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FLLL32, a curcumin analog, ameliorates intestinal injury in necrotizing enterocolitis.
Eckert, Jeffrey; Scott, Brian; Lawrence, Shelley M; Ihnat, Michael; Chaaban, Hala.
Afiliação
  • Eckert J; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
  • Scott B; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
  • Lawrence SM; Department of Pediatrics, University of Texas Health Science Center at San Antonio, San Antonio, TX.
  • Ihnat M; Department of Pediatrics, University of California San Diego, San Diego, CA.
  • Chaaban H; Department of Pharmaceutical Sciences, University of Oklahoma, College of Pharmacy, Oklahoma City, OK, USA.
J Inflamm Res ; 10: 75-81, 2017.
Article em En | MEDLINE | ID: mdl-28652797
ABSTRACT

BACKGROUND:

Necrotizing enterocolitis (NEC) is a devastating gastrointestinal disease that primarily affects premature infants. It is characterized by inflammation and leukocyte infiltration that can progress to intestinal necrosis, perforation, systemic inflammatory response, and death. In this study, we examined the effect of FLLL32, a curcumin analog, on an NEC-like neonatal intestinal injury model.

METHODS:

NEC was induced in CD-1 mice pups using the Paneth cell ablation and Klebsiella infection model. Pups were divided into sham, NEC, and NEC + FLLL32 groups. At the end of the experiment, pups were euthanized; whole blood and small intestines were harvested. Intestinal inflammatory cytokine profile, in vivo intestinal permeability using serum fluorescein isothiocyanate-dextran, and histological injury scores were compared between the groups. RESULTS AND

CONCLUSION:

FLLL32-treated pups had lower intestinal injury, improved intestinal permeability, and lower proinflammatory cytokine profiles compared to those in untreated pups with NEC. These results suggest that FLLL32 plays a protective role in NEC.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article