1988
DOI: 10.1136/gut.29.8.1042
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Further characterisation of the 'ileal brake' reflex in man--effect of ileal infusion of partial digests of fat, protein, and starch on jejunal motility and release of neurotensin, enteroglucagon, and peptide YY.

Abstract: SUMMARY Previous studies have shown that ileal infusion of partially digested triglyceride inhibits jejunal motility. The partial digest used in those studies contained a mixture of glycerol, free fatty acid, mono-, di-, and triglycerides. In Part I of the present study we have separately infused emulsions containing either glycerol 3.1 g (n=6), oleic acid 9-6 g (n=6), triolein 10 g (n=12), or medium chain triglycerides 10 g (n=6) into the ileum and have recorded the effect this has on jejunal motility. Five f… Show more

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Cited by 249 publications
(123 citation statements)
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References 20 publications
(7 reference statements)
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“…These results are consistent with the proposed release of PYY in response to ingested fat (26,27). If PYY release is mediated by an enteral, nutrient-dependent mechanism (26,28,29), it is possible that the effects of PYY infusion on appetite and body weight may be greater in animals consuming a high-fat diet.…”
Section: Discussionsupporting
confidence: 79%
“…These results are consistent with the proposed release of PYY in response to ingested fat (26,27). If PYY release is mediated by an enteral, nutrient-dependent mechanism (26,28,29), it is possible that the effects of PYY infusion on appetite and body weight may be greater in animals consuming a high-fat diet.…”
Section: Discussionsupporting
confidence: 79%
“…Other candidates include GLP-1 and PYY, which are mainly released from the distal ileum and colon and inhibit upper gastrointestinal functions including gastric emptying ("ileal brake") (26,27,31,32,48,55). Thus we hypothesized that delayed gastric emptying might be a consequence of disturbed release of CCK and/or PYY and/or GLP-1.…”
Section: Discussionmentioning
confidence: 99%
“…The ingestion of fat, which is subsequently hydrolyzed by lipases in the small intestine, is a strong stimulus of gut hormone secretion (58)(59)(60). Several GPCRs have been identified as sensors of the products of fat digestion ( Figure 2B).…”
Section: Gut Microbiota Host Defense and Eec Signalingmentioning
confidence: 99%