Determination of Endogenous Peptides with in Vitro ACE Inhibitory Activity in Normotensive Human Plasma by the Fluorometric HPLC Method
An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angiotensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3-8), ANG (4-8), ANG (5...
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| Published in | Bioscience, biotechnology, and biochemistry Vol. 61; no. 6; pp. 1052 - 1054 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Tokyo
Taylor & Francis
01.06.1997
Japan Society for Bioscience Biotechnology and Agrochemistry Oxford University Press |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0916-8451 1347-6947 1347-6947 |
| DOI | 10.1271/bbb.61.1052 |
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| Abstract | An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angiotensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3-8), ANG (4-8), ANG (5-8), and ANG (3-4), whose respective peptide concentrations were determined by our proposed naphthalene-2, 3-dialdehyde (NDA)-HPLC method to be 64 ±9, 39 ±5, 176 ± 22, and 197 ± 35 fmol/ml of plasma. |
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| AbstractList | An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angiotensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3–8), ANG (4–8), ANG (5–8), and ANG (3–4), whose respective peptide concentrations were determined by our proposed naphthalene-2, 3-dialdehyde (NDA)-HPLC method to be 64 ±9, 39 ±5, 176 ± 22, and 197 ± 35 fmol/ml of plasma. An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angio-tensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3-8), ANG (4-8), ANG (5-8), and ANG (3-4), whose respective peptide concentrations were determined by our proposed naphthalene-2, 3-dialdehyde (NDA)-HPLC method to be 64±9, 39±5, 176±22, and 197±35 fmol/ml of plasma. An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angiotensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3-8), ANG (5-8), and ANG (3-4), whose respective peptide concentrations were determined by our proposed naphthalene-2,3-dialdehyde (NDA)-HPLC method to be 64 +/- 9, 39 +/- 5, 176 +/- 22, and 197 +/- 35 fmol/ml of plasma.An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angiotensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3-8), ANG (5-8), and ANG (3-4), whose respective peptide concentrations were determined by our proposed naphthalene-2,3-dialdehyde (NDA)-HPLC method to be 64 +/- 9, 39 +/- 5, 176 +/- 22, and 197 +/- 35 fmol/ml of plasma. An in vitro degradation test of angiotensin (ANG) II or III in normotensive supine human plasma from 9 healthy male subjects confirmed the production of smaller ANG metabolites with angiotensin I-converting enzyme inhibitory activity. These metabolites were identified as ANG (3-8), ANG (5-8), and ANG (3-4), whose respective peptide concentrations were determined by our proposed naphthalene-2,3-dialdehyde (NDA)-HPLC method to be 64 +/- 9, 39 +/- 5, 176 +/- 22, and 197 +/- 35 fmol/ml of plasma. |
| Author | Matsufuji, Hiroshi Kawasaki, Terukazu Matsui, Toshiro Osajima, Yutaka |
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| Copyright | Copyright 1997 Taylor and Francis Group LLC 1997 1997 INIST-CNRS Copyright Japan Science and Technology Agency 1997 |
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| Keywords | Human Biological fluid Fluorescence detector Peptides Enzyme Metabolite HPLC chromatography Enzyme inhibitor Blood plasma Peptidases Peptidyl-dipeptidase A Angiotensin Hydrolases Peptidyl-dipeptidases ACE inhibitor Quantitative analysis |
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| SubjectTerms | ACE Adult Analytical, structural and metabolic biochemistry Angiotensin II - blood Angiotensin II - chemistry Angiotensin II - metabolism Angiotensin III - blood Angiotensin III - chemistry Angiotensin III - metabolism angiotensin metabolites Angiotensin-Converting Enzyme Inhibitors - blood Angiotensin-Converting Enzyme Inhibitors - chemistry Angiotensin-Converting Enzyme Inhibitors - metabolism Biological and medical sciences biotechnology Blood Pressure - physiology Chromatography, High Pressure Liquid enzyme inhibitors Enzymes and enzyme inhibitors fluorometry Fundamental and applied biological sciences. Psychology HPLC Humans Hydrolases In Vitro Techniques Indicators and Reagents - chemistry Male males metabolites Naphthalenes - chemistry peptides Peptides - blood peptidyl-dipeptidase A Radioimmunoassay Spectrometry, Fluorescence Supine Position |
| Title | Determination of Endogenous Peptides with in Vitro ACE Inhibitory Activity in Normotensive Human Plasma by the Fluorometric HPLC Method |
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