“…At first, des-acyl ghrelin was regarded as a nonfunctional ghrelin ligand. Desacyl ghrelin has been shown to actively participate in food intake (Asakawa et al, 2005;Chen et al, 2005a,b;Matsuda et al, 2006;Toshinai et al, 2006;Muscaritoli et al, 2007;Inhoff et al, 2008;Stengel et al, 2008), gut motility (Asakawa et al, 2005;Chen et al, 2005a,b), body size development Asakawa et al, 2005), adipogenesis (Thompson et al, 2004), insulin secretion and resistance (Broglio et al, 2004b;Gauna et al, 2004Gauna et al, , 2005Gauna et al, , 2007Iwakura et al, 2005;Qader et al, 2008;Zhang et al, 2008b;Kiewiet et al, 2009), to increase tension of guinea pig papillary muscle ex vivo (Bedendi et al, 2003), and cell proliferation and survival in vitro (Baldanzi et al, 2002;Cassoni et al, 2004Cassoni et al, , 2006Granata et al, 2006Granata et al, , 2007Filigheddu et al, 2007). A more recent study revealed that des-acyl ghrelin was secreted in a highly regulated manner in response to food deprivation in mice (Kirchner et al, 2009).…”