Literature DB >> 21987627

Ghrelin attenuates gastrointestinal epithelial damage induced by doxorubicin.

Mohamed A Fahim1, Hazem Kataya, Rkia El-Kharrag, Dena Am Amer, Basel al-Ramadi, Sherif M Karam.   

Abstract

AIM: To examine the influence of ghrelin on the regenerative potential of gastrointestinal (GI) epithelium.
METHODS: Damage to GI epithelium was induced in mice by two intravenous injections of doxorubicin (10 and 6 mg/kg). Some of the doxorubicin-treated mice received a continuous subcutaneous infusion of ghrelin (1.25 μg/h) for 10 d via implanted mini-osmotic pumps. To label dividing stem cells in the S-phase of the cell cycle, all mice received a single intraperitoneal injection of 5'-bromo-2'-deoxyuridine (BrdU) one hour before sacrifice. The stomach along with the duodenum were then removed and processed for histological examination and immunohistochemistry using anti-BrdU antibody.
RESULTS: The results showed dramatic damage to the GI epithelium 3 d after administration of chemotherapy which began to recover by day 10. In ghrelin-treated mice, attenuation of GI mucosal damage was evident in the tissues examined post-chemotherapy. Immunohistochemical analysis showed an increase in the number of BrdU-labeled cells and an alteration in their distribution along the epithelial lining in response to damage by doxorubicin. In mice treated with both doxorubicin and ghrelin, the number of BrdU-labeled cells was reduced when compared with mice treated with doxorubicin alone.
CONCLUSION: The present study suggests that ghrelin enhances the regenerative potential of the GI epithelium in doxorubicin-treated mice, at least in part, by modulating cell proliferation.

Entities:  

Keywords:  Gastro-intestinal mucosal damage; Gastrointestinal cell proliferation; Ghrelin

Mesh:

Substances:

Year:  2011        PMID: 21987627      PMCID: PMC3181446          DOI: 10.3748/wjg.v17.i33.3836

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  31 in total

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