Glucose metabolism during lactation in a fasting animal, the northern elephant seal

Am J Physiol Regul Integr Comp Physiol. 2006 Oct;291(4):R1129-37. doi: 10.1152/ajpregu.00570.2005. Epub 2006 May 4.

Abstract

Fasting is associated with a series of physiological responses that protect body tissues from degradation by efficiently using expendable energy reserves while sparing protein. Lactation requires the mobilization of maternal nutrients for milk synthesis. The rare life history trait of fasting simultaneous with lactation results in the conflicting demands of provisioning offspring while meeting maternal metabolic costs and preserving maternal tissues for her own survival and future reproduction. Certain tissues continue to require glucose for operation during fasting and might constrain tissue mobilization for lactogenesis due to a need for gluconeogenic substrates. This study investigated glucose flux, glucose cycle activity, and the influence of regulatory hormones in fasting lactating northern elephant seals. Measurements were taken early (5 days) and late (21 days) during the lactation period and, as a nonlactating comparison, after the completion of molting. Glucose cycle activity was highly variable in all study groups and did not change over lactation (P > 0.3), whereas endogenous glucose production decreased during lactation (t = -3.41, P = 0.008). Insulin and insulin-to-glucagon molar ratio decreased across lactation (t = 6.48, 4.28; P = 0.0001, 0.002), while plasma cortisol level increased (t = 4.15, P = 0.002). There were no relationships between glucose production and hormone levels. The glucose production values measured exceeded that predicted from available gluconeogenic substrate, indicating substantial glucose recycling in this species.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blood Glucose / biosynthesis
  • Blood Glucose / metabolism*
  • Body Composition / physiology
  • Fasting / metabolism*
  • Female
  • Glucagon / blood
  • Gluconeogenesis / physiology
  • Glucose / pharmacokinetics
  • Hydrocortisone / blood
  • Insulin / blood
  • Lactation / metabolism*
  • Lactic Acid / blood
  • Seals, Earless / metabolism*
  • Tritium
  • Weight Loss / physiology

Substances

  • Blood Glucose
  • Insulin
  • Tritium
  • Lactic Acid
  • Glucagon
  • Glucose
  • Hydrocortisone