在外周神经系统中对调节慢性应激诱导的内脏痛的基因进行表观遗传调控。

Epigenetic regulation of genes that modulate chronic stress-induced visceral pain in the peripheral nervous system.

作者信息

Hong Shuangsong, Zheng Gen, Wiley John W

机构信息

Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan.

Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan.

出版信息

Gastroenterology. 2015 Jan;148(1):148-157.e7. doi: 10.1053/j.gastro.2014.09.032. Epub 2014 Sep 28.

Abstract

BACKGROUND & AIMS: Chronic stress alters the hypothalamic-pituitary-adrenal axis, increases gut motility, and increases the perception of visceral pain. We investigated whether epigenetic mechanisms regulate chronic stress-induced visceral pain in the peripheral nervous systems of rats.

METHODS

Male rats were subjected to 1 hour of water avoidance stress each day, or given daily subcutaneous injections of corticosterone, for 10 consecutive days. L4-L5 and L6-S2 dorsal root ganglia (DRG) were collected and compared between stressed and control rats (placed for 1 hour each day in a tank without water). Levels of cannabinoid receptor 1 (CNR1), DNA (cytosine-5-)-methyltransferase 1 (DNMT1), transient receptor potential vanilloid type 1 (TRPV1), and EP300 were knocked down in DRG neurons in situ with small interfering RNAs. We measured DNA methylation and histone acetylation at genes encoding the glucocorticoid receptor (NR3C1), CNR1, and TRPV1. Visceral pain was measured in response to colorectal distention.

RESULTS

Chronic stress was associated with increased methylation of the Nr3c1 promoter and reduced expression of this gene in L6-S2, but not L4-L5, DRGs. Stress also was associated with up-regulation in DNMT1-associated methylation of the Cnr1 promoter and down-regulation of glucocorticoid-receptor-mediated expression of CNR1 in L6-S2, but not L4-L5, DRGs. Concurrently, chronic stress increased expression of the histone acetyltransferase EP300 and increased histone acetylation at the Trpv1 promoter and expression of the TRPV1 receptor in L6-S2 DRG neurons. Knockdown of DNMT1 and EP300 in L6-S2 DRG neurons of rats reduced DNA methylation and histone acetylation, respectively, and prevented chronic stress-induced increases in visceral pain.

CONCLUSIONS

Chronic stress increases DNA methylation and histone acetylation of genes that regulate visceral pain sensation in the peripheral nervous system of rats. Blocking epigenetic regulatory pathways in specific regions of the spinal cord might be developed to treat patients with chronic abdominal pain.

摘要

背景与目的

慢性应激会改变下丘脑 - 垂体 - 肾上腺轴,增加肠道蠕动,并增强内脏痛觉。我们研究了表观遗传机制是否在大鼠外周神经系统中调节慢性应激诱导的内脏痛。

方法

雄性大鼠连续10天每天接受1小时的水回避应激,或每天皮下注射皮质酮。收集应激大鼠和对照大鼠(每天在无水水箱中放置1小时)的L4 - L5和L6 - S2背根神经节(DRG)并进行比较。用小干扰RNA在DRG神经元中原位敲低大麻素受体1(CNR1)、DNA(胞嘧啶 - 5 -)- 甲基转移酶1(DNMT1)、瞬时受体电位香草酸亚型1(TRPV1)和EP300的水平。我们测量了编码糖皮质激素受体(NR3C1)、CNR1和TRPV1的基因的DNA甲基化和组蛋白乙酰化。通过结直肠扩张来测量内脏痛。

结果

慢性应激与L6 - S2而非L4 - L5背根神经节中Nr3c1启动子甲基化增加及该基因表达降低有关。应激还与L6 - S2而非L4 - L5背根神经节中Cnr1启动子的DNMT1相关甲基化上调以及糖皮质激素受体介导的CNR1表达下调有关。同时,慢性应激增加了组蛋白乙酰转移酶EP300的表达,并增加了L6 - S2背根神经节神经元中Trpv1启动子的组蛋白乙酰化和TRPV1受体的表达。在大鼠L6 - S2背根神经节神经元中敲低DNMT1和EP300分别降低了DNA甲基化和组蛋白乙酰化,并阻止了慢性应激诱导的内脏痛增加。

结论

慢性应激会增加大鼠外周神经系统中调节内脏痛觉的基因的DNA甲基化和组蛋白乙酰化。或许可以通过阻断脊髓特定区域的表观遗传调控途径来治疗慢性腹痛患者。

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