Badiani A, Castellano C, Oliverio A
Istituto di Psicobiologia e Psicofarmacologia del CNR, Roma, Italy.
Behav Neural Biol. 1991 Jan;55(1):123-30. doi: 10.1016/0163-1047(91)80132-x.
The locomotor behavior of unstressed and stressed mice of two inbred strains, DBA/2 and C57/BL6, was investigated. Animals were tested in a toggle-floor box apparatus, 30 min after saline or oxotremorine treatment (ip). A dose of oxotremorine that did not depress the activity of naïve mice (0.01 mg/kg) was chosen. Stressed mice were injected 24 h after either a single 2-h stress session (acute stress) or the last of 14 daily stress sessions of tube restraining (chronic stress). Acute stress did not modify the depressant effect of oxotremorine on locomotor behavior in either strain. On the contrary, chronic stress induced a clear sensitization of DBA but not C57 mice to the depressant effect of oxotremorine. These findings show that chronic stress may result in modifications of the cholinergic function, and its behavioral correlates, and that these changes are modulated by the genetic makeup.
对两个近交系小鼠DBA/2和C57/BL6在无应激和应激状态下的运动行为进行了研究。动物在腹腔注射生理盐水或氧化震颤素后30分钟,于翻转地板箱装置中进行测试。选用了一个不会抑制未处理小鼠活动的氧化震颤素剂量(0.01毫克/千克)。应激小鼠在单次2小时应激实验(急性应激)或14次每日束缚管应激实验(慢性应激)的最后一次实验后24小时注射药物。急性应激并未改变氧化震颤素对任一品系小鼠运动行为的抑制作用。相反,慢性应激使DBA小鼠而非C57小鼠对氧化震颤素的抑制作用产生明显的敏感性。这些发现表明,慢性应激可能导致胆碱能功能及其行为相关性的改变,且这些变化受基因组成的调节。