Meisel R L, Dohanich G P, McEwen B S, Pfaff D W
Neuroendocrinology. 1987 Mar;45(3):201-7. doi: 10.1159/000124726.
The present experiments sought to identify brain regions in which implants of an antiestrogen would antagonize the ability of a systemic estradiol treatment to activate sexual behavior in female rats. In experiment 1, ovariectomized female rats were implanted subcutaneously with 5-mm Silastic capsules containing a 5% concentration of estradiol and injected with 500 micrograms progesterone 2 days later, 4-5 h before testing for sexual behavior. Bilateral intracranial implants of 1% crystalline concentrations of the high-affinity antiestrogens monohydroxytamoxifen (TAM) or keoxifene placed into the ventromedial nucleus of the hypothalamus (VM) 24 h prior to estradiol treatment significantly reduced lordosis responsivity compared with control females receiving empty cannulae. Implants of 1% TAM into the medial preoptic area or medial amygdala 24 h prior to estradiol that no significant effect on lordosis. Similarly, implants of 1% TAM into the VM 12 h after estradiol had no effect on lordosis. In experiment 2, lordosis was activated by subcutaneous implants of Silastic capsules containing 1% estradiol plus 500 micrograms progesterone. In this experiment, implants of 1% TAM into the VM 24 h prior to estradiol significantly reduced lordosis only if both cannulae tips were in, or adjacent to, the VM. Females receiving intracranial 1% TAM, but whose cannulae (even unilaterally) were outside the VM, had levels of lordosis equivalent to those of control females. Increasing the concentration of intracranial TAM to 10% virtually eliminated lordosis in females with bilateral implants in the VM, whereas females receiving intracranial 10% TAM in the region of, but outside, the VM showed no evidence of a lordosis deficit.(ABSTRACT TRUNCATED AT 250 WORDS)
本实验旨在确定抗雌激素植入物可拮抗全身注射雌二醇激活雌性大鼠性行为能力的脑区。实验1中,对卵巢切除的雌性大鼠皮下植入含5%浓度雌二醇的5毫米硅橡胶胶囊,并在行为测试前4 - 5小时、2天后注射500微克孕酮。在雌二醇处理前24小时,将1%结晶浓度的高亲和力抗雌激素单羟基他莫昔芬(TAM)或凯昔芬双侧颅内植入下丘脑腹内侧核(VM),与接受空套管的对照雌性大鼠相比,显著降低了脊柱前凸反应性。在雌二醇处理前24小时,将1% TAM植入内侧视前区或内侧杏仁核,对脊柱前凸无显著影响。同样,在雌二醇处理12小时后将1% TAM植入VM,对脊柱前凸也无影响。实验2中,通过皮下植入含1%雌二醇加500微克孕酮的硅橡胶胶囊激活脊柱前凸。在本实验中,仅当两个套管尖端都在VM内或其附近时,在雌二醇处理前24小时将1% TAM植入VM才会显著降低脊柱前凸。接受颅内1% TAM但套管(即使单侧)在VM外的雌性大鼠,其脊柱前凸水平与对照雌性大鼠相当。将颅内TAM浓度提高到10%,实际上消除了VM双侧植入的雌性大鼠的脊柱前凸,而在VM区域但在其外接受颅内10% TAM的雌性大鼠没有脊柱前凸缺陷的迹象。(摘要截断于250字)