Department of Physiology, Pharmacology & Neuroscience, The Sophie Davis School of Biomedical Education, The City College of New York, The City University of New York, New York, NY 10031, USA.
School of Arts and Sciences, Emory University, Atlanta, GA 30322, USA.
Brain Sci. 2013 Apr 10;3(2):504-20. doi: 10.3390/brainsci3020504.
Cocaine is a psychostimulant in the pharmacological class of drugs called Local Anesthetics. Interestingly, cocaine is the only drug in this class that has a chemical formula comprised of a tropane ring and is, moreover, addictive. The correlation between tropane and addiction is well-studied. Another well-studied correlation is that between psychosis induced by cocaine and that psychosis endogenously present in the schizophrenic patient. Indeed, both of these psychoses exhibit much the same behavioral as well as neurochemical properties across species. Therefore, in order to study the link between schizophrenia and cocaine addiction, we used a behavioral paradigm called Acoustic Startle. We used this acoustic startle paradigm in female versus male Sprague-Dawley animals to discriminate possible sex differences in responses to startle. The startle method operates through auditory pathways in brain via a network of sensorimotor gating processes within auditory cortex, cochlear nuclei, inferior and superior colliculi, pontine reticular nuclei, in addition to mesocorticolimbic brain reward and nigrostriatal motor circuitries. This paper is the first to report sex differences to acoustic stimuli in Sprague-Dawley animals (Rattus norvegicus) although such gender responses to acoustic startle have been reported in humans (Swerdlow et al. 1997 [1]). The startle method monitors pre-pulse inhibition (PPI) as a measure of the loss of sensorimotor gating in the brain's neuronal auditory network; auditory deficiencies can lead to sensory overload and subsequently cognitive dysfunction. Cocaine addicts and schizophrenic patients as well as cocaine treated animals are reported to exhibit symptoms of defective PPI (Geyer et al., 2001 [2]). Key findings are: (a) Cocaine significantly reduced PPI in both sexes. (b) Females were significantly more sensitive than males; reduced PPI was greater in females than in males. (c) Physiological saline had no effect on startle in either sex. Thus, the data elucidate gender-specificity to the startle response in animals. Finally, preliminary studies show the effect of cocaine on acoustic startle in tandem with effects on estrous cycle. The data further suggest that hormones may play a role in these sex differences to acoustic startle reported herein.
可卡因是一种苯丙胺类药物,具有刺激精神的作用。有趣的是,可卡因是该类药物中唯一一种具有托烷环化学公式的药物,而且具有成瘾性。托烷与成瘾之间的相关性已经得到了充分的研究。另一个得到充分研究的相关性是可卡因引起的精神病与精神分裂症患者体内固有的精神病之间的关系。事实上,这两种精神病在物种之间表现出非常相似的行为和神经化学特性。因此,为了研究精神分裂症和可卡因成瘾之间的联系,我们使用了一种称为听觉惊跳的行为范式。我们在雌性和雄性斯普拉格-道利(Sprague-Dawley)动物中使用这种听觉惊跳范式,以区分对惊跳反应的可能性别差异。听觉惊跳方法通过听觉通路在大脑中运行,通过听觉皮层、耳蜗核、下丘和上丘、脑桥网状核以及中脑边缘奖赏和黑质纹状体运动回路中的感觉运动门控过程网络。尽管已经有报道称人类对听觉惊跳有性别反应(Swerdlow 等人,1997 [1]),但本文首次报道了斯普拉格-道利(Rattus norvegicus)动物对听觉刺激的性别差异。听觉惊跳方法监测前脉冲抑制(PPI)作为大脑神经元听觉网络中感觉运动门控丧失的衡量标准;听觉缺陷会导致感觉超负荷,随后导致认知功能障碍。可卡因成瘾者、精神分裂症患者以及接受可卡因治疗的动物被报道存在 PPI 缺陷的症状(Geyer 等人,2001 [2])。主要发现有:(a)可卡因显著降低了两性的 PPI。(b)女性比男性更敏感;女性的 PPI 降低幅度大于男性。(c)生理盐水对两性的惊跳均无影响。因此,这些数据阐明了动物惊跳反应的性别特异性。最后,初步研究显示,可卡因对听觉惊跳的影响与对发情周期的影响同时存在。这些数据进一步表明,激素可能在本文报道的听觉惊跳的性别差异中发挥作用。