When moving objects with a precision grip, fingertip forces normal to
the object surface (grip force) change in parallel with forces tangent
ial to the object (load force). We investigated whether voluntary wris
t actions can affect grip force independent of load force, because the
extrinsic finger muscles cross the wrist. Grip force increased with w
rist angular speed during wrist motion in the horizontal plane, and wa
s much larger than the increased tangential load at the fingertips or
the reaction forces from linear acceleration of the test object. Durin
g wrist flexion the index finger muscles in the hand and forearm incre
ased myoelectric activity; during wrist extension this myoelectric act
ivity increased little, or decreased for some subjects. The grip force
maxima coincided with wrist acceleration maxima, and grip force remai
ned elevated when subjects held the wrist in extreme flexion or extens
ion. Likewise, during isometric wrist actions the grip force increased
even though the fingertip loads remained constant. A grip force ''pul
se'' developed that increased with wrist force rate, followed by a sta
tic grip force while the wrist force was sustained. Subjects could not
suppress the grip force pulse when provided visual feedback of their
grip force. We conclude that the extrinsic hand muscles can be recruit
ed to assist the intended wrist action, yielding higher grip-load rati
os than those employed with the wrist at rest. This added drive to han
d muscles overcame any loss in muscle force while the extrinsic finger
flexors shortened during wrist flexion motion. During wrist extension
motion grip force increases apparently occurred from eccentric contra
ction of the extrinsic linger flexors. The coactivation of hand closin
g muscles with other wrist muscles also may result in part from a gene
ral motor facilitation, because grip force increased during isometric
knee extension. However, these increases were related weakly to the kn
ee force. The observed muscle coactivation, from all sources, may cont
ribute to grasp stability. For example, when transporting grasped obje
cts, upper limb accelerations simultaneously produce inertial torques
at the wrist that must be resisted, and inertial loads at the fingerti
ps from the object that must be offset by increased grip force. The mu
scle coactivation described here would cause similarly timed pulses in
the wrist force and grip force. However, grip-load coupling from this
mechanism would not contribute much to grasp stability when small wri
st forces are required, such as for slow movements or when the object'
s total resistive load is small.