Protective/restorative role of the adipose tissue-derived mesenchymal stem cells on the radioiodine-induced salivary gland damage in rats

Author:

Saylam Güleser1,Bayır Ömer1,Gültekin Salih Sinan2,Pınarlı Ferda Alparslan3,Han Ünsal4,Korkmaz Mehmet Hakan5,Sancaktar Mehmet Eser6,Tatar İlkan7,Sargon Mustafa Fevzi7,Tatar Emel Çadallı1

Affiliation:

1. University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital , Department of Otolaryngology , Head and Neck Surgery , Ankara , Turkey

2. University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital , Department of Nuclear Medicine , Ankara , Turkey

3. University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital , Department of Stem Cell and Genetic Diagnostic Center , Ankara , Turkey

4. University of Health Sciences, Dışkapı Yıldırım Beyazıt Training and Research Hospital , Department of Pathology , Ankara , Turkey

5. Yıldırım Beyazıt University, Faculty of Medicine , Department of Otolaryngology , Head and Neck Surgery , Ankara , Turkey

6. Ministry of Health, Samsun Training and Reseach Hospital , Department of Otolaryngology , Head and Neck Surgery , Samsun , Turkey

7. Hacettepe University, Faculty of Medicine , Department of Anatomy , Ankara , Turkey

Abstract

Abstract Background To analyze protective/regenerative effects of adipose tissue-derived mesenchymal stem cells (ADMSC) on 131I-Radioiodine (RAI)-induced salivary gland damage in rats. Materials and Methods Study population consisted of controls (n:6) and study groups (n:54): RAI (Group 1), ADMSC (Group 2), amifostine (Group 3), RAI+amifostine (Group 4), concomitant RAI+ADMSC (Group 5) and RAI+ADMSC after 48 h (Group 6). We used light microscopy (LM), transmission electron microscopy (TEM), and salivary gland scintigraphy (SGS), and analyzed data statistically. Results We observed the homing of ADMSC in salivary glands at 1st month on LM. RAI exposure affected necrosis, periductal fibrosis, periductal sclerosis, vascular sclerosis and the total sum score were in a statistically significant manner (P < 0.05). Intragroup comparisons with LM at 1st and 6th months revealed statistically significant improvements in Group 6 (P < 0.05) but not in Groups 4 and 5. Intergroup comparisons of the total score showed that Groups 4 and 5 in 1st month and Group 6 in 6th month had the lowest values. TEM showed vacuolization, edema, and fibrosis at 1st month, and an improvement in damage in 6th month in Groups 5 and 6. SGSs revealed significant differences for the maximum secretion ratio (Smax) (P = 0.01) and the gland-to-background ratio at a maximum count (G/BGmax) (P = 0. 01) at 1st month, for G/BGmax (P = 0.01), Smax (P = 0.01) and the time to reach the maximum count ratio over the time to reach the minimum count (Tmax/Tmin) (P = 0.03) at 6th month. 1st and 6th month scans showed differences for Smax and G/BGmax (P = 0.04), but not for Tmax/Tmin (p > 0.05). We observed a significant deterioration in gland function in group 1, whereas, mild to moderate deteriorations were seen in protective treatment groups. Conclusions Our results indicated that ADMSC might play a promising role as a protective/regenerative agent against RAI-induced salivary gland dysfunction.

Publisher

Walter de Gruyter GmbH

Subject

Radiology Nuclear Medicine and imaging,Oncology

Reference28 articles.

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