✍ Scribed by Ana F. Soares; Francisco J. Viega; Rui A. Carvalho; John G. Jones
No coin nor oath required. For personal study only.
Hepatic glycogen synthesis from intact hexose (direct pathway) relative to that from gluconeogenic precursors (indirect pathway) was quantified in ad libitum‐fed rats. Following ^2^H~2~O administration and overnight feeding, the livers were removed and glycogen ^2^H‐enrichment was measured by ^2^H NMR. Six controls and six rats rendered hyperglycemic by streptozotocin (STZ; fasting blood glucose = 385 ± 31 mg/dl) were studied. The indirect pathway contribution, estimated as glycogen hydrogen 5 relative to hydrogen 2 enrichment, was 54% ± 4% for control rats—similar to values from healthy, meal‐fed humans. In STZ‐treated rats, the indirect pathway contribution was significantly higher (68% ± 4%, P < 0.05 vs. controls), similar to that of Type 1 diabetic (T1D) patients. In conclusion, sources of hepatic glycogen synthesis in rats during ad libitum nocturnal feeding were quantified by analysis of glycogen enrichment from ^2^H~2~O. STZ caused alterations resembling the pathophysiology of hepatic glycogen synthesis in T1D patients. Magn Reson Med 61:1–5, 2009. © 2008 Wiley‐Liss, Inc.
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