Obesity Induces Artery-Specific Alterations: Evaluation of Vascular Function and Inflammatory and Smooth Muscle Phenotypic Markers.
Antonio Garcia SoaresMaria Helena Catelli de CarvalhoEliana H AkaminePublished in: BioMed research international (2017)
Vascular alterations are expected to occur in obese individuals but the impact of obesity could be different depending on the artery type. We aimed to evaluate the obesity effects on the relaxing and contractile responses and inflammatory and smooth muscle (SM) phenotypic markers in two vascular beds. Obesity was induced in C57Bl/6 mice by 16-week high-fat diet and vascular reactivity, mRNA expression of inflammatory and SM phenotypic markers, and collagen deposition were evaluated in small mesenteric arteries (SMA) and thoracic aorta (TA). Endothelium-dependent relaxation in SMA and TA was not modified by obesity. In contrast, contraction induced by depolarization and contractile agonists was reduced in SMA, whereas only contraction induced by adrenergic agonist was reduced in TA of obese mice. Obesity increased the mRNA expression of pro- and anti-inflammatory cytokines in SMA and TA. The expression of genes necessary for maintaining contractile ability was increased by obesity, but the increase was more pronounced in TA. Collagen deposition was increased in SMA, but not in TA, of obese mice. Although the endothelial function was still preserved, the SM of the two artery types was impaired by obesity, but the impairment was higher in SMA, which could be associated with SM phenotypic changes.
Keyphrases
- smooth muscle
- insulin resistance
- high fat diet induced
- weight loss
- metabolic syndrome
- type diabetes
- high fat diet
- weight gain
- adipose tissue
- skeletal muscle
- oxidative stress
- randomized controlled trial
- magnetic resonance imaging
- coronary artery
- nitric oxide
- endothelial cells
- physical activity
- dna methylation
- poor prognosis
- clinical trial
- spinal cord
- pulmonary hypertension
- pulmonary artery
- aortic valve
- blood flow
- spinal cord injury
- study protocol
- tissue engineering