The use of tetrazolium salts in the histochemical demonstration of succinic dehydrogenase activity in plant tissues

1968 ◽  
Vol 14 (1) ◽  
pp. 81-88 ◽  
Author(s):  
P. B. Gahan ◽  
M. Kalina
Keyword(s):  
Dehydrogenase Activity ◽  
Succinic Dehydrogenase ◽  
Histochemical Demonstration ◽  
Plant Tissues ◽  
Succinic Dehydrogenase Activity ◽  
Tetrazolium Salts

scholarly journals NONOSMIOPHILIC TETRAZOLIUM SALTS THAT YIELD OSMIOPHILIC, LIPOPHOBIC FORMAZANS FOR ULTRASTRUCTURAL LOCALIZATION OF DEHYDROGENASE ACTIVITY

1972 ◽  
Vol 20 (9) ◽  
pp. 685-695 ◽  
Author(s):  
MOSHE KALINA ◽  
ROBERT E. PLAPINGER ◽  
YOSHINOBU HOSHINO ◽  
ARNOLD M. SELIGMAN
Keyword(s):  
Dehydrogenase Activity ◽  
Osmium Tetroxide ◽  
Succinic Dehydrogenase ◽  
Ultrastructural Localization ◽  
Nitroblue Tetrazolium ◽  
Tetrazolium Salt ◽  
Succinic Dehydrogenase Activity ◽  
Tetrazolium Chloride ◽  
Tetrazolium Salts ◽  
Cytochemical Demonstration

Monotetrazolium salts were designed and prepared which incorporate a phthalhydrazide moiety to make them lipophobic and a benzothiazole moiety to make them react with osmium tetroxide after they are reduced to the corresponding formazans. The tetrazolium salts themselves do not react with osmium tetroxide under the conditions used for the cytochemical demonstration of enzyme activities. Although all of the new formazans, when dissolved in dimethylformamide, were reoxidized to the tetrazolium salts by osmium tetroxide, they were not reoxidized by osmium tetroxide when they were dissolved in tetrahydrofuran or precipitated by reduction in tissue, but gave dark complexes. One of the tetrazolium salts, 2-(2'-benzothiazolyl)-5-styryl-3-(4'-phthalhydrazidyl) tetrazolium chloride (BSPT), was readily reduced by succinic dehydrogenase activity, gave a formazan which produced a dark osmium complex relatively rapidly and gave good localization of succinic dehydrogenase activity on the membranes of mitochondria of rat myocardial cells. Although this tetrazolium salt (BSPT) was not photoreduced by fresh cells of Elodea to stain chloroplasts as seen with nitroblue tetrazolium or distyryl nitroblue tetrazolium, the 5-p-nitrophenyl derivative of BSPT was photoreduced by chloroplasts. The preparation of BSPT and its use in demonstrating succinic dehydrogenase activity ultracytochemically is given here. The preparation and ultracytochemical use of the 5-p-nitrophenyl derivative in chloroplasts will be published later.

scholarly journals UBIQUINONE AND PHOSPHOLIPIDS AS LIMITING FACTORS IN THE HISTOCHEMICAL DEMONSTRATION OF SUCCINIC DEHYDROGENASE ACTIVITY

1967 ◽  
Vol 15 (2) ◽  
pp. 79-82 ◽  
Author(s):  
MOSHE WOLMAN ◽  
JOSE JAIME BUBIS
Keyword(s):  
Dehydrogenase Activity ◽  
Succinic Dehydrogenase ◽  
Histochemical Demonstration ◽  
Mouse Kidney ◽  
Limiting Factors ◽  
Succinic Dehydrogenase Activity ◽  
Similar Treatment ◽  
Kidney Liver ◽  
Cryostat Sections ◽  
Long Storage

Deposition of ubiquinone and preferably of a crude phospholipid mixture and ubiquinone on cryostat sections of mouse kidney, liver and heart increased the intensity of staining for succinic dehydrogenase. A similar treatment partly restored the activity of this enzyme which was reduced by exposure to 60°C, long storage at 37°C, oxidation and treatment with lipid solvents. The restoration was present only in the case of mild noxious treatments. It is suggested that removal or structural alteration of ubiquinone and phospholipids may limit the rate of dehydrogenase activity; more drastic treatments affect the enzyme itself so that these factors cannot exert any restorative activity.

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