Diabetes-associated sleep fragmentation impairs liver and heart function via SIRT1-dependent epigenetic modulation of NADPH oxidase 4.
10.1016/j.apsb.2024.12.031
- Author:
Yuanfang GUO
1
;
Jie WANG
1
;
Dongmei ZHANG
1
;
Yufeng TANG
2
;
Quanli CHENG
3
;
Jiahao LI
1
;
Ting GAO
1
;
Xiaohui ZHANG
1
;
Guangping LU
1
;
Mingrui LIU
1
;
Xun GUAN
1
;
Xinyu TANG
1
;
Junlian GU
1
Author Information
1. School of Nursing and Rehabilitation, Cheeloo College of Medicine, Shandong University, Jinan 250012, China.
2. Department of Orthopedic Surgery, the First Affiliated Hospital of Shandong First Medical University, Jinan 250014, China.
3. Department of Cardiovascular Disease, First Hospital of Jilin University, Changchun 130021, China.
- Publication Type:Journal Article
- Keywords:
Heart disease;
Histone acetylation;
Inflammation;
Inter-organ communication;
NOX4;
Non-alcoholic fatty liver disease;
SIRT1;
Sleep fragmentation
- From:
Acta Pharmaceutica Sinica B
2025;15(3):1480-1496
- CountryChina
- Language:English
-
Abstract:
Although clinical evidence suggests that nonalcoholic fatty liver disease is an established major risk factor for heart failure, it remains unexplored whether sleep disorder-caused hepatic damage contributes to the development of cardiovascular disease (CVD). Here, our findings revealed that sleep fragmentation (SF) displayed notable hepatic detrimental phenotypes, including steatosis and oxidative damage, along with significant abnormalities in cardiac structure and function. All these pathological changes persisted even after sleep recovery for 2 consecutive weeks or more, displaying memory properties. Mechanistically, persistent higher expression of nicotinamide adenine dinucleotide phosphate oxidase 4 (NOX4) in the liver was the key initiator of SF-accelerated damage phenotypes. SF epigenetically controlled the acetylation of histone H3 lysine 27 (H3K27ac) enrichment at the Nox4 promoter and markedly increased Nox4 expression in liver even after sleep recovery. Moreover, fine coordination of the circadian clock and hepatic damage was strictly controlled by BMAL1-dependent Sirtuin 1 (Sirt1) transcription after circadian misalignment. Accordingly, genetic manipulation of liver-specific Nox4 or Sirt1, along with pharmacological intervention targeting NOX4 (GLX351322) or SIRT1 (Resveratrol), could effectively erase the epigenetic modification of Nox4 by reducing the H3K27ac level and ameliorate the progression of liver pathology, thereby counteracting SF-evoked sustained CVD. Collectively, our findings may pave the way for strategies to mitigate myocardial injury from persistent hepatic detrimental memory in diabetic patients.
