PPARγ Agonist Rosiglitazone and Antagonist GW9662: Antihypertensive Effects on Chronic Intermittent Hypoxia-Induced Hypertension in Rats.
Ningzhi ZhangFeng WeiSisi NingJialu HuHongtao ShiZhifeng YaoMinna TangYongqiao ZhangJiaxin GongJunbo GeZhaoqiang CuiPublished in: Journal of cardiovascular translational research (2024)
The increased incidence of hypertension associated with obstructive sleep apnea (OSA) presents significant physical, psychological, and economic challenges. Peroxisome proliferator-activated receptor gamma (PPARγ) plays a role in both OSA and hypertension, yet the therapeutic potential of PPARγ agonists and antagonists for OSA-related hypertension remains unexplored. Therefore, we constructed a chronic intermittent hypoxia (CIH)-induced hypertension rat model that mimics the pathogenesis of OSA-related hypertension in humans. The model involved administering PPARγ agonist rosiglitazone (RSG), PPARγ antagonist GW9662, or normal saline, followed by regular monitoring of blood pressure and thoracic aorta analysis using staining and electron microscopy. Intriguingly, our results indicated that both RSG and GW9662 appeared to potently counteract CIH-induced hypertension. In silico study suggested that GW9662's antihypertensive effect might mediated through angiotensin II receptor type 1 (AGTR1). Our findings provide insights into the mechanisms of OSA-related hypertension and propose novel therapeutic targets.
Keyphrases
- blood pressure
- obstructive sleep apnea
- hypertensive patients
- angiotensin ii
- heart rate
- positive airway pressure
- mental health
- type diabetes
- physical activity
- spinal cord
- high glucose
- aortic valve
- diabetic rats
- risk factors
- depressive symptoms
- molecular docking
- spinal cord injury
- angiotensin converting enzyme
- vascular smooth muscle cells
- sleep apnea