心理神经免疫学的研究及其思路问题

回顾并分析了心理神经免疫学的研究历史和发展,指出要深入揭示行为、精神活动是如何转化为影响健康的生理状态的奥秘,需要新的研究思路并讨论了新的研究路线     

Variability and creativity in small-sided conditioned games among elite soccer players

ObjectiveSmall-sided conditioned games (SSCG) in soccer are games with a small number of players, often played on smaller than regular pitches and with adapted rules. It has been argued that SSCG foster soccer players’ physical, technical and tactical performances and creativity. This study tested the latter conjecture by analysing video-footage of individual actions of elite soccer players in 5 v 5, 6 v 6, 7 v 7 SSCG played during regular training sessions and 11-aside training matches. Based on the ecological dynamics approach, we hypothesized that smaller formats would result in players making more individual actions. We additionally anticipated that the smaller formats players would induce a larger repertoire of actions, that is, an increased variability of actions, and that such increase in variability would be associated with more creative actions. Along the same lines, we reasoned that midfielders would make more creative actions than defenders and attackers.MethodWe categorized 3555 soccer actions on the ball and without the ball of 24 elite soccer players.ResultsPlayers produced more actions in smaller SSCG formats compared to the larger SSCG format and the 11-aside match. They also produced more different actions in SSCG than the 11-aside match. Furthermore, ten creative actions (i.e., actions that were adequate and only made by one or two players) were discerned. The creative actions emerged most often in the smaller SSCG, and were absent in the 11-aside matches. Finally, strikers, defenders and midfielders did not show reliable differences in terms of number, variability and creativity of action.ConclusionSSCG in soccer do indeed stimulate variability and creativity of individual actions. It is important to confirm whether these immediate effects of SSCG generalize across longer time scales.     

The effect of on‐ or off‐line extinction of a first‐order conditioned stimulus on a second‐order conditioned response in rats

In a water‐licking experiment with rats, the effects of the extinction of a first‐order conditioned stimulus (CS1) on the suppression of licking established for a second‐order conditioned stimulus (CS2) were explored. Extinction of the first‐order conditioned response (CR1) attenuated the conditioned suppression induced by CS2 when the rats had been allowed to lick water during the CR1 extinction phase. However, if water had been unavailable during the CR1 extinction phase, suppression by CS2 was not affected. The latter result is consistent with other studies of rats' conditioned suppression and suggests that the underlying mechanism of second‐order conditioning in this experiment is a connection between CS2 and the response elicited by CS1 rather than a CS2‐CS1 connection. The former result was interpreted as the CR1 extinction phase encouraging the rats to lick water despite the fear elicited by CS1, and thus, in testing, they licked despite the fear elicited by CS2.     

二级强化程序在药物成瘾研究中的应用

二级强化程序是一种以物质的强化效应为基础,评价药物的精神依赖性潜力的方法,将其应用到自身给药实验中,即为二级强化自身给药模型。在这个模型中,动物在条件性刺激的影响下按压杠杆以寻求药物的行为反映了其对成瘾性药物的渴求。使用二级强化程序,人们发现：条件性刺激既能够影响觅药行为的获得和保持,也能够影响这种行为的消退;伏隔核的核区、杏仁核基底外侧部和内侧前额皮层等部位在药物相关的条件性刺激诱导动物产生觅药行为的过程中起重要作用。二级强化程序的应用为开发治疗药物成瘾的物质提供了一条新思路     

Implications and refinements of the establishing operation concept

In this paper I discuss (a) three steps in the development of establishing operation (EO) terminology, (b) my early neglect of its possible relevance to applied behavior analysis, (c) the importance of functional analysis methodology for increasing awareness of EO issues, and (d) three comprehensive reviews that clarify the role of EOs in applied work. I then review and further analyze seven topics that require further clarification or that have been raised since my 1982 and 1993 articles: the EO evocative effect, deprivation and satiation, problem behavior maintained by attention, decreasing behavior evoked by a transitive conditioned establishing operation, EOs in the context of escape and avoidance, academic demand, and decreasing behavior evoked by a reflexive conditioned establishing operation.     

Pigeons may not remember the stimuli that reinforced their recent behavior

In two experiments the conditioned reinforcing and delayed discriminative stimulus functions of stimuli that signal delays to reinforcement were studied. Pigeons' pecks to a center key produced delayed-matching-to-sample trials according to a variable-interval 60-s (or 30-s in 1 pigeon) schedule (Experiment 1) or a multiple variable-interval 20-s variable-interval 120-s schedule (Experiment 2). The trials consisted of a 2-s illumination of one of two sample key colors followed by delays ranging across phases from 0.1 to 27.0 s followed in turn by the presentation of matching and nonmatching comparison stimuli on the side keys. Pecks to the key color that matched the sample were reinforced with 4-s access to grain. Under some conditions of Experiment 1, pecks to nonmatching comparison stimuli produced a 4-s blackout and the start of the next interval. Under other conditions of Experiment 1 and each condition of Experiment 2, pecks to nonmatching stimuli had no effect and trials ended only when pigeons pecked the other, matching stimulus and received food. The functions relating pretrial response rates to delays differed markedly from those relating matching-to-sample accuracy to delays. Specifically, response rates remained relatively high until the longest delays (15.0 to 27.0 s) were arranged, at which point they fell to low levels. Matching accuracy was high at short delays, but fell to chance at delays between 3.0 and 9.0 s. In Experiment 2, both matching accuracy and response rates remained high over a wider range of delays in the variable-interval 120-s component relative to the variable-interval 20-s component. The difference in matching accuracy between the components was not due to an increased tendency in the variable-interval 20-s component toward proactive interference following short intervals. Thus, under these experimental conditions the conditioned reinforcing and the delayed discriminative functions of the sample stimulus depended on the same variables (delay and variable-interval value), but were nevertheless dissociated.     

Devaluation of stimuli contingent on choice: evidence for conditioned reinforcement

Pigeons were presented a concurrent-chains schedule of reinforcement that had terminal links of equal duration. The initial links of the schedule were periodically interrupted by 15-s periods during which an extinction schedule was in effect. The extinction periods were presented on either a response-contingent or a noncontingent basis. Relative response rate for the left alternative decreased when the extinction periods were accompanied by the left terminal-link stimulus. Relative response rate for the right alternative decreased when the extinction periods were accompanied by the right terminal-link stimulus. Relative response rate varied inversely with the frequency of presentation of the extinction periods but was unaffected by presence versus absence of the response contingency in the schedule of extinction-period presentation. Furthermore, relative response rate was unaffected by presentation of extinction periods accompanied by a novel stimulus. When the extinction periods were presented after reinforcement in the left terminal link instead of as interruptions of the initial links, relative response rate for the left alternative was reduced if the postreinforcement extinction period was accompanied by the terminal-link stimulus for the left chain and reduced less if the extinction period was accompanied by the terminal-link stimulus for the right chain. The results demonstrate that the correlation between the terminal-link stimulus and extinction influenced the relative response rate in the initial link.     

A molecular analysis of choice on concurrent-chains schedules.

Six pigeons responded on concurrent-chains schedules with either independent or interdependent equal variable-interval schedules in the initial links and unequal variable-interval schedules, always in a 2:1 ratio, in the terminal links. Relative response rates in the initial links increased across conditions as initial-link duration was shortened and decreased across conditions as terminal-link duration was shortened, replicating previous findings. Responses in the initial links were recorded in 5-s bins, and local or molecular relative response rates were calculated in order to ascertain how relative response rate varied as a function of time since the onset of the initial links. Two distinct molecular patterns were found. With interdependent initial links, relative response rates for the preferred key were elevated for the first 10 or 20 s of the initial links and then declined to an asymptotic value. With independent initial links, a negative recency effect was found similar to that reported by Killeen (1970). These two molecular patterns were related to the different momentary reinforcement probabilities resulting from independent and interdependent scheduling.     

Resistance to change produced by access to fixed-delay versus variable-delay terminal links

Pigeons' responding was reinforced on a multiple schedule consisting of two two-link chain schedules presented in regular alternation. Responding in initial links (always variable-interval 60-s) produced a key-color change and access to a terminal link. The terminal link for one chain provided food after a fixed delay (fixed-interval or fixed-time); the terminal link for the other provided food after a variable delay (variable-interval or variable-time). The average duration of the terminal-link schedules was varied across conditions, but in every condition the arithmetic mean of the variable-delay terminal-link schedule was equal to the duration of the fixed delay. Response rates were higher in the initial links of the chains with the variable-delay terminal links. Response-decreasing operations (satiation, extinction) were used after performances reached asymptote. Response rates maintained by access to variable-delay terminal links tended to be more resistant to change than were rates maintained by access to fixed-delay terminal links. These results are consistent with the preference for variable- over fixed-interval terminal links observed with concurrent-chains schedules, suggesting (1) that immediacy of reinforcement influences the conditioned reinforcing potency of access to a terminal link and (2) that choice in concurrent chains and resistance of responding to change may be manifestations of the same effect of reinforcement.     

Effects on preference of reinforcement delay, number of reinforcers, and terminal-link duration

Three experiments used concurrent-chains procedures to examine the effects of reinforcement delay, number of reinforcers, and terminal-link duration on preference. In Condition 30 of Experiment 1, food was delivered after 30 seconds in each 150-second terminal link, with four additional food deliveries occurring at 30-second intervals in one of the links. In Condition 5, food was delivered after 5 seconds in each 25-second terminal link, and the four additional reinforcers were delivered at 5-second intervals. Preferences for the multiple-food chain were greater in Condition 30. In Experiment 2, the terminal link(s) providing only one reinforcer terminated immediately after delivery of the reinforcer. Preferences for the multiple-food chain were smaller than in Experiment 1. In Condition 5 of Experiment 3, food was delivered after 5, 75, 100, 125, and 150 seconds in one 150-second link and after 5 seconds in the other. Condition 50 differed only in that the first (or only) reinforcer in each link was delivered after 50 seconds instead of after 5 seconds. Preferences for the multiple-food chain were greater in Condition 50. Results of Experiments 1 and 2 do not correspond to results obtained by Moore (1979).