<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-26T15:50:15Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/96084" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/96084</identifier><datestamp>2025-08-28T14:30:45Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Martínez-Sáenz, Ana </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Recio Visedo, María Paz</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Orensanz, Luis M. </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Leite Fernandes, Vitor Samuel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Martínez Sainz, María Del Pilar</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Bustamante, Salvador </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Carballido, Joaquín </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>García-Sacristán, Albino </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Prieto Ocejo, Dolores</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Hernández Rodríguez, Medardo Vicente</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2024-01-29T13:18:43Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2024-01-29T13:18:43Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2011</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Martínez-Sáenz A, Recio P, Orensanz LM, Fernandes VS, Martínez MP, Bustamante S, et al. Role of Calcitonin Gene-Related Peptide in Inhibitory Neurotransmission to the Pig Bladder Neck. Journal of Urology 2011;186:728–35. https://doi.org/10.1016/j.juro.2011.03.142.</mods:identifier>
   <mods:identifier type="issn">0022-5347</mods:identifier>
   <mods:identifier type="doi">10.1016/j.juro.2011.03.142</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/96084</mods:identifier>
   <mods:identifier type="essn">1527-3792</mods:identifier>
   <mods:identifier type="officialurl">https://www.doi.org/10.1016/j.juro.2011.03.142</mods:identifier>
   <mods:identifier type="relatedurl">https://www.auajournals.org/doi/10.1016/j.juro.2011.03.142</mods:identifier>
   <mods:abstract>Purpose:
We studied the role of calcitonin gene-related peptide in nonadrenergic, noncholinergic neurotransmission to the pig bladder neck.

Materials and Methods:
We used immunohistochemical techniques to determine the distribution of calcitonin gene-related peptide immunoreactive fibers as well as organ baths for isometric force recording. We investigated relaxation due to endogenously released or exogenously applied calcitonin gene-related peptide in urothelium denuded phenylephrine precontracted strips treated with guanethidine, atropine and NG-nitro-L-arginine to block noradrenergic neurotransmission, muscarinic receptors and nitric oxide synthase, respectively.

Results:
Rich calcitonin gene-related peptide immunoreactive innervation was found penetrating through the adventitia and distributed in the suburothelial and muscle layers. Numerous, variable size, varicose calcitonin gene-related peptide immunopositive terminals were seen close below the urothelium. In the muscle layer calcitonin gene-related peptide immunopositive nerves usually appeared as varicose terminals running along muscle fibers. Electrical field stimulation (2 to 16 Hz) and exogenous calcitonin gene-related peptide (0.1 nM to 0.3 μM) evoked frequency and concentration dependent relaxation, respectively. Nerve responses were potentiated by capsaicin, decreased by calcitonin gene-related peptide (8–37) and abolished by tetrodotoxin, capsaicin sensitive primary afferent blockers, calcitonin gene-related peptide receptors and neuronal voltage gated Na+ channels. Calcitonin gene-related peptide-induced relaxation was potentiated by the neuronal voltage gated Ca2+ channels blocker ω-conotoxin-GVIA and decreased by calcitonin gene-related peptide (8–37). Calcitonin gene-related peptide relaxation was not modified by blockade of endopeptidases, nitric oxide synthase, guanylyl cyclase and cyclooxygenase.

Conclusions:
Results suggest that calcitonin gene-related peptide is involved in the nonadrenergic, noncholinergic inhibitory neurotransmission of the pig bladder neck, producing relaxation through neuronal and muscle calcitonin gene-related peptide receptors. Nitric oxide/cyclic guanosine monophosphate and cyclooxygenase pathways do not seem to be involved in such responses.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">metadata only access</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Role of Calcitonin Gene-Related Peptide in Inhibitory Neurotransmission to the Pig Bladder Neck</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods></metadata></record></GetRecord></OAI-PMH>