肾上腺髓质素/一氧化氮信号通路在早期糖尿病视网膜病变中的抑制作用。

Jan J Blom, Thomas J Giove, Tara L Favazza, James D Akula, William D Eldred
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引用次数: 9

摘要

一氧化氮(NO)信号通路全面参与了视觉加工,在糖尿病患者的眼睛中,NO通路的变化是可测量的。小肽肾上腺髓质素(ADM)可以激活一条信号通路,提高神经元一氧化氮合酶(nNOS)的酶活性。糖尿病患者眼内ADM水平升高,ADM可能在糖尿病视网膜病变病理中发挥作用。本研究的目的是检测抑制ADM/NO信号通路对早期糖尿病视网膜病变的影响。抑制这一途径可减少高糖视网膜培养物中NO的产生。用PKC β抑制剂ruboxistaurin治疗糖尿病小鼠5周,通过视网膜电图评估,降低了ADM mRNA水平和ADM样免疫反应性,保留了视网膜功能。本研究结果表明,抑制ADM/NO信号通路可预防早期糖尿病视网膜病变的神经元病理和功能丧失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of the adrenomedullin/nitric oxide signaling pathway in early diabetic retinopathy.

The nitric oxide (NO) signaling pathway is integrally involved in visual processing and changes in the NO pathway are measurable in eyes of diabetic patients. The small peptide adrenomedullin (ADM) can activate a signaling pathway to increase the enzyme activity of neuronal nitric oxide synthase (nNOS). ADM levels are elevated in eyes of diabetic patients and therefore, ADM may play a role in the pathology of diabetic retinopathy. The goal of this research was to test the effects of inhibiting the ADM/NO signaling pathway in early diabetic retinopathy. Inhibition of this pathway decreased NO production in high-glucose retinal cultures. Treating diabetic mice with the PKC β inhibitor ruboxistaurin for 5 weeks lowered ADM mRNA levels and ADM-like immunoreactivity and preserved retinal function as assessed by electroretinography. The results of this study indicate that inhibiting the ADM/NO signaling pathway prevents neuronal pathology and functional losses in early diabetic retinopathy.

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