Evidence map›Paper›PMID 26834613›Full record

ArticleFrontiers in human neuroscience2015

The Brain Mechanisms Underlying the Perception of Pungent Taste of Capsaicin and the Subsequent Autonomic Responses.

Shinpei Kawakami, Hajime Sato, Akihiro T Sasaki, Hiroki C Tanabe, Yumiko Yoshida, Mitsuru Saito, Hiroki Toyoda, Norihiro Sadato, Youngnam Kang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in human neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Shinpei KawakamiDepartment of Neuroscience and Oral Physiology, Graduate School of Dentistry, Osaka UniversitySuita, Japan; Morinaga & Co., Ltd., YokohamaJapan.
Hajime SatoDepartment of Neuroscience and Oral Physiology, Graduate School of Dentistry, Osaka University Suita, Japan.
Akihiro T SasakiDivision of Cerebral Integration, National Institute for Physiological SciencesOkazaki, Japan; Pathophysiological and Health Science Team, RIKEN Center for Life Science TechnologiesKobe, Japan; Department of Physiology, Graduate School of Medicine, Osaka City UniversityOsaka, Japan.
Hiroki C TanabeDepartment of Psychology, Graduate School of Environmental Studies, Nagoya University Nagoya, Japan.
Yumiko YoshidaDivision of Cerebral Integration, National Institute for Physiological Sciences Okazaki, Japan.
Mitsuru SaitoDepartment of Neuroscience and Oral Physiology, Graduate School of Dentistry, Osaka UniversitySuita, Japan; Department of Oral Physiology, Graduate School of Medical and Dental Sciences, Kagoshima UniversityKagoshima, Japan.
Hiroki ToyodaDepartment of Neuroscience and Oral Physiology, Graduate School of Dentistry, Osaka University Suita, Japan.
Norihiro SadatoDivision of Cerebral Integration, National Institute for Physiological Sciences Okazaki, Japan.
Youngnam KangDepartment of Neuroscience and Oral Physiology, Graduate School of Dentistry, Osaka University Suita, Japan.
Osaka University · JPNational Institute for Physiological Sciences · JPNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

autonomic functioncapsaicinfMRIinsular cortextaste recognition

Identifiers

PMID26834613
PMCPMC4717328
OpenAlexW2236526830

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.