IMAGING
TECHNOLOGIES
Director:
Dr. Stanley Fricke
One of the major obstacles
in translating interventions in animal models of CNS injury to future human
applications is the inability to follow changes in the CNS over time after injury
and in response to interventions. These resources are expensive in terms of
both equipment and expertise. This NCARRN provides core access to state-of-the-art
imaging, including access to expertise in designing, executing and analyzing
imaging experiments and will also provide technical assistance in gathering
pilot data.
Animal
Imaging: Magnetic Resonance Imaging
Functional magnetic imaging (fMRI) provides a novel means for following anatomical
reorganization longitudinally in vivo after injury and to define the contribution
of specific remodeling to the recovery of function observed. Investigators will
have the opportunity to use somatosensory fMRI on rat brain as a means for characterizing
plasticity after spinal cord injury and for assessing treatment outcomes. Images
are acquired on site using a 7.0 Tesla small animal magnetic resonance imaging
system (Bruker Bio-Spin, Billerica, MA). Anatomic MRI sequence protocols in
general terms consist of: (1) those which most favor the display of anatomic
resolution across the brain and spinal cord (T1-type TURBO-RARE protocol after
the administration of MnCl2), and (2) those which most favor the display of
iron-oxide content hypointensity (T2-like Gradient Echo-Fast Imaging Sequence
after the administration of MnCl2)
Animal Imaging:
MRI visualization of iron-oxide microsphere labeled neural stem cells in vivo
Our recent work (see Figure) demonstrates that MRI can be used in vitro and
in vivo to identify individual iron oxide labeled neural stem cells. Phase and
fluorescence microscopy performed after high resolution MRI confirms the iron-microsphere
label within an individual cell. MRI can be used in vivo after spinal cord injury
and transplantation to track aggregates of such cells near and at a distance
from sites of injury in both hemisection and contusion injury models. Specific
capabilities on site include: high field MRI and spectroscopy for small animal
studies using a 7.0 Tesla Bruker Bio-Spin system (Billerica, MA). This system
is housed in the Department of Neuroscience at Georgetown University and is
fully available to investigators under the NCARRN.
| RESEARCH
OPPORTUNITIES & RESOURCES |
The Small Animal Imaging
NMR Laboratory (SAIL) has extensive laboratory space in the basement of the
Research Building at Georgetown University with a main magnet room, an operators?
area, a well-equipped electronics workshop, an animal surgery, a large office
area and storage areas. The main magnet room houses a 7.0 Tesla horizontal bore
magnet (300 MHz 1H) interfaced with a Bruker spectrometer/imager running Paravision
2.1. The animal surgery unit is equipped with rodent ventilators, inhalation
anesthesia apparatus (halothane and isoflurane), infusion pumps, thermostatically
controlled heating pads, recovery humidicribs, stereotaxic devices, a blood-gas
machine, MacLab physiological monitoring of blood pressure and temperature,
as well as various surgical instruments. A separate ventilator and anesthesia
apparatus, including non-magnetic heating blankets, are dedicated for use in
the magnet room. Physiological monitoring is performed using Luxtron fluroptic
probes and respiration monitors. Dr. Stanley Fricke is the director of SAIL.
Dr. Fricke is a nuclear physicist specializing in imaging. The SAIL performs
MRI on animals that weigh less than 500 gm. Participating faculty will use the
animal MRI for studies in CNS trauma, degeneration and disease that involve
brain chemistry and morphology. The research projects as part of the NCARRN
will conduct studies with the advice and participation of Dr. Fricke.
A research-dedicated 3.0
Tesla Siemens (Erlangen, Germany) Trio whole-body MRI system with EPI (echo
planar imaging) capability is located in the Center for Functional and Molecular
Imaging (CFMI), Georgetown University Medical Center, and is available to NCARRN
participants. The gradient system has 40mT/m maximum strength with a slew-rate
of 200T/m/sec. The RF-system includes 8 parallel receiver channels each with
a 1MHz bandwidth. The Trio is also equipped with the iPAT technology (similar
to SENSE from Philips) that can be used to reduce susceptibility artifacts around
the base of the brain without increasing SAR (specific absorption ratio). The
facilities also includes 2 robot manipulators (one planar - for elbow and shoulder
studies and one wrist manipulator) that will be used for studies of motor recovery
following stroke (both to quantitatively measure recovery and also for robot-assisted
therapy). The idea is to carefully characterize the nature of the motor recovery
(assessed with the robots) in relation to neural change (measured with fMRI).
See Center
for Functional and Molecular Imaging website a GU
Last Revised 24-Aug-06 09:24 AM.
|