Complete inhibition of purinoceptor agonist-induced nociception by spinorphin, but not by morphine

Hiroshi Ueda, Shinobu Matsunaga, Makoto Inoue, Yukio Yamamoto, Tadahiko Hazato

Research output: Contribution to journalArticlepeer-review

Abstract

We found that spinorphin, a novel neuropeptide showed analgesia in a different manner compared with morphine. By measuring flexor responses induced by the intraplanter injection of substances, the presence of three different types of sensory neurons were demonstrated. Although spinorphin completely blocked 2-metylthioadenosine (2-MeS ATP, a P2X3 agonist)-induced responses, morphine did not. On the other hand, morphine-induced blockade of bradykinin (BK, a B2-receptor agonist)-responses was attenuated by pertussis toxin (PTX) treatment, whereas that of spinorphin was not. Thus it is suggested that spinorphin has a spectrum of analgesia which covers the blockade of nociception insensitive to morphine. (C) 2000 Elsevier Science Inc.

Original languageEnglish (US)
Pages (from-to)1215-1221
Number of pages7
JournalPeptides
Volume21
Issue number8
DOIs
StatePublished - Aug 2000
Externally publishedYes

Keywords

  • 2-MeS ATP
  • Bradykinin
  • Gi
  • P2X
  • PGI agonist
  • Spinorphin

ASJC Scopus subject areas

  • Biochemistry
  • Physiology
  • Endocrinology
  • Cellular and Molecular Neuroscience

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