Weir G C, Mojsov S, Hendrick G K, Habener J F
Joslin Diabetes Center, Boston, MA 02215.
Diabetes. 1989 Mar;38(3):338-42. doi: 10.2337/diab.38.3.338.
Glucagonlike peptide I (7-37) [GLP-I-(7-37)], encoded with glucagon and glucagonlike peptide II and intervening peptide II in the rat and human glucagon gene, is processed from proglucagon in both pancreas and intestine and is a potent stimulator of insulin secretion. Unequivocal insulin release from the isolated perfused rat pancreas is elicited by a 10(-11) M concentration of this peptide, and a weak response is found at 10(-12) M. We found that GLP-I-(7-37) is approximately 100 times more potent than glucagon in the stimulation of insulin secretion. Insulin release in response to GLP-I-(7-37) is highly dependent on the ambient glucose concentration; no response is detectable at a glucose concentration of 2.8 mM, and at 6.6 and 16.7 mM, insulin release is augmented by 4.7 and 22.8 ng/ml, respectively. The pattern of insulin secretion stimulated by GLP-I-(7-37) is biphasic, with an initial spike followed by a plateau of sustained release. The effects on insulin release of GLP-I-(7-36) amide, a GLP-I analogue, and GLP-I-(7-37) at concentrations of 10(-11) M were indistinguishable. We also found that GLP-I-(7-37) at 10(-9) M does not influence glucagon secretion and that glucagonlike peptide II and the intervening peptide II, two other peptides encoded by the glucagon gene, have no detectable effects on insulin secretion.
胰高血糖素样肽I(7 - 37)[GLP - I -(7 - 37)]与胰高血糖素、胰高血糖素样肽II及间隔肽II一起由大鼠和人类的胰高血糖素基因编码,在胰腺和肠道中从胰高血糖素原加工而来,是胰岛素分泌的强效刺激剂。10⁻¹¹M浓度的该肽可引起离体灌注大鼠胰腺明确的胰岛素释放,在10⁻¹²M时可发现微弱反应。我们发现,在刺激胰岛素分泌方面,GLP - I -(7 - 37)的效力约为胰高血糖素的100倍。对GLP - I -(7 - 37)的胰岛素释放高度依赖于周围葡萄糖浓度;在葡萄糖浓度为2.8 mM时未检测到反应,在6.6 mM和16.7 mM时,胰岛素释放分别增加4.7 ng/ml和22.8 ng/ml。GLP - I -(7 - 37)刺激的胰岛素分泌模式是双相的,先是一个初始峰值,随后是持续释放的平台期。浓度为10⁻¹¹M时,GLP - I类似物GLP - I -(7 - 36)酰胺和GLP - I -(7 - 37)对胰岛素释放的影响无法区分。我们还发现,10⁻⁹M的GLP - I -(7 - 37)不影响胰高血糖素分泌,并且胰高血糖素基因编码的另外两种肽,即胰高血糖素样肽II和间隔肽II,对胰岛素分泌没有可检测到的影响。