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白藜芦醇通过逆转组蛋白去乙酰化酶1(HDAC1)的表达来逆转吗啡耐受大鼠体内吗啡诱导的神经炎症。

Resveratrol reverses morphine-induced neuroinflammation in morphine-tolerant rats by reversal HDAC1 expression.

作者信息

Tsai Ru-Yin, Wang Juei-Chii, Chou Kuang-Yi, Wong Chih-Shung, Cherng Chen-Hwan

机构信息

College of Nursing and Health Sciences, Da-Yeh University, Changhua, Taiwan.

Department of Anesthesiology, Cathay General Hospital, Taipei, Taiwan.

出版信息

J Formos Med Assoc. 2016 Jun;115(6):445-54. doi: 10.1016/j.jfma.2015.05.010. Epub 2015 Jun 13.

Abstract

BACKGROUND/PURPOSE: We previously showed that subsequent intrathecal (i.t.) injection of resveratrol (30 μg) significantly reverses morphine-evoked neuroinflammation in morphine-tolerant rats. The present study examined the underlying mechanism.

METHODS

Male Wistar rats were implanted with two i.t. catheters, one of which was connected to a miniosmotic pump and used for morphine (15 μg/h) or saline infusion for 120 hours. To examine the effects on spinal cord expression of histone deacetylase 1 (HDAC1), the inflammatory cytokine tumor necrosis factor-α (TNF-α), and TNF receptor (TNFR) 1 and TNFR2 during tolerance induction, a tail-flick test was performed prior to infusion and after 24 hours, 48 hours, 72 hours, 96 hours, and 120 hours of infusion.

RESULTS

Resveratrol treatment prior to morphine challenge restored the antinociceptive effect of morphine in morphine-tolerant rats and reversed the morphine infusion-induced increase in HDAC1, TNF-α, and TNFR1 expression. Moreover, chronic morphine infusion increased TNFR1-specific expression in neuron in morphine-tolerant rat spinal cords, and this effect was almost completely inhibited by resveratrol treatment prior to morphine challenge.

CONCLUSION

Resveratrol restores the antinociceptive effect of morphine by reversing morphine infusion-induced spinal cord neuroinflammation and increase in TNFR1 expression. The reversal of the morphine-induced increase in TNFR1 expression by resveratrol is partially due to reversal of the morphine infusion-induced increase in HDAC1 expression. Resveratrol pretreatment can be used as an adjuvant in clinical pain management for patients who need long-term morphine treatment or with neuropathic pain.

摘要

背景/目的:我们之前的研究表明,随后鞘内注射白藜芦醇(30μg)可显著逆转吗啡耐受大鼠体内吗啡诱发的神经炎症。本研究探讨其潜在机制。

方法

雄性Wistar大鼠植入两根鞘内导管,其中一根连接微型渗透泵,用于以15μg/h的速度输注吗啡或生理盐水,持续120小时。为了研究在耐受诱导过程中对脊髓组蛋白去乙酰化酶1(HDAC1)、炎性细胞因子肿瘤坏死因子-α(TNF-α)以及TNF受体(TNFR)1和TNFR2表达的影响,在输注前以及输注24小时、48小时、72小时、96小时和120小时后进行甩尾试验。

结果

在吗啡激发前给予白藜芦醇治疗可恢复吗啡在吗啡耐受大鼠中的镇痛作用,并逆转吗啡输注诱导的HDAC1、TNF-α和TNFR1表达增加。此外,慢性吗啡输注增加了吗啡耐受大鼠脊髓神经元中TNFR1的特异性表达,而在吗啡激发前给予白藜芦醇治疗几乎完全抑制了这种作用。

结论

白藜芦醇通过逆转吗啡输注诱导的脊髓神经炎症和TNFR1表达增加来恢复吗啡的镇痛作用。白藜芦醇逆转吗啡诱导的TNFR1表达增加部分归因于其逆转了吗啡输注诱导的HDAC1表达增加。白藜芦醇预处理可作为辅助手段应用于需要长期吗啡治疗或患有神经性疼痛的患者的临床疼痛管理。

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