Long-term dexamethasone treatment diminishes store-operated Ca entry in salivary acinar cells.
10.1038/s41368-018-0031-0
- Author:
Yuichiro KUSUDA
1
;
Yusuke KONDO
2
;
Yuta MIYAGI
1
;
Takashi MUNEMASA
1
;
Yusuke HORI
1
;
Fumiko AONUMA
1
;
Shintaro TSUKA
1
;
Taro MUKAIBO
1
;
Chihiro MASAKI
1
;
Ryuji HOSOKAWA
1
Author Information
1. Division of Oral Reconstruction and Rehabilitation, Kyushu Dental University, Kitakyushu, Fukuoka, 803-8580, Japan.
2. Division of Oral Reconstruction and Rehabilitation, Kyushu Dental University, Kitakyushu, Fukuoka, 803-8580, Japan. r07kondo@fa.kyu-dent.ac.jp.
- Publication Type:Journal Article
- MeSH:
Acinar Cells;
drug effects;
metabolism;
Animals;
Calcium;
metabolism;
Calcium Signaling;
drug effects;
Carbachol;
pharmacology;
Dexamethasone;
therapeutic use;
Mice;
Muscarinic Agonists;
pharmacology;
Saliva;
metabolism;
Salivation;
drug effects;
Submandibular Gland;
drug effects;
metabolism
- From:
International Journal of Oral Science
2019;11(1):1-1
- CountryChina
- Language:English
-
Abstract:
Corticosteroids are used in the treatment of many diseases; however, they also induce various side effects. Dexamethasone is one of the most potent corticosteroids, and it has been reported to induce the side effect of impaired salivary gland function. This study aimed to evaluate the effects of dexamethasone on mouse submandibular gland function to gain insight into the mechanism of dexamethasone-induced salivary hypofunction. The muscarinic agonist carbachol (CCh) induced salivary secretion and was not affected by short-term dexamethasone treatment but was decreased following long-term dexamethasone administration. The expression levels of the membrane proteins Na-K-2Cl cotransporter, transmembrane member 16A, and aquaporin 5 were comparable between the control and long-term dexamethasone treatment groups. The CCh-induced increase in calcium concentration was significantly lower in the presence of extracellular Ca in the long-term dexamethasone treatment group compared to that in the control group. Furthermore, CCh-induced salivation in the absence of extracellular Ca and Ca ionophore A23187-induced salivation was comparable between the control and long-term dexamethasone treatment groups. Moreover, salivation induced by the Ca-ATPase inhibitor thapsigargin was diminished in the long-term dexamethasone treatment group. In summary, these results demonstrate that short-term dexamethasone treatment did not impair salivary gland function, whereas long-term dexamethasone treatment diminished store-operated Ca entry, resulting in hyposalivation in mouse submandibular glands.
