Shors Tracey J, Miesegaes George
Department of Psychology and Center for Collaborative Neuroscience, Rutgers University, Piscataway, NJ 08854-8020, USA.
Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13955-60. doi: 10.1073/pnas.202199999. Epub 2002 Oct 1.
Exposure to an acute stressful event can enhance learning in male rats, whereas exposure to the same event dramatically impairs performance in females. Here we tested whether the presence of sex hormones during early development organizes these opposite effects of stress on learning in males vs. females. In the first experiment, males were castrated at birth whereas females were injected with testosterone. Rats were trained as adults on the hippocampal-dependent learning task of trace eyeblink conditioning. Performance in adult males that had been castrated at birth was still enhanced by exposure to an acute stressful experience. However, adult females injected with testosterone at birth responded in the opposite direction, i.e., exposure to the stressor that typically reduces performance instead enhanced their levels of conditioning. In the second experiment, exposure to testosterone was manipulated in utero by injecting pregnant females with a testosterone antagonist. After foster rearing, adult offspring were exposed to the stressor and trained on the hippocampal-dependent learning task of trace conditioning. Although performance in adult females was unaffected by antagonizing testosterone in utero, i.e., stress still reduced performance, the enhancement of conditioning after stress in adult males was prevented. Thus, the presence of sex hormones during gestation and development organizes whether and how acute stressful experience will affect the ability to acquire new information in adulthood. As with many sexual behaviors, these cognitive responses to stress appear to be masculinized by exposure to testosterone and feminized by its absence during very early development.
暴露于急性应激事件可增强雄性大鼠的学习能力,而暴露于相同事件则会显著损害雌性大鼠的表现。在此,我们测试了早期发育过程中性激素的存在是否会导致应激对雄性和雌性学习产生的这些相反影响。在第一个实验中,雄性大鼠在出生时被阉割,而雌性大鼠则被注射睾酮。大鼠成年后接受海马体依赖的痕迹眨眼条件反射学习任务训练。出生时被阉割的成年雄性大鼠,其表现仍会因暴露于急性应激经历而得到增强。然而,出生时注射睾酮的成年雌性大鼠的反应却相反,即暴露于通常会降低表现的应激源反而提高了它们的条件反射水平。在第二个实验中,通过给怀孕的雌性大鼠注射睾酮拮抗剂来在子宫内控制睾酮的暴露。在寄养饲养后,成年后代暴露于应激源,并接受海马体依赖的痕迹条件反射学习任务训练。虽然成年雌性大鼠的表现不受子宫内睾酮拮抗的影响,即应激仍然会降低表现,但成年雄性大鼠应激后条件反射的增强却被阻止了。因此,妊娠和发育过程中性激素的存在决定了急性应激经历是否以及如何影响成年后获取新信息的能力。与许多性行为一样,这些对应激的认知反应似乎在早期发育过程中因暴露于睾酮而雄性化,因缺乏睾酮而雌性化。