том 129 издание 5 страницы 1533-1543

Corticotropin-Releasing Hormone Receptor 1 Antagonist Blocks Brain–Gut Activation Induced by Colonic Distention in Rats

Тип публикацииJournal Article
Дата публикации2005-11-10
scimago Q1
wos Q1
БС1
SJR7.195
CiteScore39.5
Impact factor25.1
ISSN00165085, 15280012
Gastroenterology
Hepatology
Краткое описание
The corticotropin-releasing hormone receptor 1 mediates stress-induced changes in colonic motor activity and emotion. We tested the hypothesis that pretreatment with JTC-017, a specific corticotropin-releasing hormone receptor 1 antagonist, blocks colorectal distention-induced hippocampal noradrenaline release and visceral perception in rats. We also investigated whether pretreatment with JTC-017 blocks acute or chronic colorectal distention-induced adrenocorticotropic hormone release, anxiety, and stress-induced changes in colonic motility.Rats were pretreated intrahippocampally with alpha-helical corticotropin-releasing hormone (1.25 microg/kg; vehicle), a nonspecific corticotropin-releasing hormone receptor antagonist, or intraperitoneally with JTC-017 (10 mg/kg). Hippocampal noradrenaline release after microdialysis and the frequency of abdominal contractions were measured in response to acute colorectal distention. Plasma adrenocorticotropic hormone levels, anxiety-related behavior, and stress-induced changes in colonic motility were evaluated after acute or chronic colorectal distention followed by exposure to an elevated plus maze.Administration of alpha-helical corticotropin-releasing hormone or JTC-017 significantly attenuated hippocampal noradrenaline release and reduced the frequency of abdominal contractions induced by acute distention. In addition, JTC-017 significantly reduced plasma adrenocorticotropic hormone and anxiety after acute distention. After chronic distention, changes in plasma adrenocorticotropic hormone and anxiety were not significant because of habituation. In contrast, a significant increase in fecal pellet output during the elevated plus maze was observed after chronic distention. This increase in fecal pellet output was blocked by pretreatment with JTC-017.Our results suggest that JTC-017, a specific corticotropin-releasing hormone receptor 1 antagonist, attenuates hippocampal noradrenaline release, visceral perception, adrenocorticotropic hormone release, and anxiety after acute colorectal distention in rats. In addition, JTC-017 blocks stress-induced changes in colonic motility after chronic colorectal distention in rats.
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Saito K. et al. Corticotropin-Releasing Hormone Receptor 1 Antagonist Blocks Brain–Gut Activation Induced by Colonic Distention in Rats // Gastroenterology. 2005. Vol. 129. No. 5. pp. 1533-1543.
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Saito K., KASAI T., Nagura Y., Ito H., Kanazawa M., Fukudo S. Corticotropin-Releasing Hormone Receptor 1 Antagonist Blocks Brain–Gut Activation Induced by Colonic Distention in Rats // Gastroenterology. 2005. Vol. 129. No. 5. pp. 1533-1543.
RIS |
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TY - JOUR
DO - 10.1053/j.gastro.2005.07.053
UR - https://doi.org/10.1053/j.gastro.2005.07.053
TI - Corticotropin-Releasing Hormone Receptor 1 Antagonist Blocks Brain–Gut Activation Induced by Colonic Distention in Rats
T2 - Gastroenterology
AU - Saito, Kumi
AU - KASAI, Toshiyuki
AU - Nagura, Yohko
AU - Ito, Hitomi
AU - Kanazawa, Motoyori
AU - Fukudo, Shin
PY - 2005
DA - 2005/11/10
PB - Elsevier
SP - 1533-1543
IS - 5
VL - 129
PMID - 16285953
SN - 0016-5085
SN - 1528-0012
ER -
BibTex |
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@article{2005_Saito,
author = {Kumi Saito and Toshiyuki KASAI and Yohko Nagura and Hitomi Ito and Motoyori Kanazawa and Shin Fukudo},
title = {Corticotropin-Releasing Hormone Receptor 1 Antagonist Blocks Brain–Gut Activation Induced by Colonic Distention in Rats},
journal = {Gastroenterology},
year = {2005},
volume = {129},
publisher = {Elsevier},
month = {nov},
url = {https://doi.org/10.1053/j.gastro.2005.07.053},
number = {5},
pages = {1533--1543},
doi = {10.1053/j.gastro.2005.07.053}
}
MLA
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Saito, Kumi, et al. “Corticotropin-Releasing Hormone Receptor 1 Antagonist Blocks Brain–Gut Activation Induced by Colonic Distention in Rats.” Gastroenterology, vol. 129, no. 5, Nov. 2005, pp. 1533-1543. https://doi.org/10.1053/j.gastro.2005.07.053.