Modulation of Sirtuin 3 by N-Acetylcysteine Preserves Mitochondrial Oxidative Phosphorylation and Restores Bisphenol A-Induced Kidney Damage in High-Fat-Diet-Fed Rats.
Anongporn KobroobSirinart KumfuSiriporn C ChattipakornOrawan WongmekiatPublished in: Current issues in molecular biology (2024)
Bisphenol A (BPA) and high-fat diets (HFD) are known to adversely affect the kidneys. However, the combined effects of both cases on kidney health and the potential benefits of N-acetylcysteine (NAC) in mitigating these effects have not been investigated. To explore these aspects, male Wistar rats were fed with HFD and allocated to receive a vehicle or BPA. At week twelve, the BPA-exposed rats were subdivided to receive a vehicle or NAC along with BPA until week sixteen. Rats fed HFD and exposed to BPA showed renal dysfunction and structural abnormalities, oxidative stress, inflammation, and mitochondrial dysfunction, with alterations in key proteins related to mitochondrial oxidative phosphorylation (OXPHOS), bioenergetics, oxidative balance, dynamics, apoptosis, and inflammation. Treatment with NAC for 4 weeks significantly improved these conditions. The findings suggest that NAC is beneficial in protecting renal deterioration brought on by prolonged exposure to BPA in combination with HFD, and modulation of sirtuin 3 (SIRT3) signaling by NAC appears to play a key role in the preservation of homeostasis and integrity within the mitochondria by enhancing OXPHOS activity, maintaining redox balance, and reducing inflammation. This study provides valuable insights into potential therapeutic strategies for preserving kidney health in the face of environmental and dietary challenges.
Keyphrases
- oxidative stress
- high fat diet
- transcription factor
- diabetic rats
- insulin resistance
- adipose tissue
- ischemia reperfusion injury
- dna damage
- human health
- induced apoptosis
- healthcare
- public health
- genome wide analysis
- mental health
- health information
- protein kinase
- risk assessment
- clinical trial
- skeletal muscle
- metabolic syndrome
- weight loss
- heat shock
- randomized controlled trial
- mass spectrometry
- high glucose
- reactive oxygen species
- endoplasmic reticulum stress
- atomic force microscopy
- combination therapy
- heat shock protein