Effect of central 5-hydroxytryptamine depletion on performance in the freeoperant psychophysical procedure: facilitation of switching, but no effecton temporal differentiation of responding
Tj. Chiang et al., Effect of central 5-hydroxytryptamine depletion on performance in the freeoperant psychophysical procedure: facilitation of switching, but no effecton temporal differentiation of responding, PSYCHOPHAR, 143(2), 1999, pp. 166-173
This experiment examined the effect of destroying the ascending 5-hydroxytr
yptaminergic (5-HTergic) pathways on timing and switching behaviour in the
free-operant psychophysical procedure. Rats received injections of 5,7-dihy
droxytryptamine into the dorsal and median raphe nuclei or sham lesions. Th
ey were trained to press levers for sucrose reinforcement; sessions consist
ed of fifty 50-s trials in which reinforcers were available on a variable-i
nterval 30-s schedule. In the first 25 s,of each trial, reinforcement was o
nly available for responses on lever A: in the Last 25 s, it was available
only for responses on lever B. In phase 1 (70 sessions) repetitive switchin
g between the levers was prevented by withdrawal of lever A after the first
response on lever B in each trial, in phase 3 (40 sessions) this constrain
t on switching was removed; in phase 3 (40 sessions) the constraint was rei
nstated. Data were collected from probe trials (four per session) in which
no reinforcers were delivered, during the last ten sessions of each phase.
In all phases, both groups showed declining response rates on lever A and i
ncreasing response rates on lever B as a function of time from the onset of
the trial. Response rate on lever BI expressed as percentage of overall re
sponse rate, could be described by a tao-parameter logistic function. Remov
al of the constraint on switching reduced the slope of the function without
changing the indifference point (time corresponding to 50% responding on l
ever B). The parameters of the timing function did not differ between the g
roups in any of the phases. However, the lesioned group showed a greater en
hancement of switching rate during phase 2 than the control group. The leve
ls of 5-HT and 5-hydroxyindoleacetic acid were reduced in the brains of the
lesioned rats, but the levels of noradrenaline and dopamine wen not altere
d. The results provide further evidence for the involvement of the ascendin
g 5-HTergic pathways in switching between response alternatives, but cast d
oubt on our previous suggestion that the effects of 5-HT depletion on tempo
ral differentiation of behaviour are mediated by facilitated switching.