Characterization of Tyr‐Leu‐Gly, a novel anxiolytic‐like peptide released from bovine αS‐casein. Issue 7 (11th April 2013)
- Record Type:
- Journal Article
- Title:
- Characterization of Tyr‐Leu‐Gly, a novel anxiolytic‐like peptide released from bovine αS‐casein. Issue 7 (11th April 2013)
- Main Title:
- Characterization of Tyr‐Leu‐Gly, a novel anxiolytic‐like peptide released from bovine αS‐casein
- Authors:
- Mizushige, Takafumi
Sawashi, Yurina
Yamada, Ayako
Kanamoto, Ryuhei
Ohinata, Kousaku - Abstract:
- Abstract : We found previously that dipeptide YL exhibits orally active anxiolytic activity comparable to diazepam. The YL sequence is often observed in the primary structure of natural food proteins. In the present study, we investigated whether YL and YL analogues are released from bovine αS ‐casein by gastrointestinal proteases. YLG, corresponding to αS1 ‐casein (aa 91–93), was more effectively released from αS ‐casein than YL by pepsin‐pancreatin digestion, mimicking gastrointestinal enzymatic conditions. Using the synthetic model peptide, we determined that trypsin cleaved the N terminus of YLG, and elastase and carboxypeptidase contributed to cleave the C‐terminus. YLG exhibited orally active anxiolytic‐like activity in the elevated plus maze and open‐field tests in mice. The anxiolytic‐like activity of YLG was inhibited by WAY100135, SCH23390 or bicuculline, antagonists of serotonin 5‐HT1A, dopamine D1, and GABAA receptors, respectively; however, YLG had no affinity for these receptors. The pepsin‐pancreatin digest of αS ‐Casein also exhibited anxiolytic‐like activity. Meanwhile, anxiolytic‐like activity of α‐casozepine, an αS1 ‐casein‐derived decapeptide with YL sequence in the N terminus, was blocked by WAY100135, SCH23390, or bicuculline, equally to YLG and YL; however, it was not detected in the pepsin‐pancreatic digest. Taken together, we found that YLG is released after pepsin‐pancreatic digestion of αS ‐casein and exhibits potent anxiolytic‐like activity viaAbstract : We found previously that dipeptide YL exhibits orally active anxiolytic activity comparable to diazepam. The YL sequence is often observed in the primary structure of natural food proteins. In the present study, we investigated whether YL and YL analogues are released from bovine αS ‐casein by gastrointestinal proteases. YLG, corresponding to αS1 ‐casein (aa 91–93), was more effectively released from αS ‐casein than YL by pepsin‐pancreatin digestion, mimicking gastrointestinal enzymatic conditions. Using the synthetic model peptide, we determined that trypsin cleaved the N terminus of YLG, and elastase and carboxypeptidase contributed to cleave the C‐terminus. YLG exhibited orally active anxiolytic‐like activity in the elevated plus maze and open‐field tests in mice. The anxiolytic‐like activity of YLG was inhibited by WAY100135, SCH23390 or bicuculline, antagonists of serotonin 5‐HT1A, dopamine D1, and GABAA receptors, respectively; however, YLG had no affinity for these receptors. The pepsin‐pancreatin digest of αS ‐Casein also exhibited anxiolytic‐like activity. Meanwhile, anxiolytic‐like activity of α‐casozepine, an αS1 ‐casein‐derived decapeptide with YL sequence in the N terminus, was blocked by WAY100135, SCH23390, or bicuculline, equally to YLG and YL; however, it was not detected in the pepsin‐pancreatic digest. Taken together, we found that YLG is released after pepsin‐pancreatic digestion of αS ‐casein and exhibits potent anxiolytic‐like activity via activation of serotonin, dopamine, and the GABA receptor system.—Mizushige, T., Sawashi, Y., Yamada, A., Kanamoto, R., Ohinata, K. Characterization of Tyr‐Leu‐Gly, a novel anxiolytic‐like peptide released from bovine αS ‐casein. FASEB J. 27, 2911‐2917 (2013). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 27:Issue 7(2013)
- Journal:
- FASEB journal
- Issue:
- Volume 27:Issue 7(2013)
- Issue Display:
- Volume 27, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 27
- Issue:
- 7
- Issue Sort Value:
- 2013-0027-0007-0000
- Page Start:
- 2911
- Page End:
- 2917
- Publication Date:
- 2013-04-11
- Subjects:
- gastrointestinal protease -- neurotransmitter -- tripeptide
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.12-225474 ↗
- 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:
- 13221.xml