How are brain-reward thresholds measured by an ICSS test?

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In summary, the conversation discusses a scientific article about the effects of alcohol addiction and withdrawal on brain-reward functioning in rats. The article explains how brain-reward thresholds are measured and monitored through ICSS (Intracranial self-stimulation) and also discusses response latencies in the experiments. The article uses the Kornetsky and Esposito procedure and findings suggest that elevations in brain reward thresholds are only detected after a prolonged period of alcohol intake. An explanation of the results is also requested.
  • #1
Lightstryk
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I'm reading a scientific article about the effects of alcohol addiction and withdrawal on brain-reward functioning in rats (file attached to this post) and am having some trouble understanding the methods used. How are brain-reward thresholds measured and monitored through ICSS? (Intracranial self-stimulation) Also, what are response latencies discussed in the experiments?

To quote the first experiment from the attached file:
"Experiment 1 Statistical analyses indicated that there were
no significant differences in the absolute baseline brain
reward thresholds or the response latencies between the
control group and the alcohol group prior to the administration
of the liquid diets or prior to any of the withdrawal
sessions (Table 1). The average alcohol intake (weeks 1–
12) was 7.3±0.3 g/kg per day. The mean blood alcohol
concentrations (BAC) on the day prior to each withdrawal
session are shown in Table 2. Introduction of the liquid
diets induced a small but significant increase in brain
reward thresholds (prior liquid diet baseline vs. withdrawal
1 baseline; Time: F1,17=5.595, p<0.03) and did not affect
the response latencies. The baseline brain reward thresholds
and the baseline response latencies remained stable from
the first withdrawal session to the fourth withdrawal
session. Throughout the experiment, the alcohol rats and
the control rats were pair-fed, and there were no differences
in the body weights of the control rats and the alcohol rats immediately prior or at the end of the liquid diet procedure
(Table 3). After a period of 3 weeks, the alcohol liquid diet
was replaced by the control diet (withdrawal session 1).
Discontinuation of the alcohol liquid diet did not affect the
brain reward thresholds (Table 4). During the withdrawal
period, the response latencies of the control rats were
slightly increased compared to those of the alcohol rats
(Table 4; Treatment: F1,17=10.904, p<0.004). After a
period of 4 weeks, the alcohol liquid diet was again
replaced by the control diet (withdrawal session 2).
Discontinuation of the alcohol liquid diet did not affect
the brain reward thresholds (Table 4). There were also no
differences between the response latencies of the control
rats and the alcohol rats during the withdrawal period
(Table 4; Time: F4,68=3.540, p<0.011). After a period of
5 weeks, the alcohol liquid diet was replaced by the control
diet (withdrawal session 3). There were no differences
between the brain reward thresholds of the control rats and
the alcohol rats during the withdrawal period (Table 4;
Time: F4,68=2.577, p<0.045). There were also no differences
between the response latencies of the control rats and
the alcohol rats during the withdrawal period. After a
period of 12 weeks, the alcohol liquid diet was replaced by
the control diet (withdrawal session 5). During this final
withdrawal period, the brain reward thresholds of the
alcohol treated rats were elevated compared to those of
the control rats (Table 4; Treatment: F1,17=7.133, p<0.016;
time: F4,68=3.940, p<0.006). These findings suggest that elevations in brain reward thresholds are only detected after a prolonged (12 weeks) period of alcohol intake. Alcohol
withdrawal did not affect the response latencies (Table 4).

If I'm not already too much of a bother, an explanation of the results would be greatly appreciated! :]

Thanks for your help!
 

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  • #3
Thanks a lot; that really helped explain the procedure. And yes, they do both use the same ICSS method.
I'm not completely clear with how they conducted each "series" of trials, but I guess I'll figure it out later (I'm tired).

Thanks again for the help!
 

1. What is an ICSS test?

An ICSS (intracranial self-stimulation) test is a behavioral neuroscience technique used to measure the rewarding effects of different stimuli on the brain. It involves the use of electrodes implanted into specific regions of the brain, which can then be activated to stimulate that area and produce a pleasurable sensation.

2. How are brain-reward thresholds measured during an ICSS test?

The brain-reward threshold is measured by gradually increasing the level of stimulation delivered to the brain through the implanted electrodes. The subject is then given the opportunity to self-administer the stimulation by pressing a lever or performing a specific action. The threshold is determined when the subject reaches a point where they are no longer motivated to continue self-administering the stimulation.

3. What are the benefits of using ICSS to measure brain-reward thresholds?

ICSS is a highly sensitive and reliable method for measuring brain-reward thresholds. It allows for precise and controlled manipulation of specific brain regions, and can be used to study the effects of drugs, environmental factors, and genetic influences on reward pathways in the brain.

4. Are there any limitations to using ICSS to measure brain-reward thresholds?

One limitation of ICSS is that it can only measure the reward threshold for a specific brain region that has been targeted for stimulation. This does not necessarily reflect the overall reward threshold of the entire brain. Also, ICSS does not take into account other factors that may influence reward, such as learning, motivation, and emotion.

5. How do the results of an ICSS test contribute to our understanding of reward pathways in the brain?

The results of an ICSS test can help identify the specific brain regions and neurochemical pathways involved in reward processing. This information is crucial for understanding the underlying mechanisms of addiction, pleasure, and motivation, and can potentially lead to the development of new treatments for substance abuse and other disorders related to reward dysfunction.

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