Abstract

The object of this study was to investigate the effect of maternal metabolic state on the activity of lipoprotein lipase (LPL) in human milk. Although the total LPL activity in milk was not significantly affected by up to three cycles of freezing and thawing, the amount of LPL associated with the cream fraction of the milk increased from an average of less than 10% to about 70% after this treatment. The enzyme was relatively stable when the milk was stored on ice, losing activity at a rate of about 1% per hour. At 37 degrees C degradation was more rapid, about 7% per hour. When LPL activity was measured in samples taken at hourly intervals by breast pump, using oxytocin to achieve a complete letdown at each pumping, activity was found to double from the first to the third pumping. Thereafter the activity was stable under fasting conditions. Hyperglycemic and euglycemic, hyperinsulinemic glucose clamp protocols were used to evaluate the effects of glucose and insulin. Both high plasma glucose and high plasma insulin in the presence of normal glucose significantly increased LPL activity within 4 hours. We conclude that, like adipose, tissue LPL, mammary LPL is regulated by plasma insulin.

Highlights

  • The object of this study was to investigate the effect of maternal metabolic state on the activity of lipoprotein lipase (LPL) in human milk

  • The effects of insulin and glucose suggest that the enzyme in human milk is subject to metabolic regulation: it is increased in response to increases in plasma insulin

  • Others have found the majority of LPL to be associated with the cream fraction of human milk [2]. They used milk that had been frozen and thawed for their determination. For this reason and to reaffirm the results of others that human milk samples could be frozen without substantial loss of LPL activity [22], we examined the effects of freezing and thawing on LPL activity and distribution

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Summary

Introduction

The object of this study was to investigate the effect of maternal metabolic state on the activity of lipoprotein lipase (LPL) in human milk. The effects of lactational stage on mammary and adipose LPL have been investigated in a number of laboratories [7, 13,14,15,16,17] and the metabolic regulation of adipose tissue LPL has received wide investigation (ll), there has been little systematic study of the metabolic regulation of the enzyme in the mammary gland or in milk Such information is important because of its possible bearing on the regulation of lipid secretion into milk. For this reason we determined the LPL activity in milk samples collected hourly during a study designed to determine the effects of short-term fasting, as well as maternal levels of insulin and glucose on human milk production

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