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Chapter 2. Prehension

Chapter 2. Prehension

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<strong>Chapter</strong> 5 - Movement Before Contact 177<br />

provides a hypothesis that lesions in parietal Area 7 could disconnect<br />

visual and somatosensory information critical for patterning of visually<br />

goal-directed movements. It is assumed that this disconnection of vi-<br />

sual and somatosensory information, and the associated distortions in<br />

sensorimotor transformations prevent alignment of the visual and pro-<br />

prioceptive maps of opposition space.<br />

Somatosensory processing through the dorsal roots of the spinal<br />

cord is essential for grip formation, as has been demonstrated with<br />

deafferentations of the arm. Experimental monkeys with dorsal root<br />

sections show a corresponding loss of grip formation (Liu &<br />

Chambers, 1971; cited by Jeannerod, 1986). Dorsal column input has<br />

been implicated as essential for proprioceptive guidance of movements<br />

to achieve ‘tactile foveation’ in pad opposition. Glendinning and col-<br />

leagues examined stumptail macaques (Macaca artoides) before and<br />

after lesions of the fasciculus cuneatus (Glendinning, Cooper, Vierck,<br />

& Leonard, 1992). For the first two weeks following surgery, mon-<br />

keys neglected the affected hand, and did not use it for climbing, lo-<br />

comotion, support, foraging, scratching or grooming. Gross arm and<br />

finger movement returned gradually over the next few months, but the<br />

monkeys retained a ‘wrist-drop’ posture, with abduction and hypoto-<br />

nia of the fingers. They were unable to perform pad opposition in the<br />

same way postoperatively. prior to surgery, the monkey approached<br />

small food objects with a highly consistent grip formation. The fin-<br />

gertips formed a small grip aperture during approach, and pad opposi-<br />

tion between the index and thumb was obtained through a multiarticu-<br />

lar pattern whereby the proximal joint flexed and the distal interpha-<br />

langeal (DIP) joint of the index finger extended to align with the op-<br />

position vector, directly through the object into the thumb pad.<br />

Videotape analysis of kinematics, and grasp outcome postoperatively<br />

revealed alterations in grip formation: either excessive or not enough<br />

finger opening, with flexion about all joints of the fingers, a marked<br />

contrast to the DIP extension at contact preoperatively. All the mon-<br />

keys used the table surface to help grasp items with fingers in opposi-<br />

tion to the palm because they were unable to oppose the thumb and<br />

forefinger successfully. Vierck (1975, 1982) had earlier revealed<br />

permanent deficits in orientation of the hand during approach and<br />

grasp of an object using pad opposition, but had not captured the<br />

kinematic changes in grip formation. These results implicate kines-<br />

thetic sensory information in the planning and execution of grip for-<br />

mation, prior to tactile contact with the object.<br />

For the interested reader, excellent reviews of the neural<br />

mechanisms in reaching and grasping are provided in the following

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