1811 The ipsilateral projection of the mental nerve to the primary somatosensory cortex through the contralateral cerebral cortex in rats

1993 ◽  
Vol 18 ◽  
pp. S198
Author(s):  
Tomio Hayama ◽  
Hisashi Ogawa
2016 ◽  
Vol 116 (4) ◽  
pp. 1795-1806 ◽  
Author(s):  
K. Sathian

Haptic sensing of objects acquires information about a number of properties. This review summarizes current understanding about how these properties are processed in the cerebral cortex of macaques and humans. Nonnoxious somatosensory inputs, after initial processing in primary somatosensory cortex, are partially segregated into different pathways. A ventrally directed pathway carries information about surface texture into parietal opercular cortex and thence to medial occipital cortex. A dorsally directed pathway transmits information regarding the location of features on objects to the intraparietal sulcus and frontal eye fields. Shape processing occurs mainly in the intraparietal sulcus and lateral occipital complex, while orientation processing is distributed across primary somatosensory cortex, the parietal operculum, the anterior intraparietal sulcus, and a parieto-occipital region. For each of these properties, the respective areas outside primary somatosensory cortex also process corresponding visual information and are thus multisensory. Consistent with the distributed neural processing of haptic object properties, tactile spatial acuity depends on interaction between bottom-up tactile inputs and top-down attentional signals in a distributed neural network. Future work should clarify the roles of the various brain regions and how they interact at the network level.


2020 ◽  
Vol 123 (5) ◽  
pp. 1944-1954 ◽  
Author(s):  
Sergey G. Khasabov ◽  
Hai Truong ◽  
Victoria M. Rogness ◽  
Kevin D. Alloway ◽  
Donald A. Simone ◽  
...  

Processing of information related to itch sensation at the level of cerebral cortex is not well understood. In this first single-unit electrophysiological study of pruriceptive cortical neurons, we show that neurons responsive to noxious and pruritic stimulation of the cheek of the face are concentrated in a small area of the dysgranular cortex, indicating that these neurons encode information related to itch and pain.


In the primary somatosensory cortex of the mouse there are approximately 35 cytoarchitectonic units, named ‘barrels’ (Woolsey & Van der Loos 1970), per hemisphere. There are also about 150 similar, but smaller, barrels. Each of the 35 large barrels is held to be the cortical endstation of the projections from one of the similar number of mystacial vibrissae on the animal’s contralateral muzzle. These barrels are arranged in a pattern that is topologically equivalent to the pattern of the whiskers. There are five rows of whiskers and of barrels, named A, B, C, D and E, and four whiskers and barrels that straddle the ends of the rows named α, β, γ and δ. Morphological data obtained from mice (Woolsey & Van der Loos 1970; Van der Loos & Woolsey 1973) together with physiological data obtained from the rat (Welker 1971) contributed to the recognition of the relation between whiskerpad and barrelfield. A whisker and its corresponding barrel bear the same letter-number combination rather as on a chessboard. (For a review, see Van der Loos (1976 b ).)In what follows, analyses referred to are on mice, unless otherwise stated.


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