摘要
The spiropiperidine, MK0677, has been exploited to characterize and expression clone the growth hormone secretagogue receptor (GHS-R). Cloning of this receptor led to identification of its natural ligands, ghrelin and adenosine. Targeted disruption of the Ghsr gene demonstrated unambiguously that the GH-releasing and orexigenic properties of ghrelin are dependent on Ghsr expression and that the orexigenic signal is mediated through neuropeptide Y and agouti-related peptide neurons. This review summarizes new developments in our understanding of the physiological roles of ghrelin and its receptor (GHS-R). Recent discoveries of the effects of ghrelin on the thymus and proinflammatory and chemotactic cytokine pathways stimulate renewed interest in potential clinical applications, which include age-associated disorders, such as metabolic disease, sarcopenia, congestive heart failure, atherosclerosis and anorexia.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 436-442 |
| 页数 | 7 |
| 期刊 | Trends in Endocrinology and Metabolism |
| 卷 | 16 |
| 期 | 9 |
| DOI | |
| 出版状态 | 已出版 - 11月 2005 |
| 已对外发布 | 是 |
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可持续发展目标 3 良好健康与福祉
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