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Petersen, Kitt Falk, Gary W. Cline, James B. Blair, and Gerald I. Shulman. between pyruvate and oxaloacetate in awake normal and 3,3â-&triiodo-Lthyronine-treated rats. Am. J. Physiol. 267 (Endocrinol. Metab. 30): E273-E277, 1994.- between pyruvate and oxaloacetate was assessed in awake 24-h fasted normal and triiodothyronine (T&treated rats. After a 20- or 60-min infusion of 13-13C]alanine (99% enriched, 12 mg/min) the 13C enrichments of liver glucose and alanine carbons were analyzed by 1.3Cand lH nuclear magnetic resonance spectroscopy and gas chromatography-mass spectrometry. from phosphoenolpyruvate to pyruvate [via pyruvate kinase (PK)] and from oxaloacetate to pyruvate [via malic enzyme (ME)] relative to the pyruvate carboxylase (PC) flux [i.e., (PK + ME)/PC] was assessed by the ratio of the 13C enrichment of C-2 alanine relative to that in C-5 glucose. In the normal rats (PK + ME)/PC was 0.26 t 0.07 (n = 7, t = 20 min) and 0.37 * 0.08 (n = 4, t = 60 min). In the T3-treated rats the (PK + ME)/PC increased four- to fivefold to 1.03 t 0.19 (n = 8, t = 20 min) and to 1.83 2 0.19 (n = 3, t = 60 min) (P < 0.05 vs. normal rats). The
AJP - Endocrinology and Metabolism – The American Physiological Society
Published: Aug 1, 1994
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