scholarly journals FLUORESCENCE METHODS FOR THE HISTOCHEMICAL DEMONSTRATION OF MONOAMINES. 3. SODIUM BOROHYDRIDE REDUCTION OF THE FLUORESCENT COMPOUNDS AS A SPECIFICITY TEST

1964 ◽  
Vol 12 (8) ◽  
pp. 582-586 ◽  
Author(s):  
HANS CORRODI ◽  
NILS-ÅKE HILLARP ◽  
GÖSTA JONSSON

It has been shown in previous papers that catecholamines and 5-hydroxytryptamine can under certain conditions be converted to highly fluorescent 6,7 - dihydroxy - 3,4 - dihydroisoquinolines and 6-hydroxy-3,4-dihydro-β-carboline respectively, and that this can be used as a highly sensitive and specific method for the histochemical demonstration of the monoamines at the cellular level. In the present paper it is shown that the fluorescent compounds are very readily reduced by sodium borohydride to the corresponding, non-fluorescent 1,2,3,4-tetrahydro-compounds—even if they are present in a non-extractable state in dried serum albumin spots or in tissue sections—and that the fluorescence can be regenerate by renewed formaldehyde treatment. The non-specific fluorescence ( e. g. autofluorescence) in tissue sections was never observed to undergo any changes on borohydride treatment. On the basis of these findings a very simple histochemical test has been worked out to check directly in the tissue section whether or not an observed fluorescence is due to the presence of the reacting monoamines.

1973 ◽  
Vol 21 (4) ◽  
pp. 293-311 ◽  
Author(s):  
KJELL FUXE ◽  
GÖSTA JONSSON

The formaldehyde fluorescence technique is a highly sensitive and specific method for the demonstration of catecholamines (CA) at the cellular level. It permits the demonstration of as little as about 5 x l0–4 pg noradrenaline, present in a single varicosity. The method can also be used for quantitative microfluorimetric studies on the CA stores at the cellular level, although a concentration-dependent quenching of the fluorescence in locations where the CA concentration is very high may impose some limitations. The sensitivity of the technique has been increased by using sections of unembedded tissue from unfixed or formalin-fixed tissue (Hökfelt and Ljungdahl). A glyoxylic acid technique, recently introduced by Axelsson and his co-workers, may prove to be an additional reliable alternative method for the demonstration of CA. Examples of neurobiologic problems that could be approached by using the formaldehyde fluorescence technique are briefly reviewed.


1968 ◽  
Vol 16 (6) ◽  
pp. 419-427 ◽  
Author(s):  
V. J. DESMET ◽  
A.-M. BULLENS ◽  
J. DE GROOTE ◽  
K. P. M. HEIRWEGH

A new technique is presented for the specific histochemical demonstration of conjugated bilirubin in tissue sections, using the diazonium salt of ethylanthranilate. The specificity of this method was proved by using test materials and cholestatic tissue sections. There was no diffusion artifact under the prescribed working conditions. The method is applicable to fresh cryostat sections and frozen sections of cold, formol-calcium-fixed tissues. The method could not be satisfactorily applied for the staining of total bilirubin. The method using 2,4-dichloraniline remains the best available technique for the histochemical demonstration of total bilirubin, while the technique with ethylanthranilate proves to be the most specific method available for the demonstration of conjugated bile pigments.


1965 ◽  
Vol 30 (7) ◽  
pp. 2241-2246 ◽  
Author(s):  
Harold Zinnes ◽  
Roger A. Comes ◽  
Francis R. Zuleski ◽  
Albert N. Caro ◽  
John Shavel

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