The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses.
In a human fMRI study, it has been demonstrated that tasting and ingesting capsaicin activate the ventral part of the middle and posterior short gyri (M/PSG) of the insula which is known as the primary gustatory area, suggesting that capsaicin is recognized as a taste. Tasting and digesting spicy f...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2016-01-01
|
Series: | Frontiers in Human Neuroscience |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fnhum.2015.00720/full |
id |
doaj-e0e2cecb6e7d4aa8969bae2a1bce4164 |
---|---|
record_format |
Article |
spelling |
doaj-e0e2cecb6e7d4aa8969bae2a1bce41642020-11-25T02:42:31ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612016-01-01910.3389/fnhum.2015.00720175391The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses.Shinpei eKawakami0Shinpei eKawakami1Hajime eSato2Akihiro T Sasaki3Akihiro T Sasaki4Akihiro T Sasaki5Hiroki C Tanabe6Yumiko eYoshida7Mitsuru eSaito8Hiroki eToyoda9Norihiro eSadato10Youngnam eKang11Osaka University Graduate School of DentistryMorinaga & Co., Ltd.Osaka University Graduate School of DentistryNational Institute for Physiological SciencesRIKEN Center for Life Science TechnologiesOsaka City University Graduate School of MedicineNagoya University Graduate School of Environmental StudiesNational Institute for Physiological SciencesOsaka University Graduate School of DentistryOsaka University Graduate School of DentistryNational Institute for Physiological SciencesOsaka University Graduate School of DentistryIn a human fMRI study, it has been demonstrated that tasting and ingesting capsaicin activate the ventral part of the middle and posterior short gyri (M/PSG) of the insula which is known as the primary gustatory area, suggesting that capsaicin is recognized as a taste. Tasting and digesting spicy foods containing capsaicin induce various physiological responses such as perspiration from face, salivation and facilitation of cardiovascular activity, which are thought to be caused through viscero-visceral autonomic reflexes. However, this does not necessarily exclude the possibility of the involvement of higher-order sensory-motor integration between the M/PSG and anterior short gyrus (ASG) known as the autonomic region of the insula. To reveal a possible functional coordination between the M/PSG and ASG, we here addressed whether capsaicin increases neural activity in the ASG as well as the M/PSG using fMRI and a custom-made taste delivery system. Twenty subjects participated in this study, and three tastant solutions: capsaicin, NaCl and artificial saliva (AS) were used. Group analyses with the regions activated by capsaicin revealed significant activations in the bilateral ASG and M/PSG. The fMRI blood oxygenation level-dependent (BOLD) signals in response to capsaicin stimulation were significantly higher in ASG than in M/PSG regardless of the side. Concomitantly, capsaicin increased the fingertip temperature significantly. Although there was no significant correlation between the fingertip temperatures and BOLD signals in the ASG or M/PSG when the contrast [Capsaicin–AS] or [Capsaicin–NaCl] was computed, a significant correlation was found in the bilateral ASG when the contrast [2×Capsaicin–NaCl–AS] was computed. In contrast, there was a significant correlation in the hypothalamus regardless of the contrasts. Furthermore, there was a significant correlation between M/PSG and ASG. These results indicate that capsaicin increases neural activity in the ASG as well as the M/PSG, suggesting that the neural coordination between the two cortical areas may be involved in autonomic responses to tasting spicy foods as reflected in fingertip temperature increases.http://journal.frontiersin.org/Journal/10.3389/fnhum.2015.00720/fullCapsaicinfMRIAutonomic Functioninsular cortextaste recognition |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shinpei eKawakami Shinpei eKawakami Hajime eSato Akihiro T Sasaki Akihiro T Sasaki Akihiro T Sasaki Hiroki C Tanabe Yumiko eYoshida Mitsuru eSaito Hiroki eToyoda Norihiro eSadato Youngnam eKang |
spellingShingle |
Shinpei eKawakami Shinpei eKawakami Hajime eSato Akihiro T Sasaki Akihiro T Sasaki Akihiro T Sasaki Hiroki C Tanabe Yumiko eYoshida Mitsuru eSaito Hiroki eToyoda Norihiro eSadato Youngnam eKang The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. Frontiers in Human Neuroscience Capsaicin fMRI Autonomic Function insular cortex taste recognition |
author_facet |
Shinpei eKawakami Shinpei eKawakami Hajime eSato Akihiro T Sasaki Akihiro T Sasaki Akihiro T Sasaki Hiroki C Tanabe Yumiko eYoshida Mitsuru eSaito Hiroki eToyoda Norihiro eSadato Youngnam eKang |
author_sort |
Shinpei eKawakami |
title |
The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. |
title_short |
The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. |
title_full |
The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. |
title_fullStr |
The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. |
title_full_unstemmed |
The brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. |
title_sort |
brain mechanisms underlying the perception of pungent taste of capsaicin and the subsequent autonomic responses. |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Human Neuroscience |
issn |
1662-5161 |
publishDate |
2016-01-01 |
description |
In a human fMRI study, it has been demonstrated that tasting and ingesting capsaicin activate the ventral part of the middle and posterior short gyri (M/PSG) of the insula which is known as the primary gustatory area, suggesting that capsaicin is recognized as a taste. Tasting and digesting spicy foods containing capsaicin induce various physiological responses such as perspiration from face, salivation and facilitation of cardiovascular activity, which are thought to be caused through viscero-visceral autonomic reflexes. However, this does not necessarily exclude the possibility of the involvement of higher-order sensory-motor integration between the M/PSG and anterior short gyrus (ASG) known as the autonomic region of the insula. To reveal a possible functional coordination between the M/PSG and ASG, we here addressed whether capsaicin increases neural activity in the ASG as well as the M/PSG using fMRI and a custom-made taste delivery system. Twenty subjects participated in this study, and three tastant solutions: capsaicin, NaCl and artificial saliva (AS) were used. Group analyses with the regions activated by capsaicin revealed significant activations in the bilateral ASG and M/PSG. The fMRI blood oxygenation level-dependent (BOLD) signals in response to capsaicin stimulation were significantly higher in ASG than in M/PSG regardless of the side. Concomitantly, capsaicin increased the fingertip temperature significantly. Although there was no significant correlation between the fingertip temperatures and BOLD signals in the ASG or M/PSG when the contrast [Capsaicin–AS] or [Capsaicin–NaCl] was computed, a significant correlation was found in the bilateral ASG when the contrast [2×Capsaicin–NaCl–AS] was computed. In contrast, there was a significant correlation in the hypothalamus regardless of the contrasts. Furthermore, there was a significant correlation between M/PSG and ASG. These results indicate that capsaicin increases neural activity in the ASG as well as the M/PSG, suggesting that the neural coordination between the two cortical areas may be involved in autonomic responses to tasting spicy foods as reflected in fingertip temperature increases. |
topic |
Capsaicin fMRI Autonomic Function insular cortex taste recognition |
url |
http://journal.frontiersin.org/Journal/10.3389/fnhum.2015.00720/full |
work_keys_str_mv |
AT shinpeiekawakami thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT shinpeiekawakami thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT hajimeesato thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT akihirotsasaki thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT akihirotsasaki thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT akihirotsasaki thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT hirokictanabe thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT yumikoeyoshida thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT mitsuruesaito thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT hirokietoyoda thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT norihiroesadato thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT youngnamekang thebrainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT shinpeiekawakami brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT shinpeiekawakami brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT hajimeesato brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT akihirotsasaki brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT akihirotsasaki brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT akihirotsasaki brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT hirokictanabe brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT yumikoeyoshida brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT mitsuruesaito brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT hirokietoyoda brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT norihiroesadato brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses AT youngnamekang brainmechanismsunderlyingtheperceptionofpungenttasteofcapsaicinandthesubsequentautonomicresponses |
_version_ |
1724773306434846720 |