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Noradrenergic pathways involved in micturition in an animal model of hydrocephalus—Implications for urinary dysfunction

dc.contributor.authorLouçano, Marta
dc.contributor.authorCoelho, Ana
dc.contributor.authorChambel, Sílvia Sousa
dc.contributor.authorPrudêncio, Cristina
dc.contributor.authorCruz, Célia Duarte
dc.contributor.authorTavares, Isaura
dc.date.accessioned2024-03-15T16:13:26Z
dc.date.available2024-03-15T16:13:26Z
dc.date.issued2024-01-18
dc.description.abstractHydrocephalus is characterized by enlargement of the cerebral ventricles, accompanied by distortion of the periventricular tissue. Patients with hydrocephalus usually experience urinary impairments. Although the underlying etiology is not fully described, the effects of hydrocephalus in the neuronal network responsible for the control of urination, which involves periventricular areas, including the periaqueductal gray (PAG) and the noradrenergic locus coeruleus (LC). In this study, we aimed to investigate the mechanisms behind urinary dysfunction in rats with kaolin-induced hydrocephalus. For that purpose, we used a validated model of hydrocephalus—the rat injected with kaolin in the cisterna magna—also presents urinary impairments in order to investigate the putative involvement of noradrenergic control from the brain to the spinal cord Onuf’s nucleus, a key area in the motor control of micturition. We first evaluated bladder contraction capacity using cystometry. Since our previous characterization of the LC in hydrocephalic animals showed increased levels of noradrenaline, we then evaluated the noradrenergic innervation of the spinal cord’s Onuf’s nucleus by measuring levels of dopamine β-hydroxylase (DBH). We also evaluated the expression of the c-Fos protooncogene, the most widely used marker of neuronal activation, in the ventrolateral PAG (vlPAG), an area that plays a major role in the control of urination by its indirect control of the LC via pontine micturition center. Hydrocephalic rats showed an increased frequency of bladder contractions and lower minimum pressure. These animals also presented increased DBH levels at the Onuf´s nucleus, along with decreased c-Fos expression in the vlPAG. The present findings suggest that impairments in urinary function during hydrocephalus may be due to alterations in descending noradrenergic modulation. We propose that the effects of hydrocephalus in the decrease of vlPAG neuronal activation lead to a decrease in the control over the LC. The increased availability of noradrenaline production at the LC probably causes an exaggerated micturition reflex due to the increased innervation of the Onuf´s nucleus, accounting for the urinary impairments detected in hydrocephalic animals. The results of the study provide new insights into the neuronal underlying mechanisms of urinary dysfunction in hydrocephalus. Further research is needed to fully evaluate the translational perspectives of the current findings.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationLouçano, M., Coelho, A., Chambel, S. S., Prudêncio, C., Cruz, C. D., & Tavares, I. (2024). Noradrenergic pathways involved in micturition in an animal model of hydrocephalus—Implications for urinary dysfunction. Biomedicines, 12(1), Artigo 1. https://doi.org/10.3390/biomedicines12010215pt_PT
dc.identifier.doi10.3390/biomedicines12010215pt_PT
dc.identifier.eissn2227-9059
dc.identifier.urihttp://hdl.handle.net/10400.22/25173
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationNORTE-01-0145-FEDER-000008pt_PT
dc.relation.publisherversionhttps://doi.org/10.3390/biomedicines12010215pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectHydrocephaluspt_PT
dc.subjectPeriaqueductal graypt_PT
dc.subjectLocus coeruleuspt_PT
dc.subjectUrinary dysfunctionpt_PT
dc.subjectNoradrenalinept_PT
dc.subjectOnuf’s nucleuspt_PT
dc.titleNoradrenergic pathways involved in micturition in an animal model of hydrocephalus—Implications for urinary dysfunctionpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage11pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleBiomedicinespt_PT
oaire.citation.volume12(1)pt_PT
person.familyNamePrudêncio
person.givenNameCristina
person.identifier1200571
person.identifier.ciencia-idC81E-F4EE-FADE
person.identifier.orcid0000-0002-9920-936X
person.identifier.scopus-author-id6508057930
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication881a8ad5-ab13-4e49-89f4-08ca61cc81e3
relation.isAuthorOfPublication.latestForDiscovery881a8ad5-ab13-4e49-89f4-08ca61cc81e3

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