Characterization of Intrinsic Optical Signal during Spreading Depolarization

2018 ◽  
Vol 08 (01) ◽  
Author(s):  
Zelong Zheng ◽  
Zhikai Cao ◽  
Jinbiao Luo ◽  
Jianping Lv
2016 ◽  
Vol 36 (12) ◽  
pp. 2051-2057 ◽  
Author(s):  
Edgar Santos ◽  
Fiorella León ◽  
Humberto Silos ◽  
Renan Sanchez-Porras ◽  
C William Shuttleworth ◽  
...  

The aim was to characterize the effects of magnesium sulfate, using i.v. bolus and local administration, using intrinsic signal imaging, and on electrocorticographic activity during the induction and propagation of spreading depolarizations in the gyrencephalic porcine brain. Local application of magnesium sulfate led to a complete inhibition of spreading depolarizations. One hour after washing out the topical magnesium sulfate, re-incidence of the spreading depolarizations was observed in 50% of the hemispheres. Those spreading depolarizations showed attenuation in hemodynamic characteristics and speed in intrinsic optical signal imaging. The electrical amplitude decreased through electrocorticographic activity. Intravenous magnesium therapy showed no significant effects on spreading depolarization incidence and characteristics.


2016 ◽  
Vol 37 (5) ◽  
pp. 1706-1719 ◽  
Author(s):  
Michael Johannes Schöll ◽  
Edgar Santos ◽  
Renan Sanchez-Porras ◽  
Modar Kentar ◽  
Markus Gramer ◽  
...  

Haemodynamic responses to spreading depolarizations (SDs) have an important role during the development of secondary brain damage. Characterization of the haemodynamic responses in larger brains, however, is difficult due to movement artefacts. Intrinsic optical signal (IOS) imaging, laser speckle flowmetry (LSF) and electrocorticography were performed in different configurations in three groups of in total 18 swine. SDs were elicited by topical application of KCl or occurred spontaneously after middle cerebral artery occlusion. Movement artefacts in IOS were compensated by an elastic registration algorithm during post-processing. Using movement-compensated IOS, we were able to differentiate between four components of optical changes, corresponding closely with haemodynamic variations measured by LSF. Compared with ECoG and LSF, our setup provides higher spatial and temporal resolution, as well as a better signal-to-noise ratio. Using IOS alone, we could identify the different zones of infarction in a large gyrencephalic middle cerebral artery occlusion pig model. We strongly suggest movement-compensated IOS for the investigation of the role of haemodynamic responses to SDs during the development of secondary brain damage and in particular to examine the effect of potential therapeutic interventions in gyrencephalic brains.


2001 ◽  
Vol 73 (3) ◽  
pp. 351-364 ◽  
Author(s):  
VERA M. FERNANDES-DE-LIMA ◽  
JOÃO E. KOGLER ◽  
JOCELYN BENNATON ◽  
WOLFGANG HANKE

The brain is an excitable media in which excitation waves propagate at several scales of time and space. ''One-dimensional'' action potentials (millisecond scale) along the axon membrane, and spreading depression waves (seconds to minutes) at the three dimensions of the gray matter neuropil (complex of interacting membranes) are examples of excitation waves. In the retina, excitation waves have a prominent intrinsic optical signal (IOS). This optical signal is created by light scatter and has different components at the red and blue end of the spectrum. We could observe the wave onset in the retina, and measure the optical changes at the critical transition from quiescence to propagating wave. The results demonstrated the presence of fluctuations preceding propagation and suggested a phase transition. We have interpreted these results based on an extrapolation from Tasaki's experiments with action potentials and volume phase transitions of polymers. Thus, the scatter of red light appeared to be a volume phase transition in the extracellular matrix that was caused by the interactions between the cellular membrane cell coat and the extracellular sugar and protein complexes. If this hypothesis were correct, then forcing extracellular current flow should create a similar signal in another tissue, provided that this tissue was also transparent to light and with a similarly narrow extracellular space. This control tissue exists and it is the crystalline lens. We performed the experiments and confirmed the optical changes. Phase transitions in the extracellular polymers could be an important part of the long-range correlations found during wave propagation in central nervous tissue.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Zsigmond Benkő ◽  
Kinga Moldován ◽  
Katalin Szádeczky-Kardoss ◽  
László Zalányi ◽  
Sándor Borbély ◽  
...  

2007 ◽  
Vol 424 (2) ◽  
pp. 133-138 ◽  
Author(s):  
Zhen Wang ◽  
Pengcheng Li ◽  
Weihua Luo ◽  
Shangbin Chen ◽  
Qingming Luo

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