scholarly journals Carbamyol phosphate synthetase 1 gene (4217C>A) polymorphism and its relation to low plasma arginine level among preterm with necrotizing enterocolitis; a single center Egyptian study

2018 ◽  
Vol 8 (5) ◽  
Author(s):  
Wesam A Mokhtar
2015 ◽  
Vol 25 (06) ◽  
pp. 520-525 ◽  
Author(s):  
Etienne Suply ◽  
Marc-David Leclair ◽  
Michel Neunlist ◽  
Jean-Christophe Roze ◽  
Cyril Flamant

2007 ◽  
Vol 293 (5) ◽  
pp. G1061-G1067 ◽  
Author(s):  
Carole Rougé ◽  
Clotilde Des Robert ◽  
Alexander Robins ◽  
Olivier Le Bacquer ◽  
Christelle Volteau ◽  
...  

To determine whether circulating citrulline can be manipulated in vivo in humans, and, if so, whether citrulline availability affects the levels of related amino acids, nitric oxide, urinary citrulline, and urea nitrogen, 10 healthy volunteers were studied on 3 separate days: 1) under baseline conditions; 2) after a 24-h treatment with phenylbutyrate (0.36 g·kg−1·day−1), a glutamine “trapping” agent; and 3) during oral l-citrulline supplementation (0.18 g·kg−1·day−1), in randomized order. Plasma, erythrocyte (RBC), and urinary citrulline concentrations were determined by gas chromatography-mass spectrometry at 3-h intervals between 1100 and 2000 on each study day. Regardless of treatment, RBC citrulline was lower than plasma citrulline, with an RBC-to-plasma ratio of 0.60 ± 0.04, and urinary citrulline excretion accounted for <1% of the citrulline load filtered by kidney. Phenylbutyrate induced an ∼7% drop in plasma glutamine ( P = 0.013), and 18 ± 14% ( P < 0.0001) and 19 ± 17% ( P < 0.01) declines in plasma and urine citrulline, respectively, with no alteration in RBC citrulline. Oral l-citrulline administration was associated with 1) a rise in plasma, urine, and RBC citrulline (39 ± 4 vs. 225 ± 44 μmol/l, 0.9 ± 0.3 vs. 6.2 ± 3.8 μmol/mmol creatinine, and 23 ± 1 vs. 52 ± 9 μmol/l, respectively); and 2) a doubling in plasma arginine level, without altering blood urea or urinary urea nitrogen excretion, and thus enhanced nitrogen balance. We conclude that 1) depletion of glutamine, the main precursor of citrulline, depletes plasma citrulline; 2) oral citrulline can be used to enhance systemic citrulline and arginine availability, because citrulline is bioavailable and very little citrulline is lost in urine; and 3) further studies are warranted to determine the mechanisms by which citrulline may enhance nitrogen balance in vivo in humans.


2018 ◽  
Vol 53 (5) ◽  
pp. 914-917 ◽  
Author(s):  
Patricio E. Lau ◽  
Stephanie M. Cruz ◽  
Elena C. Ocampo ◽  
Sushma Nuthakki ◽  
Candace C. Style ◽  
...  

2019 ◽  
Vol 51 (11) ◽  
pp. 1975-1983
Author(s):  
Ismail Selvi ◽  
Halil Basar ◽  
Numan Baydilli ◽  
Koza Murat ◽  
Ozlem Kaymaz

2020 ◽  
Vol 48 (9) ◽  
pp. 030006052095780
Author(s):  
Miao Duan ◽  
Zunhua Han ◽  
Nanqu Huang

Objective To investigate the changes in the diversity and dynamics of intestinal microflora in patients with neonatal necrotizing enterocolitis (NEC) in a single center in China. Methods In this prospective study conducted between 2016 and 2019, feces were collected from 28 neonates with NEC and 30 control neonates to analyze the species richness and Shannon’s diversity index of the bands, which were also sequenced via PCR-denaturing gradient gel electrophoresis. Results The species richness and Shannon’s diversity index were significantly lower in the NEC group than in the control group, indicating that the diversity of intestinal flora was reduced in NEC. The numbers of samples positive for Bacteroides and Klebsiella were higher in the NEC group, whereas Escherichia coli, Bifidobacterium, and Lactobacillus were less frequently detected in patients with NEC than in controls. The prevalence of intestinal bacteria normalized after the resolution of NEC. Conclusion The decrease of intestinal flora diversity in neonates with NEC, especially the decreased prevalence of probiotic bacteria, may be an important factor in the pathogenesis of NEC.


2008 ◽  
Vol 295 (5) ◽  
pp. G1092-G1103 ◽  
Author(s):  
Charlotte R. Bjornvad ◽  
Thomas Thymann ◽  
Nicolaas E. Deutz ◽  
Douglas G. Burrin ◽  
Søren K. Jensen ◽  
...  

Preterm neonates have an immature gut and metabolism and may benefit from total parenteral nutrition (TPN) before enteral food is introduced. Conversely, delayed enteral feeding may inhibit gut maturation and sensitize to necrotizing enterocolitis (NEC). Intestinal mass and NEC lesions were first recorded in preterm pigs fed enterally (porcine colostrum, bovine colostrum, or formula for 20–40 h), with or without a preceding 2- to 3-day TPN period ( n = 435). Mucosal mass increased during TPN and further after enteral feeding to reach an intestinal mass similar to that in enterally fed pigs without TPN (+60–80% relative to birth). NEC developed only after enteral feeding but more often after a preceding TPN period for both sow's colostrum (26 vs. 5%) and formula (62 vs. 39%, both P < 0.001, n = 43–170). Further studies in 3-day-old TPN pigs fed enterally showed that formula feeding decreased villus height and nutrient digestive capacity and increased luminal lactic acid and NEC lesions, compared with colostrum (bovine or porcine, P < 0.05). Mucosal microbial diversity increased with enteral feeding, and Clostridium perfringens density was related to NEC severity. Formula feeding decreased plasma arginine, citrulline, ornithine, and tissue antioxidants, whereas tissue nitric oxide synthetase and gut permeability increased, relative to colostrum (all P < 0.05). In conclusion, enteral feeding is associated with gut dysfunction, microbial imbalance, and NEC in preterm pigs, especially in pigs fed formula after TPN. Conversely, colostrum milk diets improve gut maturation and NEC resistance in preterm pigs subjected to a few days of TPN after birth.


2007 ◽  
Vol 177 (4S) ◽  
pp. 549-549
Author(s):  
Hannes Steiner ◽  
Thomas Akkad ◽  
Christian Gozzi ◽  
Brigitte Springer-Stoehr ◽  
Georg Bartsch

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