Radiation induced cell loss in rat submandibular gland and its relation togland function

Citation
Ljw. Zeilstra et al., Radiation induced cell loss in rat submandibular gland and its relation togland function, INT J RAD B, 76(3), 2000, pp. 419-429
Citations number
41
Categorie Soggetti
Experimental Biology
Journal title
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
ISSN journal
09553002 → ACNP
Volume
76
Issue
3
Year of publication
2000
Pages
419 - 429
Database
ISI
SICI code
0955-3002(200003)76:3<419:RICLIR>2.0.ZU;2-S
Abstract
Purpose: To understand early and late radiation-induced loss of function of the submandibular gland, changes in cell number were documented and correl ated with data on gland function. Modulation of the radiation effect by sia logogues was used to investigate possible mechanisms of action. Materials and methods: Rats were irradiated with a single dose of 15 Gy of X-rays after pre-treatment with either saline, the muscarinic receptor agon ists methacholine or pilocarpine, the adrenergic receptor agonist phenyleph rine or methacholine plus phenylephrine. Before and 1-240 days after irradi ation, submandibular saliva Row rate was measured. At the same time points and from comparable animals submandibular glands were carefully extirpated, weighed and prepared for light microscopic examination. Results: Soon after irradiation (< 30 days) no significant loss of cells wa s observed, whereas the gland function was severely compromized. Sialogogue pre-treatment attenuated the radiation-induced loss of gland function. At later intervals a considerable loss of acinar cells and to a lesser extent loss of granular convoluted tubule cells were observed. Gland function subs equently declined slowly. Pre-treatment with sialogogues gave transient pro tection against cell loss and loss of gland function. Conclusions: The lack of cell loss observed soon after irradiation indicate s that the observed reduction in gland function was caused by a compromised functioning of the acini. The later loss of cells is probably due to death of cells that normally proliferate, leading to a further reduced secretory capacity. Protection of gland morphology and function by sialogogues at la ter rimes must therefore involve resistance of progenitor cells to radiatio n-induced cell death.