1. Antihypertensive Effects of Artemisia scoparia Waldst in Spontaneously Hypertensive Rats and Identification of Angiotensin I Converting Enzyme Inhibitors
- Author
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Lily Jaiswal, Do Young Hwang, Kyung-Hee Park, Kyung-Sik Ham, Jae-Hak Moon, So-Young Kim, Sun-Young Park, Haeng-Ran Kim, Yang-Kyun Park, Saoraya Chanmuang, and Jeong-Yong Cho
- Subjects
Vascular Endothelial Growth Factor A ,Pharmaceutical Science ,Angiotensin-Converting Enzyme Inhibitors ,Kidney ,Analytical Chemistry ,Lipid peroxidation ,chemistry.chemical_compound ,Artemisia scoparia ,halophyte ,blood pressure ,ACE inhibitor ,phenolics ,Rats, Inbred SHR ,Drug Discovery ,biology ,medicine.anatomical_structure ,Chemistry (miscellaneous) ,Molecular Medicine ,Oxidation-Reduction ,medicine.drug ,medicine.medical_specialty ,Article ,Nitric oxide ,lcsh:QD241-441 ,lcsh:Organic chemistry ,Internal medicine ,medicine ,Animals ,Physical and Theoretical Chemistry ,Muscle, Skeletal ,Nuclear Magnetic Resonance, Biomolecular ,Antihypertensive Agents ,Dose-Response Relationship, Drug ,Plant Extracts ,Organic Chemistry ,biology.organism_classification ,Angiotensin II ,Rats ,Disease Models, Animal ,Oxidative Stress ,Endocrinology ,Blood pressure ,Artemisia ,chemistry ,Lipid Peroxidation ,rhoA GTP-Binding Protein - Abstract
We investigated the antihypertensive effects of Artemisia scoparia (AS) in spontaneously hypertensive rats (SHR). The rats were fed diets containing 2% (w/w) hot water extracts of AS aerial parts for 6 weeks. The AS group had significantly lower systolic and diastolic blood pressure levels than the control group. The AS group also had lower angiotensin I converting enzyme (ACE) activity and angiotensin II content in serum compared to the control group. The AS group showed higher vascular endothelial growth factor and lower ras homolog gene family member A expression levels in kidney compared to the control group. The AS group had significantly lower levels of plasma lipid oxidation and protein carbonyls than the control group. One new and six known compounds were isolated from AS by guided purification. The new compound was determined to be 4′-O-β-D-glucopyranoyl (E)-4-hydroxy-3-methylbut-2-enyl benzoate, based on its nuclear magnetic resonance and electrospray ionization-mass spectroscopy data.
- Published
- 2015