Eszter Farkas

Prof. Eszter Farkas

Department of Medical Physics and Informatics, Faculty of Medicine, University of Szeged, Korányi fasor 9, H-6720 Szeged, Hungary
orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 August 2001 in Progress in Neurobiology
Verified
Journal Article
Closed access
Eszter FarkasEszter Farkas
Eszter Farkas
PLPaul G.M Luiten
Paul G.M Luiten

1 April 2007 in Brain Research Reviews
Verified
Journal Article
Closed access
Eszter FarkasEszter Farkas
Eszter Farkas
PLPaul G.M. Luiten
Paul G.M. Luiten
FBFerenc Bari
Ferenc Bari

21 July 2016 in Journal of Cerebral Blood Flow & Metabolism
Verified
Journal Article
Open access
JHJed A Hartings
Jed A Hartings
CSC William Shuttleworth
C William Shuttleworth
SKSergei A Kirov
Sergei A Kirov
CACenk Ayata
Cenk Ayata
JHJason M Hinzman
Jason M Hinzman
JDJens P Dreier
Jens P Dreier
A modern understanding of how cerebral cortical lesions develop after acute brain injury is based on Aristides Leão’s historic discoveries of spreading depression and asphyxial/anoxic depolarization. Treated as separate entities for decades, we now appreciate that these events define a continuum of spreading mass depolarizations, a concept that is central to understanding their pathologic effects. Within minutes of acute severe ischemia, the onset of persistent depolarization triggers the breakdown of ion homeostasis and development of cytotoxic edema. These persistent changes are diagnosed as diffusion restriction in magnetic resonance imaging and define the ischemic core. In delayed lesion growth, transient spreading depolarizations arise spontaneously in the ischemic penumbra and induce further persistent depolarization and excitotoxic damage, progressively expanding the ischemic core. The causal role of these waves in lesion development has been proven by real-time monitoring of electrophysiology, blood flow, and cytotoxic edema. The spreading depolarization continuum further applies to other models of acute cortical lesions, suggesting that it is a universal principle of cortical lesion development. These pathophysiologic concepts establish a working hypothesis for translation to human disease, where complex patterns of depolarizations are observed in acute brain injury and appear to mediate and signal ongoing secondary damage.

20 July 2016 in Journal of Cerebral Blood Flow & Metabolism
Verified
Journal Article
Closed access
JDJens P Dreier
Jens P Dreier
MFMartin Fabricius
Martin Fabricius
CACenk Ayata
Cenk Ayata
OSOliver W Sakowitz
Oliver W Sakowitz
CSC William Shuttleworth
C William Shuttleworth
JHJed A Hartings
Jed A Hartings
Spreading depolarizations (SD) are waves of abrupt, near-complete breakdown of neuronal transmembrane ion gradients, are the largest possible pathophysiologic disruption of viable cerebral gray matter, and are a crucial mechanism of lesion development. Spreading depolarizations are increasingly recorded during multimodal neuromonitoring in neurocritical care as a causal biomarker providing a diagnostic summary measure of metabolic failure and excitotoxic injury. Focal ischemia causes spreading depolarization within minutes. Further spreading depolarizations arise for hours to days due to energy supply-demand mismatch in viable tissue. Spreading depolarizations exacerbate neuronal injury through prolonged ionic breakdown and spreading depolarization-related hypoperfusion (spreading ischemia). Local duration of the depolarization indicates local tissue energy status and risk of injury. Regional electrocorticographic monitoring affords even remote detection of injury because spreading depolarizations propagate widely from ischemic or metabolically stressed zones; characteristic patterns, including temporal clusters of spreading depolarizations and persistent depression of spontaneous cortical activity, can be recognized and quantified. Here, we describe the experimental basis for interpreting these patterns and illustrate their translation to human disease. We further provide consensus recommendations for electrocorticographic methods to record, classify, and score spreading depolarizations and associated spreading depressions. These methods offer distinct advantages over other neuromonitoring modalities and allow for future refinement through less invasive and more automated approaches.

1 June 2019 in Redox Biology
Verified
Journal Article
Open access
STStefano Tarantini
Stefano Tarantini
MVMarta Noa Valcarcel-Ares
Marta Noa Valcarcel-Ares
PTPeter Toth
Peter Toth
AYAndriy Yabluchanskiy
Andriy Yabluchanskiy
ZTZsuzsanna Tucsek
Zsuzsanna Tucsek
ZUZoltan Ungvari
Zoltan Ungvari
Adjustment of cerebral blood flow (CBF) to neuronal activity via neurovascular coupling (NVC) has an essential role in maintenance of healthy cognitive function. In aging increased oxidative stress and cerebromicrovascular endothelial dysfunction impair NVC, contributing to cognitive decline. There is increasing evidence showing that a decrease in NAD+ availability with age plays a critical role in a range of age-related cellular impairments but its role in impaired NVC responses remains unexplored. The present study was designed to test the hypothesis that restoring NAD+ concentration may exert beneficial effects on NVC responses in aging. To test this hypothesis 24-month-old C57BL/6 mice were treated with nicotinamide mononucleotide (NMN), a key NAD+ intermediate, for 2 weeks. NVC was assessed by measuring CBF responses (laser Doppler flowmetry) evoked by contralateral whisker stimulation. We found that NVC responses were significantly impaired in aged mice. NMN supplementation rescued NVC responses by increasing endothelial NO-mediated vasodilation, which was associated with significantly improved spatial working memory and gait coordination. These findings are paralleled by the sirtuin-dependent protective effects of NMN on mitochondrial production of reactive oxygen species and mitochondrial bioenergetics in cultured cerebromicrovascular endothelial cells derived from aged animals. Thus, a decrease in NAD+ availability contributes to age-related cerebromicrovascular dysfunction, exacerbating cognitive decline. The cerebromicrovascular protective effects of NMN highlight the preventive and therapeutic potential of NAD+ intermediates as effective interventions in patients at risk for vascular cognitive impairment (VCI).

24 February 2022 in Journal of Experimental Medicine
Verified
Journal Article
Open access
PDF file
ECEszter Császár
Eszter Császár
NLNikolett Lénárt
Nikolett Lénárt
CCCsaba Cserép
Csaba Cserép
KZKörnyei Zsuzsanna
Környei Zsuzsanna
RFRebeka Fekete
Rebeka Fekete
ÁDÁdám Dénes
Ádám Dénes
Microglia, the main immunocompetent cells of the brain, regulate neuronal function, but their contribution to cerebral blood flow (CBF) regulation has remained elusive. Here, we identify microglia as important modulators of CBF both under physiological conditions and during hypoperfusion. Microglia establish direct, dynamic purinergic contacts with cells in the neurovascular unit that shape CBF in both mice and humans. Surprisingly, the absence of microglia or blockade of microglial P2Y12 receptor (P2Y12R) substantially impairs neurovascular coupling in mice, which is reiterated by chemogenetically induced microglial dysfunction associated with impaired ATP sensitivity. Hypercapnia induces rapid microglial calcium changes, P2Y12R-mediated formation of perivascular phylopodia, and microglial adenosine production, while depletion of microglia reduces brain pH and impairs hypercapnia-induced vasodilation. Microglial actions modulate vascular cyclic GMP levels but are partially independent of nitric oxide. Finally, microglial dysfunction markedly impairs P2Y12R-mediated cerebrovascular adaptation to common carotid artery occlusion resulting in hypoperfusion. Thus, our data reveal a previously unrecognized role for microglia in CBF regulation, with broad implications for common neurological diseases.