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Am J Physiol Regul Integr Comp Physiol 293: R2376-R2381, 2007. First published October 3, 2007; doi:10.1152/ajpregu.00403.2007
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COMPARATIVE AND EVOLUTIONARY PHYSIOLOGY

Lipolysis and glycerol gluconeogenesis in simultaneously fasting and lactating northern elephant seals

Dorian S. Houser, Cory D. Champagne, and Daniel E. Crocker

Department of Biology, Sonoma State University, Rohnert Park, California

Submitted 9 June 2007 ; accepted in final form 29 September 2007

Adult female elephant seals (Mirounga angustirostris) combine long-term fasting with lactation and molting. Glycerol gluconeogenesis has been hypothesized as potentially meeting all of the glucose requirements of the seals during these fasts. To test this hypothesis, a primed constant infusion of [2-14C]glycerol was administered to 10 ten adult female elephant seals at 5 and 21–22 days postpartum and to 10 additional adult females immediately after the molt. Glycerol kinetics, rates of lipolysis, and the contribution of glycerol to glucose production were determined for each period. Plasma metabolite levels as well as insulin, glucagon, and cortisol were also measured. Glycerol rate of appearance was not significantly correlated with mass (P = 0.14, r2 = 0.33) but was significantly related to the percentage of glucose derived from glycerol (P < 0.01, r2 = 0.81) during late lactation. The contribution of glycerol to glucose production was <3% during each fasting period, suggesting a lower contribution to gluconeogenesis than is observed in other long-term fasting mammals. Because of a high rate of endogenous glucose production in fasting elephant seals, it is likely that glycerol gluconeogenesis still makes a substantial contribution to the substrate needs of glucose-dependent tissues. The lack of a relationship between glucoregulatory hormones and glycerol kinetics, glycerol gluconeogenesis, and metabolites supports the proposition that fasting elephant seals do not conform to the traditional insulin-glucagon model of substrate metabolism.

reesterification; lipid metabolism; lactogenesis; glucagon; insulin



Address for reprint requests and other correspondence: D. S. Houser, 7951 Shantung Dr., Santee, CA 92071 (e-mail: biomimetica{at}cox.net)




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