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Abstracts / Clinical Neurophysiology 128 (2017) e1–e163 e161

Materials & methods: 10 healthy participants were stimulated brain—D. Bragin *, O. Bragina, G. Statom, S. Hagberg, E. Nemoto
with either iTBS, cTBS or sham on F3 electrode over 3 different ses- (University of New Mexico School of Medicine, Neurosurgery,
sions. TMS-EEG was used to assess cortical excitability change via Albuquerque, United States)
TMS-evoked potentials (TEPs) and TMS-evoked oscillations.
⇑ Corresponding author.
Results: Analysis on F3 revealed increase in N120 amplitude
(p = .009) from pre to post iTBS. Cluster-based statistics showed
one significant negative cluster at N120 (p = .003), indicating Introduction: We previously showed that pulsed electromagnetic
increased amplitude at the site of stimulation and contralaterally. field (PEMF) increased microvascular blood flow and tissue oxygena-
TBS-induced changes (post - pre) were calculated and compared tion by nitric oxide-induced vasodilation in a healthy rat brain
among different TBS conditions. N120 amplitude post iTBS was high- (Bragin et al., 2015). We also showed that high intracranial pressure
er than cTBS at F3 (p = .042). (ICP) in rats caused a transition from capillary (CAP) to non-nutritive
TMS-evoked oscillations were significantly increased after iTBS in microvascular shunt (MVS) flow, tissue hypoxia and blood brain bar-
theta frequency at F3 from 50 to 250 ms (p = .044). TMS-evoked rier (BBB) degradation (Bragin et al., 2011).
oscillations among different TBS at F3 yielded higher theta power Objectives: To evaluate whether PEMF attenuates the detrimental
after iTBS compared to cTBS and sham (p < .05; Fig. 1). effects of non-nutritive MVS flow induced by high ICP.
Conclusion: This study provides some of the first evidence that TBS Materials and methods: By in vivo 2-photon laser scanning micro-
produces direct changes in cortical excitability in the prefrontal cor- scopy over the rat parietal cortex, we evaluated the effects of
tex. This may be a useful approach to optimise stimulation para- PEMF on microvascular blood flow, tissue oxygenation (NADH),
digms prior to the conduct of clinical trials. BBB permeability (dye extravasation) and neuronal necrosis (i.v. pro-
pidium Iodide) during 4 h of high ICP. Doppler cortical flux, rectal
doi:10.1016/j.clinph.2016.10.414 and cranial temperatures, ICP and arterial pressure, blood gases
and electrolytes were monitored. After baseline imaging at normal
ICP (10 mmHg), rats were subjected to high ICP (30 mmHg) by rais-
P308 ing an artificial cerebrospinal fluid reservoir connected to the cis-
The effects of cerebellar trans-cranial direct current stimulation terna magna. At ICP of 30 mmHg, PEMF was applied for 30 min
on neural network dynamics in supraspinal motor circuits during and imaging continuously performed after the treatment. Controls
motor adaptation in cats—H.T. Darch *, N.L. Cerminara, R. Apps were untreated with PEMF.
(University of Bristol, Bristol, United Kingdom) Results: PEMF decreased tissue hypoxia (NADH reduced by
14.6 ± 3.7% compared to control, n = 10 rats per group,
⇑ Corresponding author. mean ± SEM, p < 0.05). BBB damage progression was reduced as
reflected by less by 17.2 ± 5.4% dye extravasation (p < 0.05).
Recent studies of trans-cranial Direct Current stimulation (tDCS) Decreased by PEMF hypoxia reduced neuronal necrosis (15 ± 3.6%
have raised the possibility that this is a relatively simple and well in PEMF vs. 26 ± 6.2% in control, p < 0.05), consistent with dilation
tolerated method that can be used as an effective therapeutic tool of arterioles (+4.5 ± 3.2%) and an increase in capillary blood flow
to treat neurological and neuropsychiatric disorders (Grimaldir velocity (+4.7 ± 3.2%). PEMF did not completely mitigate the gradual
et al., 2016). In particular, stimulation of the cerebellum (ctDCS) in increase in MVS flow at but, as reflected by MVS/capillary ratio, the
humans has been shown to modulate a wide range of functions, transition to non-nutritive flow was reduced in the PEMF compared
including motor learning and working memory (Grimaldir et al., to the untreated rats (2.3 ± 1.1 and 3.8 ± 2.1% change per hour,
2014). Despite the increasing use of this method, there are still respectively, p < 0.05).
important knowledge gaps and controversies regarding the physio- Conclusions: PEMF
logical effects of ctDCS and the underlying neurobiological basis of reduced tissue hypoxia, BBB degradation and neuronal necrosis by
any effects remains unknown. modulating cerebral blood flow at high ICP. PEMF could be an effec-
We have examined the effects of anodal, and cathodal ctDCS on tive treatment for high ICP after severe cerebral insults.
the electrophysiological activity in the supraspinal motor network Support: Rio Grande Neurosciences.
(SMN) during prism motor adaptation of a skilled, goal-directed
movement in cats. Preliminary frequency domain analysis of the References
local field potential recorded simultaneously in cerebellar cortex
(lobule V, proximal to the ctDCS electrode), primary motor cortex, Bragin et al, J. Neurosurgery, 2015.
Bragin et al, J. Neurotrauma, 2011.
and pre-frontal cortex suggests variable effects of ctDCS on neuronal
population activity and changes in coherence between different sites
doi:10.1016/j.clinph.2016.10.416
in the SMN during motor adaptation.

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Pulsed electromagnetic field (PEMF) improves microcirculation
and reduces hypoxia and neuronal death in a hypertensive rat ⇑ Corresponding author.

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