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暴露后给予 A(1) 腺苷受体激动剂可减轻噪声性听力损失。

Post exposure administration of A(1) adenosine receptor agonists attenuates noise-induced hearing loss.

机构信息

Department of Physiology, Faculty of Medical and Health Sciences, The University of Auckland, New Zealand.

出版信息

Hear Res. 2010 Feb;260(1-2):81-8. doi: 10.1016/j.heares.2009.12.004. Epub 2009 Dec 6.

Abstract

Adenosine is a constitutive cell metabolite with a putative role in protection and regeneration in many tissues. This study was undertaken to determine if adenosine signalling pathways are involved in protection against noise injury. A(1) adenosine receptor expression levels were altered in the cochlea exposed to loud sound, suggesting their involvement in the development of noise injury. Adenosine and selective adenosine receptor agonists (CCPA, CGS-21680 and Cl-IB-MECA) were applied to the round window membrane of the cochlea 6h after noise exposure. Auditory brainstem responses measured 48h after drug administration demonstrated partial recovery of hearing thresholds (up to 20dB) in the cochleae treated with adenosine (non-selective adenosine receptor agonist) or CCPA (selective A(1) adenosine receptor agonist). In contrast, the selective A(2A) adenosine receptor agonist CGS-21680 and A(3) adenosine receptor agonist Cl-IB-MECA did not protect the cochlea from hearing loss. Sound-evoked cochlear potentials in control rats exposed to ambient noise were minimally altered by local administration of the adenosine receptor agonists used in the noise study. Free radical generation in the cochlea exposed to noise was reduced by administration of adenosine and CCPA. This study pinpoints A(1) adenosine receptors as attractive targets for pharmacological interventions to reduce noise-induced cochlear injury after exposure.

摘要

腺苷是一种组成型细胞代谢物,在许多组织的保护和再生中具有潜在作用。本研究旨在确定腺苷信号通路是否参与对抗噪声损伤的保护。在暴露于强声的耳蜗中,A1 腺苷受体表达水平发生改变,表明其参与了噪声损伤的发生。在噪声暴露后 6 小时,将腺苷和选择性腺苷受体激动剂(CCPA、CGS-21680 和 Cl-IB-MECA)应用于耳蜗的圆窗膜。给药后 48 小时测量的听觉脑干反应显示,用腺苷(非选择性腺苷受体激动剂)或 CCPA(选择性 A1 腺苷受体激动剂)处理的耳蜗的听力阈值部分恢复(高达 20dB)。相比之下,选择性 A2A 腺苷受体激动剂 CGS-21680 和 A3 腺苷受体激动剂 Cl-IB-MECA 不能保护耳蜗免受听力损失。在暴露于环境噪声的对照大鼠中,局部给予噪声研究中使用的腺苷受体激动剂对声诱发的耳蜗电位几乎没有影响。给予腺苷和 CCPA 可减少噪声暴露后耳蜗中的自由基生成。本研究指出 A1 腺苷受体是减少暴露后噪声诱导的耳蜗损伤的药物干预的有吸引力的靶标。

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