Báez M, Volosin M
Departamento de Farmacología, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina.
Pharmacol Biochem Behav. 1994 Nov;49(3):729-36. doi: 10.1016/0091-3057(94)90093-0.
The effect of corticosterone (CS) synthesis inhibition with metyrapone-a blocker of the 11 beta-hydroxylase (150 mg/kg IP)-on immobility time during the forced swim test was recorded. Immobility time was measured during a 15-min forced swim (test). Twenty-four hours later rats were subjected to an additional 5 min forced swim (retest). In one experiment, metyrapone or vehicle was administered 3 h before the initial test, while CS (0, 5, 10, or 20 mg/kg SC) was administered 1 h prior to the initial test. Metyrapone significantly reduced immobility time during both test and retest. This effect was reverted in a dose-dependent fashion by CS. In a second experiment, animals exposed to the initial test 24 h before were injected with metyrapone or vehicle 3 h before the retest, while CS (0, 10, or 20 mg/kg SC) was administered 1 h prior the retest. Metyrapone, administered before the retest, reduced immobility time and CS partially reverted metyrapone effect. In another group of animals, serum CS concentrations were evaluated before and after test and retest. In vehicle groups, the high immobility time during test and retest was associated with high CS serum concentrations poststress. In animals receiving metyrapone prior to the initial test, the reduced immobility time was related to low levels of CS after the test and an attenuated secretion following the retest. Moreover, CS (20 mg/kg) and metyrapone+CS groups had high CS levels before the test, which remained high 2 h after the test, although after the retest, both groups showed a pattern of CS secretion similar to that observed in vehicle animals.(ABSTRACT TRUNCATED AT 250 WORDS)
记录了用甲吡酮(一种11β-羟化酶阻滞剂,腹腔注射150毫克/千克)抑制皮质酮(CS)合成对强迫游泳试验中不动时间的影响。在15分钟的强迫游泳(试验)期间测量不动时间。24小时后,对大鼠进行额外5分钟的强迫游泳(重新测试)。在一项实验中,在初始试验前3小时给予甲吡酮或赋形剂,而在初始试验前1小时给予CS(0、5、10或20毫克/千克,皮下注射)。甲吡酮在试验和重新测试期间均显著减少了不动时间。CS以剂量依赖的方式逆转了这种作用。在第二项实验中,24小时前接受初始试验的动物在重新测试前3小时注射甲吡酮或赋形剂,而在重新测试前1小时给予CS(0、10或20毫克/千克,皮下注射)。在重新测试前给予甲吡酮减少了不动时间,CS部分逆转了甲吡酮的作用。在另一组动物中,在试验和重新测试前后评估血清CS浓度。在赋形剂组中,试验和重新测试期间的高不动时间与应激后高CS血清浓度相关。在初始试验前接受甲吡酮的动物中,不动时间的减少与试验后CS水平低以及重新测试后分泌减弱有关。此外,CS(20毫克/千克)组和甲吡酮+CS组在试验前CS水平较高,试验后2小时仍保持较高水平,尽管在重新测试后,两组CS分泌模式与赋形剂组动物相似。(摘要截断于250字)