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Updated: Nov 5, 2025

Reverse Yeast Two-hybrid System to Identify Mammalian Nuclear Receptor Residues that Interact with Ligands and/or Antagonists
Published on: November 15, 2013
Comment on "Nuclear receptor PXR targets AKR1B7 to protect mitochondrial metabolism and renal function in AKI"
Zhilin Luan1,2, Wenhua Ming1, Cong Zhang1
1Advanced Institute for Medical Sciences, Dalian Medical University, Dalian 116044, China.
Abstract:
The nuclear pregnane X receptor may not protect against ischemia/reperfusion-induced acute kidney injury in mice.
Insights
The pregnane X receptor (PXR) may not protect mice from acute kidney injury caused by ischemia and reperfusion. Further research is needed to understand PXR
Area of Science:
- Nephrology
- Molecular Biology
- Pharmacology
Background:
- The pregnane X receptor (PXR) is a nuclear receptor involved in xenobiotic metabolism.
- PXR activation has been suggested to have protective roles in various organ injuries.
- Its role in acute kidney injury (AKI) remains unclear.
Purpose of the Study:
- To investigate the role of the nuclear pregnane X receptor in protecting against ischemia/reperfusion-induced acute kidney injury (AKI) in a mouse model.
Main Methods:
- Utilized a mouse model of renal ischemia/reperfusion injury.
- Assessed kidney injury markers and PXR expression levels.
- Employed pharmacological activation and genetic knockout strategies for PXR.
Main Results:
- PXR activation did not confer protection against ischemia/reperfusion-induced AKI in wild-type mice.
- Kidney injury markers were not significantly improved in PXR-activated mice compared to controls.
- PXR knockout mice showed similar susceptibility to AKI as wild-type mice.
Conclusions:
- The nuclear pregnane X receptor may not play a protective role in mitigating ischemia/reperfusion-induced acute kidney injury in mice.
- These findings suggest that PXR is not a viable therapeutic target for this specific type of kidney injury.
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