Dear Users
This Thursday (4-5 pm in YNiC) there will be a talk by Dr Aneurin
Kennerley from the University of Sheffield.
http://www.sheffield.ac.uk/psychology/staff/research/aneurin-kennerley
The title of Dr Kennerley's talk is "Concurrent 7T fMRI and 2-D Optical
Imaging Spectroscopy: Towards building a forward model between neuronal
activity and the BOLD signal". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Functional magnetic resonance imaging (fMRI) has become the cornerstone
of cognitive neuroscience in recent years. The widely used Blood
Oxygenation Level Dependent (BOLD) signal is often used to interpret
changes in neuronal activation. However, at present, a biophysical
understanding of the neurovascular drivers of the BOLD signal is not
clear and thus hinders any quantitative estimation of the underlying
neuronal activity.
Neuroimaging research at the University of Sheffield drives towards
building a forward biophysical model of this complex relationship. As
part of this multidisciplinary group my research is aimed at developing
a general model of the BOLD signal which can model both intra- and
extra- vascular MR signals, across a wide range of imaging parameters,
from estimates of the haemodynamic changes.
Validation and refinement of the haemodynamic response models underlying
fMRI signals, an essential precondition for the correct interpretation
of human BOLD data requires invasive multimodal animal imaging. I have
developed an innovative in-vivo methodology for concurrent fMRI and 2D
optical imaging spectroscopy (2D-OIS) techniques for simultaneous
measurement of BOLD signal and underlying haemoglobin changes to
neuronal activation in the healthy rodent model.
Applications of this technology include: 1) Understanding of the
negative BOLD signal (Boorman et al 2010). Most researchers assume a
negative BOLD to be a result of either neuronal inhibition or vascular
steal. It is only with the simultaneous, independent measurement of
haemoglobin changes (with 2D-OIS) that one could disassociate any
possible physiological relationships; 2) Refinement of mathematical and
biophysical models of both the BOLD signal and optical imaging
spectroscopy techniques (Kennerley et.al. 2009); 3) Calibration of
non-BOLD fMRI techniques such as VASO and ASL; 4) Interpretation of
abnormal BOLD responses; specifically in disease and trauma conditions
in which either neuronal or haemodynamic breakdown could be responsible.
[1] Boorman, L.W. et.al. (2010) /Journal of Neuroscience/. /30(12):
4285-94;/ [2] Kennerley, A.J. et.al (2009) /NeuroImage 47:1608-1619/;
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Dr. Rebecca E. Millman
Science Liaison Officer
York Neuroimaging Centre
The Biocentre
York Science Park
Heslington
YO10 5DG
Tel: +44 (0) 1904 567614
Fax: +44 (0) 1904 435356