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Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats

Hypothalamo-neurohypophysial oxytocin (OXT) plays an essential role in reproduction and in several socio-physiological functions, including stress reduction, anxiety relief, feeding suppression, social recognition, and trust building. Recent studies suggest that the central OXT system is also involv...

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Autores principales: Maruyama, Takashi, Shimizu, Makiko, Ikeda, Naofumi, Baba, Kazuhiko, Yoshimura, Mitsuhiro, Ueta, Yoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469901/
https://www.ncbi.nlm.nih.gov/pubmed/36110514
http://dx.doi.org/10.3389/fphar.2022.961135
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author Maruyama, Takashi
Shimizu, Makiko
Ikeda, Naofumi
Baba, Kazuhiko
Yoshimura, Mitsuhiro
Ueta, Yoichi
author_facet Maruyama, Takashi
Shimizu, Makiko
Ikeda, Naofumi
Baba, Kazuhiko
Yoshimura, Mitsuhiro
Ueta, Yoichi
author_sort Maruyama, Takashi
collection PubMed
description Hypothalamo-neurohypophysial oxytocin (OXT) plays an essential role in reproduction and in several socio-physiological functions, including stress reduction, anxiety relief, feeding suppression, social recognition, and trust building. Recent studies suggest that the central OXT system is also involved in antinociceptive and anti-inflammatory functions. Kamikihi-to (KKT), a Japanese traditional herbal (Kampo) medicine composed of 14 herbal ingredients, is clinically prescribed for patients with psychological symptoms, including anxiety, depression, and insomnia, and it has been associated with OXT expression. We investigated the antinociceptive response and OXT expression according to sex and the effects of KKT pre administration in a rat model. We found that nociceptive responses measured via the hot plate and formalin tests were attenuated following the administration of KKT-enriched feed for 4 weeks. The observation of mRFP1 fluorescence in OXT-mRFP1 transgenic rats revealed that KKT-administered rats showed increased expression of OXT in the magnocellular and parvocellular paraventricular nucleus of the hypothalamus. Food intake in the KKT-pre-administered group significantly decreased after cholecystokinin (CCK)-8 administration. Our results suggest that KKT is involved in the attenuation of nociceptive stress in female rats by enhancing the expression of OXT in the hypothalamus.
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spelling pubmed-94699012022-09-14 Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats Maruyama, Takashi Shimizu, Makiko Ikeda, Naofumi Baba, Kazuhiko Yoshimura, Mitsuhiro Ueta, Yoichi Front Pharmacol Pharmacology Hypothalamo-neurohypophysial oxytocin (OXT) plays an essential role in reproduction and in several socio-physiological functions, including stress reduction, anxiety relief, feeding suppression, social recognition, and trust building. Recent studies suggest that the central OXT system is also involved in antinociceptive and anti-inflammatory functions. Kamikihi-to (KKT), a Japanese traditional herbal (Kampo) medicine composed of 14 herbal ingredients, is clinically prescribed for patients with psychological symptoms, including anxiety, depression, and insomnia, and it has been associated with OXT expression. We investigated the antinociceptive response and OXT expression according to sex and the effects of KKT pre administration in a rat model. We found that nociceptive responses measured via the hot plate and formalin tests were attenuated following the administration of KKT-enriched feed for 4 weeks. The observation of mRFP1 fluorescence in OXT-mRFP1 transgenic rats revealed that KKT-administered rats showed increased expression of OXT in the magnocellular and parvocellular paraventricular nucleus of the hypothalamus. Food intake in the KKT-pre-administered group significantly decreased after cholecystokinin (CCK)-8 administration. Our results suggest that KKT is involved in the attenuation of nociceptive stress in female rats by enhancing the expression of OXT in the hypothalamus. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9469901/ /pubmed/36110514 http://dx.doi.org/10.3389/fphar.2022.961135 Text en Copyright © 2022 Maruyama, Shimizu, Ikeda, Baba, Yoshimura and Ueta. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Maruyama, Takashi
Shimizu, Makiko
Ikeda, Naofumi
Baba, Kazuhiko
Yoshimura, Mitsuhiro
Ueta, Yoichi
Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats
title Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats
title_full Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats
title_fullStr Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats
title_full_unstemmed Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats
title_short Expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of Kamikihi-to in female rats
title_sort expression of oxytocin in hypothalamus and reduction of nociceptive stress following administration of kamikihi-to in female rats
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469901/
https://www.ncbi.nlm.nih.gov/pubmed/36110514
http://dx.doi.org/10.3389/fphar.2022.961135
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