gms | German Medical Science

69. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
Joint Meeting mit der Mexikanischen und Kolumbianischen Gesellschaft für Neurochirurgie

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

03.06. - 06.06.2018, Münster

The impact of hypo- and hyperthermia on Spreading Depolarization and delayed infarct progression after focal ischemia in C57BL/6 mice

Meeting Abstract

  • Leonie Schumm - Charité - Universitätsmedizin Berlin, Klinik für Neurochirurgie, Berlin, Deutschland
  • Anna Zdunczyk - Charité - Universitätsmedizin Berlin, Klinik für Neurochirurgie, Berlin, Deutschland
  • Sebastian Major - Charité - Universitätsmedizin Berlin, Klinik für Neurologie, Berlin, Deutschland
  • Nils Hecht - Charité - Universitätsmedizin Berlin, Klinik für Neurochirurgie, Berlin, Deutschland
  • Peter Vajkoczy - Charité - Universitätsmedizin Berlin, Klinik für Neurochirurgie, Berlin, Deutschland
  • Johannes Woitzik - Charité - Universitätsmedizin Berlin, Klinik für Neurochirurgie, Berlin, Deutschland

Deutsche Gesellschaft für Neurochirurgie. 69. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), Joint Meeting mit der Mexikanischen und Kolumbianischen Gesellschaft für Neurochirurgie. Münster, 03.-06.06.2018. Düsseldorf: German Medical Science GMS Publishing House; 2018. DocP217

doi: 10.3205/18dgnc557, urn:nbn:de:0183-18dgnc5578

Veröffentlicht: 18. Juni 2018

© 2018 Schumm et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Objective: Spreading depolarization (SD) occurs in high frequency in patients with malignant hemispheric stroke (MHS) and is coupled to different hyperaemic or hypoaemic blood flow responses. Body temperature is a major trigger for SDs and influences the accompanied flow coupling. Here, we investigated neurovascular coupling and occurrence of SD during systemic hypo- and hyperthermia in a later phase of experimental cerebral ischemia.

Methods: Permanent focal ischemia was performed by distal occlusion of the left middle cerebral artery (MCA) in adult, male C57BL/6 mice. Twenty-four hours after MCA occlusion, SD was generated with the potassium-chloride method. During SD, systemic hypothermia (34±1°C) or hyperthermia (38±1°C) was induced and the neurovascular response was measured by continuous laser speckle perfusion imaging. Infarction progression was evaluated by sequential MRI. Four study groups were analysed: control group without SD, SD with potassium chloride, SD with hypothermia and SD with hyperthermia.

Results: 24 hours after stroke onset we observed 0.2±0.3 SD/hour with a mean duration of 1.7±0.6 minutes. An increase of SD duration was observed in hypothermia (3.3±1.3 min; *p<0.05), as well as in hyperthermia (3.1±0.9 min; *p<0.05). Neurovascular coupling during hyperthermia was associated with a reduced cerebral blood flow increase and a shorter hyperperfusion phase (*p<0.05). Repetitive induction of SD significantly increased the stroke volume (11.6±28.4mm3; *p<0,05). In contrast, infarct progression was prevented by systemic hypothermia (1.0±2.8 mm3).

Conclusion: Systemic temperature changes have a relevant impact on late SD occurrence, the associated CBF response and secondary infarct progression.