Physico-chemical mechanism of the argyrophil I reaction
- 1 January 1982
- journal article
- research article
- Published by Springer Nature in Histochemistry and Cell Biology
- Vol. 74 (3) , 393-407
- https://doi.org/10.1007/bf00493439
Abstract
Kinetic experiments have shown that the argyrophil I reaction (the formation of metallic from ionic silver by reducing groups of the tissues) is a catalytic process. Topochemical considerations, and several reaction kinetic observations, suggest that the semi-conductor properties and the favourable chemical structure of certain sites (catalytic points) of the tissue structure play a fundamental role in the catalysis. The electrochemical half processes in the argyrophil I reaction (i.e., the transformation of tissue-bound reducing groups into their oxidized form and the reduction of silver ions into silver atoms) take place separately in space, while the electrons released in the former half reaction are transported by the semi-conduction bands of the tissue to the catalytic points where the metallic silver grains are formed.Keywords
This publication has 22 references indexed in Scilit:
- Chemical nature of the first products (nuclei) of the argyrophil stainingActa Histochemica, 1980
- Simultaneous determination of the amounts of metallic and ?reducible? silver in histologic specimensHistochemistry and Cell Biology, 1979
- MODIFICATIONS OF THE SILVER METHENAMINE TEST FOR THE ULTRASTRUCTURAL DEMONSTRATION OF CYSTINE-CONTAINING PROTEINSJournal of Histochemistry & Cytochemistry, 1972
- The electron histochemistry of cystine—containing proteins in thin transverse sections of human hairJournal of the Royal Microscopical Society, 1968
- Semiconductive properties of lipids and their possible relationship to lipid bilayer conductivityChemistry and Physics of Lipids, 1968
- THE ELECTRON-HISTOCHEMICAL DEMONSTRATION OF PHOSPHOGLYCERIDEJournal of Histochemistry & Cytochemistry, 1965
- THE HISTOCHEMICAL IDENTIFICATION OF PHOSPHOGLYCERIDES IN MYELINJournal of Neurochemistry, 1963
- SILVER IMPREGNATION OF ULTRATHIN SECTIONS FOR ELECTRON MICROSCOPYThe Journal of cell biology, 1961
- Studies of the Solubility of the Product of Argentaffin and Argyrophil ReactionsJournal of Investigative Dermatology, 1960
- Cholinesterase in the Skin of the Rat, Dog, Cat, Guinea Pig and Rabbit11From the Section of Dermatology and the Section of Pathologic Anatomy, Mayo Clinic and Mayo Foundation, Rochester, Minnesota. This study was supported in part by Public Health Service Grant No. B-1755 (C1)Journal of Investigative Dermatology, 1959