Protective Role of Antioxidant Huskless Barley Extracts on TNF-α-Induced Endothelial Dysfunction in Human Vascular Endothelial Cells.
Zhanghua LiaoHaoran CaiZekun XuJing WangChen QiuJing XieWu-Yang HuangZhongquan SuiPublished in: Oxidative medicine and cellular longevity (2018)
Oxidative stress and inflammation are considered as two key factors that contribute to the development of atherosclerosis. This study was to investigate the antioxidant capacity of huskless barley and to explore its protective functions through the regulation of the antioxidant defense and inflammatory response in human umbilical vein endothelial cells (HUVEC). The oxygen radical absorbance capacity (ORAC), ferric-reducing antioxidant power (FRAP), and 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) scavenging capacity of water and alkali extracts of the polysaccharides from nine huskless barley varieties were investigated in vitro. The antioxidant properties of the alkaline extracts were more pronounced than those of the water extracts. The results from the cell model showed that pretreatment of HUVEC with the water or alkaline extracts of the polysaccharides from the huskless barley cultivars QHH and NLGL decreased the levels of reactive oxygen species (ROS), monocyte chemotactic protein 1 (MCP-1), and vascular cell adhesion molecule 1 (VCAM-1) but increased the level of superoxide dismutase (SOD) and maintained cell viability. Huskless barley polysaccharide extracts exhibited the vasodilatory effect of inhibiting angiotensin-converting enzyme (ACE) production. These discoveries revealed the potent protective functions of barley in oxidative damage and a potential role for barley in preventing chronic inflammation in cardiovascular diseases.
Keyphrases
- oxidative stress
- endothelial cells
- diabetic rats
- angiotensin converting enzyme
- high glucose
- anti inflammatory
- reactive oxygen species
- cell adhesion
- inflammatory response
- cardiovascular disease
- dna damage
- angiotensin ii
- ischemia reperfusion injury
- induced apoptosis
- rheumatoid arthritis
- single cell
- cell death
- signaling pathway
- coronary artery disease
- type diabetes
- mesenchymal stem cells
- mass spectrometry
- drug induced
- anaerobic digestion
- hydrogen peroxide
- bone marrow
- high resolution
- binding protein
- water soluble
- cardiovascular risk factors
- metabolic syndrome
- lps induced
- toll like receptor
- amyotrophic lateral sclerosis
- atomic force microscopy
- pluripotent stem cells