1988
DOI: 10.1016/s0016-5085(88)80070-2
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Stress-Induced Gastrointestinal Secretory and Motor Responses in Rats Are Mediated by Endogenous Corticotropin-Releasing Factor

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Cited by 224 publications
(165 citation statements)
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“…Stressors have been shown to affect secretion of gastric acid, which may in turn influence survival of ingested pathogens. Lenz et al showed that restraint stress significantly increased or decreased gastric acidity, depending upon temperature (Lenz et al, 1988). Another effect of stress on GI function is a reduction in motility.…”
Section: Microbial Endocrinologymentioning
confidence: 99%
“…Stressors have been shown to affect secretion of gastric acid, which may in turn influence survival of ingested pathogens. Lenz et al showed that restraint stress significantly increased or decreased gastric acidity, depending upon temperature (Lenz et al, 1988). Another effect of stress on GI function is a reduction in motility.…”
Section: Microbial Endocrinologymentioning
confidence: 99%
“…27 Indeed, induction of gastric lesions in rodents by sociopsychological stress is useful as an experimental model to assess the anxiolytic activity of novel drugs and the anxiolytic potency of a drug may be predicted by its anti-ulcer effect. 28 While the role of corticotropin-releasing hormone (CRH) in mediating the stress-induced alteration of gastrointestinal secretory and motor responses is fairly established, [29][30][31] its role in the pathogenesis of stress ulcer has been debatable. 32,33 CRH is a 41-amino acid peptide that was first isolated as the principal hypothalamic hormone that mobilizes the pituitary-adrenal responses to stress 34 and subsequently identified as a key player in the behavioral and autonomic responses to stress in rodents 35 and nonhuman primates.…”
Section: Introductionmentioning
confidence: 99%
“…31 Central administration of peptide CRH receptor antagonists prevents the gastrointestinal secretory and motor responses elicited by either stress or exogenous CRH in a dose-dependent fashion. 30,38 The clinical development of nonpeptide antagonists which cross the blood-brain barrier to reset brain CRH-R1 for the treatment of anxiety 40 and melancholic depression 41 is currently the focus of extensive research. We have recently reported that oral administration of antalarmin, a member of this novel family of drugs, attenuates neuroendocrine and behavioral responses to stress in primates.…”
Section: Introductionmentioning
confidence: 99%
“…inhibited gastric emptying in rats, and this effect of CRF was prevented by i.v. antiserum to CRF but not altered by bretylium (a noradrenergic blocker) or chorisondamine (a ganglionic blocking agent) (Lenz et al, 1988). The overall results of the study suggest that TF may show an antianorectic effect by acting as a CRF antagonist.…”
Section: Effects Of Tf and Its Constituents On Fluoxetine-induced Anomentioning
confidence: 70%