Evaluation of in-vitro neuronal protection by poloxamer 188 following simulated traumatic brain injury

Dissertation, Universitätsmedizin der Universität Greifswald, 2021

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Bibliographische Detailangaben
1. Verfasser: Meyer, Luise Johanna Cornelia (VerfasserIn)
Körperschaft: Universität Greifswald (Grad-verleihende Institution)
Weitere Verfasser: Hahnenkamp, Klaus (AkademischeR BetreuerIn), Tzabazis, Alexander (AkademischeR BetreuerIn)
Format: UnknownFormat
Sprache:eng
Veröffentlicht: Greifswald 2020
Schlagworte:
Hochschulschrift > Schädel-Hirn-Trauma > Schlaganfall > Hypoxie > Nervenzelle > Copolymere > Poloxamer > In vitro
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Zusammenfassung:Dissertation, Universitätsmedizin der Universität Greifswald, 2021
Ischämischer Insult, Neuron, Sauerstoffmangel, Schädelhirntrauma, Copolymer, Hypoxie, In-vitro, Ischämie-Reperfusions-Schaden, Kompression, Poloxamer 188
I/R injury occurs during stroke and TBI. It represents a complex pathological event including several processes that can lead to cell membrane disruption, cellular dysfunction and death. The reintroduction of blood flow after the ischemic event may cause detrimental injury to the brain beyond the harm caused by ischemia itself and, therefore, represents a clinical challenge. This so-called I/R injury damages cells in a variety of ways including poration of cell membranes. Hence, methods to improve the endogenous membrane resealing capacity are crucial to prevent neuronal injury. In the present work, treatment during reoxygenation with the probably most studied CCMS, P188, was investigated in an in-vitro simulation of stroke and TBI in primary isolated cortical mouse neurons. P188 offers a unique hydrophilic/lipophilic character that has been reported to protect different cells and tissues in various experimental settings against I/R and mechanical injury by sealing membranes. The aim of this study was to establish an in-vitro stroke and TBI model and further investigate if P188 directly interacts with neurons after compression and H/R (simulated I/R) injury, when administered at the start of reoxygenation. The outcome of this treatment was evaluated in regard to cell number/viability, mitochondrial viability, membrane damage by LDH release and FM1-43 incorporation as well as activation of apoptosis by Caspase 3. It could be demonstrated that 5 hours hypoxia ± compression ...
Beschreibung:Literaturverzeichnis: Blatt 62-72
Beschreibung:xi, 82 Blätter
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