Bast Tobias, Feldon Joram
Behavioral Neurobiology Laboratory, The Swiss Federal Institute of Technology Zurich, Schorenstrasse 16, CH 8603 Schwerzenbach, Switzerland.
Prog Neurobiol. 2003 Jul;70(4):319-45. doi: 10.1016/s0301-0082(03)00112-6.
While the hippocampus makes unique contributions to memory, it has also long been associated with sensorimotor processes, i.e. innate processes involving control of motor responses to sensory stimuli. Moreover, hippocampal dysfunction has been implicated in neuropsychiatric diseases, such as schizophrenia and anxiety disorders, primarily characterized by non-mnemonic deficits in the processing of and responding to sensory information. This review is concerned with the hippocampal modulation of three sensorimotor processes in rats-locomotor activity, prepulse inhibition (PPI) of the startle reflex, and the startle reflex itself-whose alterations are related to human psychosis or anxiety disorders. Its main purpose is to present and discuss the picture emerging from studies examining the effects of pharmacological manipulations of the dorsal and ventral hippocampus by local drug microinfusions. While a role of the hippocampus in regulating locomotor activity, PPI, and startle reactivity has also been suggested based on the effects of hippocampal lesions, the microinfusion studies have revealed additional important details of this role and suggest modifications of notions based on lesion studies. In summary, the microinfusion studies corroborate that hippocampal mechanisms can directly influence locomotor activity, PPI, and startle reactivity, and that aberrant hippocampal function may contribute to neuropsychiatric diseases, in particular psychosis. The relation between different sensorimotor processes and hippocampal neurotransmission, the role of ventral and dorsal hippocampus, and the extrahippocampal mechanisms mediating the hippocampal modulation of different sensorimotor processes can partly be dissociated. Thus, the hippocampal modulation of these sensorimotor processes appears to reflect multiple operations, rather than one unitary operation.
虽然海马体对记忆有独特贡献,但长期以来它也与感觉运动过程相关,即涉及控制对感觉刺激的运动反应的先天过程。此外,海马体功能障碍与神经精神疾病有关,如精神分裂症和焦虑症,其主要特征是在处理和响应感觉信息方面存在非记忆缺陷。本综述关注大鼠的三种感觉运动过程——自发活动、惊吓反射的前脉冲抑制(PPI)以及惊吓反射本身——海马体对它们的调节,这些过程的改变与人类精神病或焦虑症有关。其主要目的是呈现和讨论通过局部药物微量注射对背侧和腹侧海马体进行药理学操作的研究中出现的情况。虽然基于海马体损伤的影响也有人提出海马体在调节自发活动、PPI和惊吓反应性方面的作用,但微量注射研究揭示了这一作用的其他重要细节,并建议对基于损伤研究的观念进行修正。总之,微量注射研究证实海马体机制可直接影响自发活动、PPI和惊吓反应性,并且海马体功能异常可能导致神经精神疾病,尤其是精神病。不同感觉运动过程与海马体神经传递之间的关系、腹侧和背侧海马体的作用以及介导海马体对不同感觉运动过程调节的海马体外机制可以部分地被区分。因此,海马体对这些感觉运动过程的调节似乎反映了多种操作,而不是单一的操作。