Cortical projections to the red nucleus and the brain stem in the rhesus monkey

2016 ◽  
Vol 1645 ◽  
pp. 28-30 ◽  
Author(s):  
Roger N. Lemon
1967 ◽  
Vol 4 (2-3) ◽  
pp. 151-188 ◽  
Author(s):  
Henricus G.J.M. Kuypers ◽  
Donald G. Lawrence

1947 ◽  
Vol 3 (1) ◽  
pp. 55-67 ◽  
Author(s):  
Marcel Monnier ◽  
George Sander
Keyword(s):  

2014 ◽  
Vol 111 (5) ◽  
pp. 1027-1032 ◽  
Author(s):  
Jing Wu ◽  
Wenchao Wang ◽  
Joshua Dominic Rizak ◽  
Zhengbo Wang ◽  
Jianhong Wang ◽  
...  

Recent developments in neuron recording techniques include the invention of some fragile electrodes. The fragility of these electrodes impedes their successful use in deep brain recordings because it is difficult to penetrate the electrodes through the dura mater, especially the tentorium cerebelli (TC) enclosing the cerebellum and brain stem. This paper reports a new method to pierce the TC for inserting fragile electrodes into the inferior colliculus of rhesus monkeys. Briefly, a unique tool kit, consisting of needles with sharp tips, a guide tube and an “impactor,” was used in a multistep protocol to pierce the TC. The impactor provided a brief force that quickly thrusts the needles through the meninges without causing significant damage to the brain tissue under the TC. Using this novel approach, tetrodes were successfully implanted into the inferior colliculus of a rhesus monkey and neuronal discharge signals were recorded. This method, which is simple, convenient and economical, allows neurophysiologists to study the electrophysiological characteristics of deep brain structures under the TC with advanced, albeit fragile, electrodes.


1983 ◽  
Vol 50 (4) ◽  
pp. 743-769 ◽  
Author(s):  
P. Rudomin ◽  
I. Jimenez ◽  
M. Solodkin ◽  
S. Duenas

The present series of investigations was aimed to disclose the possible sites of action of excitatory and inhibitory inputs on tho-interneuron pathway mediating the primary afferent depolarization (PAD) of group I afferents of extensor muscles in the cat spinal cord. To this end we compared the effects produced by stimulation of segmental and descending pathways on the PAD generated either by stimulation of group I fibers of flexor muscles or by intraspinal microstimulation. It was assumed that under the appropriate conditions the PAD produced by intraspinal microstimulation results from the activation of the last-order interneurons in the PAD pathway and may, therefore, allow detection pathway. The PAD of single group I afferent fibers was determined in barbiturate-anesthetized preparations by measuring the test stimulus current required to maintain a constant probability of antidromic firing. This was achieved by means of a feedback system that continuously adjusted the test stimulus current to the required values. The PAD of individual group Ia gastrocnemius soleus (GS) fibers that is produced by activation of the low-threshold afferents of the posterior biceps and semitendinosus nerve was found to be inhibited by conditioning stimulation of the relatively low-threshold cutaneous fibers and also by stimulation of supraspinal structures such as the ipsilateral brain stem reticular formation, the contralateral red nucleus, and the contralateral pyramidal tract. In contrast, the PAD of group Ia fibers produced by microstimulation applied in the intermediate nucleus could be inhibited only by stimulation of the brain stem reticular formation but not by stimulation of the other descending inputs presently tested or by stimulation of cutaneous nerves. PAD of group Ia fibers was produced also by microstimulation applied within the motor nucleus. However, in most fibers the resulting PAD could not be inhibited either by stimulation of the brain stem reticular formation, the red nucleus, the pyramidal tract, or cutaneous nerves. Stimulation of cutaneous and of flexor muscle nerves of the brain stem reticular formation, the red nucleus, and the pyramidal tract all produced PAD of the group Ib GS fibers.(ABSTRACT TRUNCATED AT 400 WORDS)


1973 ◽  
Vol 64 ◽  
pp. 442-445 ◽  
Author(s):  
Z.A. Tamarova ◽  
A.I. Shapovalov ◽  
L. Vyklicky´

Sign in / Sign up

Export Citation Format

Share Document