Nagaya Noritoshi, Kojima Masakazu, Kangawa Kenji
Department of Regenerative Medicine and Tissue Engineering, National Cardiovascular Center Research Institute, Osaka.
Intern Med. 2006;45(3):127-34. doi: 10.2169/internalmedicine.45.1402. Epub 2006 Mar 1.
Ghrelin is a novel growth hormone (GH)-releasing peptide, isolated from the stomach, which has been identified as an endogenous ligand for GH secretagogue receptor. The discovery of ghrelin indicates that the release of GH from the pituitary might be regulated not only by hypothalamic GH-releasing hormone, but also by ghrelin derived from the stomach. This peptide also stimulates food intake and induces adiposity through GH-independent mechanisms. In addition, ghrelin acts directly on the central nervous system to decrease sympathetic nerve activity. Thus, ghrelin plays important roles for maintaining GH release and energy homeostasis. Repeated administration of ghrelin improves body composition, muscle wasting, functional capacity, and sympathetic augmentation in cachectic patients with heart failure or chronic obstructive pulmonary disease. These results suggest that ghrelin has anti-cachectic effects through GH-dependent and independent mechanisms. Thus, administration of ghrelin may be a new therapeutic strategy for the treatment of cardiopulmonary-associated cachexia.
胃饥饿素是一种从胃中分离出的新型生长激素(GH)释放肽,已被确定为生长激素促分泌素受体的内源性配体。胃饥饿素的发现表明,垂体生长激素的释放可能不仅受下丘脑生长激素释放激素的调节,还受源自胃的胃饥饿素的调节。这种肽还通过不依赖生长激素的机制刺激食物摄入并诱导肥胖。此外,胃饥饿素直接作用于中枢神经系统以降低交感神经活动。因此,胃饥饿素在维持生长激素释放和能量稳态方面发挥着重要作用。反复给予胃饥饿素可改善心力衰竭或慢性阻塞性肺疾病恶病质患者的身体组成、肌肉萎缩、功能能力和交感神经亢进。这些结果表明,胃饥饿素通过依赖生长激素和不依赖生长激素的机制具有抗恶病质作用。因此,给予胃饥饿素可能是治疗心肺相关恶病质的一种新的治疗策略。