2nd Department of Propedeutic Surgery, University of Athens, Medical School, Laiko General Hospital, Athens, Greece.
Med Sci Monit. 2010 Jul;16(7):RA147-62.
Ghrelin is a 28 amino acid peptide, identified in the stomach of rats and humans, in 1999. It is an endogenous ligand of the growth hormone secretagogue receptor (GHS-R) that strongly stimulates release of growth hormone at the hypothalamus-pituitary axis. In humans, ghrelin exerts a variety of different endocrine and paracrine actions; from increasing food intake (orexigenic effect) to modulating energy homeostasis. It has been proved that ghrelin affects bone metabolism acting by an autocrine/paracrine mode, independent of GH/IGF-1 axis. Recently, ghrelin was identified in osteoblasts, stimulating proliferation and inhibiting apoptosis. Its expression also was confirmed in rat and human cartilage, being prevalently localized in the proliferative and maturative zone of the epiphyseal growth plate (which further supports the hypothesis of ghrelin's action as a growth factor for chondrocytes). Ghrelin also inhibits prostaglandin and/or leukotriene synthesis. Lately, ghrelin promotes osteogenesis of intramembranous bone and improves the repair of calvarial bone defect in rats in vivo. This review summarizes the effects of ghrelin on bone and cartilage metabolism, analyzes its direct and indirect actions on bone cells, and presents the clinical implication for its use.
胃饥饿素是一种 28 个氨基酸组成的肽,于 1999 年在大鼠和人类的胃中被发现。它是生长激素促分泌素受体(GHS-R)的内源性配体,强烈刺激下丘脑-垂体轴生长激素的释放。在人类中,胃饥饿素发挥着多种不同的内分泌和旁分泌作用;从增加食物摄入(食欲作用)到调节能量平衡。已经证明,胃饥饿素通过自分泌/旁分泌模式影响骨代谢,而不依赖于 GH/IGF-1 轴。最近,胃饥饿素在成骨细胞中被鉴定出来,刺激增殖并抑制细胞凋亡。其表达也在大鼠和人软骨中得到证实,主要定位于骺板的增殖和成熟区(这进一步支持了胃饥饿素作为软骨细胞生长因子的作用假说)。胃饥饿素还抑制前列腺素和/或白三烯的合成。最近,胃饥饿素促进膜内骨的成骨作用,并改善大鼠体内颅骨骨缺损的修复。本文综述了胃饥饿素对骨和软骨代谢的影响,分析了其对骨细胞的直接和间接作用,并提出了其临床应用的意义。