Changes in the blood serotonin concentration in rabbits during prolonged electrical stimulation of the anterior part of the hypothalamus

1967 ◽  
Vol 63 (5) ◽  
pp. 454-456
Author(s):  
N. L. Vekshina
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Sangjun Lee ◽  
Jimin Park ◽  
Jinuk Kwon ◽  
Dong Hwan Kim ◽  
Chang-Hwan Im

AbstractTransorbital electrical stimulation (tES) has been studied as a new noninvasive method for treating intractable eye diseases by delivering weak electrical current to the eye through a pair of electrodes attached to the skin around the eye. Studies have reported that the therapeutic effect of tES is determined by the effective stimulation of retinal cells that are densely distributed in the posterior part of the retina. However, in conventional tES with a pair of electrodes, a greater portion of the electric field is delivered to the anterior part of the retina. In this study, to address this issue, a new electrode montage with multiple electrodes was proposed for the effective delivery of electric fields to the posterior retina. Electric field analysis based on the finite element method was performed with a realistic human head model, and optimal injection currents were determined using constrained convex optimization. The resultant electric field distributions showed that the proposed multi-channel tES enables a more effective stimulation of the posterior retina than the conventional tES with a pair of electrodes.


The functional organization of the brain of Sepia has been investigated by electrical stimulation. As a result several new divisions of the brain have been made. The pedal ganglion has been shown to consist of four parts: (1) the anterior chromatophore lobes innervating the skin and muscles of the anterior part of the head and arm s; (2) the anterior pedal lobe innervating the arms and tentacles; (3) the posterior pedal lobe innervating the funnel, collar and retractor muscles of the head; (4) the lateral pedal lobes innervating the muscles of the eyes and tissues of the orbits. The palliovisceral (or visceral) ganglion, apart from the magnocellular lobe demonstrated by Young (1939), is shown here to consist of (1) a central palliovisceral lobe innervating the mantle, funnel and viscera ; (2) a pair of lobes innervating the muscles of the fins; (3) a pair of posterior chromatophore lobes innervating the muscles of the chromatophores and skin of the mantle, fin and back of the head; (4) a pair of vasomotor lobes. Because of these new divisions the three main groupings of the suboesophageal neural tissue are now referred to as the anterior, middle and posterior suboesophageal masses corresponding to the old brachial, pedal and palliovisceral divisions. The suboesophageal centres are classified as lower motor centres and intermediate motor centres, depending on the kind of response they give to electrical stimulation and their peripheral connexions. In the supraoesophageal lobes, higher motor centres and silent areas are recognized. The silent areas include the vertical, superior frontal, subvertical, precommissural and dorsal basal lobes. Of the higher motor centres the anterior basal lobe is primarily concerned with the positioning of the head, arms and eyes, particularly during movements involving changes in direction while swimming. Such manoeuvres are brought about by the anterior basal lobe control over the fins and position of the funnel. The posterior basal lobe is here shown to consist of six main divisions: (1) the sub vertical lobe; (2) the dorsal basal lobes; (3) the precommissural lobe; (4) the medial basal lobe; (5) the lateral basal lobe; (6) the interbasal lobe. The medial, lateral and interbasal lobes are higher motor centres. The lateral and medial basal lobes control movements of the chromatophores and skin; the medial basal lobe controls swimming, breathing, fin movements and various visceral functions. The interbasal lobe controls the movements of the tentacles. The optic nerves and the optic lobes, at their periphery, are electrically inexcitable. Electrical stimulation of the centre of the optic lobes evokes all the responses that can be obtained from the other higher m otor centres. The results are discussed in term s of Sanders & Young’s (1940) physiological classification of the brain. A further category intermediate motor centre is recognized. Summary lists of the responses of each lobe are given on pages 516, 520, 525.


In recent years Miller (8) and fulton (6) among other authors have produced valuable reviews of the question of cerebellar function. Of primary importance in investigating cerebellar activity by stimulation of its cortex is the fundamental observation of Sherrington (12) that faradisation of the rostral surface produces ipsilateral inhibition of inhibition of decerebrate rigidity. Latterly this observation has been confirmed and amplified by Bremer (1) and by Miller and Banting (7) among others. Electrical stimulation of the anterior lobe inhibits posture in ipsilateral antigravity muscles augments lobe produces spasticity of antigravity muscles on one or both sides. In the pigeon, Which lacks a pyramidal tract, Bremer and Ley (2) Have obtained similar results by excision of, or by stimulation of, the cerebellar cortes. Pollock and Davis (10) have produced similar results in cats by rendering anæmic the anterior part of the cerebellum at the same time as the precollicular neuraxis. Rademaker's animals, from which the entire cerebellum had been ablated, were observed for many months(11) and throughout that time hypertonicity of antigravity muscles was a prominent feature of their symptoms. More recently, Miller and Laughton (9) have described the result of stimulating, not the cerebellar cortex, but the nuclei themselves, which were exposed by ablation of overlying nerve tissue. We proposed therefore to extend these observations by use of a dead-beat recording mechanism, namely, the Sherrington myograph.


Sign in / Sign up

Export Citation Format

Share Document