Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?

Depression and diabetes are serious diseases with an increasing global prevalence. Intriguingly, recent meta-analyses have highlighted an asymmetrical relationship between the two conditions as depressed patients were found to display a higher risk of developing type 2 diabetes than those individual...

Full description

Bibliographic Details
Main Authors: Pomytkin, I, Cline, B, Anthony, D, Steinbusch, H, Lesch, K, Strekalova, T
Format: Journal article
Language:English
Published: 2015
_version_ 1797053522063130624
author Pomytkin, I
Cline, B
Anthony, D
Steinbusch, H
Lesch, K
Strekalova, T
author_facet Pomytkin, I
Cline, B
Anthony, D
Steinbusch, H
Lesch, K
Strekalova, T
author_sort Pomytkin, I
collection OXFORD
description Depression and diabetes are serious diseases with an increasing global prevalence. Intriguingly, recent meta-analyses have highlighted an asymmetrical relationship between the two conditions as depressed patients were found to display a higher risk of developing type 2 diabetes than those individuals suffering from diabetes are to become depressed. Based on recent findings, we favor a hypothesis where by decreased peripheral serotonin (5-HT) transporter (5-HTT) function is a reciprocal risk factor for the co-morbidity of depression and diabetes, as it can trigger inflammatory pathogenetic mechanisms of both conditions. Higher intestinal levels of 5-HT and 5-HT3 receptor stimulation lead to increased intestinal permeability in 5-HTT deficient mice, which is viewed one of the most relevant animal models of depression. We hypothesize that this leakage of bacterial endotoxins can activate both central and peripheral Toll-like receptor 4 (TLR4), which inhibits insulin signaling and IRS1/PI3K/Akt and thus, contribute to the pathogenesis of diabetes and depression that are associated with this pathway. Antidepressant therapies, which also suppress intestinal 5-HTT, may have potentiating effects on the association between depression and diabetes. It is also of interest that high carbohydrate and fat intake ("cafeteria-type diet") increases intestinal 5-HT leading to TLR4 activation. Thus, endotoxaemia and inflammation owing to increased intestinal 5-HT may underpin the depression and diabetes association, where the risk of the latter pathology becomes particularly preeminent after the onset of depression and not vice versa. The evidence presented here shows the further investigation into peripheral mechanisms that linked diabetes to depression is clearly warranted.
first_indexed 2024-03-06T18:44:56Z
format Journal article
id oxford-uuid:0e2df8a1-74c3-41de-87a2-9151ce591ea3
institution University of Oxford
language English
last_indexed 2024-03-06T18:44:56Z
publishDate 2015
record_format dspace
spelling oxford-uuid:0e2df8a1-74c3-41de-87a2-9151ce591ea32022-03-26T09:44:34ZEndotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:0e2df8a1-74c3-41de-87a2-9151ce591ea3EnglishSymplectic Elements at Oxford2015Pomytkin, ICline, BAnthony, DSteinbusch, HLesch, KStrekalova, TDepression and diabetes are serious diseases with an increasing global prevalence. Intriguingly, recent meta-analyses have highlighted an asymmetrical relationship between the two conditions as depressed patients were found to display a higher risk of developing type 2 diabetes than those individuals suffering from diabetes are to become depressed. Based on recent findings, we favor a hypothesis where by decreased peripheral serotonin (5-HT) transporter (5-HTT) function is a reciprocal risk factor for the co-morbidity of depression and diabetes, as it can trigger inflammatory pathogenetic mechanisms of both conditions. Higher intestinal levels of 5-HT and 5-HT3 receptor stimulation lead to increased intestinal permeability in 5-HTT deficient mice, which is viewed one of the most relevant animal models of depression. We hypothesize that this leakage of bacterial endotoxins can activate both central and peripheral Toll-like receptor 4 (TLR4), which inhibits insulin signaling and IRS1/PI3K/Akt and thus, contribute to the pathogenesis of diabetes and depression that are associated with this pathway. Antidepressant therapies, which also suppress intestinal 5-HTT, may have potentiating effects on the association between depression and diabetes. It is also of interest that high carbohydrate and fat intake ("cafeteria-type diet") increases intestinal 5-HT leading to TLR4 activation. Thus, endotoxaemia and inflammation owing to increased intestinal 5-HT may underpin the depression and diabetes association, where the risk of the latter pathology becomes particularly preeminent after the onset of depression and not vice versa. The evidence presented here shows the further investigation into peripheral mechanisms that linked diabetes to depression is clearly warranted.
spellingShingle Pomytkin, I
Cline, B
Anthony, D
Steinbusch, H
Lesch, K
Strekalova, T
Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?
title Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?
title_full Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?
title_fullStr Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?
title_full_unstemmed Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?
title_short Endotoxaemia resulting from decreased serotonin tranporter (5-HTT) function: A reciprocal risk factor for depression and insulin resistance?
title_sort endotoxaemia resulting from decreased serotonin tranporter 5 htt function a reciprocal risk factor for depression and insulin resistance
work_keys_str_mv AT pomytkini endotoxaemiaresultingfromdecreasedserotonintranporter5httfunctionareciprocalriskfactorfordepressionandinsulinresistance
AT clineb endotoxaemiaresultingfromdecreasedserotonintranporter5httfunctionareciprocalriskfactorfordepressionandinsulinresistance
AT anthonyd endotoxaemiaresultingfromdecreasedserotonintranporter5httfunctionareciprocalriskfactorfordepressionandinsulinresistance
AT steinbuschh endotoxaemiaresultingfromdecreasedserotonintranporter5httfunctionareciprocalriskfactorfordepressionandinsulinresistance
AT leschk endotoxaemiaresultingfromdecreasedserotonintranporter5httfunctionareciprocalriskfactorfordepressionandinsulinresistance
AT strekalovat endotoxaemiaresultingfromdecreasedserotonintranporter5httfunctionareciprocalriskfactorfordepressionandinsulinresistance