Literature DB >> 6184702

A fragment of substance P with specific central activity: SP(1-7).

J M Stewart, M E Hall, J Harkins, R C Frederickson, L Terenius, T Hökfelt, W A Krivoy.   

Abstract

Amino-terminal fragments of substance P (SP), SP(1-7) and SP(1-8), were found to produce naloxone-reversible antinociception in the mouse similar to that produced by SP. Similar to SP, these peptides produce antinociception only within a narrow dose range. They have no activity on smooth muscle or blood pressure. These results suggest that contrary to peripheral effects of SP, which are mediated by receptors which recognize the carboxy-terminal part of the SP molecule, certain central actions of SP are mediated by receptors which recognize the amino-terminal part of the SP molecule. SP may be metabolized to this active fragment prior to its action at these receptors.

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Year:  1982        PMID: 6184702     DOI: 10.1016/0196-9781(82)90027-4

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  7 in total

1.  Hydrolysis of substance P in the presence of the osteosarcoma cell line SaOS-2: release of free amino acids.

Authors:  Antonella Cavazza; Mario Marini; L Giorgio Roda; Umberto Tarantino; Angela Valenti
Journal:  Neurochem Res       Date:  2011-08-21       Impact factor: 3.996

2.  The NK1 receptor is essential for the full expression of noxious inhibitory controls in the mouse.

Authors:  H Bester; C De Felipe ; S P Hunt
Journal:  J Neurosci       Date:  2001-02-01       Impact factor: 6.167

3.  Identification of substance P precursor forms in human brain tissue.

Authors:  F Nyberg; P le Grevés; L Terenius
Journal:  Proc Natl Acad Sci U S A       Date:  1985-06       Impact factor: 11.205

4.  Influence of substance P and fragments on passive avoidance behavior.

Authors:  O Gaffori; J M Stewart; D de Wied
Journal:  Experientia       Date:  1984-01-15

Review 5.  Sequence-specific effects of neurokinin substance P on memory, reinforcement, and brain dopamine activity.

Authors:  J P Huston; R U Hasenöhrl; F Boix; P Gerhardt; R K Schwarting
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

6.  The dipeptide Phe-Phe amide attenuates signs of hyperalgesia, allodynia and nociception in diabetic mice using a mechanism involving the sigma receptor system.

Authors:  Masahiro Ohsawa; Anna Carlsson; Megumi Asato; Takayuki Koizumi; Yuki Nakanishi; Rebecca Fransson; Anja Sandström; Mathias Hallberg; Fred Nyberg; Junzo Kamei
Journal:  Mol Pain       Date:  2011-10-31       Impact factor: 3.395

7.  Profound loss of neprilysin accompanied by decreased levels of neuropeptides and increased CRP in ulcerative colitis.

Authors:  Zeynep Gök Sargın; Nuray Erin; Gokhan Tazegul; Gülsüm Özlem Elpek; Bülent Yıldırım
Journal:  PLoS One       Date:  2017-12-12       Impact factor: 3.240

  7 in total

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