Department of Psychology, University of Tromsø, 9037 Tromsø, Norway.
Behav Brain Res. 2012 Apr 21;230(1):11-20. doi: 10.1016/j.bbr.2012.01.048. Epub 2012 Feb 1.
Ovariectomized females were given an infusion in the medial preoptic area (MPOA) of a viral vector carrying either a shRNA directed against the estrogen receptor α (ERα) or luciferase. The females were subjected to a test for sexual incentive motivation immediately followed by a test for receptivity and proceptive behaviors. Two weeks later they were tested in the light/dark choice procedure, and after another 2 weeks they were subjected to a test in a brightly lit open field. Finally, the females were given free access to a running wheel for 88h. The females were treated with estradiol benzoate (EB), 18 or 1.5μg/kg, in randomized order 52h before each test except the running wheel. In that experiment, they were given EB 48h after introduction into the wheel cage. They were given progesterone, 1mg/rat, about 4h before all tests, except the running wheel. The shRNA reduced the number of ERα with 83%. Females with few ERα in the MPOA showed increased lordosis quotient after the 1.5μg/kg dose of EB. There was no effect on proceptive behaviors or on rejections. When given the 18μg/kg EB dose, there was no difference between females with few preoptic ERα and controls. In the test for sexual incentive motivation, females with few preoptic ERα approached the castrated male incentive more than controls, regardless of EB dose. They also moved a shorter distance. In the light/dark choice test as well as in the open field, females with few ERα in the MPOA showed signs of reduced fear/anxiety, since they spent more time in the light part of the dark/light box and in the center of the open field. Finally, the data from the running wheel showed that females with few preoptic ERα failed to show enhanced activity after treatment with EB. These data show that the preoptic ERα inhibits lordosis in females with an intermediate level of receptivity while it fails to do so in fully receptive females. The ERα in the MPOA seems to be necessary for selective approach to a sexual incentive. Finally, activation of this receptor appears to have anxiogenic effects in the procedures employed here. A hypothesis for how all these actions of the preoptic ERα contributes to efficient reproductive behavior is outlined.
去卵巢雌性动物被给予在中脑前腹内侧核(MPOA)中输注携带针对雌激素受体α(ERα)或荧光素酶的 shRNA 的病毒载体。雌性动物立即接受性激励动机测试,然后接受接受性和前摄性行为测试。两周后,它们在明暗选择程序中进行测试,两周后在明亮的开阔场中进行测试。最后,雌性动物可以自由使用跑步轮 88 小时。雌性动物用苯甲酸雌二醇(EB)处理,以随机顺序在每次测试前 52 小时,除了跑步轮,以 18 或 1.5μg/kg 给予,在该实验中,它们在引入车轮笼后 48 小时给予 EB。在所有测试前约 4 小时给予孕激素,1mg/大鼠,除了跑步轮。MPOA 中 ERα 数量减少 83%。MPOA 中 ERα 数量较少的雌性动物在接受 1.5μg/kg EB 剂量后,发情指数增加。对前摄性行为或拒绝没有影响。当给予 18μg/kg EB 剂量时,MPOA 中 ERα 较少的雌性动物与对照动物没有区别。在性激励动机测试中,无论 EB 剂量如何,MPOA 中 ERα 较少的雌性动物比对照动物更接近去势雄性激励。它们移动的距离也较短。在明暗选择测试以及开阔场中,MPOA 中 ERα 较少的雌性动物表现出恐惧/焦虑减少的迹象,因为它们在明暗箱的亮部和开阔场的中心花费更多时间。最后,跑步轮的数据显示,MPOA 中 ERα 较少的雌性动物在接受 EB 治疗后未能表现出活动增强。这些数据表明,中脑前腹内侧核的 ERα 抑制了具有中等接受能力的雌性动物的发情,而在完全接受的雌性动物中则不能抑制发情。MPOA 中的 ERα 似乎对选择性接近性激励是必要的。最后,激活该受体似乎在本实验中使用的程序中具有焦虑作用。概述了中脑前腹内侧核 ERα 的所有这些作用如何有助于有效的生殖行为的假设。