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[蛙皮素与各种中枢作用药物之间的拮抗作用特征:通过小鼠动态活动进行的研究]

[Characteristics of antagonism between ceruletide and various central-acting drugs: investigation by means of ambulatory activity in mice].

作者信息

Ida I, Asami T, Kuribara H, Machiyama Y, Tadokoro S

机构信息

Division for Behavior Analysis, Gunma University School of Medicine, Maebashi, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1990 Dec;96(6):333-41. doi: 10.1254/fpj.96.6_333.

Abstract

Behavioral characteristics of ceruletide, a cholecystokinin-like decapeptide, were investigated by means of ambulatory activity in mice. Ceruletide at 100 and 300 micrograms/kg, i.p. slightly but significantly decreased the mouse's activity for 20 min. Therefore, 100 micrograms/kg of ceruletide was used in the experiment of combined administration with the central-acting drugs. Ceruletide reduced the increased activity which was produced by methamphetamine (2 mg/kg, s.c.), ephedrine (80 mg/kg, i.p.), methylphenidate (4 mg/kg, s.c.), cocaine (20 mg/kg, s.c.), mazindol (2.5 mg/kg, s.c.), apomorphine (0.5 mg/kg, s.c.), bromocriptine (8 mg/kg, i.p.), scopolamine (0.5 mg/kg, s.c.), caffeine (10 mg/kg, s.c.) and morphine (20 mg/kg, s.c.) with different potencies and durations. The mice that had experienced ceruletide at 3 micrograms/kg for 5 times at intervals of 3-4 days demonstrated a significant increase in the sensitivity to methamphetamine, although the same treatment with 10-300 micrograms/kg of ceruletide was without effect. On the other hand, when 3-300 micrograms/kg of ceruletide was combined with 2 mg/kg of methamphetamine, the development of reverse tolerance to the ambulation-increasing effect of methamphetamine was inhibited dependently on the doses of ceruletide. However, the reverse tolerance to methamphetamine once established was scarcely modified by ceruletide when it was administered afterwards.

摘要

通过小鼠的动态活动研究了一种胆囊收缩素样十肽——蛙皮素的行为特征。腹腔注射100和300微克/千克的蛙皮素可使小鼠的活动在20分钟内略有但显著下降。因此,在与中枢作用药物联合给药的实验中使用了100微克/千克的蛙皮素。蛙皮素降低了由甲基苯丙胺(2毫克/千克,皮下注射)、麻黄碱(80毫克/千克,腹腔注射)、哌醋甲酯(4毫克/千克,皮下注射)、可卡因(20毫克/千克,皮下注射)、马吲哚(2.5毫克/千克,皮下注射)、阿扑吗啡(0.5毫克/千克,皮下注射)、溴隐亭(8毫克/千克,腹腔注射)、东莨菪碱(0.5毫克/千克,皮下注射)、咖啡因(10毫克/千克,皮下注射)和吗啡(20毫克/千克,皮下注射)产生的活动增加,其效力和持续时间各不相同。每隔3 - 4天以3微克/千克的剂量给小鼠注射5次蛙皮素后,小鼠对甲基苯丙胺的敏感性显著增加,尽管用10 - 300微克/千克的蛙皮素进行相同处理没有效果。另一方面,当3 - 300微克/千克的蛙皮素与2毫克/千克的甲基苯丙胺联合使用时,对甲基苯丙胺增加活动作用的反向耐受性的发展依赖于蛙皮素的剂量而受到抑制。然而,一旦建立起对甲基苯丙胺的反向耐受性,之后注射蛙皮素几乎不会对其产生改变。

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