazakhstan Marat Ospanov Medical University, 68 Maresyev St., Aktobe 030000, Kazakhstan.
Abstract:
A compelling body of evidence links pesticide exposure to human diseases. The liver plays a central role in the detoxification of pesticides, suggesting intense pesticide-liver cell interactions. A growing body of studies highlighted in this review supports the contribution of pesticides of various chemical classes to the development of non-alcoholic fatty liver disease (NAFLD), alcohol-associated liver disease (ALD), liver cirrhosis, viral hepatitis, hepatocellular carcinoma, etc., via disrupting lipid and carbohydrate metabolism and redox homeostasis, promoting endoplasmic reticulum stress and mitochondrial dysfunction, as well as stimulating apoptosis, fibrosis, and inflammation. In this review, we systematically illustrated an underappreciated mechanism of pesticide-induced overall and hepatic toxicity, i.e., the ability to induce non-apoptotic regulated cell death (RCD) pathways such as ferroptosis, necroptosis, and pyroptosis. Our analysis indicates that pesticides are implicated in driving liver diseases by inducing ferroptosis, necroptosis, and pyroptosis. Non-apoptotic RCDs mediate pesticide-induced liver steatosis and fibrosis. Furthermore, these cell death modalities fuel inflammation through the promotion of pro-inflammatory cytokine production and the generation of damage-associated molecular patterns. Understanding of deeper mechanisms of pesticide-induced effects on the non-apoptotic cell death machinery and subsequent immunogenic effects in liver pathology might help develop novel preventive strategies to reduce liver damage.
Insights
Pesticide exposure contributes to liver diseases by triggering specific cell death pathways. Understanding these mechanisms, including ferroptosis, necroptosis, and pyroptosis, can help prevent liver damage.
Area of Science:
- Environmental Toxicology
- Hepatology
- Cell Biology
Background:
- Pesticide exposure is linked to various human diseases.
- The liver is crucial for pesticide detoxification, making it susceptible to pesticide-induced damage.
- Pesticides contribute to liver conditions like NAFLD, ALD, cirrhosis, and cancer.
Purpose of the Study:
- To systematically review the role of non-apoptotic regulated cell death (RCD) pathways in pesticide-induced liver toxicity.
- To highlight ferroptosis, necroptosis, and pyroptosis as underappreciated mechanisms of pesticide-induced liver damage.
- To explore how these RCDs contribute to liver steatosis, fibrosis, and inflammation.
Main Methods:
- Systematic review of existing literature on pesticide exposure and liver disease.
- Analysis of studies investigating pesticide-induced cell death mechanisms.
- Examination of the link between non-apoptotic RCDs and liver pathology markers.
Main Results:
- Pesticides induce liver diseases by activating ferroptosis, necroptosis, and pyroptosis.
- Non-apoptotic RCDs are key mediators of pesticide-induced liver steatosis and fibrosis.
- These cell death pathways promote inflammation via cytokine production and DAMPs release.
Conclusions:
- Pesticide-induced liver toxicity involves non-apoptotic regulated cell death pathways.
- Targeting ferroptosis, necroptosis, and pyroptosis may offer novel strategies for preventing pesticide-related liver damage.
- Further understanding of RCDs and immunogenic effects is crucial for developing preventive measures.
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