The objective of the Core unit is to provide continued high quality analytical support for the metabolic studies in the PERC.
This aim can be achieved efficiently and in a cost-effective way, by having a centralized Core facility utilized by a number of investigators. This is particularly necessary for stable isotope and mass spectrometry, because of the complicated nature of methods and the high cost of purchasing and maintaining the necessary equipment. Over the past several years, all of these objectives have been successfully achieved. The Core Metabolism Laboratories have had a major impact on the productivity and the quality of research of various investigators in the PERC. The GC-MS Laboratory has developed new innovative stable isotope methods for the study of metabolism in the pregnant subject and the newborn infants. Analytical techniques for the following stable isotope labelled substrates are established in our laboratories: glucose, urea, alanine, leucine, lysine, serine and glycine, lactate, palmitic acid, glycerol, and ketones. All of the methods are now routine analysis. In addition, the analytical technique for the measurement of 13C enrichment of blood bicarbonate has been refined. A more recent addition has been the quantitative analysis of a-keto acids of branched-chain amino acids on GC-MS & HPLC. These techniques were important in order to measure the precursor pool enrichment for quantifying protein synthesis. Services provided will include sample analysis, help in interpretation, supervision and consultation. The Core is also responsible for the maintenance and adequate functioning of the sophisticated analytical instruments. All of the metabolism protocols utilizing stable isotope tracers will use the Core Laboratory.

Project Start
Project End
Budget Start
Budget End
Support Year
19
Fiscal Year
1996
Total Cost
Indirect Cost
Koontz, M B; Gunzler, D D; Presley, L et al. (2014) Longitudinal changes in infant body composition: association with childhood obesity. Pediatr Obes 9:e141-4
Kalhan, Satish C; Marczewski, Susan E (2012) Methionine, homocysteine, one carbon metabolism and fetal growth. Rev Endocr Metab Disord 13:109-19
Kim, Jaeyeon; Saidel, Gerald M; Kalhan, Satish C (2008) A computational model of adipose tissue metabolism: evidence for intracellular compartmentation and differential activation of lipases. J Theor Biol 251:523-40
Durnwald, Celeste; Huston-Presley, Larraine; Amini, Saied et al. (2004) Evaluation of body composition of large-for-gestational-age infants of women with gestational diabetes mellitus compared with women with normal glucose tolerance levels. Am J Obstet Gynecol 191:804-8
Okereke, Ndubueze C; Uvena-Celebrezze, Jennifer; Hutson-Presley, Larraine et al. (2002) The effect of gender and gestational diabetes mellitus on cord leptin concentration. Am J Obstet Gynecol 187:798-803
Catalano, P M; Kirwan, J P (2001) Maternal factors that determine neonatal size and body fat. Curr Diab Rep 1:71-7
Uvena-Celebrezze, J; Catalano, P M (2000) The infant of the woman with gestational diabetes mellitus. Clin Obstet Gynecol 43:127-39
Catalano, P M; Huston, L; Amini, S B et al. (1999) Longitudinal changes in glucose metabolism during pregnancy in obese women with normal glucose tolerance and gestational diabetes mellitus. Am J Obstet Gynecol 180:903-16
Lewy, V D; Danadian, K; Arslanian, S (1999) Determination of body composition in African-American children: validation of bioelectrical impedence with dual energy X-ray absorptiometry. J Pediatr Endocrinol Metab 12:443-8
Kalhan, S C; Rossi, K Q; Gruca, L L et al. (1998) Relation between transamination of branched-chain amino acids and urea synthesis: evidence from human pregnancy. Am J Physiol 275:E423-31

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