Antimuscarinic effects of antihistamines : Quantitative evaluation by receptor-binding assay.

  • KUBO Nobuo
    Department of Pharmacology, Kobe University School of Medicine
  • SHIRAKAWA Osamu
    Department of Pharmacology, Kobe University School of Medicine
  • KUNO Takayoshi
    Department of Pharmacology, Kobe University School of Medicine
  • TANAKA Chikako
    Department of Pharmacology, Kobe University School of Medicine

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抄録

Quantitative evaluation of antimuscarinic effects of antihistamines (H1and H2-receptor antagonists) was carried out using a receptor-binding assay. The inhibition constants (K1 values) of twenty seven H1-receptor antagonists, one related antidepressant and three H2-receptor antagonists at H1-receptors and muscarinic receptors in the bovine cerebral cortex were determined. All the H2receptor antagonists examined showed very low affinity for the muscarinic receptors. On the other hand, some H1-receptor antagonists (mequitazine, cyproheptazine, clemastine, diphenylpyraline, promethazine, homochlorcyclizine and alimemazine) had high affinity for the muscarinic receptors (K1=5.0-38 nM). Another group of H1 -receptor antagonists (mepyramine, terfenadine, metapyrilen, azelastine, hydroxyzine and meclizine) had low affinity for the muscarinic receptors (K1=3, 600-30, 000 nM). Thus, a broad range of antimuscarinic potencies among the antihistamines was demonstrated. These results should provide helpful information with regard to the clinical and experimental use of antihistamines.

収録刊行物

  • Jpn.J.Pharmacol.

    Jpn.J.Pharmacol. 43 (3), 277-282, 1987

    公益社団法人 日本薬理学会

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詳細情報 詳細情報について

  • CRID
    1390282679265135872
  • NII論文ID
    130000833420
  • DOI
    10.1254/jjp.43.277
  • COI
    1:CAS:528:DyaL2sXhvVyrt7g%3D
  • ISSN
    13473506
    00215198
    http://id.crossref.org/issn/00215198
  • PubMed
    2884340
  • Web Site
    https://search.jamas.or.jp/link/ui/1988162500
  • 本文言語コード
    en
  • データソース種別
    • JaLC
    • Crossref
    • PubMed
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

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