Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System
Antidopaminergic gastrointestinal prokinetics are indeed commonly used to treat gastrointestinal motility disorders, although the precise role of dopaminergic transmission in the gut is still unclear. Since dopamine transporter (DAT) is involved in several brain disorders by modulating extracellular...
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doaj-b58e2508d9c24eb9a974031a723bafe42021-04-24T23:01:45ZengMDPI AGBiomedicines2227-90592021-04-01946546510.3390/biomedicines9050465Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous SystemSilvia Cerantola0Valentina Caputi1Gabriella Contarini2Maddalena Mereu3Antonella Bertazzo4Annalisa Bosi5Davide Banfi6Dante Mantini7Cristina Giaroni8Maria Cecilia Giron9Department of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, ItalyDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, ItalyDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95131 Catania, ItalyDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, ItalyDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, ItalyDepartment of Medicine and Surgery, University of Insubria, 21100 Varese, ItalyDepartment of Medicine and Surgery, University of Insubria, 21100 Varese, ItalyIRCCS San Camillo Hospital, 30126 Venice, ItalyDepartment of Medicine and Surgery, University of Insubria, 21100 Varese, ItalyDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, 35131 Padova, ItalyAntidopaminergic gastrointestinal prokinetics are indeed commonly used to treat gastrointestinal motility disorders, although the precise role of dopaminergic transmission in the gut is still unclear. Since dopamine transporter (DAT) is involved in several brain disorders by modulating extracellular dopamine in the central nervous system, this study evaluated the impact of DAT genetic reduction on the morpho-functional integrity of mouse small intestine enteric nervous system (ENS). In DAT heterozygous (DAT<sup>+/−</sup>) and wild-type (DAT<sup>+/+</sup>) mice (14 ± 2 weeks) alterations in small intestinal contractility were evaluated by isometrical assessment of neuromuscular responses to receptor and non-receptor-mediated stimuli. Changes in ENS integrity were studied by real-time PCR and confocal immunofluorescence microscopy in longitudinal muscle-myenteric plexus whole-mount preparations (). DAT genetic reduction resulted in a significant increase in dopamine-mediated effects, primarily via D1 receptor activation, as well as in reduced cholinergic response, sustained by tachykininergic and glutamatergic neurotransmission via NMDA receptors. These functional anomalies were associated to architectural changes in the neurochemical coding and S100β immunoreactivity in small intestine myenteric plexus. Our study provides evidence that genetic-driven DAT defective activity determines anomalies in ENS architecture and neurochemical coding together with ileal dysmotility, highlighting the involvement of dopaminergic system in gut disorders, often associated to neurological conditions.https://www.mdpi.com/2227-9059/9/5/465dopamine transporterenteric nervous systemsmall intestineneuromuscular contractilityconfocal microscopy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Silvia Cerantola Valentina Caputi Gabriella Contarini Maddalena Mereu Antonella Bertazzo Annalisa Bosi Davide Banfi Dante Mantini Cristina Giaroni Maria Cecilia Giron |
spellingShingle |
Silvia Cerantola Valentina Caputi Gabriella Contarini Maddalena Mereu Antonella Bertazzo Annalisa Bosi Davide Banfi Dante Mantini Cristina Giaroni Maria Cecilia Giron Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System Biomedicines dopamine transporter enteric nervous system small intestine neuromuscular contractility confocal microscopy |
author_facet |
Silvia Cerantola Valentina Caputi Gabriella Contarini Maddalena Mereu Antonella Bertazzo Annalisa Bosi Davide Banfi Dante Mantini Cristina Giaroni Maria Cecilia Giron |
author_sort |
Silvia Cerantola |
title |
Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System |
title_short |
Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System |
title_full |
Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System |
title_fullStr |
Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System |
title_full_unstemmed |
Dopamine Transporter Genetic Reduction Induces Morpho-Functional Changes in the Enteric Nervous System |
title_sort |
dopamine transporter genetic reduction induces morpho-functional changes in the enteric nervous system |
publisher |
MDPI AG |
series |
Biomedicines |
issn |
2227-9059 |
publishDate |
2021-04-01 |
description |
Antidopaminergic gastrointestinal prokinetics are indeed commonly used to treat gastrointestinal motility disorders, although the precise role of dopaminergic transmission in the gut is still unclear. Since dopamine transporter (DAT) is involved in several brain disorders by modulating extracellular dopamine in the central nervous system, this study evaluated the impact of DAT genetic reduction on the morpho-functional integrity of mouse small intestine enteric nervous system (ENS). In DAT heterozygous (DAT<sup>+/−</sup>) and wild-type (DAT<sup>+/+</sup>) mice (14 ± 2 weeks) alterations in small intestinal contractility were evaluated by isometrical assessment of neuromuscular responses to receptor and non-receptor-mediated stimuli. Changes in ENS integrity were studied by real-time PCR and confocal immunofluorescence microscopy in longitudinal muscle-myenteric plexus whole-mount preparations (). DAT genetic reduction resulted in a significant increase in dopamine-mediated effects, primarily via D1 receptor activation, as well as in reduced cholinergic response, sustained by tachykininergic and glutamatergic neurotransmission via NMDA receptors. These functional anomalies were associated to architectural changes in the neurochemical coding and S100β immunoreactivity in small intestine myenteric plexus. Our study provides evidence that genetic-driven DAT defective activity determines anomalies in ENS architecture and neurochemical coding together with ileal dysmotility, highlighting the involvement of dopaminergic system in gut disorders, often associated to neurological conditions. |
topic |
dopamine transporter enteric nervous system small intestine neuromuscular contractility confocal microscopy |
url |
https://www.mdpi.com/2227-9059/9/5/465 |
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