Blom Jan J, Giove Thomas J, Favazza Tara L, Akula James D, Eldred William D
Department of Biology, Boston University, Boston, MA USA.
J Ocul Biol Dis Infor. 2011 Jun;4(1-2):70-82. doi: 10.1007/s12177-011-9072-8. Epub 2012 Jan 12.
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.
一氧化氮(NO)信号通路完整地参与视觉处理,并且在糖尿病患者的眼睛中可检测到NO通路的变化。小肽肾上腺髓质素(ADM)可激活一条信号通路,以增加神经元型一氧化氮合酶(nNOS)的酶活性。糖尿病患者眼睛中的ADM水平升高,因此,ADM可能在糖尿病视网膜病变的病理过程中起作用。本研究的目的是测试抑制早期糖尿病视网膜病变中ADM/NO信号通路的效果。抑制该通路可降低高糖视网膜培养物中的NO生成。用蛋白激酶Cβ抑制剂鲁比前列酮治疗糖尿病小鼠5周,可降低ADM mRNA水平和ADM样免疫反应性,并通过视网膜电图评估保留视网膜功能。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中的神经元病理改变和功能丧失。