Vagus Nerve Stimulation Attenuates Acute Skeletal Muscle Injury Induced by Ischemia-Reperfusion in Rats.
Yifeng ZhangHewei LiMenglong WangGuannan MengZhenya WangJielin DengMeng WangQianqian ZhangSheng-Li YangHong JiangPublished in: Oxidative medicine and cellular longevity (2019)
Vagus nerve stimulation (VNS) has been shown to attenuate ischemia-reperfusion (I/R) injury in multiple organs. The present study aimed at investigating whether VNS could exert protective effects against I/R injury in the skeletal muscle. Male Sprague-Dawley rats were randomly divided into 3 groups: the control, I/R, and I/R+VNS groups. The skeletal muscle I/R (SMI/R) model was induced by occlusion of the left femoral artery for 2.5 hours followed by reperfusion for 2 hours. The vagal nerve trunk was separated, and VNS was performed during the whole I/R process. The intensity of VNS was optimized in each rat to obtain a 10% reduction in the heart rate relative to the value before stimulation. After the experiment, the blood sample and left gastrocnemius muscle tissues were collected for histological examination, biochemical analysis, and molecular biological detection. During the I/R process, VNS significantly reduced cellular apoptosis, necrosis, and inflammatory cell infiltration compared to sham VNS. The VNS treatment also decreased the inflammatory response, alleviated oxidative stress, and improved vascular endothelial function (p < 0.05 for each). In contrast, the I/R group showed an opposite effect compared to the control group. The present study indicated that VNS could protect against SMI/R injury by suppressing excessive inflammation, alleviating oxidative stress, and preserving vascular endothelial function.
Keyphrases
- oxidative stress
- skeletal muscle
- heart rate
- inflammatory response
- insulin resistance
- diabetic rats
- dna damage
- heart rate variability
- ischemia reperfusion injury
- gene expression
- blood pressure
- induced apoptosis
- magnetic resonance
- coronary artery disease
- stem cells
- computed tomography
- liver failure
- bone marrow
- cell proliferation
- atrial fibrillation
- metabolic syndrome
- intensive care unit
- mesenchymal stem cells
- lipopolysaccharide induced
- acute coronary syndrome
- left ventricular
- cell therapy
- cerebral ischemia
- physical activity
- sensitive detection
- heat shock
- acute ischemic stroke
- cell cycle arrest
- double blind
- peripheral nerve