Serotonin receptors and their association with the immune system in the gastrointestinal tract of weaning piglets.

5-HT Gut health Immunity Inflammation Piglet Serotonin Weaning

Journal

Porcine health management
ISSN: 2055-5660
Titre abrégé: Porcine Health Manag
Pays: England
ID NLM: 101684126

Informations de publication

Date de publication:
28 Jan 2022
Historique:
received: 30 08 2021
accepted: 19 12 2021
entrez: 29 1 2022
pubmed: 30 1 2022
medline: 30 1 2022
Statut: epublish

Résumé

Immune cell activation and perpetuation of inflammation have been attributed to the neurotransmitter serotonin (5-hydroxytryptamine; 5-HT). Our hypothesis was that the 5-HT system plays a role in GI health and immunity in post-weaning piglets. A disruption of the 5-HT system post-weaning with transcriptional upregulation of 5-HT receptors may be linked to increased cytokine mRNA abundance and immune system activation. The objective of this exploratory study was to assess the relationship between 5-HT receptor expression and immune system biomarkers in piglets at 1 (n = 9) and 15 (n = 10) days post-weaning. The mRNA transcript abundance of three 5-HT receptors (5-HTR3, 5-HTR4, and 5-HTR7) measured in jejunum and colon tissues were used to determine the relationship with the immune system and jejunal morphometry at 2 timepoints post-weaning using correlations, mixed models, and multivariate analysis techniques. Overall, 5-HT receptor mRNA expression decreased from day 1 to day 15 post-weaning. Time × tissue interactions showed the lowest 5-HTR3 expression in the colon and lower 5-HTR7 expression in the jejunum at 15 days post-weaning. 5-HTR3 and 5-HTR4 expression were negatively associated with pro-inflammatory (IFN-ɣ) and anti-inflammatory (IL-10 and IL-12β) cytokines in jejunum, and with TNF-α in the colon at 1-day post-weaning. At 15 days post-weaning, 5-HTR3 in the colon was negatively associated with pro-inflammatory (IL-1α, IL-1β, TNF-α, IL-8, and IFN-ɣ) and anti-inflammatory (IL-10 and IL-12β) cytokines. Furthermore, 5-HTR7 expressed a predominantly pro-inflammatory profile (IFN-α, IL-1α, IL-1β, IL-8, TNF-α and IL-12α) in the jejunum at the same timepoint, whereas colonic 5-HTR7 expression was negatively correlated with IL-1α, IL-1β, IL-10 and TGF-β. Lastly, positive correlations were found for increased expression of 5-HTR4 receptor with villus height, 5-HTR7 receptor expression and crypt depth, and increased expression of 5-HTR3 and 5-HTR4 receptor with villus height to crypt depth ratio at 1-day post-weaning. The 5-HT receptor mRNA abundance was associated with the immune system and intestinal morphometry in piglets. The 5-HT receptors were highly expressed at weaning in both jejunum and colon tissues relative to 15 days post-weaning. Although a clear relationship between immune system and 5-HTR expression is observed, particularly at day 15, a cause-consequence cannot be proven with current data. Further research is warranted to elucidate the effects of 5-HT on gastrointestinal inflammation during the weaning process in piglets, which could be the basis for new interventions to ease weaning stress.

Sections du résumé

BACKGROUND BACKGROUND
Immune cell activation and perpetuation of inflammation have been attributed to the neurotransmitter serotonin (5-hydroxytryptamine; 5-HT). Our hypothesis was that the 5-HT system plays a role in GI health and immunity in post-weaning piglets. A disruption of the 5-HT system post-weaning with transcriptional upregulation of 5-HT receptors may be linked to increased cytokine mRNA abundance and immune system activation.
METHODS METHODS
The objective of this exploratory study was to assess the relationship between 5-HT receptor expression and immune system biomarkers in piglets at 1 (n = 9) and 15 (n = 10) days post-weaning. The mRNA transcript abundance of three 5-HT receptors (5-HTR3, 5-HTR4, and 5-HTR7) measured in jejunum and colon tissues were used to determine the relationship with the immune system and jejunal morphometry at 2 timepoints post-weaning using correlations, mixed models, and multivariate analysis techniques.
RESULTS RESULTS
Overall, 5-HT receptor mRNA expression decreased from day 1 to day 15 post-weaning. Time × tissue interactions showed the lowest 5-HTR3 expression in the colon and lower 5-HTR7 expression in the jejunum at 15 days post-weaning. 5-HTR3 and 5-HTR4 expression were negatively associated with pro-inflammatory (IFN-ɣ) and anti-inflammatory (IL-10 and IL-12β) cytokines in jejunum, and with TNF-α in the colon at 1-day post-weaning. At 15 days post-weaning, 5-HTR3 in the colon was negatively associated with pro-inflammatory (IL-1α, IL-1β, TNF-α, IL-8, and IFN-ɣ) and anti-inflammatory (IL-10 and IL-12β) cytokines. Furthermore, 5-HTR7 expressed a predominantly pro-inflammatory profile (IFN-α, IL-1α, IL-1β, IL-8, TNF-α and IL-12α) in the jejunum at the same timepoint, whereas colonic 5-HTR7 expression was negatively correlated with IL-1α, IL-1β, IL-10 and TGF-β. Lastly, positive correlations were found for increased expression of 5-HTR4 receptor with villus height, 5-HTR7 receptor expression and crypt depth, and increased expression of 5-HTR3 and 5-HTR4 receptor with villus height to crypt depth ratio at 1-day post-weaning.
CONCLUSIONS CONCLUSIONS
The 5-HT receptor mRNA abundance was associated with the immune system and intestinal morphometry in piglets. The 5-HT receptors were highly expressed at weaning in both jejunum and colon tissues relative to 15 days post-weaning. Although a clear relationship between immune system and 5-HTR expression is observed, particularly at day 15, a cause-consequence cannot be proven with current data. Further research is warranted to elucidate the effects of 5-HT on gastrointestinal inflammation during the weaning process in piglets, which could be the basis for new interventions to ease weaning stress.

Identifiants

pubmed: 35090573
doi: 10.1186/s40813-022-00250-5
pii: 10.1186/s40813-022-00250-5
pmc: PMC8796611
doi:

Types de publication

Journal Article

Langues

eng

Pagination

8

Informations de copyright

© 2022. The Author(s).

Références

Am J Physiol Gastrointest Liver Physiol. 2002 May;282(5):G877-93
pubmed: 11960784
Curr Opin Pharmacol. 2011 Feb;11(1):29-33
pubmed: 21393060
Br J Nutr. 2012 Jun;107(12):1776-86
pubmed: 21936967
Brain Behav Immun. 2000 Sep;14(3):219-24
pubmed: 10970681
J Anim Sci. 2006 Apr;84(4):963-71
pubmed: 16543575
Neuropsychopharmacology. 2019 Sep;44(10):1742-1751
pubmed: 30959513
Biochim Biophys Acta. 2008 Feb;1780(2):134-44
pubmed: 18082146
Histochem Cell Biol. 1999 Oct;112(4):257-63
pubmed: 10550609
Biogerontology. 2013 Feb;14(1):21-45
pubmed: 23100172
J Nutr Biochem. 2010 Jun;21(6):468-75
pubmed: 19428234
Free Radic Biol Med. 2014 Apr;69:377-89
pubmed: 24524998
Int Immunol. 2005 May;17(5):599-606
pubmed: 15802305
Physiol Rep. 2019 Nov;7(21):e14278
pubmed: 31724827
J Pharmacol Exp Ther. 2003 Jul;306(1):355-62
pubmed: 12682218
Vet Immunol Immunopathol. 2006 Jun 15;111(3-4):187-98
pubmed: 16621019
Gastroenterology. 2002 Jul;123(1):217-26
pubmed: 12105850
J Immunol. 2004 May 15;172(10):6011-9
pubmed: 15128784
PLoS One. 2013 Apr 24;8(4):e59838
pubmed: 23637741
J Immunol. 2013 May 1;190(9):4795-804
pubmed: 23554310
J Nutr. 2004 Mar;134(3):641-7
pubmed: 14988461
PLoS One. 2009 Jul 31;4(7):e6453
pubmed: 19649285
J Cell Physiol. 2008 Nov;217(2):301-6
pubmed: 18651566
Acta Physiol (Oxf). 2015 Mar;213(3):561-74
pubmed: 25439045
World J Gastroenterol. 2014 Nov 7;20(41):15216-32
pubmed: 25386070
Nat Cell Biol. 2018 Aug;20(8):909-916
pubmed: 30038251
Comp Biochem Physiol A Mol Integr Physiol. 2004 Apr;137(4):757-65
pubmed: 15123184
Br J Pharmacol. 2012 Nov;167(6):1362-8
pubmed: 22758653
Pharmacol Biochem Behav. 1990 Oct;37(2):219-25
pubmed: 2080185
Neurogastroenterol Motil. 2015 Jul;27(7):899-905
pubmed: 26095115
Free Radic Biol Med. 2017 May;106:196-207
pubmed: 28216386
Biochimie. 2019 Jun;161:56-64
pubmed: 29909048
Acta Histochem. 2009;111(1):35-41
pubmed: 18550155
J Nutr Biochem. 2008 Jan;19(1):8-15
pubmed: 17434724
Am J Physiol Gastrointest Liver Physiol. 2006 Nov;291(5):G803-11
pubmed: 16728728
ACS Chem Neurosci. 2017 May 17;8(5):920-931
pubmed: 28288510
J Immunol Methods. 2005 Nov 30;306(1-2):16-27
pubmed: 16223507
Vet Immunol Immunopathol. 2004 Dec 8;102(3):199-216
pubmed: 15507306
Vet Res. 2009 May-Jun;40(3):23
pubmed: 19236838
Nucleic Acids Res. 2001 May 1;29(9):e45
pubmed: 11328886
J Anim Sci. 2021 Apr 1;99(4):
pubmed: 33640983
Virus Res. 2008 Dec;138(1-2):89-96
pubmed: 18796318
Gastroenterology. 2009 Dec;137(6):2074-83
pubmed: 19747920
J Nutr. 1999 Mar;129(3):613-9
pubmed: 10082764
Eur J Histochem. 2016 Dec 28;60(4):2689
pubmed: 28076934
Am J Physiol. 1999 Nov;277(5):G922-8
pubmed: 10564096
PLoS One. 2016 Mar 29;11(3):e0150216
pubmed: 27022727
Gastroenterology. 2007 Jan;132(1):397-414
pubmed: 17241888
Mol Metab. 2018 May;11:70-83
pubmed: 29576437
Nat Rev Gastroenterol Hepatol. 2017 Jul;14(7):412-420
pubmed: 28487547
Gastroenterology. 2009 Nov;137(5):1649-60
pubmed: 19706294
Biochim Biophys Acta. 2014 Nov;1843(11):2563-2582
pubmed: 24892271
Acta Histochem. 2002;104(2):185-92
pubmed: 12086339
Toxicol Pathol. 2014 Jan;42(1):54-66
pubmed: 24436039
Comp Biochem Physiol A Mol Integr Physiol. 2008 Jan;149(1):51-8
pubmed: 17997116
J Virol. 2017 Jan 3;91(2):
pubmed: 27852848

Auteurs

Lluís Fabà (L)

Trouw Nutrition R&D, Boxmeer, The Netherlands. lluis.faba.camats@trouwnutrition.com.

Nienke de Groot (N)

Trouw Nutrition Innovation, Amersfoort, The Netherlands.

Guillermo Ramis (G)

Dpto. Producción Animal, Facultad de Veterinaria, Universidad de Murcia, Murcia, Spain.

Carolina G Cabrera-Gómez (CG)

Dpto. Producción Animal, Facultad de Veterinaria, Universidad de Murcia, Murcia, Spain.

John Doelman (J)

Trouw Nutrition R&D, Boxmeer, The Netherlands.

Classifications MeSH