Reano Simone, Graziani Andrea, Filigheddu Nicoletta
Department of Translational Medicine, Università del Piemonte Orientale 'A. Avogadro', Novara, Italy.
Curr Opin Clin Nutr Metab Care. 2014 May;17(3):236-40. doi: 10.1097/MCO.0000000000000049.
Muscle wasting is a comorbidity often associated with a wide range of disorders that severely affects patient prognosis and quality of life. Ghrelin, through its receptor GHSR-1a, stimulates appetite and growth hormone (GH) release. Several studies indicate that ghrelin administration is a valid treatment for cachexia because it improves muscle mass and function, likely by restoring a positive energy balance.
In addition to its GHSR-1a-mediated effects on muscle mass, ghrelin acts directly on skeletal muscle, wherein it exerts a protective activity against muscle wasting. This direct activity is independent of GHSR-1a and is shared by the unacylated form of ghrelin, which does not bind GHSR-1a and is devoid of the effects on appetite and GH release.
Both the acylated and unacylated forms of ghrelin might have therapeutic potential for the treatment of skeletal muscle wasting.
肌肉萎缩是一种常与多种疾病相关的合并症,严重影响患者预后和生活质量。胃饥饿素通过其受体GHSR-1a刺激食欲和生长激素(GH)释放。多项研究表明,给予胃饥饿素是治疗恶病质的有效方法,因为它可能通过恢复正能量平衡来改善肌肉质量和功能。
除了其通过GHSR-1a对肌肉质量产生的作用外,胃饥饿素还直接作用于骨骼肌,在其中发挥抗肌肉萎缩的保护活性。这种直接活性独立于GHSR-1a,且未酰化形式的胃饥饿素也具有此活性,未酰化的胃饥饿素不与GHSR-1a结合,且没有对食欲和GH释放的作用。
胃饥饿素的酰化和未酰化形式可能都具有治疗骨骼肌萎缩的潜力。