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Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice

BACKGROUND: Atherosclerosis is a multifactorial process. Emerging evidence highlights a role of the enzyme heparanase in various disease states, including atherosclerosis formation and progression. OBJECTIVE: The aim of the study was to investigate the effect of heparanase inhibition on blood pressu...

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Autores principales: Hamoud, Shadi, Shekh Muhammad, Rabia, Abu-Saleh, Niroz, Hassan, Ahmad, Zohar, Yaniv, Hayek, Tony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684525/
https://www.ncbi.nlm.nih.gov/pubmed/29226146
http://dx.doi.org/10.1155/2017/7357495
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author Hamoud, Shadi
Shekh Muhammad, Rabia
Abu-Saleh, Niroz
Hassan, Ahmad
Zohar, Yaniv
Hayek, Tony
author_facet Hamoud, Shadi
Shekh Muhammad, Rabia
Abu-Saleh, Niroz
Hassan, Ahmad
Zohar, Yaniv
Hayek, Tony
author_sort Hamoud, Shadi
collection PubMed
description BACKGROUND: Atherosclerosis is a multifactorial process. Emerging evidence highlights a role of the enzyme heparanase in various disease states, including atherosclerosis formation and progression. OBJECTIVE: The aim of the study was to investigate the effect of heparanase inhibition on blood pressure, blood glucose levels, and oxidative stress in apoE−/− mice. METHODS: Male apoE−/− mice were divided into two groups: one treated by the heparanase inhibitor PG545, administered intraperitoneally weekly for seven weeks, and the other serving as control group (injected with saline). Blood pressure was measured a day before sacrificing the animals. Serum glucose levels and lipid profile were measured. Assessment of oxidative stress was performed as well. RESULTS: PG545 significantly lowered blood pressure and serum glucose levels in treated mice. It also caused significant reduction of the serum oxidative stress. For safety concerns, liver enzymes were assessed, and PG545 caused significant elevation only of alanine aminotransferase, but not of the other hepatic enzymes. CONCLUSION: Heparanase inhibition by PG545 caused marked reduction of blood pressure, serum glucose levels, and oxidative stress in apolipoprotein E deficient mice, possibly via direct favorable metabolic and hemodynamic changes caused by the inhibitor. Possible hepatotoxic and weight wasting effects are subject for future investigation.
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spelling pubmed-56845252017-12-10 Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice Hamoud, Shadi Shekh Muhammad, Rabia Abu-Saleh, Niroz Hassan, Ahmad Zohar, Yaniv Hayek, Tony Biomed Res Int Research Article BACKGROUND: Atherosclerosis is a multifactorial process. Emerging evidence highlights a role of the enzyme heparanase in various disease states, including atherosclerosis formation and progression. OBJECTIVE: The aim of the study was to investigate the effect of heparanase inhibition on blood pressure, blood glucose levels, and oxidative stress in apoE−/− mice. METHODS: Male apoE−/− mice were divided into two groups: one treated by the heparanase inhibitor PG545, administered intraperitoneally weekly for seven weeks, and the other serving as control group (injected with saline). Blood pressure was measured a day before sacrificing the animals. Serum glucose levels and lipid profile were measured. Assessment of oxidative stress was performed as well. RESULTS: PG545 significantly lowered blood pressure and serum glucose levels in treated mice. It also caused significant reduction of the serum oxidative stress. For safety concerns, liver enzymes were assessed, and PG545 caused significant elevation only of alanine aminotransferase, but not of the other hepatic enzymes. CONCLUSION: Heparanase inhibition by PG545 caused marked reduction of blood pressure, serum glucose levels, and oxidative stress in apolipoprotein E deficient mice, possibly via direct favorable metabolic and hemodynamic changes caused by the inhibitor. Possible hepatotoxic and weight wasting effects are subject for future investigation. Hindawi 2017 2017-10-26 /pmc/articles/PMC5684525/ /pubmed/29226146 http://dx.doi.org/10.1155/2017/7357495 Text en Copyright © 2017 Shadi Hamoud et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hamoud, Shadi
Shekh Muhammad, Rabia
Abu-Saleh, Niroz
Hassan, Ahmad
Zohar, Yaniv
Hayek, Tony
Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice
title Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice
title_full Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice
title_fullStr Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice
title_full_unstemmed Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice
title_short Heparanase Inhibition Reduces Glucose Levels, Blood Pressure, and Oxidative Stress in Apolipoprotein E Knockout Mice
title_sort heparanase inhibition reduces glucose levels, blood pressure, and oxidative stress in apolipoprotein e knockout mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684525/
https://www.ncbi.nlm.nih.gov/pubmed/29226146
http://dx.doi.org/10.1155/2017/7357495
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