Abstract
1. Rabbit plasma enzymes that degrade angiotensin I are inhibited completely by the combination of 2,3-dimercaptopropan-1-ol (10mm), EDTA (10mm) and chlorhexidine gluconate (0.005%, w/v). These compounds do not modify the reaction of renin with renin substrate and are termed the selective inhibitors. 2. The renin substrate concentration of plasma can be measured as angiotensin I content by incubating plasma plus the selective inhibitors with renin for a time sufficient to allow complete utilization of renin substrate. 3. This reaction obeys first-order kinetics to substrate concentrations of at least 1000ng. of angiotensin I content/ml. In general, the renin substrate concentrations of normal rabbit plasmas are less than 1000ng. of angiotensin I content/ml. Thus the time required for the complete release of angiotensin I from normal plasma is inversely related to renin activity and is independent of renin substrate concentration. 4. A method for the assay of renin substrate, taking these reaction kinetics into account, is presented.
MeSH Terms
Alcohols
Angiotensin II/analysis
Animals
Chemical Phenomena
Chemistry
Chromatography, Gel
Countercurrent Distribution
Edetic Acid
Gluconates
Heparin
Kidney/physiology
Kinetics
Mercury
Methods
Nephrectomy
Rabbits
Renin/antagonists & inhibitors,blood
Chemicals
Alcohols
Gluconates
Angiotensin II
Heparin
Edetic Acid
Renin
Mercury
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ryan J W
McKenzie J K
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16 references, click to expand
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