-transparent.png){kind=logo}
1. Inhibitory post-synaptic potentials evoked by adequate stimulation of group Ia muscle spindle afferents of homonymous and synergistic muscles and by selective electrical stimulation of tendon organ afferents were analysed in motoneurones of triceps surae and plantaris. 2. Selective activation of Ia afferents was verified to occur with brief stretches of triceps surae and plantaris 35 micrometer or less in amplitude with an initial muscle tension of 5 N; stretches of 30--35 micrometer were estimated to activate 80--90% of Ia afferents in these muscles. Under the same conditions the lowest thresholds for group Ib tendon organ afferents were about 40 micrometer. 3. Stretches less than or equal to 30 micrometer evoked i.p.s.p.s in 80% of triceps surae and plantaris motoneurones; lowest thresholds for evoking i.p.s.p.s wef triceps surae and plantaris motoneurones; lowest thresholds for evoking i.p.s.p.s were 10 micrometer or less. However, such low thresholds for stretch-evoked i.p.s.p.s, lower than the thresholds for activation of Ib afferents, were found mainly in spinalized, unanaesthetized (after decerebration) or lightly anaesthetized animals. The latencies of these i.p.s.p.s indicated disynaptic and trisynaptic coupling between Ia afferents and motoneurones. The i.p.s.p.s were evoked (i) from the homonymous and synergistic muscles stretched together, (ii) from the homonymous muscles alone and (iii) from the synergistic muscles alone. 4. Control experiments showed that i.p.s.p.s could be evoked by stretches sub-threshold for discharging motoneurones, thus showing that those i.p.s.p.s were not mediated by Renshaw cells. The stretch-evoked i.p.s.p.s disappeared after sectioning the nerves from the corresponding muscles, further excluding their mediation by afferents other than group Ia afferents from thf stretched muscle. 5. In order to selectively activate tendon organ afferents, thresholds for excitation of Ia afferents by electrical stimuli were increased to a level above the threshold for Ib afferents by prolonged muscle vibration (Coppin, Jack & MacLennan, 1970). I.p.s.p.s evoked by stimuli near threshold for Ib afferents appeared with latencies indicating disynaptic coupling. Later (trisynaptic) components of Ib i.p.s.p.s required somewhat stronger stimuli. 6. Amplitudes of Ia i.p.s.p.s evoked by muscle stretches activating about 80% of muscle spindle afferents were compared with amplitudes of Ib i.p.s.p.s due to less than 50% of tendon organ afferents of the same muscles. The Ia i.p.s.p.s were much smaller (16--35%) than the Ib i.p.s.p.s. The amplitudes of such Ia and Ib i.p.s.p.s constituted about 10 and 25--66%, respectively, of the maximal i.p.s.p.s evoked by electrical stimulation of all group I afferents. 7. We conclude that inhibition of motoneurones may be evoked from Ia muscle spindle afferents from homonymous and synergistic muscles as well as from Ib tendon organ afferents...
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
July 1981,
The Journal of physiology,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
July 1981,
The Journal of physiology,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
September 1989,
The Journal of physiology,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
April 1980,
Neuroscience letters,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
December 1981,
The Journal of physiology,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
October 1957,
Experientia,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
April 1972,
Acta physiologica Scandinavica,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
February 1984,
Neuroscience letters,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
February 1987,
The Journal of physiology,
E E Fetz, and
E Jankowska, and
T Johannisson, and
J Lipski
March 1981,
The Journal of physiology,
