The Evolution of Surface Species in NiW/Al2O3Catalysts in Various Stages of Sulfidation: A Quasiin-SituHigh Resolution Transmission Electron Microscopic Investigation

1998 ◽  
Vol 179 (2) ◽  
pp. 443-450 ◽  
Author(s):  
H.R. Reinhoudt ◽  
A.D. van Langeveld ◽  
P.J. Kooyman ◽  
R.M. Stockmann ◽  
R. Prins ◽  
...  
Keyword(s):  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Surface Species ◽  
Electron Microscopic ◽  
Transmission Electron ◽  
Transmission Electron Microscopic

Morphological Evidence for Reinnervation in the Adult Mammalian Central Nervous System

1977 ◽  
Vol 35 ◽  
pp. 630-631
Author(s):  
R. H. Seall ◽  
R. E. Kingsley
Keyword(s):  
Spinal Cord ◽  
Microscopic Investigation ◽  
Electron Microscopic Investigation ◽  
Morphological Evidence ◽  
Electron Microscopic ◽  
Experimental Procedure ◽  
Regeneration Time ◽  
Transmission Electron ◽  
Transmission Electron Microscopic ◽  
Proximal Stump

It has been shown that the adult mammalian CNS is capable of axonal sprouting and limited regeneration in response to injury, but this regeneration is interrupted by the scar produced in the lesioned area by proliferating glia. Experiments by Barnes and Worrall (1) demonstrated that the proximal stump of a ventral root when grafted to a ganglionectomized dorsal root is capable of reinnervating the spinal cord without interference by the glia, and is capable of forming new functional synapses within the spinal cord. In an effort to provide anatomical verification for this physiological study, we repeated their experimental procedure. A transmission electron microscopic investigation of the spinal cord where the dorsal roots terminate was undertaken in an attempt to identify these reinnervating axons and newly formed synapses. Regeneration time was varied from 8 to 16 weeks. In order to identify reinnervating from normal tissue, the graft was lesioned 3 or 4 days prior to preparation of the spinal cord for electron microscopy.

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