Tsumura Kampo Research Laboratories, Tsumura & Co., Ibaraki 300-1192, Japan.
Int J Mol Sci. 2021 Apr 5;22(7):3763. doi: 10.3390/ijms22073763.
Growth hormone secretagogue receptor 1a (GHS-R1a), which is one of the G protein-coupled receptors (GPCRs), is involved in various physiological actions such as energy consumption, growth hormone secretion promoting action, and cardiovascular protective action. The ligand was searched for as an orphan receptor for a while, but the ligand was found to be acylated ghrelin (ghrelin) discovered by Kangawa and Kojima et al. in 1999. Recently, it has also been reported that dysregulation of GHS-R1a mediates reduced feeding in various diseases. On the other hand, since the physiological effects of ghrelin have been studied exclusively in male mice, few studies have been conducted on gender differences in ghrelin reactivity. In this review, we describe (1) the characteristics of GHS-R1a, (2) the role of ghrelin in hypophagia due to stress or anticancer drugs, and (3) the gender differences in the physiological effects of GHS-R1a and the influence of stress on it.
生长激素促分泌素受体 1a(GHS-R1a)是 G 蛋白偶联受体(GPCR)之一,参与能量消耗、生长激素分泌促进作用和心血管保护作用等各种生理作用。该配体曾被作为孤儿受体进行过一段时间的研究,但配体是由 Kangawa 和 Kojima 等人于 1999 年发现的酰化 ghrelin(ghrelin)。最近,也有报道称 GHS-R1a 的失调介导了各种疾病中摄食量的减少。另一方面,由于 ghrelin 的生理作用仅在雄性小鼠中进行了研究,因此对 ghrelin 反应的性别差异的研究较少。在这篇综述中,我们描述了(1)GHS-R1a 的特征,(2)ghrelin 在应激或抗癌药物引起的摄食减少中的作用,以及(3)GHS-R1a 的生理作用的性别差异以及应激对其的影响。