Changes in Spontaneous Neuronal Firing in Cerebellum Red Nucleus and Raphe Nuclear Complex During Convulsive Activity

Author(s):  
Augusto Fernández-Guardiola ◽  
Carlos M. Contreras ◽  
Jose M. Calvo ◽  
Fructuoso Ayala ◽  
Simon Brailowsky ◽  
...  
2000 ◽  
Vol 163 (1) ◽  
pp. 253-263 ◽  
Author(s):  
L. Ciranna ◽  
F. Licata ◽  
G. Li Volsi ◽  
F. Santangelo
Keyword(s):  

2016 ◽  
Vol 110 ◽  
pp. 29-36 ◽  
Author(s):  
Yoshihide Satoh ◽  
Ken’Ichi Ishizuka ◽  
Mutsumi Takahashi ◽  
Shin-ichi Iwasaki

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Kathleen Ruchalski ◽  
Gasser M. Hathout

The midbrain represents the uppermost portion of the brainstem, containing numerous important nuclei and white matter tracts, most of which are involved in motor control, as well as the auditory and visual pathways. Notable midbrain nuclei include the superior and inferior colliculus nuclei, red nucleus, substantia nigra, oculomotor nuclear complex, and trochlear nucleus. In addition, white matter tracts include the brachium conjunctivum, medial and lateral lemniscus, spinothalamic tracts, and the fiber tracts within the cerebral peduncles. Although neurologically vital, many of these small midbrain nuclei and white matter tracts are not easily individually identified on neuroimaging. However, given their diverse functions, midbrain pathology often leads to distinct clinical syndromes. A review and understanding of the location and relationships between the different midbrain nuclei and fiber tracts will allow more precise correlation of radiologic findings with patient pathology and symptomatology. Particular syndromes associated with midbrain pathology include the Weber, Claude, Benedikt, Nothnagel, and Parinaud syndromes. The oculomotor and trochlear cranial nerves also reside at this level. An understanding of their functions as well as their projected courses from the midbrain towards the eye allows identification of distinct locations which are particularly vulnerable to pathology.


Author(s):  
R H. Selinfreund ◽  
A. H. Cornell-Bell

Cellular electrophysiological properties are normally monitored by standard patch clamp techniques . The combination of membrane potential dyes with time-lapse laser confocal microscopy provides a more direct, least destructive rapid method for monitoring changes in neuronal electrical activity. Using membrane potential dyes we found that spontaneous action potential firing can be detected using time-lapse confocal microscopy. Initially, patch clamp recording techniques were used to verify spontaneous electrical activity in GH4\C1 pituitary cells. It was found that serum depleted cells had reduced spontaneous electrical activity. Brief exposure to the serum derived growth factor, IGF-1, reconstituted electrical activity. We have examined the possibility of developing a rapid fluorescent assay to measure neuronal activity using membrane potential dyes. This neuronal regeneration assay has been adapted to run on a confocal microscope. Quantitative fluorescence is then used to measure a compounds ability to regenerate neuronal firing.The membrane potential dye di-8-ANEPPS was selected for these experiments. Di-8- ANEPPS is internalized slowly, has a high signal to noise ratio (40:1), has a linear fluorescent response to change in voltage.


Author(s):  
Eva B. Krammer ◽  
Martin F. Lischka ◽  
Thomas P. Egger ◽  
Maria Riedl ◽  
Helmut Gruber

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