Literature DB >> 12466148

Intestinal alkaline phosphatase release is not associated with chylomicron formation.

Andromeda M Nauli1, Shuqin Zheng, Qing Yang, Ronggui Li, Ronald Jandacek, Patrick Tso.   

Abstract

Intestinal alkaline phosphatase (IAP) is one of the major sources of alkaline phosphatase in circulation. It is secreted into the intestinal lumen, serum, and lymph. After the ingestion of lipid, lymphatic alkaline phosphatase secretion increases significantly. We have found that the nonabsorbable fat olestra is unable to stimulate lymphatic alkaline phosphatase secretion. We also found that the hydrophobic surfactant Pluronic L-81, which blocks chylomicron formation, fails to inhibit this increase in lymphatic alkaline phosphatase secretion. These results suggest that it is the lipid uptake into the mucosa and/or reesterification to form triacylglycerols, but not the formation of chylomicrons, that is necessary for the stimulation of the secretion of alkaline phosphatase into the lymph.

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Year:  2002        PMID: 12466148     DOI: 10.1152/ajpgi.00482.2002

Source DB:  PubMed          Journal:  Am J Physiol Gastrointest Liver Physiol        ISSN: 0193-1857            Impact factor:   4.052


  9 in total

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Review 7.  Assay format as a critical success factor for identification of novel inhibitor chemotypes of tissue-nonspecific alkaline phosphatase from high-throughput screening.

Authors:  Thomas D Y Chung; Eduard Sergienko; José Luis Millán
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8.  Chylomicrons produced by Caco-2 cells contained ApoB-48 with diameter of 80-200 nm.

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  9 in total

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