2025-02-24T04:43:05-05:00 DEBUG: VuFindSearch\Backend\Solr\Connector: Query fl=%2A&wt=json&json.nl=arrarr&q=id%3A%22oai%3Aojs.pkp.sfu.ca%3Aarticle-511%22&qt=morelikethis&rows=5
2025-02-24T04:43:05-05:00 DEBUG: VuFindSearch\Backend\Solr\Connector: => GET http://localhost:8983/solr/biblio/select?fl=%2A&wt=json&json.nl=arrarr&q=id%3A%22oai%3Aojs.pkp.sfu.ca%3Aarticle-511%22&qt=morelikethis&rows=5
2025-02-24T04:43:05-05:00 DEBUG: VuFindSearch\Backend\Solr\Connector: <= 200 OK
2025-02-24T04:43:05-05:00 DEBUG: Deserialized SOLR response

ПЭО-1500 ингибирует Са2+-АТРазу эритроцитов человека

Human erythrocyte Ca2+-ATPase provides the maintenance and regulation of intercellular calcium level. Change in its functional activity under cryopreservation plays an important role in cell survival and structural integrity preservation. PEO-1500 exocellular cryoprotectant inhibits erythrocyte Ca2+...

Full description

Saved in:
Bibliographic Details
Main Authors: Zemlyanskikh, N. G., Nikolchenko, A. Yu., Babijchuk, L. A.
Format: Article
Language:English
Published: Publishing House ‘Akademperiodyka’ of the National Academy of Sciences of Ukraine; Institute for Problems of Cryobiology and Cryomedicine 2007
Subjects:
Online Access:https://cryo.org.ua/journal/index.php/probl-cryobiol-cryomed/article/view/511
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Human erythrocyte Ca2+-ATPase provides the maintenance and regulation of intercellular calcium level. Change in its functional activity under cryopreservation plays an important role in cell survival and structural integrity preservation. PEO-1500 exocellular cryoprotectant inhibits erythrocyte Ca2+-ATPase activity at incubation stage but the following freeze-thawing cycle (–196...37°C) in its presence does not affect the settled regimen of this enzyme functioning. The inhibition caused by PEO-1500 effect has a reversible character and the erythrocyte Ca2+-ATPase activity is recovered after its dilution in cell suspension that is essential for cryopreserved cell normal functioning in blood bed after transfusion. The inhibition of Ca2+-ATPase activity is apparently associated to physical and chemical membrane modification under this compound effect.