Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension

Background and Purpose: Human chymase (h-chymase) is a serine protease that forms local angiotensin II and has been proven to be related to onset of hypertension, arteriosclerosis, and post myocardial infarction cardiac remodeling. Since no chymase inhibitor was clinically available, an extensive sc...

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Main Authors: Keisuke Okamura, Rieko Kuroda, Kaori Nagata, Hidenori Urata
Format: Article
Language:English
Published: Taylor & Francis Group 2019-11-01
Series:Clinical and Experimental Hypertension
Subjects:
Online Access:http://dx.doi.org/10.1080/10641963.2018.1545847
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author Keisuke Okamura
Rieko Kuroda
Kaori Nagata
Hidenori Urata
author_facet Keisuke Okamura
Rieko Kuroda
Kaori Nagata
Hidenori Urata
author_sort Keisuke Okamura
collection DOAJ
description Background and Purpose: Human chymase (h-chymase) is a serine protease that forms local angiotensin II and has been proven to be related to onset of hypertension, arteriosclerosis, and post myocardial infarction cardiac remodeling. Since no chymase inhibitor was clinically available, an extensive screening for inhibition of h-chymase in three different extracts (water, hot water,  and ethanol) of approximately 800 food ingredients had been performed and we identified Polygonum hydropiper L (Polygonum). Using a dried and powdered Polygonum, we conducted a prospective, single-arm, pilot study to investigate its safety and antihypertensive effect in subjects with normal high blood pressure to moderate hypertension. Methods: First, a single oral dose of Polygonum powder (4000 mg) was administered to assess acute toxicity. Then, a pilot study was conducted in 11 subjects using the sequence of placebo and Polygonum for 2 weeks each. The dose of Polygonum was increased sequentially (200–2000 mg/day). Home blood pressure and pulse rate were monitored. Results: Oral administration of Polygonum (4000 mg) did not cause any adverse events. In the dose-escalation phase, evening systolic blood pressure was significantly decreased at 800 mg, 2000 mg doses post-treatment (p < 0.05, and p < 0.05, respectively). Depressor responders to Polygonum intake had significantly higher salt intake in spot urine (p < 0.05). No adverse events or reactions occurred. Conclusion: This was the first investigation that an h-chymase inhibitory Polygonum intake for safety and tolerability was proven and, in addition, chymase inhibitory Polygonum appeared to have depressor effect especially in a hypertensive subject with excessive salt intake.
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spelling doaj.art-0537be9a6352404bbe79ba51765f271a2023-09-19T15:19:28ZengTaylor & Francis GroupClinical and Experimental Hypertension1064-19631525-60062019-11-0141871772510.1080/10641963.2018.15458471545847Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertensionKeisuke Okamura0Rieko Kuroda1Kaori Nagata2Hidenori Urata3Fukuoka University Chikushi HospitalBiotechnology and Food Research Institute Fukuoka Industrial Technology CenterNutrition for Life AssociationFukuoka University Chikushi HospitalBackground and Purpose: Human chymase (h-chymase) is a serine protease that forms local angiotensin II and has been proven to be related to onset of hypertension, arteriosclerosis, and post myocardial infarction cardiac remodeling. Since no chymase inhibitor was clinically available, an extensive screening for inhibition of h-chymase in three different extracts (water, hot water,  and ethanol) of approximately 800 food ingredients had been performed and we identified Polygonum hydropiper L (Polygonum). Using a dried and powdered Polygonum, we conducted a prospective, single-arm, pilot study to investigate its safety and antihypertensive effect in subjects with normal high blood pressure to moderate hypertension. Methods: First, a single oral dose of Polygonum powder (4000 mg) was administered to assess acute toxicity. Then, a pilot study was conducted in 11 subjects using the sequence of placebo and Polygonum for 2 weeks each. The dose of Polygonum was increased sequentially (200–2000 mg/day). Home blood pressure and pulse rate were monitored. Results: Oral administration of Polygonum (4000 mg) did not cause any adverse events. In the dose-escalation phase, evening systolic blood pressure was significantly decreased at 800 mg, 2000 mg doses post-treatment (p < 0.05, and p < 0.05, respectively). Depressor responders to Polygonum intake had significantly higher salt intake in spot urine (p < 0.05). No adverse events or reactions occurred. Conclusion: This was the first investigation that an h-chymase inhibitory Polygonum intake for safety and tolerability was proven and, in addition, chymase inhibitory Polygonum appeared to have depressor effect especially in a hypertensive subject with excessive salt intake.http://dx.doi.org/10.1080/10641963.2018.1545847chymasepolygonum hydropiper langiotensin iiblood pressurehypertensionserine endopeptidase
spellingShingle Keisuke Okamura
Rieko Kuroda
Kaori Nagata
Hidenori Urata
Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension
Clinical and Experimental Hypertension
chymase
polygonum hydropiper l
angiotensin ii
blood pressure
hypertension
serine endopeptidase
title Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension
title_full Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension
title_fullStr Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension
title_full_unstemmed Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension
title_short Prospective single-arm observational study of human chymase inhibitor Polygonum hydropiper L in subjects with hypertension
title_sort prospective single arm observational study of human chymase inhibitor polygonum hydropiper l in subjects with hypertension
topic chymase
polygonum hydropiper l
angiotensin ii
blood pressure
hypertension
serine endopeptidase
url http://dx.doi.org/10.1080/10641963.2018.1545847
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AT kaorinagata prospectivesinglearmobservationalstudyofhumanchymaseinhibitorpolygonumhydropiperlinsubjectswithhypertension
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