The Effect of Different Routes of Injection of Bone Marrow Mesenchymal Stem Cells on Parotid Glands of Rats Receiving Cisplatin: A Comparative Study.
- Author:
Eman HANY
1
;
Mohammed A SOBH
;
Mazen T ABOU ELKHIER
;
Heba M ELSABAA
;
Ahmed R ZAHER
Author Information
- Publication Type:Comparative Study ; Original Article
- Keywords: Parotid gland; Chemotherapy; Bone marrow; Stem cells; Transmission electron microscopy; Immunohistochemistry
- MeSH: Animals; Bone Marrow*; Cisplatin*; Drug Therapy; Immunohistochemistry; Iron; Mesenchymal Stromal Cells*; Microscopy, Electron, Transmission; Parotid Gland*; Proliferating Cell Nuclear Antigen; Rats*; Rats, Sprague-Dawley; Salivary Glands; Stem Cells
- From:International Journal of Stem Cells 2017;10(2):169-178
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND AND OBJECTIVES: Cisplatin is a powerful antitumor chemotherapeutic agent that is widely used in the treatment of many cancers but it has many side effects on many organs including salivary glands. Bone marrow is considered to be a rich environment that comprises many types of stem cells of which BMSCs (Bone marrow mesenchymal stem cells) are the most studied with potentiality to differentiate into many cell types. This study was conducted to evaluate the effect of different routes of injection of BMSCs on parotid glands of rats receiving cisplatin. METHODS AND RESULTS: Sprague-Dawley rats were divided into 3 groups: a negative control group receiving phosphate buffered saline, a positive control group receiving cisplatin, and an experimental group where rats received cisplatin and then received iron oxide-labeled BMSCs by either intravenous or intraparotid routes or both. Animals were sacrificed at periods of 3,6,10 and 15 days after cisplatin injection, then histological, ultrastructural and immunohistochemical studies were done. The experimental stem cell treated group showed better histological features and increased PCNA proliferation index when compared to the control. The systemic and combination groups showed better results than the local group. Iron oxide-labeled cells were detected with Prussian blue stain. CONCLUSIONS: This study proved that BMSCs can improve cisplatin induced cytotoxicity in parotid glands. Systemic administration showed to have a better effect than local intraparotid administration and comparable effect to combined administration.
