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Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study

Deep sea water (DSW), originally pumped from the Pacific Rim off the coast of Hualien County (Taiwan), and its mineral constituents, were concentrated by a low-temperature vacuum evaporation system to produce a hardness of approximately 400,000 mg/L of seawater mineral concentrate. The primary compo...

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Autores principales: Sheu, Ming-Jyh, Chou, Pei-Yu, Lin, Wen-Hsin, Pan, Chun-Hsu, Chien, Yi-Chung, Chung, Yun-Lung, Liu, Fon-Chang, Wu, Chieh-Hsi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721228/
https://www.ncbi.nlm.nih.gov/pubmed/23774889
http://dx.doi.org/10.3390/md11062183
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author Sheu, Ming-Jyh
Chou, Pei-Yu
Lin, Wen-Hsin
Pan, Chun-Hsu
Chien, Yi-Chung
Chung, Yun-Lung
Liu, Fon-Chang
Wu, Chieh-Hsi
author_facet Sheu, Ming-Jyh
Chou, Pei-Yu
Lin, Wen-Hsin
Pan, Chun-Hsu
Chien, Yi-Chung
Chung, Yun-Lung
Liu, Fon-Chang
Wu, Chieh-Hsi
author_sort Sheu, Ming-Jyh
collection PubMed
description Deep sea water (DSW), originally pumped from the Pacific Rim off the coast of Hualien County (Taiwan), and its mineral constituents, were concentrated by a low-temperature vacuum evaporation system to produce a hardness of approximately 400,000 mg/L of seawater mineral concentrate. The primary composition of this seawater mineral concentrate was ionic magnesium (Mg(2+)), which was approximately 96,000 mg/L. Referring to the human recommended daily allowance (RDA) of magnesium, we diluted the mineral concentrate to three different dosages: 0.1 × DSW (equivalent to 3.75 mg Mg(2+)/kg DSW); 1 × DSW (equivalent to 37.5 mg Mg(2+)/kg DSW); and 2 × DSW (equivalent to 75 mg Mg(2+)/kg DSW). Additionally, a magnesium chloride treatment was conducted for comparison with the DSW supplement. The study indicated that 0.1 × DSW, 1 × DSW and 2 × DSW decreased the systolic and diastolic pressures in spontaneous hypertensive rats in an eight-week experiment. DSW has been shown to reduce serum lipids and prevent atherogenesis in a hypercholesterolemic rabbit model. Our results demonstrated that 1 × DSW and 2 × DSW significantly suppressed the serum cholesterol levels, reduced the lipid accumulation in liver tissues, and limited aortic fatty streaks. These findings indicated that the antiatherogenic effects of DSW are associated with 5′-adenosine monophosphate-activated protein kinase (AMPK) stimulation and the consequent inhibition of phosphorylation of acetyl-CoA carboxylase (ACC) in atherosclerotic rabbits. We hypothesize that DSW could potentially be used as drinking water because it modulates blood pressure, reduces lipids, and prevents atherogenesis.
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spelling pubmed-37212282013-07-24 Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study Sheu, Ming-Jyh Chou, Pei-Yu Lin, Wen-Hsin Pan, Chun-Hsu Chien, Yi-Chung Chung, Yun-Lung Liu, Fon-Chang Wu, Chieh-Hsi Mar Drugs Article Deep sea water (DSW), originally pumped from the Pacific Rim off the coast of Hualien County (Taiwan), and its mineral constituents, were concentrated by a low-temperature vacuum evaporation system to produce a hardness of approximately 400,000 mg/L of seawater mineral concentrate. The primary composition of this seawater mineral concentrate was ionic magnesium (Mg(2+)), which was approximately 96,000 mg/L. Referring to the human recommended daily allowance (RDA) of magnesium, we diluted the mineral concentrate to three different dosages: 0.1 × DSW (equivalent to 3.75 mg Mg(2+)/kg DSW); 1 × DSW (equivalent to 37.5 mg Mg(2+)/kg DSW); and 2 × DSW (equivalent to 75 mg Mg(2+)/kg DSW). Additionally, a magnesium chloride treatment was conducted for comparison with the DSW supplement. The study indicated that 0.1 × DSW, 1 × DSW and 2 × DSW decreased the systolic and diastolic pressures in spontaneous hypertensive rats in an eight-week experiment. DSW has been shown to reduce serum lipids and prevent atherogenesis in a hypercholesterolemic rabbit model. Our results demonstrated that 1 × DSW and 2 × DSW significantly suppressed the serum cholesterol levels, reduced the lipid accumulation in liver tissues, and limited aortic fatty streaks. These findings indicated that the antiatherogenic effects of DSW are associated with 5′-adenosine monophosphate-activated protein kinase (AMPK) stimulation and the consequent inhibition of phosphorylation of acetyl-CoA carboxylase (ACC) in atherosclerotic rabbits. We hypothesize that DSW could potentially be used as drinking water because it modulates blood pressure, reduces lipids, and prevents atherogenesis. MDPI 2013-06-17 /pmc/articles/PMC3721228/ /pubmed/23774889 http://dx.doi.org/10.3390/md11062183 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Sheu, Ming-Jyh
Chou, Pei-Yu
Lin, Wen-Hsin
Pan, Chun-Hsu
Chien, Yi-Chung
Chung, Yun-Lung
Liu, Fon-Chang
Wu, Chieh-Hsi
Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study
title Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study
title_full Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study
title_fullStr Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study
title_full_unstemmed Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study
title_short Deep Sea Water Modulates Blood Pressure and Exhibits Hypolipidemic Effects via the AMPK-ACC Pathway: An in Vivo Study
title_sort deep sea water modulates blood pressure and exhibits hypolipidemic effects via the ampk-acc pathway: an in vivo study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3721228/
https://www.ncbi.nlm.nih.gov/pubmed/23774889
http://dx.doi.org/10.3390/md11062183
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