Journal articles on the topic 'Rats – Psychology'

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1

Kuper, Adam. "Of rats and psychology students." Nature 397, no. 6717 (January 1999): 312–13. http://dx.doi.org/10.1038/16839.

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2

Sclafani, Anthony. "Eating rates in normal and hypothalamic hyperphagic rats." Physiology & Behavior 55, no. 3 (March 1994): 489–94. http://dx.doi.org/10.1016/0031-9384(94)90105-8.

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3

Blumberg, Mark S., and Greta Sokoloff. "Do infant rats cry?" Psychological Review 108, no. 1 (2001): 83–95. http://dx.doi.org/10.1037/0033-295x.108.1.83.

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4

Killeen, Peter R. "Rats, responses and reinforcers: Using a little psychology on our subjects." Behavioral and Brain Sciences 17, no. 1 (March 1994): 157–72. http://dx.doi.org/10.1017/s0140525x00033860.

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5

Fox, Andrew T., John R. Smethells, and Mark P. Reilly. "Flash rate discrimination in rats: Rate bisection and generalization peak shift." Journal of the Experimental Analysis of Behavior 100, no. 2 (July 22, 2013): 211–21. http://dx.doi.org/10.1002/jeab.36.

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6

Galef, Bennett G., Elaine E. Whiskin, and Christopher S. Horn. "What observer rats don’t learn about foods from demonstrator rats." Animal Learning & Behavior 27, no. 3 (September 1999): 316–22. http://dx.doi.org/10.3758/bf03199730.

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7

Hunt, Maree J., and Anne C. Macaskill. "Student Responses to Active Learning Activities With Live and Virtual Rats in Psychology Teaching Laboratories." Teaching of Psychology 44, no. 2 (February 8, 2017): 160–64. http://dx.doi.org/10.1177/0098628317692632.

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Taking an ethical approach to using nonhuman animals in teaching requires assessment of the learning benefits of using animals and how these compare to the benefits of alternative teaching practices. It is also important to consider whether students have ethical reservations about completing exercises with animals. We compared upper level undergraduate students’ evaluations of psychology laboratories using live rats with their evaluations of using a virtual rat (Sniffy). Students reported that the live-rat labs were ethically acceptable and that working with live rats enhanced their learning to a greater extent than working with Sniffy. These results support the retention of laboratories using live rats in psychology courses.
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8

Gunn, Kenneth P. "Rats' consumption rates after short breaks in food availability within meals." Learning and Motivation 20, no. 3 (August 1989): 295–321. http://dx.doi.org/10.1016/0023-9690(89)90010-6.

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9

Bradshaw, C. M., and E. Szabadi. "Herrnstein's Equation: Data from 110 Rats." Psychological Reports 73, no. 3_suppl (December 1993): 1355–61. http://dx.doi.org/10.2466/pr0.1993.73.3f.1355.

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110 rats were trained under a series of variable-interval schedules of sucrose reinforcement (0.6 M, 50 μl), covering a wide range of scheduled interreinforcement intervals. Response and reinforcement rates recorded during the last five sessions of exposure to each schedule were used to fit Herrnstein's (1970) hyperbolic ‘response strength’ equation to the data from each rat The equation accounted for >80% of the data variance in 90%, and >90% of the variance in 60% of the sample. The distribution of the values of Rmax, the asymptote of the hyperbolic curve, did not depart significantly from normality. However, the distribution of the values of KH, the reinforcement rate needed to maintain the half-maximum response rate, was markedly skewed; logarithmically transformed values of KH conformed to a normal distribution. The data provide further support for the applicability of Herrnstein's equation to variable-interval performance; it is suggested that studies involving comparison of the parameters of the equation between groups of subjects should adopt logarithmic transformation of the values of KH.
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10

Wanchisen, Barbara A., Glen E. Sutphin, Seth A. Balogh, and Thomas A. Tatham. "Lasting Effects of a Behavioral History of Low-Rate Responding in Rats." Learning and Motivation 29, no. 2 (May 1998): 220–35. http://dx.doi.org/10.1006/lmot.1997.1000.

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11

Sédat, Jacques. "L'Homme aux rats." Topique 108, no. 3 (2009): 103. http://dx.doi.org/10.3917/top.108.0103.

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12

Hensch, S. A., and C. Donald Heth. "Evaluation of Behavior in a Stochastic Choice Setting." Psychological Reports 64, no. 1 (February 1989): 80–82. http://dx.doi.org/10.2466/pr0.1989.64.1.80.

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This note presents a result obtained during a study of concurrent variable-interval choice by rats. The evidence suggests that an animal may be able to optimize reward rate in a changing environment and that animals are sensitive to daily fluctuations in reward rates.
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13

Lefrancois, Janet R., and Barbara Metzger. "LOW-RESPONSE-RATE CONDITIONING HISTORY AND FIXED-INTERVAL RESPONDING IN RATS." Journal of the Experimental Analysis of Behavior 59, no. 3 (May 1993): 543–49. http://dx.doi.org/10.1901/jeab.1993.59-543.

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14

Boer, Douglas P., W. Frank Epling, W. David Pierce, and James C. Russell. "Suppression of food deprivation-induced high-rate wheel running in rats." Physiology & Behavior 48, no. 2 (August 1990): 339–42. http://dx.doi.org/10.1016/0031-9384(90)90324-w.

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15

Ronca, April E., and Jeffrey R. Alberts. "Heart rate development and sensory-evoked cardiac responses in perinatal rats." Physiology & Behavior 47, no. 6 (June 1990): 1075–82. http://dx.doi.org/10.1016/0031-9384(90)90355-8.

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16

Dailey, William, Sharon B. Wigal, and Abram Amsel. "Effects of photic stimulation on heart rate of infant rats." International Journal of Psychophysiology 3, no. 3 (January 1986): 183–204. http://dx.doi.org/10.1016/0167-8760(86)90027-9.

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17

Gibson, Evelyn, and Phil Reed. "Stimulus Over-selectivity in Rats." Journal of Autism and Developmental Disorders 35, no. 6 (December 2005): 851–59. http://dx.doi.org/10.1007/s10803-005-0030-9.

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18

Richardson, Rick, David C. Riccio, and Drew Smoller. "Counterconditioning of memory in rats." Animal Learning & Behavior 15, no. 3 (September 1987): 321–26. http://dx.doi.org/10.3758/bf03205025.

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19

Gaffan, E. A., and A. L. Woolmore. "Complex Visual Learning by Rats." Learning and Motivation 27, no. 4 (November 1996): 375–99. http://dx.doi.org/10.1006/lmot.1996.0022.

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20

Hamilton, Kristen R., Marc N. Potenza, and Neil E. Grunberg. "Lewis rats have greater response impulsivity than Fischer rats." Addictive Behaviors 39, no. 11 (November 2014): 1565–72. http://dx.doi.org/10.1016/j.addbeh.2014.02.008.

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21

Navarre, Brittany M., Jillian D. Laggart, and Rebecca M. Craft. "Anhedonia in postpartum rats." Physiology & Behavior 99, no. 1 (January 2010): 59–66. http://dx.doi.org/10.1016/j.physbeh.2009.10.011.

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22

Schmajuk, Nestor A., and Beth A. Christiansen. "Eyeblink conditioning in rats." Physiology & Behavior 48, no. 5 (November 1990): 755–58. http://dx.doi.org/10.1016/0031-9384(90)90221-o.

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23

Hackenberg, Timothy D., Lauren Vanderhooft, Jasmine Huang, Madeline Wagar, Jordan Alexander, and Lavinia Tan. "Social preference in rats." Journal of the Experimental Analysis of Behavior 115, no. 3 (March 13, 2021): 634–49. http://dx.doi.org/10.1002/jeab.686.

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24

Galef, Bennett G., Elaine E. Whiskin, and Edita Bielavska. "Interaction with demonstrator rats changes observer rats' affective responses to flavors." Journal of Comparative Psychology 111, no. 4 (1997): 393–98. http://dx.doi.org/10.1037/0735-7036.111.4.393.

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25

Bowers, Robin L., Michelle Harris-Peterson, Matthew S. Mollenhauer, Carol DeVolder, David D. Avery, and Ralph W. Richards. "Bombesin Improves Rats' Operant Responding Maintained by a Differential-Reinforcement-of-Low-Rates Schedule of Food Reinforcement." Psychological Reports 66, no. 1 (February 1990): 131–38. http://dx.doi.org/10.2466/pr0.1990.66.1.131.

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26

Riccio, Alexandra P., and Bruce D. Goldman. "Circadian rhythms of body temperature and metabolic rate in naked mole-rats." Physiology & Behavior 71, no. 1-2 (October 2000): 15–22. http://dx.doi.org/10.1016/s0031-9384(00)00280-8.

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27

Gawley, Donald J., William Timberlake, and Gary A. Lucas. "Anticipatory drinking in rats: Compensatory adjustments in the local rate of intake." Physiology & Behavior 42, no. 3 (January 1988): 297–302. http://dx.doi.org/10.1016/0031-9384(88)90086-8.

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28

Malet-Karas, Aurore, Marion Noulhiane, and Valérie Doyère. "Dynamics of Spatio-Temporal Binding in Rats." Timing & Time Perception 7, no. 1 (January 11, 2019): 27–47. http://dx.doi.org/10.1163/22134468-20181124.

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Time and space are commonly approached as two distinct dimensions, and rarely combined together in a single task, preventing a comparison of their interaction. In this project, using a version of a timing task with a spatial component, we investigate the learning of a spatio-temporal rule in animals. To do so, rats were placed in front of a five-hole nose-poke wall in a Peak Interval (PI) procedure to obtain a reward, with two spatio-temporal combination rules associated with different to-be-timed cues and lighting contexts. We report that, after successful learning of the discriminative task, a single Pavlovian session was sufficient for the animals to learn a new spatio-temporal association. This was seen as evidence for a beneficial transfer to the new spatio-temporal rule, as compared to control animals that did not experience the new spatio-temporal association during the Pavlovian session. The benefit was observed until nine days later. The results are discussed within the framework of adaptation to a change of a complex associative rule involving interval timing processes.
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29

Satinder, K. Paul, and Robert A. McGowan. "Hippocampal Lesions and Open-Field Defecation in Rats." Psychological Reports 56, no. 2 (April 1985): 627–30. http://dx.doi.org/10.2466/pr0.1985.56.2.627.

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Effects of dorsal and ventral hippocampal lesions on open-field defecation of rats were investigated. Based on presurgical testing, matched groups from both sexes were either lesioned or sham-operated. Compared to respective presurgical scores the postsurgical defecation score decreased significantly in the sham-operated group but remained the same in the hippocampally lesioned group. Results were discussed in terms of habituation and the inverted-U arousal function.
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30

Rudski, Jeffrey. "Naloxone Decreases Responding for Conditioned Reinforcement in Rats." Psychological Reports 100, no. 1 (February 2007): 263–69. http://dx.doi.org/10.2466/pr0.100.1.263-269.

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That opioids can mediate unconditioned reinforcement is well established, but there is little evidence indicating whether they modify conditioned reinforcement. Here, a tone which initially served as a discriminative stimulus for the availability of water reinforcement was established as a conditioned stimulus. When later given a choice between pressing a lever producing the tone (but not water) or one which produced no effect, rats chose the tone-producing lever 66% of the time. Naloxone (3.0 mg/kg) reduced overall responding and completely eliminated the preference for the tone-producing lever. Results are briefly discussed in terms of the importance of understanding mechanisms serving conditioned reinforcement.
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31

Nakajima, Sadahiko. "Further Evidence for Swimming‐Based Pica in Rats." Japanese Psychological Research 62, no. 1 (December 18, 2018): 39–50. http://dx.doi.org/10.1111/jpr.12243.

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32

Nakajima, Sadahiko, and Nobuyuki Kawai. "Failure of Retrospective Inference in Rats' Taste Aversion." Japanese Psychological Research 39, no. 2 (May 1997): 87–97. http://dx.doi.org/10.1111/1468-5884.00042.

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33

MINERVINI, VANESSA, CHAD M. GALUSKA, and DAVID R. MAGUIRRE. "WITHIN-SESSION CHANGES IN RATS´ FOOD-DEMAND ELASTICITY." Revista Mexicana de Análisis de la Conducta 39, no. 1 (June 1, 2013): 35–61. http://dx.doi.org/10.5514/rmac.v39.i1.63909.

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34

Sclafani, Anthony, Karen Ackroff, Graciela Elizalde, François Lucas, Jeffrey W. Nissenbaum, and Catalina Perez. "Learned flavor preferences in rats." Appetite 12, no. 3 (June 1989): 236. http://dx.doi.org/10.1016/0195-6663(89)90274-2.

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35

Brown, L. M., P. T. Cooney, C. N. Miller, and D. J. Clegg. "Proestrus rats on a high-fat diet have less central inflammation than male rats." Appetite 52, no. 3 (June 2009): 821. http://dx.doi.org/10.1016/j.appet.2009.04.031.

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36

Klump, Kelly L., Elaine B. Sinclair, Britny A. Hildebrandt, Deborah A. Kashy, Shannon O’Connor, Megan E. Mikhail, Kristen M. Culbert, Alexander Johnson, and Cheryl L. Sisk. "The Disruptive Effects of Estrogen Removal Before Puberty on Risk for Binge Eating in Female Rats." Clinical Psychological Science 8, no. 5 (July 2, 2020): 839–56. http://dx.doi.org/10.1177/2167702620921343.

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Recent research suggests that estrogen is protective against binge eating in adult females and that pubertal estrogen may be critical for these effects. Nonetheless, to date, no study has examined the role of pubertal estrogen in adult binge-eating phenotypes in females, potentially because of difficulties experimentally manipulating estrogen in humans to examine causal effects. We used a novel animal model to examine whether estrogen removal before puberty (via prepubertal ovariectomy, or P-OVX) increased rates of binge-eating-prone (BEP) phenotypes in adulthood in female rats. Seventy-seven P-OVX rats and 79 intact rats were followed from prepuberty into adulthood and phenotyped for BEP status in adulthood. Results showed significantly increased rates (~2–8 times higher) of adult BEP phenotypes in P-OVX compared with intact rats. Findings confirm that estrogen removal substantially increases later risk for binge eating in females, potentially by disrupting typical adolescent brain development.
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37

Rowland, Neil. "Of rats and men." Behavioral and Brain Sciences 8, no. 2 (July 1985): 346. http://dx.doi.org/10.1017/s0140525x0002104x.

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38

Wertz, Frederick J. "Of Rats and Psychologists." Theory & Psychology 4, no. 2 (May 1994): 165–97. http://dx.doi.org/10.1177/0959354394042002.

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39

Skottun, Bernt Christian. "Rats, dyslexia, and the magnocellular system." Cortex 46, no. 6 (June 2010): 799. http://dx.doi.org/10.1016/j.cortex.2009.12.006.

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40

Dickinson, Anthony, Nigel Wood, and Janice W. Smith. "Alcohol Seeking by Rats: Action or Habit?" Quarterly Journal of Experimental Psychology Section B 55, no. 4b (October 2002): 331–48. http://dx.doi.org/10.1080/0272499024400016.

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In two experiments, we examined the relative susceptibility to outcome devaluation of lever pressing by rats for either a 10% ethanol solution or food pellets. The rats were trained to press different levers for these two reinforcers using a sucrose-substitution procedure. An aversion was then conditioned from either the ethanol solution or the food pellets by pairing consumption with illness induced by lithium chloride. When instrumental performance was subsequently tested in extinction, the rats pressed less on the pellet lever if the pellets, rather than the ethanol, had been devalued by aversion conditioning. By contrast, performance on the ethanol lever was unaffected by whether the ethanol or pellets were devalued. Moreover, noncontingent presentations of the devalued reinforcer had no impact on test performance. The differential resistance to outcome devaluation suggests that, in contrast to food seeking, alcohol seeking is a stimulus-response habit rather than a goal-directed action mediated by a representation of the action-outcome contingency.
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41

Bevins, Rick A., and John J. B. Ayres. "Rats’ location during conditioned suppression training." Animal Learning & Behavior 20, no. 1 (March 1992): 8–16. http://dx.doi.org/10.3758/bf03199941.

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42

Santucci, Anthony C., and F. Robert Treichler. "Concurrent object-discrimination learning in rats." Animal Learning & Behavior 18, no. 3 (September 1990): 295–301. http://dx.doi.org/10.3758/bf03205289.

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43

Santi, Angelo, Lorraine Weise, and Dwayne Kuiper. "Memory for event duration in rats." Learning and Motivation 26, no. 1 (February 1995): 83–100. http://dx.doi.org/10.1016/0023-9690(95)90012-8.

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44

Mook, Douglas G., and Sue Wagner. "Adjustment to intermittent access in rats drinking saccharin: II. Adjustment of lapping rate." Physiology & Behavior 45, no. 2 (February 1989): 299–305. http://dx.doi.org/10.1016/0031-9384(89)90131-5.

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45

Wan, Ruiqian, Michaela Diamant, Wybren de Jong, and David de Wied. "Changes in heart rate and body temperature during passive avoidance behavior in rats." Physiology & Behavior 47, no. 3 (March 1990): 493–99. http://dx.doi.org/10.1016/0031-9384(90)90115-k.

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46

Keene, Christopher S., and David J. Bucci. "Automated measure of conditioned orienting behavior in rats." Behavior Research Methods 39, no. 2 (May 2007): 303–8. http://dx.doi.org/10.3758/bf03193161.

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47

Bonardi, Charlotte, and Dómhnall J. Jennings. "The effects of stimulus distribution form during trace conditioning." Quarterly Journal of Experimental Psychology 72, no. 2 (January 1, 2018): 285–97. http://dx.doi.org/10.1080/17470218.2017.1367017.

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Three experiments examined the effect of distribution form of the trace interval on trace conditioning. In Experiments 1 and 2, two groups of rats were conditioned to a fixed-duration conditioned stimulus (CS) in a trace interval procedure; rats in Group Fix received a fixed-duration trace interval, whereas for rats in Group Var the trace interval was of variable duration. Responding during the CS was higher in Group Var than in Group Fix, whereas during the trace interval this difference in responding reversed—Group Fix showed higher response rates than Group Var. Experiment 3 examined whether the greater response rate observed during the CS in Group Var was due to a performance effect or the acquisition of greater associative strength by the CS. Following trace conditioning, the rats from Experiment 1 underwent a second phase of delay conditioning with the same CS; a 5-s auditory stimulus was presented in compound with the last 5 s of the 15-s CS, and the unconditioned stimulus (US) was delivered at the offset of the CSs. On test with the auditory stimulus alone, subjects in Group Var showed lower response rates during the auditory stimulus than subjects in Group Fix. We interpreted these findings as evidence that the superior responding in Group Var during the CS was a result of it acquiring greater associative strength than in Group Fix.
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48

Mattingly, Bruce A., James E. Gotsick, and E. Brooks Applegate. "Serotonin, Septal Lesions, and Shock-Escape Learning in Rats." Psychological Reports 58, no. 1 (February 1986): 3–9. http://dx.doi.org/10.2466/pr0.1986.58.1.3.

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The involvement of reduced serotonin in deficient leverpress, shock-escape performance of rats with septal lesions was assessed in two studies. In Exp. 1, rats were treated with either para-chlorophenylalanine (PCPA) or saline and then tested in a leverpress, shock-escape task. In Exp. 2, rats with septal lesions and sham-operated control rats were treated daily with either 5-hydroxytryptophan (5HTP) or saline and tested on the same shock-escape task. Primary findings were as follows: (a) rats treated with PCPA learned to escape shock as quickly as saline control rats; (b) the shock-escape performance of rats with septal lesions was significantly inferior to that of control rats; and (c) the administration of 5HTP did not significantly improve the performance of either lesioned or control rats. These results suggest that the reduction of brain serotonin induced by septal lesions is not involved in the deficient shock-escape performance of septal-lesioned rats.
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49

Manzo, J., M. I. Vazquez, M. R. Cruz, M. E. Hernandez, P. Carrillo, and P. Pacheco. "Fertility ratio in male rats." Physiology & Behavior 68, no. 5 (March 2000): 611–18. http://dx.doi.org/10.1016/s0031-9384(99)00219-x.

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50

Dewasmes, G., C. Duchamp, and Y. Minaire. "Sleep changes in fasting rats." Physiology & Behavior 46, no. 2 (August 1989): 179–84. http://dx.doi.org/10.1016/0031-9384(89)90252-7.

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