Topographical representation of peripheral branches of the facial nerve within the facial nucleus: A HRP study in the cat

1978 ◽  
Vol 8 (1) ◽  
pp. 5-8 ◽  
Author(s):  
Mamoru Kume ◽  
Masanori Uemura ◽  
Kojyuro Matsuda ◽  
Ryotaro Matsushima ◽  
Noboru Mizuno
Keyword(s):  
1972 ◽  
Vol 43 (2) ◽  
pp. 662-667 ◽  
Author(s):  
N. Iwata ◽  
S.T. Kitai ◽  
S. Olson
Keyword(s):  

PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0241315
Author(s):  
Joji Kunihiro ◽  
Hiroaki Nabeka ◽  
Hiroyuki Wakisaka ◽  
Kana Unuma ◽  
Md. Sakirul Islam Khan ◽  
...  

Neurotrophic factor prosaposin (PS) is a precursor for saposins A, B, C, and D, which are activators for specific sphingolipid hydrolases in lysosomes. Both saposins and PS are widely contained in various tissues. The brain, skeletal muscle, and heart cells predominantly contain unprocessed PS rather than saposins. PS and PS-derived peptides stimulate neuritogenesis and increase choline acetyltransferase activity in neuroblastoma cells and prevent programmed cell death in neurons. We previously detected increases in PS immunoactivity and its mRNA in the rat facial nucleus following facial nerve transection. PS mRNA expression increased not only in facial motoneurons, but also in microglia during facial nerve regeneration. In the present study, we examined the changes in immunoreactivity of the PS receptors GPR37 and GPR37L1 in the rat facial nucleus following facial nerve transection. Following facial nerve transection, many small Iba1- and glial fibrillary acidic protein (GFAP)-positive cells with strong GPR37L1 immunoreactivity, including microglia and astrocytes, were observed predominately on the operated side. These results indicate that GPR37 mainly works in neurons, whereas GPR37L1 is predominant in microglia or astrocytes, and suggest that increased PS in damaged neurons stimulates microglia or astrocytes via PS receptor GPR37L1 to produce neurotrophic factors for neuronal recovery.


Autoimmunity ◽  
1992 ◽  
Vol 13 (2) ◽  
pp. 117-126 ◽  
Author(s):  
Tomas Olsson ◽  
Per Diener ◽  
Åke Ljungdahl ◽  
Bo Höjeberg ◽  
Peter H. Van Der Meide ◽  
...  

Neurosurgery ◽  
2002 ◽  
Vol 50 (2) ◽  
pp. 355-363 ◽  
Author(s):  
David Choi ◽  
Geoffrey Raisman

ABSTRACT OBJECTIVE After facial nerve repair, involuntary movement of part of the face during voluntary movement of another part of the face is common. We describe an animal model of facial nerve lesion, repair, and regeneration that demonstrates abnormal organization of the facial nucleus; this model may be used to study synkinesis. METHODS In 18 rats, the facial nerve was cut completely, proximal to the parotid gland, and immediately sutured end-to-end. After a period of regeneration of 1 to 10 months, retrograde fluorescence labeling of the distal branches of the facial nerve was performed. The distribution of the tracers in the facial nucleus was assessed in both the lesioned animals and in a nonlesioned group (n = 20). RESULTS In the control animals, muscle groups were somatotopically represented in the facial nucleus. After lesioning, repair, and regeneration, the somatotopy of the facial nucleus was disrupted. Axons projected from the facial nucleus to incorrect peripheral muscle groups, and aberrant branches were observed to simultaneously innervate different subdivisions of the facial nerve. The numbers of aberrant axons and branches did not change significantly during periods of regeneration ranging from 1 to 10 months. CONCLUSION Our model provides a clear demonstration of the failure of adult facial nerve axons to make correct connections with their distal targets during regeneration. This model may be used to assess strategies aimed at minimizing synkinesis and, by assessing histology together with behavior, provides a more robust model than those previously described.


1987 ◽  
Vol 78 (3) ◽  
pp. 283-287 ◽  
Author(s):  
Takahiro Satoda ◽  
Osamu Takahashi ◽  
Takashi Tashiro ◽  
Ryotaro Matsushima ◽  
Masanori Uemura-Sumi ◽  
...  

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