Masticatory rhythm in intracellular potential of trigeminal motoneurons induced by stimulation of orbital cortex and amygdala in cats
Masticatory rhythm in intracellular potential of trigeminal motoneurons induced by stimulation of orbital cortex and amygdala in cats
复制标题
刺激猫眶皮层和杏仁核诱导的三叉神经元细胞内电位的咀嚼节律
DOI:
10.1016/0006-8993(78)90738-2
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发表时间:
1978
期刊:
影响因子:
2.9
通讯作者:
Yoshihiro Kubo
中科院分区:
文献类型:
--
作者:
Yasuhisa Nakamura;Yoshihiro Kubo
Fig. 1. Centrally induced masticatory rhythm in jaw-closer motoneurons. AD were obtained from the same cat. A and C: EMG recorded from right masseteric (top) and right anterior digastric muscles (middle) and jaw movement (bottom) induced by repetitive stimulation of left orbital gyrus (40/sec, 0.3 msec in duration, 6 V)(A) and of left lateral amygdaloid nucleus (40/see, 0.3 msec, 6 V)(C). Bars with arrows in C indicate periods of complete biting (a and b) and tonic clenching (c). B and D: intracellular records from a left jaw-closer motoneuron of rhythmical potential evoked by stimulation of orbital gyrus (B) and lateral amygdaloid nucleus on the left side (D). B and D were recorded after immobilization of the animal by application of the same stimulation as in A and C, respectively. Broken lines in B and D represent resting intracellular potential level (--56 mV). The jaw-closer motoneuron shown in B and D was identified by monosynaptic EPSPs and spike potentials evoked by stimulation of left trigeminal mesencephalic nucleus (1/sec, 0.1 msec, 4 V, two shocks in 2 msec interval) and by short-latency IPSPs evoked by left inferior alveolar nerve stimulation (1/sec, 0.03 msec, 7 V), as shown respectively in E and F, in which records consist of 5 superimposed traces. GK-intracellular responses of another jaw-closer motoneuron to stimulation of left orbital gyrus (40/sec, 0.3 msec, 8 V) in an immobilized cat. Broken lines in GK show resting potential level (--53 mV). H and I: records in a faster sweep and a higher gain of parts marked by upper horizontal bars in G. Upward arrows in H and I indicate gradual increase in the second hyperpolarizing potential. J and K: superimposed successive records in a still faster sweep and a higher gain of parts marked by lower horizontal bars in G. In J, intracellular potential level shifted gradually in depolarizing direction from resting level as indicated by upward arrow and then in hyperpolarizing direction as shown by downward arrow; in K, intracellular potential level shifted in depolarizing direction from bottom to top traces as shown by upward arrow. Upward arrow below J indicates approximate time of peak of second hyperpolarizing potential. Spike potentials in D and HK are truncated. Upward arrows in AD and G and downward arrow in G indicate onset and cessation of repetitive stimulation, respectively. Dots in H and I indicate time of stimulus application. Voltage calibrations of 400/~ V and 1 mV in A apply respectively to top and middle records in A and C. Upper (CL) and lower (OP) horizontal bars in bottom records of A and C represent respectively closed and maximal opening position of the mandible. Time bases in B and F apply respectively to AD and E and F; voltage calibrations in B and F apply respectively to B, D and E, F. Time bases and voltage calibrations in I and K apply respectively to H, I and J, K.