Abstract

The liver’s high metabolic activity and detoxification functions generate reactive oxygen species, mainly through oxidative phosphorylation in the mitochondria of hepatocytes. In contrast, it also has a potent antioxidant mechanism for counterbalancing the oxidant’s effect and relieving oxidative stress. PAS kinase (PASK) is a serine/threonine kinase containing an N-terminal Per-Arnt-Sim (PAS) domain, able to detect redox state. During fasting/feeding changes, PASK regulates the expression and activation of critical liver proteins involved in carbohydrate and lipid metabolism and mitochondrial biogenesis. Interestingly, the functional inactivation of PASK prevents the development of a high-fat diet (HFD)-induced obesity and diabetes. In addition, PASK deficiency alters the activity of other nutrient sensors, such as the AMP-activated protein kinase (AMPK) and the mammalian target of rapamycin (mTOR). In addition to the expression and subcellular localization of nicotinamide-dependent histone deacetylases (SIRTs). This review focuses on the relationship between oxidative stress, PASK, and other nutrient sensors, updating the limited knowledge on the role of PASK in the antioxidant response. We also comment on glucagon-like peptide 1 (GLP-1) and its collaboration with PASK in preventing the damage associated with hepatic oxidative stress. The current knowledge would suggest that PASK inhibition and/or exendin-4 treatment, especially under fasting conditions, could ameliorate disorders associated with excess oxidative stress.

Highlights

  • The liver is a vital organ for adapting to nutritional changes by responding appropriately to achieve metabolic and energy homeostasis through its role in the storage and redistribution of carbohydrates, proteins, vitamins, and lipids.2

  • These findings suggest that PAS kinase (PASK) inhibition and exendin-4 treatment might help to promote antioxidant responses to control hepatic oxidative stress and avoid and prevent their harmful effects

  • Its high metabolic activity logically leads to the production of reactive oxygen species (ROS), which in turn is balanced by hepatic antioxidant mechanisms

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Summary

Introduction

The liver is a vital organ for adapting to nutritional changes (e.g., fasting/feeding states) by responding appropriately to achieve metabolic and energy homeostasis through its role in the storage and redistribution of carbohydrates, proteins, vitamins, and lipids

Liver Metabolic Functions and Detoxification
ROS and Antioxidant Defense
Hepatic Oxidative Stress and Nutritional Status
AMPK and mTOR
Sirtuin Family
PASK Deficiency Reduces Hepatic Oxidative Stress
GLP-1 Role in Oxidative Stress
Findings
Conclusions
Full Text
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