Synthesis of Granuliberin-R and Various Fragment Peptides and Their Histamine-Releasing Activities

Granuliberin-R and various fragment peptides were synthesized and their histaminereleasing activities were examined. The relative potencies of granuliberin-R, H-Phe-Gly-Phe-Leu-Pro-Ile-Tyr-Arg-Arg-Pro-Ala-Ser-NH2, as liberators of histamine from mast cells are very similar to those of substance P an...

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Veröffentlicht in:Chemical & pharmaceutical bulletin 1980/03/25, Vol.28(3), pp.887-892
Hauptverfasser: KITADA, CHIEKO, ASHIDA, YASUKO, MAKI, YOSHITAKA, FUJINO, MASAHIKO, HIRAI, YUKO, YASUHARA, TADASHI, NAKAJIMA, TERUMI, TAKEYAMA, MASAHARU, KOYAMA, KANAME, YAJIMA, HARUAKI
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Sprache:eng
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Zusammenfassung:Granuliberin-R and various fragment peptides were synthesized and their histaminereleasing activities were examined. The relative potencies of granuliberin-R, H-Phe-Gly-Phe-Leu-Pro-Ile-Tyr-Arg-Arg-Pro-Ala-Ser-NH2, as liberators of histamine from mast cells are very similar to those of substance P and bradykinin. Studies on the histamine-releasing activity of various fragment peptides of granuliberin-R showed that a 4-amino acid central sequence, -Ile-Tyr-Arg-Arg-, is the minimum requirement for the releasing action of this frog skin peptide.
ISSN:0009-2363
1347-5223
DOI:10.1248/cpb.28.887