Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats

Abstract Background Disturbances in coronary microcirculatory function, such as the endothelial glycocalyx, are early hallmarks in the development of obesity and insulin resistance. Accordingly, in the present study myocardial microcirculatory perfusion during rest and stress was assessed following...

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Main Authors: Judith van Haare, M. Eline Kooi, Jurgen W. G. E. van Teeffelen, Hans Vink, Jos Slenter, Hanneke Cobelens, Gustav J. Strijkers, Dennis Koehn, Mark J. Post, Marc van Bilsen
Format: Article
Language:English
Published: BMC 2017-04-01
Series:Cardiovascular Diabetology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12933-017-0525-7
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author Judith van Haare
M. Eline Kooi
Jurgen W. G. E. van Teeffelen
Hans Vink
Jos Slenter
Hanneke Cobelens
Gustav J. Strijkers
Dennis Koehn
Mark J. Post
Marc van Bilsen
author_facet Judith van Haare
M. Eline Kooi
Jurgen W. G. E. van Teeffelen
Hans Vink
Jos Slenter
Hanneke Cobelens
Gustav J. Strijkers
Dennis Koehn
Mark J. Post
Marc van Bilsen
author_sort Judith van Haare
collection DOAJ
description Abstract Background Disturbances in coronary microcirculatory function, such as the endothelial glycocalyx, are early hallmarks in the development of obesity and insulin resistance. Accordingly, in the present study myocardial microcirculatory perfusion during rest and stress was assessed following metformin or sulodexide therapy in a rat model of diet-induced obesity. Additionally, the effect of degradation of the glycocalyx on myocardial perfusion was assessed in chow-fed rats. Methods Rats were fed a high fat diet (HFD) for 8 weeks and were divided into a group without therapy, and groups that received the anti-diabetic drug metformin or the glycocalyx-stabilizing drug sulodexide in their drinking water during the last 4 weeks of the feeding period. Myocardial microvascular perfusion was determined using first-pass perfusion MRI before and after adenosine infusion. The effect of HFD on microcirculatory properties was also assessed by sidestream darkfield (SDF) imaging of the gastrocnemius muscle. In an acute experimental setting, hyaluronidase was administered to chow-fed control rats to determine the effect of enzymatical degradation of the glycocalyx on myocardial perfusion. Results HFD-rats developed central obesity and insulin sensitivity was reduced as evidenced by the marked reduction in insulin-induced phosphorylation of Akt in both cardiac and gastrocnemius muscle. We confirmed our earlier findings that the robust increase in myocardial perfusion in chow-fed rats after an adenosine challenge (+56%, p = 0.002) is blunted in HFD rats (+8%, p = 0.68). In contrast, 4-weeks treatment with metformin or sulodexide partly restored the increase in myocardial perfusion during adenosine infusion in HFD rats (+81%, p = 0.002 and +37%, p = 0.02, respectively). Treating chow-fed rats acutely with hyaluronidase, to enzymatically degrade the glyocalyx, completely blunted the increase in myocardial perfusion during stress. Conclusions In early stages of HFD-induced insulin resistance myocardial perfusion becomes compromised, a process that can be countered by treatment with both metformin and sulodexide. The adverse effect of acute glycocalyx degradation and protective effect of long-term sulodexide administration on myocardial perfusion provides indirect evidence, suggesting a role for the glycocalyx in preserving coronary microvascular function in pre-diabetic animals.
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spelling doaj.art-4d31223b8ab24fe6a83d2f6a26359e232022-12-21T17:43:24ZengBMCCardiovascular Diabetology1475-28402017-04-0116111310.1186/s12933-017-0525-7Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese ratsJudith van Haare0M. Eline Kooi1Jurgen W. G. E. van Teeffelen2Hans Vink3Jos Slenter4Hanneke Cobelens5Gustav J. Strijkers6Dennis Koehn7Mark J. Post8Marc van Bilsen9Department of Physiology, Maastricht UniversityDepartment of Radiology and Nuclear Medicine, Maastricht UniversityDepartment of Physiology, Maastricht UniversityDepartment of Physiology, Maastricht UniversityDepartment of Radiology and Nuclear Medicine, Maastricht UniversityDepartment of Physiology, Maastricht UniversityBiomedical Engineering and Physics, Academic Medical CenterPie Medical ImagingDepartment of Physiology, Maastricht UniversityDepartment of Physiology, Maastricht UniversityAbstract Background Disturbances in coronary microcirculatory function, such as the endothelial glycocalyx, are early hallmarks in the development of obesity and insulin resistance. Accordingly, in the present study myocardial microcirculatory perfusion during rest and stress was assessed following metformin or sulodexide therapy in a rat model of diet-induced obesity. Additionally, the effect of degradation of the glycocalyx on myocardial perfusion was assessed in chow-fed rats. Methods Rats were fed a high fat diet (HFD) for 8 weeks and were divided into a group without therapy, and groups that received the anti-diabetic drug metformin or the glycocalyx-stabilizing drug sulodexide in their drinking water during the last 4 weeks of the feeding period. Myocardial microvascular perfusion was determined using first-pass perfusion MRI before and after adenosine infusion. The effect of HFD on microcirculatory properties was also assessed by sidestream darkfield (SDF) imaging of the gastrocnemius muscle. In an acute experimental setting, hyaluronidase was administered to chow-fed control rats to determine the effect of enzymatical degradation of the glycocalyx on myocardial perfusion. Results HFD-rats developed central obesity and insulin sensitivity was reduced as evidenced by the marked reduction in insulin-induced phosphorylation of Akt in both cardiac and gastrocnemius muscle. We confirmed our earlier findings that the robust increase in myocardial perfusion in chow-fed rats after an adenosine challenge (+56%, p = 0.002) is blunted in HFD rats (+8%, p = 0.68). In contrast, 4-weeks treatment with metformin or sulodexide partly restored the increase in myocardial perfusion during adenosine infusion in HFD rats (+81%, p = 0.002 and +37%, p = 0.02, respectively). Treating chow-fed rats acutely with hyaluronidase, to enzymatically degrade the glyocalyx, completely blunted the increase in myocardial perfusion during stress. Conclusions In early stages of HFD-induced insulin resistance myocardial perfusion becomes compromised, a process that can be countered by treatment with both metformin and sulodexide. The adverse effect of acute glycocalyx degradation and protective effect of long-term sulodexide administration on myocardial perfusion provides indirect evidence, suggesting a role for the glycocalyx in preserving coronary microvascular function in pre-diabetic animals.http://link.springer.com/article/10.1186/s12933-017-0525-7ObesityEndothelial dysfunctionMyocardial perfusionCardiac functionGlycocalyxMetformin
spellingShingle Judith van Haare
M. Eline Kooi
Jurgen W. G. E. van Teeffelen
Hans Vink
Jos Slenter
Hanneke Cobelens
Gustav J. Strijkers
Dennis Koehn
Mark J. Post
Marc van Bilsen
Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats
Cardiovascular Diabetology
Obesity
Endothelial dysfunction
Myocardial perfusion
Cardiac function
Glycocalyx
Metformin
title Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats
title_full Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats
title_fullStr Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats
title_full_unstemmed Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats
title_short Metformin and sulodexide restore cardiac microvascular perfusion capacity in diet-induced obese rats
title_sort metformin and sulodexide restore cardiac microvascular perfusion capacity in diet induced obese rats
topic Obesity
Endothelial dysfunction
Myocardial perfusion
Cardiac function
Glycocalyx
Metformin
url http://link.springer.com/article/10.1186/s12933-017-0525-7
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