2002
DOI: 10.1016/s0304-4017(01)00635-5
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Excretory/secretory products of Haemonchus contortus inhibit aminopyrine accumulation by rabbit gastric glands in vitro

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Cited by 16 publications
(15 citation statements)
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“…H. contortus excretory/secretory products (ES), which are released by GINs to their environment, consist of diverse bioactive components, including chemotaxins, metabolic end-products, enzymes, immunomodulators and growth factors. ES has been reported to inhibit acid secretion in vitro [191], as well as restrain the enterochromaffin-like cells, which may indirectly cause diminished acid secretion by parietal cells [187; 192]. Ovine gastrointestinal nematode chemotaxins recruit granulocytes in vitro [193], which could be another way of damaging parietal cells in vivo [163; 167].…”
mentioning
confidence: 99%
“…H. contortus excretory/secretory products (ES), which are released by GINs to their environment, consist of diverse bioactive components, including chemotaxins, metabolic end-products, enzymes, immunomodulators and growth factors. ES has been reported to inhibit acid secretion in vitro [191], as well as restrain the enterochromaffin-like cells, which may indirectly cause diminished acid secretion by parietal cells [187; 192]. Ovine gastrointestinal nematode chemotaxins recruit granulocytes in vitro [193], which could be another way of damaging parietal cells in vivo [163; 167].…”
mentioning
confidence: 99%
“…Ammonia, a principal nitrogenous excretory product of parasites (Barrett 1981), is cytotoxic and inhibits acid secretion in dispersed rabbit gastric glands (Fryklund et al 1990;Hagen et al 1997;Merkelbach et al 2002) and in amphibian gastric mucosa (Hagen et al 2000). The weak base also reduces proliferation of cells in culture (Hassell et al 1991;Schneider et al 1996) and induces cell damage (Barer et al 1988;Smoot et al 1990) and cell vacuolation (De Duve et al 1974;Ohkuma and Poole 1981;Xu et al 1990;Cover et al 1991).…”
Section: Discussionmentioning
confidence: 93%
“…Emergence and lifecycle progression to L4 coincides with the inhibition of gastric acid secretion but direct transfer of adult nematodes into the abomasum of sheep can mimic both the rapid rise in abomasal pH and the equally rapid recovery when parasites are removed by anthelmintic treatment (Simpson et al 1997). This, together with the observation that ES products from adult H. contortus inhibit aminopyrine accumulation by isolated rabbit gastric glands (Merkelbach et al 2002), suggests that excreted or secreted products of the parasites may interfere directly with parietal cell function (Anderson et al 1985;Simpson et al 1997;Scott et al 2000) and also that this activity might be common to ES products derived from different lifecycle stages. The mechanisms responsible remain uncertain but seem to be a crucial step for host pathology as well as worm survival (Haag 1995;Stringfellow 1986).…”
Section: Introductionmentioning
confidence: 80%
“…The lack of effect in vitro of ES products of both H. contortus and O. circumcincta (Lawton et al 2002) on gastrin secretion as well as on pepsinogen secretion (unless the fundic tissue is obtained from sheep previously exposed to parasites) (Scott and McKellar 1998) suggests that parasite survival may depend more on acid inhibition than on hypergastrinaemia and pepsinogenaemia in the host. We have shown that H. contortus ES products inhibit aminopyrine accumulation by gastric glands (a measure of acid secretion) (Merkelbach et al 2002), therefore, understanding how abomasal parasites inhibit and kill parietal cells may reveal a key component of the host-parasite interaction which may be amenable to blocking as a novel anthelmintic strategy.…”
Section: Discussionmentioning
confidence: 98%