scholarly journals Glycine Metabolism

1966 ◽  
Vol 241 (1) ◽  
pp. 206-209
Author(s):  
Sigrid M. Klein ◽  
Richard D. Sagers
Keyword(s):  
1990 ◽  
Vol 80 (3) ◽  
pp. 487-491 ◽  
Author(s):  
David J. Oliver ◽  
Michel Neuburger ◽  
Jacques Bourguignon ◽  
Roland Douce

1967 ◽  
Vol 242 (2) ◽  
pp. 301-305 ◽  
Author(s):  
Sigrid M. Klein ◽  
Richard D. Sagers
Keyword(s):  

2011 ◽  
Vol 107 (11) ◽  
pp. 1635-1644 ◽  
Author(s):  
Isabelle D. Kalmar ◽  
Martin W. A. Verstegen ◽  
Klaus Maenner ◽  
Jurgen Zentek ◽  
Godelieve Meulemans ◽  
...  

N,N-dimethylglycine (DMG) is a tertiary amino acid that naturally occurs as an intermediate metabolite in choline-to-glycine metabolism. The objective of the present trial was to evaluate tolerance, safety and bioaccumulation of dietary DMG in broilers when supplemented at 1 g and 10 g Na-DMG/kg. A feeding trial was conducted using 480 1-d-old broiler chicks that were randomly allocated to twenty-four pens and fed one of three test diets added with 0, 1 or 10 g Na-DMG/kg during a 39 d growth period. Production performance was recorded to assess tolerance and efficacy of the supplement. At the end of the trial, toxicity was evaluated by means of haematology, plasma biochemistry and histopathology of liver, kidney and heart (n12), whereas bioaccumulation was assessed on breast meat, liver, blood, kidney and adipose tissue (n8). Carcass traits were similar between the control and 1 g Na-DMG/kg feed groups (P>0·05), but the feed:gain ratio was significantly improved at 1 g Na-DMG/kg feed compared with the control or the 10-fold dose (P = 0·008). Histological examinations showed no pathological effects and results of haematology and plasma biochemistry revealed similar values between the test groups (P>0·05). Bioaccumulation occurred at the 10-fold dose, but the resulting DMG content in breast meat was comparable with, for instance, wheat bran and much lower than uncooked spinach. In conclusion, DMG at 1 g Na-DMG/kg improved the feed:gain ratio in broilers without DMG being accumulated in consumer parts. Furthermore, dietary supplementation with DMG up to 10 g Na-DMG/kg did not induce toxicity or impaired performance in broilers.


2015 ◽  
Vol 171 ◽  
pp. 26-31 ◽  
Author(s):  
Azhar Alhasawi ◽  
Zachary Castonguay ◽  
Nishma D. Appanna ◽  
Christopher Auger ◽  
Vasu D. Appanna

1985 ◽  
Vol 77 (2) ◽  
pp. 374-378 ◽  
Author(s):  
Michal Neeman ◽  
Dvora Aviv ◽  
Hadassa Degani ◽  
Esra Galun

2013 ◽  
Vol 32 (2) ◽  
pp. 95-103 ◽  
Author(s):  
Joanna L. Mulligan

Nonketotic hyperglycinemia (NKH) is an autosomal recessive inborn error of glycine metabolism. In this article, I will present the case of baby girl S. who presented to the emergency room on Day 4 of life with severe lethargy, seizures, and respiratory depression requiring mechanical ventilation. A diagnosis of NKH was made secondary to elevated plasma and cerebrospinal fluid glycine concentrations. I will review the pathophysiology of NKH, methods of diagnosis, and the differential diagnosis. There are a variety of different pharmacologic and alternative therapies for NKH. Despite these treatments, the prognosis for infants with NKH is poor, with severe neurologic impairment, intractable seizures, and death common before 5 years of age. I will address the role of the advanced practice nurse in caring for an infant with NKH including clinical, educational, and research implications.


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