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Alicia Flores
Objectives 1
Siegel (1997)
1.
“A frequent finding is that pharmacological conditioned responses are opposite in
direction to the unconditioned responses of the drugs upon which they are based.
Thus, if blood sugar level is repeatedly increased by administrations of epinephrine
or glucose, the administration procedure not followed by the hyperglycemic agent
leads to a decrease in blood sugar” (Seigel, 1997, p. 2). Given this example, what is
the unconditioned stimulus (US or UCS), the conditioned stimulus, the
unconditioned response, and the conditioned response? (See Pierce et al., 2023, for
additional information).
Unconditioned Stimulus: Drug administration procedure
Conditioned Stimulus: Administration of epinephrine
Unconditioned Response: Blood sugar decreases
Conditioned Response: Blood sugar increases
2.
In Seigel (1997), what was the dependent variable in Experiment 1 and how was it
measured?
The dependent variable in Experiment 1 was the rats’ level of pain tolerance.
Level of pain tolerance was measured using a version of Randall and Selitto’s paw-
pressure analgesiometer, which applies increasing pressure to a rat’s paw.
3.
What was the purpose of Experiment 1 in Seigel (1997)?
The purpose of Experiment 1 was to confirm the reliability of earlier findings that
morphine tolerance gradually increases/pain tolerance decreases due to the effects of
extinction, when using a different analgesic assessment.
To see if rats can be conditioned to elicit
4.
In Experiment 1 of Seigel (1997), what was the difference between Group M-REST-
M and Group M-P-M in terms of the procedures?
In terms of procedure, a difference in treatment occurred during the 12-day
interval between morphine sessions 6 and 7. Group M-REST-M were left undisturbed in
their home cages during this interval, whereas Group M-P-M received daily placebo tests
where they were injected with saline and their analgesia level was assessed.
5.
During the second series of Experiment 1 of Seigel (1997), how did the results of
Group M-REST-M and Group M-P-M differ in terms of their paw-withdrawal
threshold?
During the second series of Experiment 1 the M-REST-M group continued to
show a low paw-withdrawal threshold, whereas Group M-P-M began showing a high
paw-withdrawal threshold. (higher tolerance to pain)
6.
What was the purpose of Experiment 2 in Seigel (1997)?
The purpose of Experiment 2 was to investigate whether extinction (placebos
given) establishes tolerance.
Alicia Flores
Objectives 1
7.
In Experiment 2 of Seigel (1997), what was the difference between Group M-REST-
M and Group M-P-M in terms of the procedures?
In terms of procedure, a difference between both groups happened on day 2 of
morphine injections. Group M-REST-M were left undisturbed in their home cages,
whereas Group M-P-M received 4 placebo sessions, but no analgesia measurement.
During this time, rats were placed on the analgesiometer with the noise of the motor
occurring, but no pressure being applied.
8.
During the second morphine administration of Experiment 2 of Seigel (1997), how
did the results of Group M-REST-M and Group M-P-M differ in terms of their paw-
withdrawal threshold? (Hint: what happened at 45 min)
In terms of paw-withdrawal threshold, after 45 minutes, Group M-P-M’s paw-
withdrawal threshold was higher (significantly less sensitive to paw-pressure stimulation)
than Group M-Rest-M’s.
9.
In Seigel (1997), what was the dependent variable in Experiment 3 and how was it
measured?
The dependent variable in Experiment 3 was the rat’s pain sensitivity. This
dependent variable was measured by the rat being placed on a testing surface (hot plate)
for 30 seconds and noting how much time passes before the rat reacts (jumping and paw
licking).
10. What was the purpose of Experiment 3 of Seigel (1997)?
The purpose of Experiment 3 was to investigate if pre-exposure to administration
ritual (before pairing) would delay the development of tolerance.
11. In Experiment 3 of Seigel (1997), what was the difference between Group 18P and
Group 1P in terms of the procedures?
In terms of procedure, the difference between Group 18P and Group 1P occurred
during the pre-exposure phase. Group 18P received 18 pre-exposure cues and were then
taken into the testing room and placed on the hot plate. Group 1P only received one pre-
exposure cue and were left undisturbed for 17 days before receiving it.
12. In Experiment 3 of Seigel (1997), how did the results between Group 18P and Group
1P differ?
In experiment 3, the results between both groups in the pre-exposure phase were
different because the subjects’ response time in Group 1P was significantly longer than
that of the last preexposure session for Group 18P. During the tolerance acquisition
phase, high response delays occurred for the first administration of the injection however,
when these delays decreased, the decrease was more rapid for Group 1P than for Group
18P. (more exposure to rituals slows more tolerance)
13. What was the purpose of Experiment 4 of Seigel (1997)?
Alicia Flores
Objectives 1
The purpose of Experiment 4 was to investigate if partial pairing schedule, paired
with pre-exposure to administration cues, would also delay the development of tolerance.
(How often does pairing have to occur? 100% or 25%)
14. In Experiment 4 of Seigel (1997), what was the difference between Group CRF and
Group PRF in terms of the procedures?
In terms of procedure,
these two groups received different levels of reinforcement
and different treatment. Group CRF received a continuous pairing schedule, and when
they did not receive an injection, they were left undisturbed in their home cages. Group
PRF received partial reinforcement (25% schedule), and on each day in between drug
administrations, received saline injections and pre-exposure cues.
15. In Experiment 4 of Seigel (1997), how did the results differ across Group CRF and
Group PRF?
When referring to the results of experiment 4, Group PRF, which had more
experience with administration cues, differed from Group CRF because they were slower
to respond to the heat (increased pain tolerance).
Tolerance was quicker in group CRF
(who received no pre-exposure) than in Group PRF (pre-exposure given).
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