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Stop Animal
Exploitation NOW!
S. A. E. N.
"Exposing the truth to wipe
out animal experimentation"

Government Grants Promoting Cruelty to Animals
University of Minnesota, Minneapolis, MN
TIMOTHY J. EBNER - Primate Testing - 2006
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Grant Number: 5R01NS031530-13
Project Title: Encoding of Reach-to-Grasp in the Primary Motor
Cortex
PI Information: PROFESSOR TIMOTHY J. EBNER,
ebner001@tc.umn.edu
Abstract:
The global problem addressed by this proposal is how does the central
nervous system (CNS) control a structure as complex as the primate hand?
To begin to address this question, four Specific Aims are proposed that
address three outstanding issues in the neural control of
reach-to-grasp. The studies will use chronic single unit recordings in
the primary motor cortex (M1) of monkeys trained to perform various
reach-to-grasp movements. Extensive monitoring of arm and hand
kinematics, grasp forces and the activity of arm and extrinsic/intrinsic
muscles of the hand will be done. Statistical and analytical tools
including regression analyses and data reduction techniques will be used
to extract the neural representation of hand shape/object shape,
kinematics, grasp forces and EMG activity. First, findings from
psychophysical, lesion, and electrophysiological studies suggest that
the CNS, at least in part, reduces the number of degrees of freedom by
controlling the hand as a unit. Specific Aims 1 and 2 will address the
hypothesis that neurons in the hand area of M1 encode and control hand
shape/object properties, reflecting this global control of the hand.
Second, early investigations into hand movements categorized prehension
into two broad classes, power and precision grip and more elaborate
classification systems followed. A prediction of these categorical
schemes is that the CNS explicitly controls grasp type. More recent
psychophysical studies, however, suggest that a strict division of hand
posture into power and precision grasps does not occur. Specific Aim 3
will test the alternative hypothesis that power and precision are part
of a continuum of hand postures in which hand shape is primarily
controlled. A third major contemporary hypothesis is that reach and
grasp are controlled by two independent but coupled channels: a
"transport" channel that extracts information about the spatial location
of objects to guide the reach and a "manipulation" channel that extracts
information about the intrinsic properties of the object such as size
and shape to guide hand shape. Although psychophysical results suggest
that the two components are coupled, there is virtually no single unit
data addressing this question. In Specific Aim 4 the hypothesis is
tested that the reach and grasp components are coupled at the neuronal
level in M1. In general understanding how the CNS controls prehension is
a critical step in understanding human movements. In the future
understanding the signals controlling grasp could prove useful for
controlling prosthetic devices in patients with brain injury.
Thesaurus Terms:
arm, hand, limb movement, motor cortex, neural information processing,
psychomotor function biomechanics, body physical characteristic, form
/pattern perception, neuron, visual feedback, visual stimulus, wrist
Macaca mulatta, behavior test, electromyography, histology,
microelectrode, robotics, single cell analysis, stereotaxic technique
Institution: UNIVERSITY OF MINNESOTA TWIN CITIES
450 MCNAMARA ALUMNI CENTER, MINNEAPOLIS, MN 554552070
Fiscal Year: 2006
Department: NEUROSCIENCE
Project Start: 01-JAN-1994
Project End: 30-JUN-2008
ICD: NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
IRG: IFCN
Purkinje Cells Signal Hand Shape and Grasp Force
During Reach-to-Grasp in the Monkey
Carolyn R. Mason*, Claudia M. Hendrix* and Timothy J. Ebner
Department of Neuroscience, University of Minnesota, Minneapolis,
Minnesota
Submitted 11 May 2005; accepted in final form 6 September 2005
J Neurophysiol 95: 144-158, 2006. First published September 14, 2005
Two rhesus monkeys (1 female "G" at 5.2 kg, 1 male "L" at 6.8 kg)
were trained to reach and grasp objects with an overhand grasp using
specified force levels (Ojakangas and Ebner 1992 ). The animals sat in a
primate chair with their heads fixed forward and facing a computer
monitor (Fig. 1A). The animals initiated a trial by placing their hand
on a start-pad located by their side. A "go" cue signaled the animals to
reach ( 15 cm) and grasp the target object. The go cue also indicated
the required grasp force level to be generated and maintained for that
trial. As a result, the monkeys had a priori knowledge of the required
force level before initiating the reach. Once the grasp was initiated, a
red slider bar provided visual feedback of the grasp force being
generated. If the monkeys successfully initiated and maintained the
specified force level for 1.4 s, they received a juice reward. At the
completion of 25 successful trials, the object was changed. The monkeys
were not able to see their hands or the objects. However, before
initiating the first trial of each block, the animals were allowed to
identify the target object through touch. Therefore the animals were
aware of the target object to be used before the initiation of a new
block of trials.
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Please email: TIMOTHY J. EBNER,
ebner001@tc.umn.edu to protest the inhumane use of animals in this
experiment. We would also love to know about your efforts with this
cause:
saen@saenonline.org
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Rats, mice, birds, amphibians and other animals have
been excluded from coverage by the Animal Welfare Act. Therefore research
facility reports do not include these animals. As a result of this
situation, a blank report, or one with few animals listed, does not mean
that a facility has not performed experiments on non-reportable animals. A
blank form does mean that the facility in question has not used covered
animals (primates, dogs, cats, rabbits, guinea pigs, hamsters, pigs,
sheep, goats, etc.). Rats and mice alone are believed to comprise over 90%
of the animals used in experimentation. Therefore the majority of animals
used at research facilities are not even counted.
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