1992
DOI: 10.1007/bf01990961
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The short term effect of peripherally administered brain-gut peptides on gastric acid secretion in rats

Abstract: Certain brain gut-peptides are known to either stimulate or inhibit gastric acid secretion in several species after direct injection into the central nervous system. However there is inconsistency of published results on the gastric acid secretory response to some of these peptides after peripheral administration in different experimental systems. Seven peptides, namely neurotensin (NT), substance P, cholecystokinin (CCK), thyrotropin releasing hormone (TRH), human calcitonin (hCT), rat calcitonin-gene-related… Show more

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Cited by 8 publications
(3 citation statements)
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“…It is likely that such functional differentiation is also present in the gastric myenteric plexus, because studies on the innervation pattern of the musculature and the mucosa of the guinea-pig stomach have revealed differences in the distribution and density of ChAT-, NPY-, SP-and NOS-positive nerve fibres (Schultzberg et al 1980;Furness et al 1983Furness et al , 1994Keast et al 1985;Mawe et al 1989). In addition, transmitters used by the ENS, such as acetylcholine, NO, SP or NPY, modulate gastric motility (Milenov and Golenhofen 1983;Jin et al 1993;Meulemans et al 1993;, mucosal blood flow (Saperas et al 1995;Chen et al 1993;Holzer 1995;Tepperman and Whittle 1991), acid secretion (Hersey and Sachs 1995;Tsai and Cheng 1990;Zanelli et al 1992;Penner et al 1993), pepsinogen secretion (Hirschowitz and Sachs 1969;Vigna et al 1989;Kitsukawa et al 1996;Raufman and Singh 1991), bicarbonate secretion (Fändriks 1986;Bilski and Konturek 1994;Takeuchi et al 1993) and mucus secretion (Brown et al 1992;Price et al 1994).…”
Section: Introductionmentioning
confidence: 98%
“…It is likely that such functional differentiation is also present in the gastric myenteric plexus, because studies on the innervation pattern of the musculature and the mucosa of the guinea-pig stomach have revealed differences in the distribution and density of ChAT-, NPY-, SP-and NOS-positive nerve fibres (Schultzberg et al 1980;Furness et al 1983Furness et al , 1994Keast et al 1985;Mawe et al 1989). In addition, transmitters used by the ENS, such as acetylcholine, NO, SP or NPY, modulate gastric motility (Milenov and Golenhofen 1983;Jin et al 1993;Meulemans et al 1993;, mucosal blood flow (Saperas et al 1995;Chen et al 1993;Holzer 1995;Tepperman and Whittle 1991), acid secretion (Hersey and Sachs 1995;Tsai and Cheng 1990;Zanelli et al 1992;Penner et al 1993), pepsinogen secretion (Hirschowitz and Sachs 1969;Vigna et al 1989;Kitsukawa et al 1996;Raufman and Singh 1991), bicarbonate secretion (Fändriks 1986;Bilski and Konturek 1994;Takeuchi et al 1993) and mucus secretion (Brown et al 1992;Price et al 1994).…”
Section: Introductionmentioning
confidence: 98%
“…The involvement of tachykinins in regulation of acid secretion has primarily been studied in rats. Intravenous infusion of SP had no effect on basal acid secretion in rats in vivo [73,74], but inhibited the stimulatory effect of electrical stimulation of the vagus nerves [74]. In an isolated rat gastric fundus preparation SP also did not affect basal acid secretion, but augmented the stimulatory effect of histamine [75].…”
Section: Review Articlementioning
confidence: 99%
“…Different effects of tachykinins have been found in different experimental models. Infusion of substance P (SP) had no effect on basal or bethanechol stimulated acid secretion in rats in vivo (Yokotani & Fujiwara 1985, Zanelli et al 1992, but inhibited vagally induced acid secretion (Yokotani & Fujiwara 1985). However, SP failed to in¯uence basal as well as acetylcholine stimulated acid secretion in dispersed rat parietal cells (Schepp et al 1990).…”
mentioning
confidence: 99%