A reconsideration of the evidence for Escherichia coli STa (heat stable) enterotoxin-driven fluid secretion: a new view of STa action and a new paradigm for fluid absorption

Authors
Citation
Ml. Lucas, A reconsideration of the evidence for Escherichia coli STa (heat stable) enterotoxin-driven fluid secretion: a new view of STa action and a new paradigm for fluid absorption, J APPL MICR, 90(1), 2001, pp. 7-26
Citations number
95
Categorie Soggetti
Biology,Microbiology
Journal title
JOURNAL OF APPLIED MICROBIOLOGY
ISSN journal
13645072 → ACNP
Volume
90
Issue
1
Year of publication
2001
Pages
7 - 26
Database
ISI
SICI code
1364-5072(200101)90:1<7:AROTEF>2.0.ZU;2-S
Abstract
A review of the evidence for Escherichia coli STa causing fluid secretion i n vivo leads to the conclusion that the concept of STa acting through enhan ced chloride secretion in order to derange intestinal function is unproven. However, a consistent effect of STa in the small intestine is on Na+/H+ ex change, leading to interruption of luminal acidification. A model for the a ction of STa, involving inhibition of Na+/H+ exchange, is proposed which ex plains the ability of STa to reduce absorption in vivo but its inability to cause secretion in vice in contrast to its apparent secretory effect in vi tro. The apparent ability to demonstrate secretion in vitro is shown to der ive from methodologies which do not involve measurement of mass transport o f water but instead, infer it from in vitro and in vivo proxy measurements. The ill vitro demonstration of notional secretion after STa exposure can b e reconciled with the proposed new model for fluid absorption in that cell swelling is argued to arise as a transient consequence of STa challenge fol lowed by regulatory volume decrease. Evidence for this derangement model is presented in the form of observations derived from acute in vivo physiolog ical studies and clinical studies on patients without the exchanger. This p rocess of appraisal of the evidence for the mechanism of action of STa has led to a new model for fluid absorption. This is based on the formation of hypotonicity at the brush border luminal surface rather than hypertonicity within the lateral spaces as required by the present standing gradient mode l of fluid absorption. Evidence from the literature is presented for this n ew paradigm of water absorption, which may only be relevant for small intes tine and other tissues that have Na+/H+ exchangers in contact with HCO3--co ntaining solutions but which may also be generalizable to all mammalian abs orbing epithelial membranes.