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D-氨基酸氧化酶在实验性疼痛模型中的双重作用。

Dual role of D-amino acid oxidase in experimental pain models.

机构信息

Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala, 147002 India.

Vallabhbhai Patel Chest Institute, New Delhi, India.

出版信息

Eur J Pharmacol. 2019 Jul 15;855:98-102. doi: 10.1016/j.ejphar.2019.05.001. Epub 2019 May 3.

Abstract

D-amino acid oxidase (DAAO) is an astroglial enzyme abundantly present in the pain sensing regions including brain and spinal cord. There have been studies indicating an upregulation and increased activity of DAAO in different pain models. Furthermore, the upregulation of DAAO also results in the development of morphine tolerance as well as morphine-induced hyperalgesia. Accordingly, the knockdown of DAAO gene or pharmacological inhibition of DAAO reduces pain, reverses tolerance to morphine and hyperalgesia. The pain inducing actions of DAAO are related to augmented production of (hydrogen peroxide) HO, pro-inflammatory cytokines and activation of (Transient receptor protein Ankyrin-1) TRPA1 channels. On the other hand, exogenously administrated DAAO has also been shown to attenuate the pain in different pain models. The pain attenuating actions of DAAO enzyme has been linked to extensive metabolism of D-serine, which may not be able to activate NMDA receptor and trigger pain. The current review highlights the pain attenuating and pain inducing role of DAAO in experimental studies.

摘要

D-氨基酸氧化酶(DAAO)是一种丰富存在于疼痛感应区域(包括大脑和脊髓)的星形胶质细胞酶。有研究表明,在不同的疼痛模型中,DAAO 的表达上调和活性增加。此外,DAAO 的上调也导致吗啡耐受和吗啡诱导的痛觉过敏的发展。因此,DAAO 基因的敲低或 DAAO 的药理学抑制可减轻疼痛,逆转吗啡耐受和痛觉过敏。DAAO 的致痛作用与(过氧化氢)HO、促炎细胞因子的产生增加和(锚蛋白-1)TRPA1 通道的激活有关。另一方面,也有研究表明,外源性给予 DAAO 可减轻不同疼痛模型中的疼痛。DAAO 酶的镇痛作用与 D-丝氨酸的广泛代谢有关,D-丝氨酸可能无法激活 NMDA 受体并引发疼痛。本综述强调了 DAAO 在实验研究中的镇痛和致痛作用。

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