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Lithium acts to modulate abnormalities at behavioral, cellular, and molecular levels in sleep deprivation-induced mania-like behavior
被引:25
作者:
Andrabi, Mutahar
[1
]
Andrabi, Muatar Maknoon
[2
]
Kunjunni, Remesh
[1
]
Sriwastva, Mukesh
[1
]
Bose, Samrat
[3
]
Sagar, Rajesh
[4
]
Srivastava, Achal Kumar
[5
]
Mathur, Rashmi
[3
]
Jain, Suman
[3
]
Subbiah, Vivekanandhan
[1
]
机构:
[1] All India Inst Med Sci, Dept Neurobiochem, New Delhi 110029, India
[2] NHS Fdn Trust, Hillingdon Hosp, Dept Geriatr Med, London, England
[3] All India Inst Med Sci, Dept Physiol, New Deihl, India
[4] All India Inst Med Sci, Dept Psychiat, New Delhi, India
[5] All India Inst Med Sci, Dept Neurol, New Delhi, India
关键词:
BDNF;
circadian clock;
HAT;
HDAC;
mania;
oxidative stress;
REM sleep deprivation;
WHITE-MATTER MICROSTRUCTURE;
CLOCK GENE-EXPRESSION;
ANIMAL-MODEL;
BIPOLAR DISORDER;
CIRCADIAN GENES;
MOOD DISORDERS;
ENERGY-METABOLISM;
BRAIN;
DEACETYLASE;
BDNF;
D O I:
10.1111/bdi.12838
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background Ample amount of data suggests role of rapid eye movement (REM) sleep deprivation as the cause and effect of mania. Studies have also suggested disrupted circadian rhythms contributing to the pathophysiology of mood disorders, including bipolar disorder. However, studies pertaining to circadian genes and effect of lithium treatment on clock genes are scant. Thus, we wanted to determine the effects of REM sleep deprivation on expression of core clock genes and determine whether epigenetics is involved. Next, we wanted to explore ultrastructural abnormalities in the hippocampus. Moreover, we were interested to determine oxidative stress, tumor necrosis factor-alpha (TNF-alpha), and brain-derived neurotrophic factor levels in the central and peripheral systems. Methods Rats were sleep deprived by the flower pot method and were then analyzed for various behaviors and biochemical tests. Lithium was supplemented in diet. Results We found that REM sleep deprivation resulted in hyperactivity, reduction in anxiety-like behavior, and abnormal dyadic social interaction. Some of these behaviors were sensitive to lithium. REM sleep deprivation also altered circadian gene expression and caused significant imbalance between histone acetyl transferase/histone deacetylase (HAT/HDAC) activity. Ultrastructural analysis revealed various cellular abnormalities. Lipid peroxidation and increased TNF-alpha levels suggested oxidative stress and ongoing inflammation. Circadian clock genes were differentially modulated with lithium treatment and HAT/HDAC imbalance was partially prevented. Moreover, lithium treatment prevented myelin fragmentation, disrupted vasculature, necrosis, inflammation, and lipid peroxidation, and partially prevented mitochondrial damage and apoptosis. Conclusions Taken together, these results suggest plethora of abnormalities in the brain following REM sleep deprivation, many of these changes in the brain may be target of lithium's mechanism of action.
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页码:266 / 280
页数:15
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