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Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction

BACKGROUND: Vasculogenic erectile dysfunction (VED) is considered as a common complication among people with type 2 diabetes (T2D). We tested whether changes in fatty acid (FAs) classes measured in erythrocytes are associated with increased risk of diabetic VED along with related risk factors. METHO...

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Autores principales: Ben Khedher, Mohamed Raâfet, Bouhajja, Houda, Haj Ahmed, Samia, Abid, Mohamed, Jamoussi, Kamel, Hammami, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727868/
https://www.ncbi.nlm.nih.gov/pubmed/29233142
http://dx.doi.org/10.1186/s12944-017-0637-9
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author Ben Khedher, Mohamed Raâfet
Bouhajja, Houda
Haj Ahmed, Samia
Abid, Mohamed
Jamoussi, Kamel
Hammami, Mohamed
author_facet Ben Khedher, Mohamed Raâfet
Bouhajja, Houda
Haj Ahmed, Samia
Abid, Mohamed
Jamoussi, Kamel
Hammami, Mohamed
author_sort Ben Khedher, Mohamed Raâfet
collection PubMed
description BACKGROUND: Vasculogenic erectile dysfunction (VED) is considered as a common complication among people with type 2 diabetes (T2D). We tested whether changes in fatty acid (FAs) classes measured in erythrocytes are associated with increased risk of diabetic VED along with related risk factors. METHODS: We assessed erythrocyte FAs composition, lipid peroxidation parameters and inflammatory cytokines among 72 T2D men with VED, 78 T2D men without VED and 88 healthy volunteers with similar age. Biochemical, hepatic, lipid and hormonal profiles were measured. RESULTS: T2D people with VED had significant decrease in the indexes of Δ6-desaturase and elongase activities compared to the other studied groups. The same group of participants displayed lower erythrocytes levels of dihomo-γ-linolenic acid (C20:3n-6) (P < .001), precursor of the messenger molecule PGE1 mainly involved in promoting erection. Moreover, absolute SFAs concentration and HOMA IR levels were higher in T2D people with VED when compared to controls and associated with impaired NO concentration (1.43 vs 3.30 ng/L, P < .001). Our results showed that IL-6 and TNF-α were significantly increased and positively correlated with MDA levels only in T2D people with VED (r = 0.884, P = .016 and r = 0.753, P = .035; respectively) suggesting a decrease in the relative availability of vasodilator mediators and an activation of vasoconstrictors release. CONCLUSION: Our findings show that the deranged FAs metabolism represents a potential marker of VED in progress, or at least an indicator of increased risk within men with T2D.
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spelling pubmed-57278682017-12-18 Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction Ben Khedher, Mohamed Raâfet Bouhajja, Houda Haj Ahmed, Samia Abid, Mohamed Jamoussi, Kamel Hammami, Mohamed Lipids Health Dis Research BACKGROUND: Vasculogenic erectile dysfunction (VED) is considered as a common complication among people with type 2 diabetes (T2D). We tested whether changes in fatty acid (FAs) classes measured in erythrocytes are associated with increased risk of diabetic VED along with related risk factors. METHODS: We assessed erythrocyte FAs composition, lipid peroxidation parameters and inflammatory cytokines among 72 T2D men with VED, 78 T2D men without VED and 88 healthy volunteers with similar age. Biochemical, hepatic, lipid and hormonal profiles were measured. RESULTS: T2D people with VED had significant decrease in the indexes of Δ6-desaturase and elongase activities compared to the other studied groups. The same group of participants displayed lower erythrocytes levels of dihomo-γ-linolenic acid (C20:3n-6) (P < .001), precursor of the messenger molecule PGE1 mainly involved in promoting erection. Moreover, absolute SFAs concentration and HOMA IR levels were higher in T2D people with VED when compared to controls and associated with impaired NO concentration (1.43 vs 3.30 ng/L, P < .001). Our results showed that IL-6 and TNF-α were significantly increased and positively correlated with MDA levels only in T2D people with VED (r = 0.884, P = .016 and r = 0.753, P = .035; respectively) suggesting a decrease in the relative availability of vasodilator mediators and an activation of vasoconstrictors release. CONCLUSION: Our findings show that the deranged FAs metabolism represents a potential marker of VED in progress, or at least an indicator of increased risk within men with T2D. BioMed Central 2017-12-12 /pmc/articles/PMC5727868/ /pubmed/29233142 http://dx.doi.org/10.1186/s12944-017-0637-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ben Khedher, Mohamed Raâfet
Bouhajja, Houda
Haj Ahmed, Samia
Abid, Mohamed
Jamoussi, Kamel
Hammami, Mohamed
Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
title Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
title_full Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
title_fullStr Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
title_full_unstemmed Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
title_short Role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
title_sort role of disturbed fatty acids metabolism in the pathophysiology of diabetic erectile dysfunction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727868/
https://www.ncbi.nlm.nih.gov/pubmed/29233142
http://dx.doi.org/10.1186/s12944-017-0637-9
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