Abstract

Xenobiotic nuclear receptors (NR) are intracellular players involved in an increasing number of physiological processes. Examined and characterized in peripheral organs where they govern metabolic, transport and detoxification mechanisms, accumulating data suggest a functional expression of specific NR at the neurovascular unit (NVU). Here, we focus on the Constitutive Androstane Receptor (CAR), expressed in detoxifying organs such as the liver, intestines and kidneys. By direct and indirect activation, CAR is implicated in hepatic detoxification of xenobiotics, environmental contaminants, and endogenous molecules (bilirubin, bile acids). Importantly, CAR participates in physiological stress adaptation responses, hormonal and energy homeostasis due to glucose and lipid sensing. We next analyze the emerging evidence supporting a role of CAR in NVU cells including the blood–brain barrier (BBB), a key vascular interface regulating communications between the brain and the periphery. We address the emerging concept of how CAR may regulate specific P450 cytochromes at the NVU and the associated relevance to brain diseases. A clear understanding of how CAR engages during pathological conditions could enable new mechanistic, and perhaps pharmacological, entry-points within a peripheral–brain axis.

Highlights

  • CAR Governs Detoxification MechanismsThe Constitutive Androstane Receptor (CAR), a key nuclear receptor (subfamily 1, group I, member 3 (NR1i3)), displays a prominent functional expression in peripheral organs and an emerging role in the brain

  • Recent data reported a prolipogenic effect of CAR, inducing hepatic lipid accumulation upon its activation [98]. This occurs through the induction of hepatic lipogenic genes, including patatin-like phospholipase domain-containing protein 3 (Pnpla3), a gene whose polymorphism is associated with the pathogenesis of non-alcoholic fatty liver diseases (NAFLD)

  • A role of CAR was recently demonstrated in mediating a kidney-liver cross-talk in Acute kidney injury (AKI) which is characterized by the sudden impairment of kidney function [107]

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Summary

Introduction

The Constitutive Androstane Receptor (CAR), a key nuclear receptor (subfamily 1, group I, member 3 (NR1i3)), displays a prominent functional expression in peripheral organs and an emerging role in the brain. (SULT), and efflux and uptake transporters such as multidrug resistance mutation 1 (MDR1), multidrug resistance proteins (MRPS), and organic-anion-transporting polypeptides (OATP) [6,7] Via these enzymes and transporters, CAR governs the detoxification of endogenous bile acids and bilirubin, which can cause hepato-toxicity if accumulated [8,9]. This evidence outlines CAR as a player regulating key metabolic and transporter machineries involved in a myriad of endogenous and protective cellular processes, applicable to peripheral organs and the brain. We here review how CAR, through key peripheral and central functions, acts as a stress sensor engaging and responding to toxic, environmental, or metabolic insults

CAR Has a Particular Mechanism of Action
Functional Roles of CAR in Peripheral Organs
CAR as an Endobiotic Stress Sensor
CAR as a Regulator of Steroid and Thyroid Hormones
CAR as a Sensor of Fasting and Caloric Restriction
CAR as a Glucose Sensor
CAR as a Lipid Sensor
CAR as a Hypoxia Sensor
CAR Intestinal Response to Inflammatory Stress
CAR Protects from Acute Kidney Injury
Functional Roles of CAR in the Brain
CAR and Brain Disease Conditions
Conclusions
Findings
Modulation of CAR
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