Department for Innovation in Biological, Agro-food and Forest systems (DIBAF), University of Tuscia, Viterbo, Italy.
Curr Neuropharmacol. 2013 Jan;11(1):95-101. doi: 10.2174/157015913804999423.
The multiplicity of peptidergic receptors and of the transduction pathways they activate offers the possibility of important advances in the development of specific drugs for clinical treatment of central nervous system disorders. Among them, retinal ischemia is a common clinical entity and, due to relatively ineffective treatment, remains a common cause of visual impairment and blindness. Ischemia is a primary cause of neuronal death, and it can be considered as a sort of final common pathway in retinal diseases leading to irreversible morphological damage and vision loss. Neuropeptides and their receptors are widely expressed in mammalian retinas, where they exert multifaceted functions both during development and in the mature animal. In particular, in recent years somatostatin and pituitary adenylate cyclase activating peptide have been reported to be highly protective against retinal cell death caused by ischemia, while data on opioid peptides, angiotensin II, and other peptides have also been published. This review provides a rationale for harnessing the peptidergic receptors as a potential target against retinal neuronal damages which occur during ischemic retinopathies.
多种肽能受体及其激活的转导途径为开发针对中枢神经系统疾病的临床治疗的特定药物提供了可能。其中,视网膜缺血是一种常见的临床病症,由于治疗效果相对不理想,它仍然是导致视力损害和失明的常见原因。缺血是神经元死亡的主要原因,可以将其视为导致视网膜疾病发生不可逆形态损伤和视力丧失的最终共同途径。神经肽及其受体在哺乳动物视网膜中广泛表达,在视网膜发育和成熟过程中发挥着多方面的作用。特别是,近年来发现生长抑素和垂体腺苷酸环化酶激活肽对由缺血引起的视网膜细胞死亡具有高度的保护作用,而关于阿片肽、血管紧张素 II 和其他肽的数据也已发表。本综述提供了利用肽能受体作为针对缺血性视网膜病变期间发生的视网膜神经元损伤的潜在靶标的基本原理。