dc.contributor.author
Salameh, A.
dc.contributor.author
Greimann, W.
dc.contributor.author
Vollroth, M.
dc.contributor.author
Dhein, S.
dc.contributor.author
Bahramsoltani, Mahtab
dc.contributor.author
Dahnert, I.
dc.date.accessioned
2018-06-08T10:18:22Z
dc.date.available
2017-05-29T09:08:04.338Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/20215
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-23521
dc.description.abstract
Since the invention of the heart-lung machine paediatric cardiac surgery
developed rapidly. For correction of complex cardiac malformations the
application of a cardio-pulmonary bypass (CPB) has become indispensable but
possible negative effects of this technique should not be neglected.
Especially, both bypassed organs i.e. heart and lung are not perfused during
the procedure and therefore are threatened by ischemia and reperfusion injury.
Additionally, CPB was developed with a non-pulsatile flow but there are
clinical observations that pulsatile flow might be superior with improved
patient outcomes. Thus, the aim of our study was to evaluate the effect of CPB
on lung structure and to assess whether different flow modalities (pulsatile
vs. non-pulsatile flow) or application of the antibiotic minocycline might be
advantageous. Thirty five piglets of four weeks age were examined and divided
into five experimental groups: control (no CPB) without or with minocycline,
CPB (non-pulsatile flow) without or with minocycline and CPB with pulsatile
flow. CPB was performed for 90 min followed by a 120 min reperfusion and
recovery phase. Thereafter, adenosine triphosphate-content of lung biopsies
and histology was carried out. We found that CPB was associated with a
significant thickening of alveolar wall accompanied by an infiltration of
neutrophil leucocytes. Moreover, markers for hypoxia, apoptosis, nitrosative
stress, inflammation and DNA damage were significantly elevated after CPB.
These cellular damages could be partially inhibited by minocycline or
pulsatile flow. Both, minocycline and pulsatile flow attenuate lung damage
after CPB.
en
dc.rights.uri
http://www.jpp.krakow.pl/
dc.subject
cardio-pulmonary bypass
dc.subject
adenosine triphosphate
dc.subject
tumor necrosis factor-alpha
dc.subject
poly-ADP-ribose
dc.subject
bronchial epithelium
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit
dc.title
Lung protection in cardio-pulmonary bypass
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Journal of Physiology and Pharmacology. - 68 (2017), 1, S. 99-116
dcterms.bibliographicCitation.url
http://www.jpp.krakow.pl/
refubium.affiliation
Veterinärmedizin
de
refubium.mycore.fudocsId
FUDOCS_document_000000027070
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000008241
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1899-1505