Pancreatic enzymes digest obstructive meconium from cystic fibrosis pig intestines
Gopinathan Gangadharan Nambiar, Sussette Gonzalez Szachowicz, Christian F. Zirbes, Jared J. Hill, Linda S. Powers, David K. Meyerholz, Ian M. Thornell, David A. Stoltz, Anthony J. Fischer

TL;DR
Pancreatic enzymes can break down intestinal blockages in newborns with cystic fibrosis, offering a potential non-surgical treatment.
Contribution
The study demonstrates that pancreatic enzymes effectively digest obstructive meconium in a cystic fibrosis pig model.
Findings
Pancreatic enzymes significantly increased pigment release and reduced meconium solids in CF pigs.
N-acetylcysteine worsened digestion, while dithiothreitol had no improvement.
Pancreatic enzymes worked best at neutral pH in isotonic saline.
Abstract
Meconium ileus (MI) is a life-threatening obstruction of the intestines affecting ∼15% of newborns with cystic fibrosis (CF). Current medical treatments for MI often fail, requiring surgical intervention. MI typically occurs in newborns with pancreatic insufficiency from CF. Meconium contains mucin glycoprotein, a potential substrate for pancreatic enzymes or mucolytics. Our study aim was to determine whether pancreatic enzymes in combination with mucolytic treatments dissolve obstructive meconium using the CF pig model. We collected meconium from CF pigs at birth and submerged it in solutions with and without pancreatic enzymes, including normal saline, 7% hypertonic saline, and the reducing agents N-acetylcysteine (NAC) and dithiothreitol (DTT). We digested meconium at 37 °C with agitation, and measured meconium pigment release by spectrophotometry and residual meconium solids by…
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Taxonomy
TopicsCystic Fibrosis Research Advances · Infant Nutrition and Health · Infant Development and Preterm Care
