Hainer V, Urbánek J, Malec B, Krejcik L
Horm Metab Res. 1981 Aug;13(8):451-3. doi: 10.1055/s-2007-1019298.
Glucagon-induced growth hormone (GH) secretion was studied in healthy subjects under basal conditions (n = 18), and when treated with TRH (n = 10), cyproheptadine (n = 8) and pimozide (n = 6). With glucagon alone, the mean serum GH level significantly increased at 150 minutes and at 180 minutes. TRH administered as a bolus injection completely suppressed the GH response to glucagon. Cyproheptadine pretreatment resulted in a substantial suppression of the GH response to glucagon. A significant difference between basal and post-cyproheptadine GH levels was observed at 150 minutes after glucagon. Pimozide pretreatment was followed by a reduction of GH response to glucagon, but the difference between control and pimozide-treated groups was not significant. In conclusion, it is proposed that glucagon-induced GH secretion is at least partly mediated via serotoninergic mechanisms while significant dopaminergic involvement does not seem probable. It is further suggested that TRH plays a substantial inhibitory role in glucagon-stimulated SH secretion.
在基础状态下(n = 18)以及接受促甲状腺激素释放激素(TRH)(n = 10)、赛庚啶(n = 8)和匹莫齐特(n = 6)治疗时,对健康受试者进行了胰高血糖素诱导的生长激素(GH)分泌研究。单独使用胰高血糖素时,血清GH平均水平在150分钟和180分钟时显著升高。静脉注射TRH完全抑制了GH对胰高血糖素的反应。赛庚啶预处理导致对胰高血糖素的GH反应显著受到抑制。在注射胰高血糖素后150分钟时,观察到基础状态和赛庚啶处理后GH水平之间存在显著差异。匹莫齐特预处理后GH对胰高血糖素的反应降低,但对照组和匹莫齐特治疗组之间的差异不显著。总之,有人提出胰高血糖素诱导的GH分泌至少部分是通过5-羟色胺能机制介导的,而多巴胺能的显著参与似乎不太可能。进一步表明,TRH在胰高血糖素刺激的GH分泌中起重要的抑制作用。