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氟哌啶醇治疗会引起DNA甲基化的组织和性别特异性变化:一项使用大鼠的对照研究。

Haloperidol treatment induces tissue- and sex-specific changes in DNA methylation: a control study using rats.

作者信息

Shimabukuro Morihiro, Jinno Yoshihiro, Fuke Chiaki, Okazaki Yuji

机构信息

Department of Molecular Biology, Ryukyu University School of Medicine, Okinawa, Japan.

出版信息

Behav Brain Funct. 2006 Nov 29;2:37. doi: 10.1186/1744-9081-2-37.

Abstract

BACKGROUND

We previously found that there is a subtle difference in the global methylation state of blood leukocyte DNA between male subjects with and without schizophrenia. The aim of the current study was to determine whether this difference was a primary effect of the disease state, or a secondary effect of antipsychotics administered to these patients.

METHODS

We examined the methyl cytosine (mC) content of DNA from the leukocytes, brain, and liver of rats using high performance liquid chromatography. A total of 40 male and female rats received for 21 days daily injection of haloperidol or vehicle solution alone.

RESULTS

In control rats injected with buffer only, there was a sex-dependent difference in mC content in leukocyte DNA (male > female; P = 0.028, n = 10), similar to our previous observations in human peripheral leukocytes. No difference in mC content between the sexes was observed in the brain or liver in buffer-treated animals. Haloperidol treatment slightly decreased the mC content of leukocytes in male rats, but unexpectedly, increased the mC content of leukocytes in females. We observed a trend toward a higher level of mC in the liver in both sexes following haloperidol treatment, compared to buffer-treated animals. In contrast, haloperidol treatment resulted in a decrease in mC content in the brain in females, and this difference was statistically significant (P = 0.026).

CONCLUSION

These results indicate that haloperidol can affect DNA methylation states in the brain, as well as in certain other tissues, and raise the possibility that antipsychotic drugs play a role in the observed disparity in mC content in male subjects with and without schizophrenia.

摘要

背景

我们之前发现,患精神分裂症与未患精神分裂症的男性受试者之间,血液白细胞DNA的整体甲基化状态存在细微差异。本研究的目的是确定这种差异是疾病状态的主要影响,还是给予这些患者的抗精神病药物的次要影响。

方法

我们使用高效液相色谱法检测了大鼠白细胞、大脑和肝脏中DNA的甲基胞嘧啶(mC)含量。总共40只雄性和雌性大鼠每天接受氟哌啶醇或单独的赋形剂溶液注射,持续21天。

结果

在仅注射缓冲液的对照大鼠中,白细胞DNA中的mC含量存在性别差异(雄性>雌性;P = 0.028,n = 10),这与我们之前在人类外周血白细胞中的观察结果相似。在接受缓冲液处理的动物中,大脑或肝脏中未观察到两性之间mC含量的差异。氟哌啶醇治疗使雄性大鼠白细胞的mC含量略有下降,但出乎意料的是,增加了雌性大鼠白细胞的mC含量。与接受缓冲液处理的动物相比,我们观察到氟哌啶醇治疗后两性肝脏中的mC水平均有升高趋势。相比之下,氟哌啶醇治疗导致雌性大鼠大脑中的mC含量下降,且这种差异具有统计学意义(P = 0.026)。

结论

这些结果表明,氟哌啶醇可影响大脑以及某些其他组织中的DNA甲基化状态,并增加了抗精神病药物在患精神分裂症与未患精神分裂症男性受试者中观察到的mC含量差异中起作用的可能性。

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