Webbläsaren som du använder stöds inte av denna webbplats. Alla versioner av Internet Explorer stöds inte längre, av oss eller Microsoft (läs mer här: * https://www.microsoft.com/en-us/microsoft-365/windows/end-of-ie-support).

Var god och använd en modern webbläsare för att ta del av denna webbplats, som t.ex. nyaste versioner av Edge, Chrome, Firefox eller Safari osv.

ATP Depletion and Cell Death in the Neonatal Lamb Ductus Arteriosus.

Författare

  • Max Levin
  • Seth Goldbarg
  • Anders Lindqvist
  • Karl Swärd
  • Christine Roman
  • Bao Mei Liu
  • Lillemor Mattsson Hultén
  • Jan Borén
  • Ronald I Clyman

Summary, in English

Postnatal constriction of the full-term ductus arteriosus produces cell death and remodeling of the ductus wall. Using a bioluminescence imaging technique, we found that after birth, the lamb ductus develops ATP, glucose, and glycogen depletion in addition to hypoxia. In vitro studies showed that cell death correlates best with ATP depletion and is most marked when both glucose and oxygen are severely depleted; in addition, the degree of ATP depletion found in vivo is sufficient to account for the extensive degree of cell death that occurs after birth. Under hypoxic conditions, the immature ductus is more capable of preserving its ATP supply than the mature ductus as a result of increased glucose availability, glycogen stores, and glucose utilization. However, the immature ductus is just as susceptible as the mature ductus to ATP depletion when glucose supplies are restricted. The extensive degree of cell death that occurs in the newborn ductus after birth is associated primarily with ATP depletion. The increased glycolytic capacity of the immature ductus may enable it to tolerate episodes of hypoxia and nutrient shortage, making it more resistant to developing postnatal cell death and permanent closure.

Avdelning/ar

Publiceringsår

2005

Språk

Engelska

Sidor

801-805

Publikation/Tidskrift/Serie

Pediatric Research

Volym

57

Issue

6

Dokumenttyp

Artikel i tidskrift

Förlag

International Pediatric Foundation Inc.

Ämne

  • Pediatrics

Status

Published

Forskningsgrupp

  • Islet cell physiology
  • Vascular Physiology
  • Cellular Biomechanics

ISBN/ISSN/Övrigt

  • ISSN: 1530-0447