» Articles » PMID: 3962597

Exogenous Silver in Dorsal Root Ganglia, Peripheral Nerve, Enteric Ganglia, and Adrenal Medulla

Overview
Specialty Neurology
Date 1986 Jan 1
PMID 3962597
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Following intraperitoneal (i.p.) or oral administration of silver salts, the anatomic distribution of silver in the peripheral nervous system (PNS) has been studied. The structures examined were dorsal root ganglia, peripheral nerve (N. ischiadicus), enteric ganglia, and adrenal medulla. Four days after an i.p. injection of silver lactate, silver deposits were found in these structures. The silver content remained stable during the observation period (45 days). The localization of silver deposits in the orally treated animals was independent of the administered silver salt (silver nitrate or silver lactate). The silver deposits in neurons and chromaffin cells were located in the cytoplasm. In all organs silver was present in large amounts in connective tissue membranes, macrophage-like cells, vascular basal laminae, and supporting cells. Satellite cells of the dorsal root ganglia were always heavily stained, while less stain was present in Schwann cells of the peripheral nerves. Intracellular deposits were invariably located in lysosomes, whereas extracellular grains were found in connective tissue fibers and basement membranes.

Citing Articles

Elemental biomapping of human tissues suggests toxic metals such as mercury play a role in the pathogenesis of cancer.

Pamphlett R, Bishop D Front Oncol. 2024; 14:1420451.

PMID: 38974240 PMC: 11224479. DOI: 10.3389/fonc.2024.1420451.


Mercury in the human adrenal medulla could contribute to increased plasma noradrenaline in aging.

Pamphlett R, Kum Jew S, Doble P, Bishop D Sci Rep. 2021; 11(1):2961.

PMID: 33536525 PMC: 7858609. DOI: 10.1038/s41598-021-82483-y.


Silver affects viability and structure of cultured mouse peritoneal macrophages and peroxidative capacity of whole mouse liver.

Rungby J, Hultman P Arch Toxicol. 1987; 59(6):408-12.

PMID: 3606385 DOI: 10.1007/BF00316206.


Simultaneous ultrastructural demonstration of heavy metals (silver, mercury) and acid phosphatase.

Thorlacius-Ussing O, Moller Graabaek P Histochem J. 1986; 18(11-12):639-46.

PMID: 3558002 DOI: 10.1007/BF01675299.


Effects of selenium on toxicity and ultrastructural localization of silver in cultured macrophages.

Rungby J, Ellermann-Eriksen S, Danscher G Arch Toxicol. 1987; 61(1):40-5.

PMID: 3439873 DOI: 10.1007/BF00324546.

References
1.
Scott Jr W . Silver uptake in brains of chronically gamma-irradiated rats: a study by neutron activation analysis. Radiat Res. 1967; 31(3):522-8. View

2.
Danscher G, Moller-Madsen B . Silver amplification of mercury sulfide and selenide: a histochemical method for light and electron microscopic localization of mercury in tissue. J Histochem Cytochem. 1985; 33(3):219-28. DOI: 10.1177/33.3.2579122. View

3.
DEMPSEY E, WISLOCKI G . An electron microscopic study of the blood-brain barrier in the rat, employing silver nitrate as a vital stain. J Biophys Biochem Cytol. 1955; 1(3):245-56. PMC: 2223811. DOI: 10.1083/jcb.1.3.245. View

4.
Rungby J, Danscher G . Hypoactivity in silver exposed mice. Acta Pharmacol Toxicol (Copenh). 1984; 55(5):398-401. DOI: 10.1111/j.1600-0773.1984.tb02001.x. View

5.
Nathanson J, Bloom F . Heavy metals and adenosine cyclic 3',5'-monophosphate metabolism: possible relevance to heavy metal toxicity. Mol Pharmacol. 1976; 12(3):390-8. View