Hermansen K, Kappelgaard A M
Acta Endocrinol (Copenh). 1987 Apr;114(4):589-94. doi: 10.1530/acta.0.1140589.
The 40 aminoacids residue of pancreatic growth hormone-releasing hormone stimulates the secretion of insulin, glucagon, an somatostatin from the pancreas. To determine whether this stimulation of islet hormone secretion is mediated via adrenergic or cholinergic receptor sites, we studied the effects of 30 nmol/l of the growth hormone-releasing hormone on the release of insulin, glucagon, and somatostatin in the presence of either alpha-adrenergic (phentolamine), beta-adrenergic (propranolol) or cholinergic (atropine) blocking agents. The responses to the growth hormone-releasing hormone were not significantly modified by adrenergic or cholinergic blockers. The findings rule out an interaction with adrenergic and cholinergic receptors on islet cells. It is at present unknown whether the growth hormone-releasing hormone stimulates islet hormone secretion via an interaction with specific growth hormone-releasing hormone receptors or vasoactive intestinal peptide receptors.
胰腺生长激素释放激素的40个氨基酸残基可刺激胰腺分泌胰岛素、胰高血糖素和生长抑素。为了确定这种对胰岛激素分泌的刺激是否通过肾上腺素能或胆碱能受体介导,我们研究了在存在α-肾上腺素能阻滞剂(酚妥拉明)、β-肾上腺素能阻滞剂(普萘洛尔)或胆碱能阻滞剂(阿托品)的情况下,30 nmol/l生长激素释放激素对胰岛素、胰高血糖素和生长抑素释放的影响。肾上腺素能或胆碱能阻滞剂并未显著改变对生长激素释放激素的反应。这些发现排除了与胰岛细胞上的肾上腺素能和胆碱能受体相互作用的可能性。目前尚不清楚生长激素释放激素是否通过与特定的生长激素释放激素受体或血管活性肠肽受体相互作用来刺激胰岛激素分泌。