
pmid: 896796
SummaryAnti-renin and hypotensive effects of synthetic PEs were examined.(i) Eighteen PEs including optical isomers were newly synthesized. Arachidonic acid, linolenic acid, and stearic acid were substituted at the positions of β, γ, or both. Natural PE was extracted from porcine kidney, and the lyso form was prepared by treatment of phospholipase A.(ii) Anti-renin activity of these compounds was determined using high-renin plasma obtained from the dog. The inhibition of renin activity was expressed as a percentage of the reduction in the production rate of angiotensin I as measured by radioimmunoassay.(iii) The inhibitory effects of PE(β-C18=3, γ-C18) series, d- and DL-PE(β-C20=4, γ-C18), and dl- and l-PE(β-C18, γ-C20=4) were greater than that of the natural PE, but did not exceed the effect of lyso-PE.(iv) Hypotensive effect was evaluated in conscious normotensive, spontaneously hypertensive, and renal hypertensive rats by daily im injection of the test compounds.(v) Following repeated administration of...
Structure-Activity Relationship, Dogs, Hypertension, Renal, Phosphatidylethanolamines, Renin, Animals, Blood Pressure, Stereoisomerism
Structure-Activity Relationship, Dogs, Hypertension, Renal, Phosphatidylethanolamines, Renin, Animals, Blood Pressure, Stereoisomerism
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