Period3 modulates the NAD+-SIRT3 axis to alleviate depression-like behaviour by enhancing NAMPT activity in mice

Abstract

Introduction

PER3 deficiency is associated with depression-like behaviors, but the underlying mechanisms remain unclear.

Objectives

This study aims to elucidate the role and mechanism of PER3 in regulating depression-like behaviors in mice.

Methods

Depression-like behaviors were assessed using the sucrose preference test, tail suspension test, and forced swimming test. Metabolomic analysis was conducted on hippocampal tissues from Per3 knockout mice using chromatography-mass spectrometry. The regulatory role of PER3 on the expression of nicotinamide phosphoribosyltransferase (Nampt) was investigated through co-immunoprecipitation and chromatin immunoprecipitation assays.

Results

Metabolomic analysis revealed that Per3 deficiency disrupts mitochondrial function, as evidenced by reduced activities of key tricarboxylic acid (TCA) cycle enzymes (succinate dehydrogenase, citrate synthase, and α-ketoglutarate dehydrogenase), diminished expression of mitochondrial respiratory chain complexes I-V, and decreased nicotinamide adenine dinucleotide (NAD)⁺ levels in Per3 knockout mice. Supplementation with the NAD⁺ precursor nicotinamide (NAM) rescued mitochondrial function and alleviated depression-like behaviors in Per3 knockout mice. Similar effects were observed with intraperitoneal administration of the NAMPT activator P7C3-A20, while these effects were abolished by the NAMPT inhibitor FK866. Mechanistically, PER3 was found to regulate Nampt expression by binding to E-box elements within its intronic regions in conjunction with BMAL1. This interaction enhanced NAD⁺ production, activating SIRT3 to mitigate mitochondrial dysfunction in Per3 knockout mice.

Conclusions

These findings uncover a novel mechanism by which PER3 ameliorates depressive behaviors through the regulation of NAMPT-controlled NAD⁺ levels and mitochondrial function, underscoring the critical role of PER3 in depression-related pathophysiology.