lcl诱导的视听提示厌恶与反应测量和CS-US间隔的关系

Alvin M. Berk, Ralph R. Miller
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引用次数: 13

摘要

在对312只成年白化病大鼠进行的4项实验中,利用运动回避和饮酒抑制来监测空间线索与注射毒物或生理盐水之间的习得关联。从无可摄取物质的双室梭箱的一侧取出后立即注射高渗LiCl或高渗NaCl的大鼠,随后表现出该一侧的运动回避。其他接受同样训练的动物,随后在与注射配对的隔间或与非注射配对的隔间中提供新的液体,对饮酒的抑制没有差异。当注射等渗时,注射氯化钠的动物既没有表现出进食厌恶,也没有表现出运动厌恶,而注射氯化钠的动物在出现任何运动回避之前表现出特定部位的不愿喝水。当从治疗配对的隔室中取出后4分钟给药时,licl注射大鼠比运动位置偏好更快地出现了歧视性饮酒抑制,而nacl注射大鼠则没有表现出歧视性饮酒抑制。在进入治疗配对室前4分钟注射LiCl或NaCl的动物,通过摄取或运动测量均未显示明显的获得。试验类型、注射剂的性质和浓度以及注射时间之间的相互作用,不能用单一关联的不同反应阈值来解释,可以解释为在短CS-US间隔形成的高渗诱导的躯体疼痛关联对运动活动的影响,以及在短CS-US间隔或长CS-US间隔形成的毒素诱导的内脏疼痛关联对摄入行为的影响。当两者都可能以较短的间歇刺激出现时,急性躯体痛明显掩盖了内脏痛。在最近刺激等效假设失败的情况下,考虑了有关特定USs信息表现的强效反应系统的一些含义。
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LiCl-induced aversions to audiovisual cues as a function of response measure and CS—US interval

In four experiments using 312 adult albino rats, locomotor avoidance and suppression of drinking were used to monitor learned associations between spatial cues and injections of poison or saline. Rats injected with hypertonic LiCl or hypertonic NaCl immediately upon removal from one side of a two-compartment shuttlebox free of ingestible substances later showed locomotor avoidance of that side. Other animals that were identically trained and later offered novel fluids in either the compartment paired with injection or the compartment paired with noninjection did not differentially suppress drinking. When injections were isotonic, the NaCl-injected animals displayed neither ingestive nor locomotor aversions while the LiCl-injected animals showed a place-specific reluctance to drink before any locomotor avoidance appeared. When injections were administered 4 min after removal from the treatment-paired compartment, LiCl-injected rats developed discriminated suppression of drinking more rapidly than locomotor position preferences whereas NaCl-injected rats displayed no acquisition. Animals injected with LiCl or NaCl 4 min before being placed into the treatment-paired compartment showed no significant acquisition by either ingestive or locomotor measure. These interactions between type of test, nature and concentration of injected agent, and time of injection, not explicable in terms of different response thresholds for a single association, are interpreted as the consequence of hypertonically induced somatic pain associations formed at short CS—US intervals being prepotent to affect locomotor activity, and toxin-induced visceral pain associations formed at short or long CS—US intervals being prepotent to affect ingestive behavior. When both were potentially present with short interstimulus intervals, acute somatic pain apparently overshadowed visceral pain. Some implications of prepotent response systems for the manifestation of information about specific USs are considered in the light of recent failures of the stimulus equivalence hypothesis.

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