Department of Clinical Medicine, Sapienza University, viale dell'Università 37, 00185 Rome, Italy.
Curr Pharm Des. 2012;18(31):4749-54. doi: 10.2174/138161212803216906.
The growth hormone secretagogue receptor (GHS-R) is a component of the ghrelin signaling pathway and is involved in mediating the pleiotropic effects of ghrelin. Two isoforms have been identified, but only GHS-R1a binds with acyl ghrelin and transduces its message. However, the inactive variant of GHS-R, GHS-R1b, appears to play a critical role in modulating the activity of GHS-R1a by forming heterodimeric complexes which attenuates trafficking of the active variant to the cell surface. The molecular mechanisms of signal transduction are complex and are specific of the tissues where GHS-R1a is expressed. The potent induction of GH secretion and the stimulation of appetite are the most intensively studied functions of GHS-R1a. However, the tissue distribution of GHS-R1a extends beyond the pituitary and the hypothalamus, and reflects the different biological functions of the ghrelin/GHS-R system. GHS-R1a is also expressed in other brain areas, in the pancreas, adipose tissue, immune cells and cardiovascular system, and modulates learning and memory, glucose and lipid metabolism, inflammatory response and cardiac performance. The pleiotropic effects of the ghrelin/GHS-R system suggest their exploitation to prevent and treat a number of clinical conditions. Among many other syndromes and diseases, cancer cachexia, aging related cognitive decline, obesity and diabetes may significantly benefit from the use of GHS-R1a agonists or antagonists.
生长激素促分泌素受体(GHS-R)是胃饥饿素信号通路的组成部分,参与介导胃饥饿素的多种效应。已经鉴定出两种同工型,但只有 GHS-R1a 与酰基胃饥饿素结合并转导其信息。然而,GHS-R 的无活性变体 GHS-R1b 似乎通过形成异二聚体复合物在调节 GHS-R1a 的活性方面发挥关键作用,从而减弱活性变体向细胞表面的运输。信号转导的分子机制很复杂,并且特定于表达 GHS-R1a 的组织。GH 分泌的强烈诱导和食欲的刺激是 GHS-R1a 研究最深入的功能。然而,GHS-R1a 的组织分布不仅局限于垂体和下丘脑,还反映了胃饥饿素/GHS-R 系统的不同生物学功能。GHS-R1a 也在其他脑区、胰腺、脂肪组织、免疫细胞和心血管系统中表达,并调节学习和记忆、葡萄糖和脂质代谢、炎症反应和心脏功能。胃饥饿素/GHS-R 系统的多种效应表明可以利用它们来预防和治疗多种临床病症。在许多其他综合征和疾病中,癌症恶病质、与衰老相关的认知能力下降、肥胖和糖尿病可能会从 GHS-R1a 激动剂或拮抗剂的使用中显著获益。