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Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models

In the present study, the effect of intrathecal (i.t.) or intracerebroventricular (i.c.v.) administration with cholera toxin (CTX) on the blood glucose level was examined in ICR mice. The i.t. treatment with CTX alone for 24 h dose-dependently increased the blood glucose level. However, i.c.v. treat...

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Autores principales: Sim, Yun-Beom, Park, Soo-Hyun, Kang, Yu-Jung, Kim, Sung-Su, Kim, Chea-Ha, Kim, Su-Jin, Jung, Jun-Sub, Ryu, Ohk-Hyun, Choi, Moon-Gi, Choi, Seong-Soo, Suh, Hong-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634094/
https://www.ncbi.nlm.nih.gov/pubmed/23626479
http://dx.doi.org/10.4196/kjpp.2013.17.2.163
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author Sim, Yun-Beom
Park, Soo-Hyun
Kang, Yu-Jung
Kim, Sung-Su
Kim, Chea-Ha
Kim, Su-Jin
Jung, Jun-Sub
Ryu, Ohk-Hyun
Choi, Moon-Gi
Choi, Seong-Soo
Suh, Hong-Won
author_facet Sim, Yun-Beom
Park, Soo-Hyun
Kang, Yu-Jung
Kim, Sung-Su
Kim, Chea-Ha
Kim, Su-Jin
Jung, Jun-Sub
Ryu, Ohk-Hyun
Choi, Moon-Gi
Choi, Seong-Soo
Suh, Hong-Won
author_sort Sim, Yun-Beom
collection PubMed
description In the present study, the effect of intrathecal (i.t.) or intracerebroventricular (i.c.v.) administration with cholera toxin (CTX) on the blood glucose level was examined in ICR mice. The i.t. treatment with CTX alone for 24 h dose-dependently increased the blood glucose level. However, i.c.v. treatment with CTX for 24 h did not affect the blood glucose level. When mice were orally fed with D-glucose (2 g/kg), the blood glucose level reached to a maximum level at 30 min and almost returned to the control level at 120 min after D-glucose feeding. I.c.v. pretreatment with CTX increased the blood glucose level in a potentiative manner, whereas i.t. pretreatment with CTX increased the blood glucose level in an additive manner in a D-glucose fed group. In addition, the blood glucose level was increased in formalin-induced pain animal model. I.c.v. pretreatment with CTX enhanced the blood glucose level in a potentiative manner in formalin-induced pain animal model. On the other hand, i.t. pretreatment with CTX increased the blood glucose level in an additive manner in formalin-induced pain animal model. Our results suggest that CTX administered supraspinally or spinally differentially modulates the regulation of the blood glucose level in D-glucose fed model as well as in formalin-induced pain model.
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spelling pubmed-36340942013-04-26 Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models Sim, Yun-Beom Park, Soo-Hyun Kang, Yu-Jung Kim, Sung-Su Kim, Chea-Ha Kim, Su-Jin Jung, Jun-Sub Ryu, Ohk-Hyun Choi, Moon-Gi Choi, Seong-Soo Suh, Hong-Won Korean J Physiol Pharmacol Original Article In the present study, the effect of intrathecal (i.t.) or intracerebroventricular (i.c.v.) administration with cholera toxin (CTX) on the blood glucose level was examined in ICR mice. The i.t. treatment with CTX alone for 24 h dose-dependently increased the blood glucose level. However, i.c.v. treatment with CTX for 24 h did not affect the blood glucose level. When mice were orally fed with D-glucose (2 g/kg), the blood glucose level reached to a maximum level at 30 min and almost returned to the control level at 120 min after D-glucose feeding. I.c.v. pretreatment with CTX increased the blood glucose level in a potentiative manner, whereas i.t. pretreatment with CTX increased the blood glucose level in an additive manner in a D-glucose fed group. In addition, the blood glucose level was increased in formalin-induced pain animal model. I.c.v. pretreatment with CTX enhanced the blood glucose level in a potentiative manner in formalin-induced pain animal model. On the other hand, i.t. pretreatment with CTX increased the blood glucose level in an additive manner in formalin-induced pain animal model. Our results suggest that CTX administered supraspinally or spinally differentially modulates the regulation of the blood glucose level in D-glucose fed model as well as in formalin-induced pain model. The Korean Physiological Society and The Korean Society of Pharmacology 2013-04 2013-04-10 /pmc/articles/PMC3634094/ /pubmed/23626479 http://dx.doi.org/10.4196/kjpp.2013.17.2.163 Text en Copyright © 2013 The Korean Physiological Society and The Korean Society of Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sim, Yun-Beom
Park, Soo-Hyun
Kang, Yu-Jung
Kim, Sung-Su
Kim, Chea-Ha
Kim, Su-Jin
Jung, Jun-Sub
Ryu, Ohk-Hyun
Choi, Moon-Gi
Choi, Seong-Soo
Suh, Hong-Won
Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models
title Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models
title_full Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models
title_fullStr Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models
title_full_unstemmed Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models
title_short Effect of Cholera Toxin Administered Supraspinally or Spinally on the Blood Glucose Level in Pain and D-Glucose Fed Animal Models
title_sort effect of cholera toxin administered supraspinally or spinally on the blood glucose level in pain and d-glucose fed animal models
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634094/
https://www.ncbi.nlm.nih.gov/pubmed/23626479
http://dx.doi.org/10.4196/kjpp.2013.17.2.163
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