Beales I L, Calam J
Department of Gastroenterology, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.
Exp Physiol. 1996 Nov;81(6):1039-41. doi: 10.1113/expphysiol.1996.sp003988.
The ability of the proglucagon-derived peptides oxyntomodulin and truncated glucagon-like peptide-1 (7-36)amide to stimulate somatostatin release from cultured rabbit fundic D-cells was assessed. Significant stimulation of somatostatin release was seen with both peptides at 10 nM. Potentiation of the stimulatory action of cholecystokinin was seen with both peptides at both 100 pM and 10 nM. The paracrine release of somatostatin from fundic D-cells may explain the acid inhibitory actions of the enteroglucagons. The different small bowel-derived peptides may interact at the level of the D-cell to regulate gastric acid secretion.
对源自胰高血糖素原的肽类——胃抑制肽和截短的胰高血糖素样肽-1(7-36)酰胺刺激培养的兔胃底D细胞释放生长抑素的能力进行了评估。两种肽在10 nM时均能显著刺激生长抑素的释放。在100 pM和10 nM浓度下,两种肽均能增强胆囊收缩素的刺激作用。胃底D细胞旁分泌释放生长抑素可能解释了肠胰高血糖素的胃酸抑制作用。不同的源自小肠的肽可能在D细胞水平相互作用以调节胃酸分泌。