Angelino Elia, Reano Simone, Ferrara Michele, Agosti Emanuela, Graziani Andrea, Filigheddu Nicoletta
Department of Translational Medicine, University of Piemonte Orientale, Via Solaroli 17, 28100 Novara, Italy.
Int J Endocrinol. 2015;2015:385682. doi: 10.1155/2015/385682. Epub 2015 Apr 16.
Fibrosis can affect almost all tissues and organs, it often represents the terminal stage of chronic diseases, and it is regarded as a major health issue for which efficient therapies are needed. Tissue injury, by inducing necrosis/apoptosis, triggers inflammatory response that, in turn, promotes fibroblast activation and pathological deposition of extracellular matrix. Acylated and unacylated ghrelin are the main products of the ghrelin gene. The acylated form, through its receptor GHSR-1a, stimulates appetite and growth hormone (GH) release. Although unacylated ghrelin does not bind or activate GHSR-1a, it shares with the acylated form several biological activities. Ghrelin peptides exhibit anti-inflammatory, antioxidative, and antiapoptotic activities, suggesting that they might represent an efficient approach to prevent or reduce fibrosis. The aim of this review is to summarize the available evidence regarding the effects of acylated and unacylated ghrelin on different pathologies and experimental models in which fibrosis is a predominant characteristic.
纤维化可影响几乎所有组织和器官,它通常代表慢性疾病的终末期,被视为一个需要有效治疗方法的重大健康问题。组织损伤通过诱导坏死/凋亡引发炎症反应,进而促进成纤维细胞活化和细胞外基质的病理性沉积。酰化和去酰化胃饥饿素是胃饥饿素基因的主要产物。酰化形式通过其受体GHSR-1a刺激食欲和生长激素(GH)释放。虽然去酰化胃饥饿素不结合或激活GHSR-1a,但它与酰化形式具有多种共同的生物学活性。胃饥饿素肽具有抗炎、抗氧化和抗凋亡活性,表明它们可能是预防或减轻纤维化的有效方法。本综述的目的是总结关于酰化和去酰化胃饥饿素对以纤维化为主要特征的不同病理和实验模型影响的现有证据。