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Delay in the recovery of normal sleep-wake cycle after disruption of the light-dark cycle in mice: a bipolar disorder-prone animal model?

Jung SH, Park JM, Moon E, Chung YI, Lee BD, Lee YM, Kim JH, Kim SY, Jeong HJ - Psychiatry Investig (2014)

Bottom Line: During the dark cycle on the 16th experimental day, their general locomotor activities were measured in an open field for 120 minutes after an injection of quinpirole (0.5 mg/kg, s.c.).The individual differences in the recovery rate of the baseline sleep-wake cycle were noted after 3 days of switching the LD cycle.Given that the quinpirole-induced hyperactivity is an animal model of bipolar disorder, our results suggest individuals who have difficulties in recovery from circadian rhythm disruption may be vulnerable to bipolar disorder.

View Article: PubMed Central - PubMed

Affiliation: Department of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.

ABSTRACT

Objective: Disruption of the circadian rhythm is known as a provoking factor for manic episodes. Individual differences exist in the recovery rate from disruption in the general population. To develop a screening method to detect individuals vulnerable to bipolar disorder, the authors observed the relationship between the recovery of the normal sleep-wake cycle after switching the light-dark (LD) cycle and quinpirole-induced hyperactivity in mice.

Methods: Sixteen male mice (age of 5 weeks, weight 28-29 gm) were subjected to a circadian rhythm disruption protocol. Sleep-wake behaviors were checked every 5 min for a total duration of 15 days, i.e., 2 days of baseline observations, 3 days of LD cycle changes, and 10 days of recovery. During the dark cycle on the 16th experimental day, their general locomotor activities were measured in an open field for 120 minutes after an injection of quinpirole (0.5 mg/kg, s.c.).

Results: The individual differences in the recovery rate of the baseline sleep-wake cycle were noted after 3 days of switching the LD cycle. Fifty percent (n=8) of the mice returned to the baseline cycle within 6 days after normalizing the LD cycle (early recovery group). The locomotor activities of mice that failed to recover within 6 days (delayed recovery group) were significantly higher (mean rank=12.25) than those of the early recovery group (mean rank=4.75, u=62.0, p=0.001, Mann-Whitney U test).

Conclusion: Given that the quinpirole-induced hyperactivity is an animal model of bipolar disorder, our results suggest individuals who have difficulties in recovery from circadian rhythm disruption may be vulnerable to bipolar disorder.

No MeSH data available.


Related in: MedlinePlus

Locomotor activities in the open field test after quinpirole injection. Locomotor activities of mice failed to recover in 6 days (delayed recovery group) were significantly higher (mean±SD=846.9±335.1, mean rank=12.25) than those of the early recovery group (mean±SD=265.5±44.8, mean rank=4.75). *Mann-Whitney U test, u=62.0, p=0.001, two-tailed.
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Figure 2: Locomotor activities in the open field test after quinpirole injection. Locomotor activities of mice failed to recover in 6 days (delayed recovery group) were significantly higher (mean±SD=846.9±335.1, mean rank=12.25) than those of the early recovery group (mean±SD=265.5±44.8, mean rank=4.75). *Mann-Whitney U test, u=62.0, p=0.001, two-tailed.

Mentions: Fifty percent (n=8) of the mice returned to the baseline cycle in 6 days after normalizing the light-dark cycle (early recovery group). Locomotor activities of mice that failed to recover in 6 days (delayed recovery group) were significantly higher (mean±SD=846.9±335.1, mean rank=12.25) than those of the early recovery group (mean±SD=265.5±44.8, mean rank=4.75; Mann-Whitney U test, u=62.0, p=0.001)(Figure 2).


Delay in the recovery of normal sleep-wake cycle after disruption of the light-dark cycle in mice: a bipolar disorder-prone animal model?

Jung SH, Park JM, Moon E, Chung YI, Lee BD, Lee YM, Kim JH, Kim SY, Jeong HJ - Psychiatry Investig (2014)

Locomotor activities in the open field test after quinpirole injection. Locomotor activities of mice failed to recover in 6 days (delayed recovery group) were significantly higher (mean±SD=846.9±335.1, mean rank=12.25) than those of the early recovery group (mean±SD=265.5±44.8, mean rank=4.75). *Mann-Whitney U test, u=62.0, p=0.001, two-tailed.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4225215&req=5

Figure 2: Locomotor activities in the open field test after quinpirole injection. Locomotor activities of mice failed to recover in 6 days (delayed recovery group) were significantly higher (mean±SD=846.9±335.1, mean rank=12.25) than those of the early recovery group (mean±SD=265.5±44.8, mean rank=4.75). *Mann-Whitney U test, u=62.0, p=0.001, two-tailed.
Mentions: Fifty percent (n=8) of the mice returned to the baseline cycle in 6 days after normalizing the light-dark cycle (early recovery group). Locomotor activities of mice that failed to recover in 6 days (delayed recovery group) were significantly higher (mean±SD=846.9±335.1, mean rank=12.25) than those of the early recovery group (mean±SD=265.5±44.8, mean rank=4.75; Mann-Whitney U test, u=62.0, p=0.001)(Figure 2).

Bottom Line: During the dark cycle on the 16th experimental day, their general locomotor activities were measured in an open field for 120 minutes after an injection of quinpirole (0.5 mg/kg, s.c.).The individual differences in the recovery rate of the baseline sleep-wake cycle were noted after 3 days of switching the LD cycle.Given that the quinpirole-induced hyperactivity is an animal model of bipolar disorder, our results suggest individuals who have difficulties in recovery from circadian rhythm disruption may be vulnerable to bipolar disorder.

View Article: PubMed Central - PubMed

Affiliation: Department of Psychiatry, Pusan National University Hospital, Busan, Republic of Korea.

ABSTRACT

Objective: Disruption of the circadian rhythm is known as a provoking factor for manic episodes. Individual differences exist in the recovery rate from disruption in the general population. To develop a screening method to detect individuals vulnerable to bipolar disorder, the authors observed the relationship between the recovery of the normal sleep-wake cycle after switching the light-dark (LD) cycle and quinpirole-induced hyperactivity in mice.

Methods: Sixteen male mice (age of 5 weeks, weight 28-29 gm) were subjected to a circadian rhythm disruption protocol. Sleep-wake behaviors were checked every 5 min for a total duration of 15 days, i.e., 2 days of baseline observations, 3 days of LD cycle changes, and 10 days of recovery. During the dark cycle on the 16th experimental day, their general locomotor activities were measured in an open field for 120 minutes after an injection of quinpirole (0.5 mg/kg, s.c.).

Results: The individual differences in the recovery rate of the baseline sleep-wake cycle were noted after 3 days of switching the LD cycle. Fifty percent (n=8) of the mice returned to the baseline cycle within 6 days after normalizing the LD cycle (early recovery group). The locomotor activities of mice that failed to recover within 6 days (delayed recovery group) were significantly higher (mean rank=12.25) than those of the early recovery group (mean rank=4.75, u=62.0, p=0.001, Mann-Whitney U test).

Conclusion: Given that the quinpirole-induced hyperactivity is an animal model of bipolar disorder, our results suggest individuals who have difficulties in recovery from circadian rhythm disruption may be vulnerable to bipolar disorder.

No MeSH data available.


Related in: MedlinePlus