Duodenal Ca2+ absorption is not stimulated by calcitriol during early postnatal development of pigs

Author:

Schroeder Bernd1,Dahl Maria Regina2,Breves Gerhard1

Affiliation:

1. Department of Physiology, School of Veterinary Medicine, D-30173 Hannover; and

2. Department of Veterinary Physiology, Justus Liebig University, 35392 Giessen, Germany

Abstract

The role of calcitriol in stimulating intestinal active Ca2+ absorption during postnatal life was studied in newborn, suckling, and weaned control (Con) piglets and piglets suffering from inherited calcitriol deficiency (Def piglets). In addition, a group of Def piglets was treated with vitamin D3(Def-D3 piglets), which normalized plasma calcitriol levels. Regardless of age, duodenal calbindin-D9k concentrations ranged between 1,839 and 2,846 μg/g mucosa in Con piglets, between 821 and 1,219 μg/g mucosa in Def piglets, and between 2,960 and 3,692 μg/g mucosa in Def-D3 animals. In weaned animals, active Ca2+absorption as calculated from in vitro45Ca2+flux rate measurements in Ussing chambers could be related to calbindin-D9k levels. Thus active Ca2+ absorption was completely absent in Def animals but was reconstituted in Def-D3 animals. In contrast, in newborn Def piglets active Ca2+absorption functioned normally despite the low plasma calcitriol and mucosal calbindin-D9k levels and could not be affected by treatment with vitamin D3. Similar results were obtained from suckling Def piglets. The microtubule-disrupting agent colchicine caused significant inhibition of transepithelial net Ca2+ absorption in duodenal epithelia from newborn piglets without exerting an effect in suckling and weaned animals. Colchicine had no effect on Ca2+ uptake across the brush border membrane of mucosal enterocytes or on glucose-dependent electrogenic net ion flux rates in duodenal preparations from newborn Con piglets. In conclusion, our findings reveal intestinal active Ca2+ absorption during early postnatal life of pigs that involves calcitriol-independent mechanisms and that may include intact microtubule actions.

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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