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(Journal of Nutrition. 2001;131:2101-2104.)
© 2001 The American Society for Nutritional Sciences


Research Communication

Gastric Digestion of Bovine Lactoferrin In Vivo in Adults1

Freddy J. Troost*2, Jan Steijns{dagger}, Wim H. M. Saris* and Robert-Jan M. Brummer**

* Department of Human Biology, Nutrition and Toxicology Institute Maastricht, Universiteitssingel, Maastricht, The Netherlands; {dagger} DMV International, Center of Expertise Nutrition, Bornsesteeg, Wageningen, The Netherlands; and ** Department of Gastroenterology, Nutrition and Toxicology Institute Maastricht, University Hospital Maastricht, AZ Maastricht, The Netherlands

2To whom correspondence should be addressed. E-mail: f.troost{at}hb.unimaas.nl

Lactoferrin (LF), an iron-binding glycoprotein present in milk and other endocrine and exocrine secretions, may exert a number of physiologic effects in the intestines. To study the effects of oral LF supplementation in vivo in the gastrointestinal tract, information about the gastric survival of LF in vivo is important. We tested 12 healthy volunteers (age 21 ± 0.3 y) on 3 separate d according to a randomized, cross-over design. A test drink containing 4.5 g of bovine LF (20% iron-saturated LF; apoLF) in the presence of a gastric pH buffer (0.1 mol/L sodium citrate/citric acid; apoLFbuf), apoLF without the buffer (apoLF) or iron-saturated LF (holoLF) was administered into the stomach using nasogastric intubation. Gastric emptying rate, determined by a marker dilution technique, did not differ among any of these drinks. Gastric survival of LF, analyzed by gel permeation chromatography under denaturing conditions, was 64%, 62% and 79% after consumption of the apoLFbuf, apoLF and holoLF test drinks, respectively. Addition of the gastric pH buffer initially lowered intragastric pH because of its hydroxide buffering effect. However, it did not elevate intragastric pH over a prolonged period and thereby inhibit intragastric LF breakdown. We conclude that after oral administration, substantial amounts of apoLF and holoLF survive gastric transit.


KEY WORDS: • lactoferrin • breakdown • gastric emptying • biological activity • stomach




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