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α2-肾上腺素能受体拮抗剂对5-羟色胺1A受体激动剂抑制小鼠中1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(DOI)诱导的头部震颤的影响。

The effects of alpha 2-adrenoceptor antagonists on the inhibition of 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI)-induced head shakes by 5-HT1A receptor agonists in the mouse.

作者信息

Dursun S M, Handley S L

机构信息

Pharmaceutical Sciences Institute, Aston University, Birmingham.

出版信息

Br J Pharmacol. 1993 Aug;109(4):1046-52. doi: 10.1111/j.1476-5381.1993.tb13727.x.

Abstract
  1. 8-Hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT), gepirone, buspirone and ipsapirone dose-dependently antagonized the head-shakes induced by 1-(2,5-dimethoxy 4-iodophenyl)-2-amino propane hydrochloride (DOI) (1.0 mg kg-1) in mice, when these agents were given i.p. 10 min beforehand. 2. para-Chlorophenylalanine (pCPA) abolished the effect of 8-OH-DPAT (0.1 mg kg-1) and of buspirone (1.0 mg kg-1). (+/-)-Pindolol (5.0 mg kg-1) also antagonized the effect of 8-OH-DPAT (0.1 mg kg-1). 3. The alpha 2-adrenoceptor antagonists, RX811059 (1.0 mg kg-1), idazoxan (0.5 mg kg-1), yohimbine (1.0 mg kg-1) and 1-(2-pyrimidinyl)-piperazine (1-PP) (2.0 mg kg-1) i.p. prevented the antagonistic effect of 8-OH-DPAT (0.1 mg kg-1) on DOI-head-shakes. 4. Orally-administered buspirone, given 60 min beforehand, only reduced DOI-head-shakes at doses of 60 mg kg-1 and above. However, when buspirone (1.0 mg kg-1) was administered orally twice daily for 21 days, DOI-head-shakes were significantly reduced when tested 60 min after the first daily dose on days 5, 12 and 21 and 48 h after withdrawal. 5. A single oral dose of buspirone (1.0 mg kg-1) strongly antagonized DOI-head-shakes when given 24 h after the last of 4 daily doses of 1-PP (2.0 mg kg-1, p.o.) but had no effect on DOI-head-shakes 24 h after the last of 4 daily doses of water (p.o.). 6. A single oral dose of 1-PP (2.0 mg kg-1) abolished the inhibitory effect of i.p. buspirone(1.0 mg kg-1) on DOI-head-shakes in mice which had received water (p.o.) daily on the 4 previous days but not in mice which had received 1-PP (2.0mg kg-1, p.o.) on these days.7. The ability of 5-HT1A receptor agonists to antagonize DOI-head-shakes may be due to an effect at presynaptic 5-HT receptors. It is suggested that 1-PP, formed from buspirone, may act at a2-adrenoceptors to prevent acutely administered oral buspirone from antagonizing DOI-head shakes, but that tolerance occurs to this effect of I-PP, thus revealing the inhibitory effect of buspirone when the latter is given repeatedly.
摘要
  1. 8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)、吉哌隆、丁螺环酮和伊沙匹隆在预先腹腔注射10分钟后,对盐酸1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷(DOI)(1.0毫克/千克)诱导的小鼠头部震颤具有剂量依赖性拮抗作用。2. 对氯苯丙氨酸(pCPA)消除了8-OH-DPAT(0.1毫克/千克)和丁螺环酮(1.0毫克/千克)的作用。(±)-吲哚洛尔(5.0毫克/千克)也拮抗了8-OH-DPAT(0.1毫克/千克)的作用。3. α2-肾上腺素能受体拮抗剂RX811059(1.0毫克/千克)、咪唑克生(0.5毫克/千克)、育亨宾(1.0毫克/千克)和1-(2-嘧啶基)-哌嗪(1-PP)(2.0毫克/千克)腹腔注射可预防8-OH-DPAT(0.1毫克/千克)对DOI-头部震颤的拮抗作用。4. 预先60分钟口服丁螺环酮,仅在剂量为60毫克/千克及以上时可减少DOI-头部震颤。然而,当丁螺环酮(1.0毫克/千克)每日口服两次,持续21天时,在第5、12和21天首次每日给药后60分钟以及撤药后48小时进行测试时,DOI-头部震颤显著减少。5. 在每日4次口服1-PP(2.0毫克/千克)的最后一次给药后24小时给予单次口服剂量的丁螺环酮(1.0毫克/千克),可强烈拮抗DOI-头部震颤,但在每日4次口服水的最后一次给药后24小时给予丁螺环酮对DOI-头部震颤无影响。6. 单次口服剂量的1-PP(2.0毫克/千克)消除了腹腔注射丁螺环酮(1.0毫克/千克)对在前4天每日口服水的小鼠DOI-头部震颤的抑制作用,但对在这些天口服1-PP(2.0毫克/千克)的小鼠无此作用。7. 5-HT1A受体激动剂拮抗DOI-头部震颤的能力可能归因于对突触前5-羟色胺受体的作用。提示由丁螺环酮形成的1-PP可能作用于α2-肾上腺素能受体以阻止急性口服丁螺环酮拮抗DOI-头部震颤,但对1-PP的这种作用会产生耐受性,从而在反复给予丁螺环酮时显示出其抑制作用。

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