Characterization of soy‐deprestatin, a novel orally active decapeptide that exerts antidepressant‐like effects via gut–brain communication. Issue 2 (4th January 2018)
- Record Type:
- Journal Article
- Title:
- Characterization of soy‐deprestatin, a novel orally active decapeptide that exerts antidepressant‐like effects via gut–brain communication. Issue 2 (4th January 2018)
- Main Title:
- Characterization of soy‐deprestatin, a novel orally active decapeptide that exerts antidepressant‐like effects via gut–brain communication
- Authors:
- Mori, Yukiha
Asakura, Saho
Yamamoto, Akane
Odagiri, Saori
Yamada, Daisuke
Sekiguchi, Masayuki
Wada, Keiji
Sato, Masaru
Kurabayashi, Atsushi
Suzuki, Hideyuki
Kanamoto, Ryuhei
Ohinata, Kousaku - Abstract:
- Abstract : We found that the orally administered thermolysin digest of β‐conglycinin exhibits antidepressant‐like effects in tail suspension and forced swim tests in mice. A comprehensive peptide analysis of the digest using liquid chromatography/mass spectrometry was performed, and LSSTQAQQSY emerged as a candidate antidepressant‐like peptide. Orally administered synthetic LSSTQAQQSY exhibited antidepressant‐like effects at a dose of 0.3 mg/kg; therefore, we named the decapeptide soy‐deprestatin. In contrast, intraperitoneally administered soy‐deprestatin was ineffective. We then hypothesized that it acted on the gut, and its signal was transferred to the brain. Indeed, orally administered soy‐deprestatin exhibited antidepressant‐like activity in sham‐treated, but not vagotomized, mice. Oral administration of soy‐deprestatin also increased the c‐Fos expression in the nucleus of the solitary tract, which receives inputs from the vagus nerve. These results suggested that the antidepressant‐like effects were mediated by the vagus nerve. Thermolysin digest‐ and soy‐deprestatin–induced antidepressant‐like effects were also blocked by antagonists of serotonin 5‐HT1A, dopamine D1, or GABAA receptors. We also clarified the order of receptor activation as 5‐HT1A, D1, and GABAA, using selective agonists and antagonists. Taken together, soy‐deprestatin may exhibit antidepressant‐like effects after oral administration via a novel pathway mediated by 5‐HT1A, followed by D1 and GABAAAbstract : We found that the orally administered thermolysin digest of β‐conglycinin exhibits antidepressant‐like effects in tail suspension and forced swim tests in mice. A comprehensive peptide analysis of the digest using liquid chromatography/mass spectrometry was performed, and LSSTQAQQSY emerged as a candidate antidepressant‐like peptide. Orally administered synthetic LSSTQAQQSY exhibited antidepressant‐like effects at a dose of 0.3 mg/kg; therefore, we named the decapeptide soy‐deprestatin. In contrast, intraperitoneally administered soy‐deprestatin was ineffective. We then hypothesized that it acted on the gut, and its signal was transferred to the brain. Indeed, orally administered soy‐deprestatin exhibited antidepressant‐like activity in sham‐treated, but not vagotomized, mice. Oral administration of soy‐deprestatin also increased the c‐Fos expression in the nucleus of the solitary tract, which receives inputs from the vagus nerve. These results suggested that the antidepressant‐like effects were mediated by the vagus nerve. Thermolysin digest‐ and soy‐deprestatin–induced antidepressant‐like effects were also blocked by antagonists of serotonin 5‐HT1A, dopamine D1, or GABAA receptors. We also clarified the order of receptor activation as 5‐HT1A, D1, and GABAA, using selective agonists and antagonists. Taken together, soy‐deprestatin may exhibit antidepressant‐like effects after oral administration via a novel pathway mediated by 5‐HT1A, followed by D1 and GABAA systems. This is the first orally active peptide demonstrating antidepressant‐like effects via gut–brain communication.—Mori, Y., Asakura, S., Yamamoto, A., Odagiri, S., Yamada, D., Sekiguchi, M., Wada, K., Sato, M., Kurabayashi, A., Suzuki, H., Kanamoto, R., Ohinata, K. Characterization of soy‐deprestatin, a novel orally active decapeptide that exerts antidepressant‐like effects via gut–brain communication. FASEB J. 32, 568–575 (2018). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 32:Issue 2(2018)
- Journal:
- FASEB journal
- Issue:
- Volume 32:Issue 2(2018)
- Issue Display:
- Volume 32, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 32
- Issue:
- 2
- Issue Sort Value:
- 2018-0032-0002-0000
- Page Start:
- 568
- Page End:
- 575
- Publication Date:
- 2018-01-04
- Subjects:
- vagus nerve -- serotonin 5‐HT1A -- dopamine D1 -- GABAA
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201700333RR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13219.xml