Binding Characteristics of a Histamine H3-Receptor Antagonist, [3H]5-Methylthioperamide: Comparison with [3H](R)α-Methylhistamine Binding to Rat Tissues

Kazuhiko Yanai, Jong Hoon Ryu, Naruhiko Sakai, Takehiko Watanabe, Toshihiro Takahashi, Ren Iwata, Tatsuo Ido, Kazuki Murakami

Research output: Contribution to journalArticlepeer-review

35 Citations (Scopus)

Abstract

The release and synthesis of neuronal histamine are regulated by histaminergic autoreceptors named as histamine H3 receptors. The development of radiolabeled histamine H3 antagonists is needed to characterize the binding of antagonists to these receptors. Here we describe the binding characteristics of a new histamine H3-receptor antagonist, [3H]S-methylthioperamide (SMT), to rat tissues, and compare its binding with that of [3H](R)α-methylhistamine ((R)αMH), a selective histamine H3-receptor agonist. The binding of [3H]SMT to the membranes of rat forebrain was found to be stereoselective, saturable, reversible and temperature-dependent. Saturation binding experiments indicated a single class of high affinity sites for [3H]SMT in forebrain membranes (KD = 2.1 nM, Bmax=24.3 pmol/g of tissue at 4°C). The Bmax was approximately 3 times that of [3H](R)αMH binding to rat forebrain membranes (KD = 2.5 nM, Bmax = 7.3 pmol/g of tissue at 25 oC). Autoradiographic images of [3H]SMT binding in the brain were essentially the same as those of [3H](R)αMH. [3H]SMT also bound appreciably to peripheral tissues (the liver, adrenal, stomach, ileum, kidney, lung and bladder), whereas the [3H](R)αMH bindings to these peripheral tissues were negligible. These results indicate that [3H]SMT binds to H3 receptors primarily in the central nervous system, and that it also has high affinity toward non-H3 receptors, probably hemoproteins, in peripheral tissues.

Original languageEnglish
Pages (from-to)107-112
Number of pages6
JournalJapanese Journal of Pharmacology
Volume65
Issue number2
DOIs
Publication statusPublished - 1994

Keywords

  • Binding
  • Histamine
  • Histamine H3 receptor
  • [3H](R)α-Methylhistamine
  • [3H]5-Methylthioperamide

ASJC Scopus subject areas

  • Pharmacology

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