Laboratory of Regulation in Metabolism and Behavior, Faculty of Agriculture, Kyushu University, Fukuoka, Japan.
R&I Center, Kyowa Hakko Bio Co., Ltd., Ibaraki, Japan.
J Vet Med Sci. 2022 Sep 12;84(9):1283-1287. doi: 10.1292/jvms.22-0125. Epub 2022 Jul 26.
l-Ornithine is known to stimulate growth hormone (GH) release in mammals. Here, we demonstrated that increases in plasma GH levels after oral administration of l-ornithine were first observed 150 min after administration, and the elevated levels were sustained for more than 90 min in mice. The increase was significantly delayed compared with the reported timing of plasma and tissue levels of l-ornithine after administration. The l-ornithine-induced increase in GH release was completely blocked by [D-Lys]-GHRP-6, a ghrelin receptor antagonist, but not by cyclosomatostatin or JV-1-38, antagonists of somatostatin and GH-releasing hormone, respectively. These results suggest the involvement of ghrelin receptor-mediated pathways in l-ornithine-induced increases in GH release.
鸟氨酸已知可刺激哺乳动物生长激素 (GH) 的释放。在这里,我们证明,口服鸟氨酸后,血浆 GH 水平的升高首先在给药后 150 分钟观察到,并且升高水平在小鼠中持续超过 90 分钟。与报道的给药后鸟氨酸的血浆和组织水平的时间相比,增加明显延迟。[D-Lys]-GHRP-6,一种胃饥饿素受体拮抗剂,完全阻断了鸟氨酸诱导的 GH 释放增加,但环缩氨酸或 JV-1-38 分别是生长抑素和生长激素释放激素的拮抗剂,不能阻断。这些结果表明,鸟氨酸诱导的 GH 释放增加涉及胃饥饿素受体介导的途径。