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Beneficial effects of Etanercept on experimental necrotizing enterocolitis
Authors:Sadık Yurttutan  Ramazan Ozdemir  Fuat Emre Canpolat  Mehmet Yekta Oncel  Hatice Germen Unverdi  Bülent Uysal  Ömer Erdeve  Ugur Dilmen
Affiliation:1. Neonatal Intensive Care Unit, Zekai Tahir Burak Maternity Teaching Hospital, 06110, Hamam?nü/Ankara, Turkey
2. Division of Neonatology, Department of Pediatrics, In?nü University School of Medicine, Malatya, Turkey
3. Department of Pathology, Ankara Etlik Ihtisas Training and Research Hospital, Ankara, Turkey
4. Department of Physiology, Gulhane Military Medical Academy, Ankara, Turkey
5. Division of Neonatology, Department of Pediatrics, Ankara University School of Medicine, Ankara, Turkey
6. Department of Pediatrics, Y?ld?r?m Beyaz?t University School of Medicine, Ankara, Turkey
Abstract:

Purpose

Tissue damage in necrotizing enterocolitis (NEC) of infants occurs as a result of an uncontrolled inflammatory response. The aim of this study was to investigate any potential anti-inflammatory effects that Etanercept may have on the inflammatory response in an experimental NEC model in newborn rats.

Methods

Newborn pups were randomized into three groups immediately after birth (Control, NEC + Placebo and NEC + Etanercept). Pups in the NEC + Placebo and NEC + Etanercept groups were subjected to an NEC-inducing protocol (hypercarbia, hypothermia and hyperoxia) twice a day for 3 days. Pups in the NEC + Etanercept group were given an intraperitoneal injection of Etanercept. Rats were harvested for biochemical and histopathological examinations.

Results

The histopathological injury score of rats in the NEC + Placebo group was significantly higher compared to the NEC + Etanercept and Control groups (p < 0.05 for both comparisons). Tissue levels of tumor necrosis factor-α, interleukin-1β, and malondialdehyde were higher in the placebo group compared to the Etanercept group.

Conclusion

Our results suggest that Etanercept attenuates intestinal tissue damage in NEC by reducing inflammation and blocking the production of free-oxygen radicals, while also reducing tissue levels of tumor necrosis factor-α and interleukin-1β.
Keywords:
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