Metabolomics of Artichoke Bud Extract in Spontaneously Hypertensive Rats.
Zhi-Bin WangShi-Long JiangShao-Bo LiuJing-Bo PengShuo HuXu WangWei ZhuoTong LiuJi-Wei GuoHong-Hao ZhouZhi-Quan YangXiao-Yuan MaoZhao-Qian LiuPublished in: ACS omega (2021)
Hypertension adversely affects the quality of life in humans across modern society. Studies have attributed increased reactive oxygen species production to the pathophysiology of hypertension. So far, a specific drug to control the disease perfectly has not been developed. However, artichoke, an edible vegetable, plays an essential role in treating many diseases due to its potent antioxidant activities. The objective of this study is to evaluate the effect of artichoke bud extract (ABE) on heart tissue metabolomics of hypertensive rats. Spontaneously hypertensive rats and Wistar-Kyoto (WKY) rats were divided into six groups, then exposed to different doses comprising ABE, Enalapril Maleate, or 1% carboxylmethyl cellulose for 4 weeks. Their blood pressures were recorded at 0, 2, 3, and 4 weeks after the start of the test period. Thereafter, all rats were anesthetized, and blood was collected from their cardiac apexes. Then, we measured the levels for 15 kinds of serum biochemical parameters. An established orthogonal partial least square-discriminant analysis model completed the metabolomic analysis. Hypertensive rats in the ABE group exhibited well-controlled blood pressure, relative to those in the model group. Specifically, artichoke significantly lowered serum levels for total protein (TP), albumin (ALB), and uric acid (UA) in the hypertensive rats. This effect involved the action of eight metabolites, including guanine, 1-methylnicotinamide, p-aminobenzoic acid, NAD, NADH, uridine 5'-monophosphate, adenosine monophosphate, and methylmalonic acid. Collectively, these findings suggest that ABE may play a role in affecting oxidative stress and purine, nicotinate, and nicotinamide metabolism.
Keyphrases
- blood pressure
- oxidative stress
- uric acid
- reactive oxygen species
- anti inflammatory
- mass spectrometry
- metabolic syndrome
- ms ms
- heart rate
- dna damage
- heart failure
- ischemia reperfusion injury
- induced apoptosis
- type diabetes
- gestational age
- weight loss
- binding protein
- blood glucose
- small molecule
- data analysis
- endoplasmic reticulum stress
- glycemic control
- heat shock protein