Impairment of passive avoidance performance in SART-stressed mice and the action of drugs.

  • NISHIMURA Yoshitaka
    Department of Pharmacology, Faculty of Pharmacy, Kinki University
  • HATA Taeko
    Department of Pharmacology, Faculty of Pharmacy, Kinki University
  • KAWABATA Atsufumi
    Department of Pharmacology, Faculty of Pharmacy, Kinki University
  • ITOH Eiji
    Department of Pharmacology, Faculty of Pharmacy, Kinki University
  • KITA Tomitaro
    Department of Pharmacology, Faculty of Pharmacy, Kinki University

抄録

In order to investigate the behavioral characteristics of the SART-stressed (repeated cold-stressed) animal, a model of dysautonomia, step-down passive avoidance performance was examined in SART-stressed mice. SART-stressed mice exhibited a shortened test trial latency and a decreased incidence of maximum latency of 300 sec, but no change in the training latency. These alterations were blocked by single administration of chlorpromazine or carpipramine prior to the training trial. Repeated, but not single treatments with neurotropin and hopantenate improved the impaired performance due to SART stress. On the other hand, alprazolam and diazepam were ineffective by either mode of administration. Thus, SART-stressed mice appear to have impairment in the process of acquisition of a passive avoidance task.

収録刊行物

  • Jpn.J.Pharmacol.

    Jpn.J.Pharmacol. 49 (1), 111-117, 1989

    公益社団法人 日本薬理学会

被引用文献 (3)*注記

もっと見る

キーワード

詳細情報 詳細情報について

  • CRID
    1390001204290436352
  • NII論文ID
    130000832351
  • DOI
    10.1254/jjp.49.111
  • COI
    1:CAS:528:DyaL1MXovVCrtw%3D%3D
  • ISSN
    13473506
    00215198
  • PubMed
    2724672
  • 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

問題の指摘

ページトップへ