Effect of cadmium chloride and Cd-metallothionein on the nervous tissue culture

1983 ◽  
Vol 16 (1-2) ◽  
pp. 95-101 ◽  
Author(s):  
Sugawara Naoki ◽  
Aoshima Keiko ◽  
Kasuya Minoru
2020 ◽  
Vol 189 ◽  
pp. 110040 ◽  
Author(s):  
Patricia Azevedo ◽  
Nicole Pavan Butolo ◽  
Luciano Delmondes de Alencar ◽  
Hellen Maria Soares-Lima ◽  
Victor Ribeiro Sales ◽  
...  

1996 ◽  
Vol 122 (1) ◽  
pp. 728-730
Author(s):  
Yu. V. Bobryshev ◽  
S. A. Dambinova ◽  
N. G. Pavlova ◽  
N. N. Konstantinova ◽  
O. V. Pavlov ◽  
...  

1998 ◽  
Vol 29 (1-2) ◽  
pp. 173
Author(s):  
D.D. Orlovskaya ◽  
V.M. Buravlev ◽  
N.A. Uranova

1969 ◽  
Vol 14 (6) ◽  
pp. 607-615 ◽  
Author(s):  
A. Ghadirian

The addicting influence of morphine sulfate on the nervous tissue of new-born rabbits and puppies was studied by using the tissue culture technique. Certain low concentrations of morphine seemed to stimulate the growth of the cells as mitosis and proliferation increased. Nerve cells subjected to morphine sulfate developed increasing tolerance and physical dependence, which was tested through the processes of exposure to higher concentrations of morphine sulfate, withdrawal and reintroduction of this drug to the tissue cultures. Symbols in Figures MS: morphine sulfate DIV: days in vitro T.T.: number of test tubes RMS: reintroduction of morphine sulfate


Author(s):  
Adrian F. van Dellen

The morphologic pathologist may require information on the ultrastructure of a non-specific lesion seen under the light microscope before he can make a specific determination. Such lesions, when caused by infectious disease agents, may be sparsely distributed in any organ system. Tissue culture systems, too, may only have widely dispersed foci suitable for ultrastructural study. In these situations, when only a few, small foci in large tissue areas are useful for electron microscopy, it is advantageous to employ a methodology which rapidly selects a single tissue focus that is expected to yield beneficial ultrastructural data from amongst the surrounding tissue. This is in essence what "LIFTING" accomplishes. We have developed LIFTING to a high degree of accuracy and repeatability utilizing the Microlift (Fig 1), and have successfully applied it to tissue culture monolayers, histologic paraffin sections, and tissue blocks with large surface areas that had been initially fixed for either light or electron microscopy.


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