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STAINING PROCEDURE FOR PARAFFIN OF FORMALIN FIXED CENTRAL NERVOUS TISSUE.(PRELIMINARY REPORT) Fujimori Mrsao 1,3 , Narita Minoru 2,3 1Surgical Clinic, Tokyo Univ. Medical School. Surgical. Department 2Pathological Institute, Tokyo Univ. Med. School. Surgical. Department, Izumibashi Hospital 3,Izumibashi Hospital pp.208-214
Published Date 1952/7/1
DOI https://doi.org/10.11477/mf.1406200288
  • Abstract
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Proceding of formalin fixing paraffin sectioned material to perchase for the various const-ructionof central nervous system. I tried a certain particular stain, and was able to get some considerable results. So I report it on this paper.

(I) Staining for axis-cylinder.

a) Silver impregnation for axis-cylinder.

1) Remove paraffin from section and place in;

2) 5% ammoniac iodine potassium solution, half to an hour at 55-60 C grade.

3) 30% formalin for 1 minute.

4) 10% silver nitric acid, 15 minutes at 55-60 C grade.

5) and deoxydation in 20% formalin.

6) 3 times diluted Gros-Schultze's ammo niac silver fluid, 15 minutes at 55-60 C grade.

7) Deoxydation in 20% formalin.

8) And follow the precedent of Bielscho-wsky's method. (Gold chloride etc.) b) Hematoxylin staining for axis-cylinder. This procedure on cut sections of the cerebellum, pons, and of medulla oblon-gata is described, allowing Sargent's he-matoxylin, is worked excellent consequ-ence.

(Ⅱ) Staining for medullary sheath.

I deviced four methods, however, one of what altered of Kulschitzky's method was most available for this purpose.

1) Remove paraffin by xylol.

2) 5% Iron alum, 15 minuites.

3) Kulschitzy's hematoxylin, 20 to 30 minu-tes at 55-60 C grade.

4) Differentiate in lithion-ferricyan potas-sium.

5) Dehydrate and mount.

(III) For Nissl staining

This method should be proceded with original solution of Wrights' was deluted 3 times by Giordano buffer solution, and be differentiated by absolute alcohol.

(IV) Staining for glia fibrils.

a) The manner specialized in using of Mallo-ry's hematoxylin.

1) Of high grade acidfied acetic acid copper solution, an hour to one and half hours at 37 C grade.

2) 0.3% permanganic acid potassium, 30 minuites to an hour.

3) 1.0% oxalic acid, 30 mminuites and place in;

4) Mallory's hematoxylin, 10 hours or over at 37℃ grade.

5) Dehydrate and mount.

b) Method in using of victoriablue. 1) Excessively acidfied saturation acetic acid copper solution, one and half to two hours at 37 C grade.

2) 0.3% permanganic acid potassium, an hour or over.

3) 1.0% oxalic aJid, 30 minuites.

4) 1.0% victoaiablue, 4 to 5 hours or over at 37℃ grade.

5) After the manner of the Weifert's me-thod. (Iodine-iodic potassium solution and anilin-xylol. etc.)


Copyright © 1952, Igaku-Shoin Ltd. All rights reserved.

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