Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function (Articolo in rivista)

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  • Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1152/ajpheart.00718.2012 (literal)
Alternative label
  • Baragatti B. [ 1,2 ] ; Ciofini E. [ 1 ] ; Sodini D. [ 1 ] ; Luin S. [ 3,4 ] ; Scebba F. [ 1 ] ; Coceani F. [ 1,2 ] (2013)
    Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function
    in American journal of physiology. Heart and circulatory physiology; AMER CHEMICAL SOC, WASHINGTON (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Baragatti B. [ 1,2 ] ; Ciofini E. [ 1 ] ; Sodini D. [ 1 ] ; Luin S. [ 3,4 ] ; Scebba F. [ 1 ] ; Coceani F. [ 1,2 ] (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 304 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • [ 1 ] Scuola Super Sant Anna, Inst Life Sci, I-56127 Pisa, Italy [ 2 ] CNR, Inst Clin Physiol, Pisa, Italy [ 3 ] Scuola Normale Super Pisa, Lab Natl Enterprise NanoSci & NanoTechnol, Pisa, Italy [ 4 ] CNR, Ist Nanosci, Pisa, Italy (literal)
Titolo
  • Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function (literal)
Abstract
  • Baragatti B, Ciofini E, Sodini D, Luin S, Scebba F, Coceani F. Hydrogen sulfide in the mouse ductus arteriosus: a naturally occurring relaxant with potential EDHF function. Am J Physiol Heart Circ Physiol 304: H927-H934, 2013. First published February 1, 2013; doi:10.1152/ajpheart.00718.2012.-We have previously reported that bradykinin relaxes the fetal ductus arteriosus via endothelium-derived hyperpolarizing factor (EDHF) when other naturally occurring relaxants (prostaglandin E-2, nitric oxide, and carbon monoxide) are suppressed, but the identity of the agent could not be ascertained. Here, we have examined in the mouse whether hydrogen sulfide (H2S) is a relaxant of the ductus and, if so, whether it may also function as an EDHF. We found in the vessel transcripts for the H2S synthetic enzymes, cystathionine-gamma-lyase (CSE) and cystathionine-beta-synthase (CBS), and the presence of these enzymes was confirmed by immunofluorescence microscopy. CSE and CBS were distributed across the vessel wall with the former prevailing in the intimal layer. Both enzymes occurred within the endoplasmic reticulum of endothelial and muscle cells, whereas only CSE was located also in the plasma membrane. The isolated ductus contracted to inhibitors of CSE (D,L-propargylglycine, PPG) and CBS (amino-oxyacetic acid), and PPG contraction was attenuated by removal of the endothelium. EDHF-mediated bradykinin relaxation was curtailed by both PPG and amino-oxyacetic acid, whereas the relaxation to sodium nitroprusside was not affected by either treatment. The H2S donor sodium hydrogen sulfide (NaHS) was also a potent, concentration-dependent relaxant. We conclude that the ductus is endowed with a H2S system exerting a tonic relaxation. In addition, H2S, possibly via an overriding CSE source, qualifies as an EDHF. These findings introduce a novel vasoregulatory mechanism into the ductus, with implications for antenatal patency of the vessel and its transitional adjustments at birth. (literal)
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