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Protective Effect of Alpha-Lipoic Acid on Salivary Dysfunction in a Mouse Model of Radioiodine Therapy-Induced Sialoadenitisopen access

Authors
Jung, Jung HwaKim, Jin HyunJung, Myeong HeeKim, Seung WonJeong, Bae KwonWoo, Seung Hoon
Issue Date
Jun-2020
Publisher
MDPI
Keywords
alpha lipoic acid; Thyroid; RI; complications; salivary gland
Citation
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.21, no.11, pp 1 - 12
Pages
12
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume
21
Number
11
Start Page
1
End Page
12
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/6583
DOI
10.3390/ijms21114136
ISSN
1661-6596
1422-0067
Abstract
Radioiodine (RI) therapy is known to cause salivary gland (SG) dysfunction. The effects of antioxidants on RI-induced SG damage have not been well described. This study was performed to investigate the radioprotective effects of alpha lipoic acid (ALA) administered prior to RI therapy in a mouse model of RI-induced sialadenitis. Four-week-old female C57BL/6 mice were divided into four groups (n = 10 per group): group I, normal control; group II, ALA alone (100 mg/kg); group III, RI alone (0.01 mCi/g body weight, orally); and group IV, ALA + RI (ALA at 100 mg/kg, 24 h and 30 min before RI exposure at 0.01 mCi/g body weight). The animals in these groups were divided into two subgroups and euthanized at 30 or 90 days post-RI treatment. Changes in salivary Tc-99m pertechnetate uptake and excretion were tracked by single-photon emission computed tomography. Salivary histological examinations and TUNEL assays were performed. The Tc-99m pertechnetate excretion level recovered in the ALA treatment group. Salivary epithelial (aquaporin 5) cells of the ALA + RI group were protected from RI damage. The ALA + RI group exhibited more mucin-containing parenchyma and less fibrotic tissues than the RI only group. Fewer apoptotic cells were observed in the ALA + RI group compared to the RI only group. Pretreatment with ALA before RI therapy is potentially beneficial in protecting against RI-induced salivary dysfunction.
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