Level D· Scientific groundwork from lab and animal studiesLaboratory StudyPubMedOpen access

Protective/restorative Role of the Adipose Tissue-derived Mesenchymal Stem Cells on the Radioiodine-induced Salivary Gland Damage in Rats.

Saylam G., Bayır Ö., Gültekin SS., Pınarlı FA., Han Ü., Korkmaz MH.

Laboratory Study, published in Radiol Oncol (2017) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Laboratory Study
Journal
Radiol Oncol (2017)
Country
Poland
Reported sample size
—
Source database
PubMed
PMID
28959167
PMCID
PMC5611995
DOI
10.1515/raon-2017-0022
Citations
11

Abstract (original English)

To analyze protective/regenerative effects of adipose tissue-derived mesenchymal stem cells (ADMSC) on 131 I-Radioiodine (RAI)-induced salivary gland damage in rats. 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. We observed the homing of ADMSC in salivary glands at 1 st 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 1 st and 6 th 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 1 st month and Group 6 in 6 th month had the lowest values. TEM showed vacuolization, edema, and fibrosis at 1 st month, and an improvement in damage in 6 th 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 1 st month, for G/BGmax ( P = 0.01), Smax ( P = 0.0

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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