๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The initiation of osteodentin formation in the rat incisor after adriamycin administration

โœ Scribed by Karim, A. C.


Publisher
John Wiley and Sons
Year
1985
Tongue
English
Weight
934 KB
Volume
213
Category
Article
ISSN
0003-276X

No coin nor oath required. For personal study only.

โœฆ Synopsis


In order to study the initiation of osteodentin formation in rat incisors, animals were injected intravenously with adriamycin (5 mg/kg body weight), and killed from 2 to 7 days after injection by perfusion with a 2.5% buffered glutaraldehyde solution. Control animals, injected with only physiological saline, were treated in the same manner.

Three days after adriamycin injection aggregations of mesenchymal cells were observed along the mesial and lateral walls of the pulp chamber. Between 3 days and 7 days osteodentin production was observed at the sites where the mesenchymal aggregations were previously observed. Electron microscopic observations revealed that the cells involved in the aggregates were larger and contained more profiles of rough endoplasmic reticulum and secretion granules than the unaffected pulp cells. The osteodentin matrix first appeared as a scant deposition of collagen fibers between the cells. As more collagen fibers were deposited the matrix became much denser. Some cells that initially formed the mesenchymal aggregates were completely enclosed by the increased deposition of the matrix.

It therefore appears that osteodentin formation, as observed in the rat incisor pulp after adriamycin administration, is the result of an abnormal differentiation of pulp mesenchymal cells.


๐Ÿ“œ SIMILAR VOLUMES


Pharmacokinetics of desethylamiodarone i
โœ Anooshirvan Shayeganpour; Dalia A. Hamdy; Dion R. Brocks ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 124 KB ๐Ÿ‘ 1 views

## Abstract The pharmacokinetics of desethylamiodarone (DEA), the active metabolite of amiodarone (AM), were studied in the rat after administration of AM or preformed metabolite. Rats received 10โ€‰mg/kg of either intravenous or oral AM HCl or DEA base. Blood samples were obtained via a surgically i

Toxicokinetics of chloroethanol in the r
โœ W. Grunow; H. -J. Altmann ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Springer-Verlag ๐ŸŒ English โš– 512 KB

The excretion and tissue distribution of 14C-labelled chloroethanol were studied in rats following single oral administration of 5 and 50 mg/kg body weight. At both dose levels, the radioactivity was rapidly eliminated, mainly in the urine. On the first day after application of 5 mg/kg body weight,