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本文引用的文献

1
Lithium augmentation of the effects of desipramine in a mouse model of treatment-resistant depression: a role for hippocampal cell proliferation.锂增强去甲丙咪嗪在治疗抵抗性抑郁症小鼠模型中的作用:海马细胞增殖的作用。
Neuroscience. 2013 Jan 3;228:36-46. doi: 10.1016/j.neuroscience.2012.09.072. Epub 2012 Oct 13.
2
The mouse forced swim test.小鼠强迫游泳试验。
J Vis Exp. 2012 Jan 29(59):e3638. doi: 10.3791/3638.
3
An investigation of whether there are sex differences in certain behavioural and neurochemical parameters in the rat.研究大鼠某些行为和神经化学参数是否存在性别差异。
Behav Brain Res. 2012 Apr 1;229(1):289-300. doi: 10.1016/j.bbr.2011.12.036. Epub 2012 Jan 2.
4
Behavioral differences in black Swiss mice from separate colonies: implications for modeling domains of mania.来自不同群体的黑色瑞士小鼠的行为差异:对躁狂症建模领域的启示。
Behav Pharmacol. 2012 Apr;23(2):211-4. doi: 10.1097/FBP.0b013e32834f9e4e.
5
Lithium-induced effects on adult hippocampal neurogenesis are topographically segregated along the dorso-ventral axis of stressed mice.锂诱导的成年海马神经发生的影响沿应激小鼠的背腹轴呈地形分离。
Neuropharmacology. 2012 Jan;62(1):247-55. doi: 10.1016/j.neuropharm.2011.07.015. Epub 2011 Jul 22.
6
Antidepressant-like responses to lithium in genetically diverse mouse strains.锂在遗传多样性的小鼠品系中产生抗抑郁样反应。
Genes Brain Behav. 2011 Jun;10(4):434-43. doi: 10.1111/j.1601-183X.2011.00682.x. Epub 2011 Mar 1.
7
Pharmacogenetics of lithium response in bipolar disorder.双相障碍锂反应的药物遗传学。
Pharmacogenomics. 2010 Oct;11(10):1439-65. doi: 10.2217/pgs.10.127.
8
Lithium's emerging role in the treatment of refractory major depressive episodes: augmentation of antidepressants.锂在治疗难治性重度抑郁发作中的新作用:抗抑郁药增效。
Neuropsychobiology. 2010;62(1):36-42. doi: 10.1159/000314308. Epub 2010 May 7.
9
Shock-induced aggression in mice is modified by lithium.锂可改变小鼠的休克诱导性攻击行为。
Pharmacol Biochem Behav. 2010 Jan;94(3):380-6. doi: 10.1016/j.pbb.2009.09.020. Epub 2009 Oct 1.
10
Recurrence risk in bipolar manic-depressive disorders after discontinuing lithium maintenance treatment: an overview.锂维持治疗停药后双相情感障碍躁狂发作的复发风险:概述。
Clin Drug Investig. 1998;15(4):337-51. doi: 10.2165/00044011-199815040-00010.

不同品系小鼠对锂治疗的抗抑郁样反应差异:性别、母性照顾和混合遗传背景的影响。

Differential antidepressant-like response to lithium treatment between mouse strains: effects of sex, maternal care, and mixed genetic background.

机构信息

Department of Psychiatry, University of Maryland School of Medicine, Rm. 934D MSTF, 685 W. Baltimore St., Baltimore, MD 21201, USA.

出版信息

Psychopharmacology (Berl). 2013 Aug;228(3):411-8. doi: 10.1007/s00213-013-3045-5. Epub 2013 Mar 17.

DOI:10.1007/s00213-013-3045-5
PMID:23503701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3707960/
Abstract

BACKGROUND

Lithium is a mood stabilizer with both antidepressant and antimanic properties, however its mechanism of action is unclear. Identifying the genetic factors that influence lithium's therapeutic actions will be an important step to assist in identifying such mechanisms. We previously reported that lithium treatment of male mice has antidepressant-like effects in the C57BL/6J strain but that such effects were absent in the BALB/cJ strain.

OBJECTIVES

This study aimed to assess the roles of both genetic and non-genetic factors such as sex and non-shared environmental conditions that may mediate differential behavioral responses to lithium.

METHODS

Mice were treated with lithium for 10 days and then tested in the forced swim test followed by lithium discontinuation and retesting to assess effects of lithium withdrawal. We also assessed effects of sex and cross-fostering on lithium response between the C57BL/6J and BALB/cJ strains, and antidepressant-like effects of lithium in the hybrid CB6F1/J strain that is derived from C57BL/6J and BALB/cJ parental strains.

RESULTS

Neither sex nor maternal care significantly influenced the differential antidepressant-like response to lithium. Withdrawal from lithium treatment reversed antidepressant-like effects in the C57BL/6J strain but had no effects in BALB/cJ mice. Lithium treatment did not result in antidepressant-like effects in the CB6F1/J strain.

CONCLUSIONS

Genetic factors are likely primarily responsible for differential antidepressant-like effects of lithium in the C57BL/6J and BALB/cJ strains. Future studies identifying such genetic factors may help to elucidate the neurobiological mechanisms of lithium's therapeutic actions.

摘要

背景

锂是一种具有抗抑郁和抗躁狂作用的心境稳定剂,但其作用机制尚不清楚。确定影响锂治疗作用的遗传因素将是协助确定这些机制的重要步骤。我们之前报道过,锂治疗雄性小鼠在 C57BL/6J 品系中具有抗抑郁作用,但在 BALB/cJ 品系中则没有。

目的

本研究旨在评估遗传和非遗传因素(如性别和非共享环境条件)在介导对锂的不同行为反应中的作用。

方法

小鼠用锂治疗 10 天,然后进行强迫游泳试验,随后停止锂治疗并重新测试,以评估锂停药的影响。我们还评估了性别和交叉寄养对 C57BL/6J 和 BALB/cJ 品系之间锂反应的影响,以及锂在源自 C57BL/6J 和 BALB/cJ 亲本品系的杂交 CB6F1/J 品系中的抗抑郁作用。

结果

性别和母婴照顾都没有显著影响锂的抗抑郁样反应的差异。锂治疗的停药逆转了 C57BL/6J 品系的抗抑郁样作用,但对 BALB/cJ 小鼠没有影响。锂治疗在 CB6F1/J 品系中没有导致抗抑郁样作用。

结论

遗传因素可能是锂在 C57BL/6J 和 BALB/cJ 品系中产生抗抑郁样作用的主要原因。未来确定这些遗传因素的研究可能有助于阐明锂治疗作用的神经生物学机制。