TY - JOUR
T1 - Single oral administration of flavan 3-ols induces stress responses monitored with stress hormone elevations in the plasma and paraventricular nucleus
AU - Fujii, Yasuyuki
AU - Suzuki, Kenta
AU - Hasegawa, Yahiro
AU - Nanba, Fumio
AU - Toda, Toshiya
AU - Adachi, Takahiro
AU - Taira, Shu
AU - Osakabe, Naomi
N1 - Funding Information:
This work was supported by a grant from the Cross-Ministerial Strategic Innovation Promotion Program (SIP) , Urgent Project for Development and Diffusion of Innovative Technology towards Realization of the Aggressive Agriculture, Forestry, and Fisheries, Council for Science, Technology and Innovation, Cabinet Office, Government of Japan.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/8/24
Y1 - 2018/8/24
N2 - We previously confirmed that postprandial alterations in the circulation and metabolism after a single oral dose of flavan 3-ols (mixture of catechin and catechin oligomers) were involved in an increase in sympathetic nervous activity. However, it is well known that, in response to various stresses, activation of the hypothalamic-pituitary-adrenal (HPA) axis occurs together with sympathetic nerve activity, which is associated with activation of the sympathetic-adrenal-medullary (SAM) axis. In this study, we examined whether the HPA axis was activated after a single dose of flavan 3-ols. We administered an oral dose of 10 or 50 mg/kg flavan 3-ols to male ICR mice, removed the brains, and fixed them in paraformaldehyde-phosphate buffer. Other animals that were treated similarly were decapitated, and blood was collected. In the paraventricular nucleus (PVN), c-fos mRNA expression increased significantly at 15 min after administration of either 10 or 50 mg/kg flavan 3-ols. Corticotropin-releasing hormone (CRH) mRNA expression levels significantly increased at 240 min after administration of 10 mg/kg flavan 3-ols, and at 60 min after administration of 50 mg/kg flavan 3-ols. Plasma corticosterone levels were also significantly increased at 240 min after ingestion of 50 mg/kg flavan 3-ols. In this experiment, we confirmed that the ingestion of flavan 3-ols acted as a stressor in mammals with activation both the SAM and HPA axes.
AB - We previously confirmed that postprandial alterations in the circulation and metabolism after a single oral dose of flavan 3-ols (mixture of catechin and catechin oligomers) were involved in an increase in sympathetic nervous activity. However, it is well known that, in response to various stresses, activation of the hypothalamic-pituitary-adrenal (HPA) axis occurs together with sympathetic nerve activity, which is associated with activation of the sympathetic-adrenal-medullary (SAM) axis. In this study, we examined whether the HPA axis was activated after a single dose of flavan 3-ols. We administered an oral dose of 10 or 50 mg/kg flavan 3-ols to male ICR mice, removed the brains, and fixed them in paraformaldehyde-phosphate buffer. Other animals that were treated similarly were decapitated, and blood was collected. In the paraventricular nucleus (PVN), c-fos mRNA expression increased significantly at 15 min after administration of either 10 or 50 mg/kg flavan 3-ols. Corticotropin-releasing hormone (CRH) mRNA expression levels significantly increased at 240 min after administration of 10 mg/kg flavan 3-ols, and at 60 min after administration of 50 mg/kg flavan 3-ols. Plasma corticosterone levels were also significantly increased at 240 min after ingestion of 50 mg/kg flavan 3-ols. In this experiment, we confirmed that the ingestion of flavan 3-ols acted as a stressor in mammals with activation both the SAM and HPA axes.
KW - Corticosterone
KW - Corticotropin-releasing hormone
KW - Flavan 3-ols
KW - Hypothalamic-pituitary-adrenal axis
KW - Stress
UR - http://www.scopus.com/inward/record.url?scp=85048704776&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85048704776&partnerID=8YFLogxK
U2 - 10.1016/j.neulet.2018.06.015
DO - 10.1016/j.neulet.2018.06.015
M3 - Article
C2 - 29902479
AN - SCOPUS:85048704776
SN - 0304-3940
VL - 682
SP - 106
EP - 111
JO - Neuroscience Letters
JF - Neuroscience Letters
ER -