Oxyntomodulin stimulates intestinal glucose uptake in rats.
Oxyntomodulin stimulates intestinal glucose uptake in rats.
复制标题
泌酸调节素刺激大鼠肠道葡萄糖的摄取。
DOI:
10.1053/gast.1997.v112.pm9178688
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发表时间:
1997
期刊:
影响因子:
29.4
通讯作者:
ReeveJr,JR
中科院分区:
文献类型:
--
作者:
Collie,NL;Zhu,Z;Jordan,S;ReeveJr,JR
BACKGROUND & AIMSEnteroglucagon peptides have long been proposed as mediators of intestinal adaptation, including mucosal growth and nutrient absorptive capacity. The hypothesis that infusions of oxyntomodulin, a bioactive form of enteroglucagon, would stimulate glucose and amino acid uptake was tested and its effects were compared with those of glucagon.METHODSRats were infused intravenously via minipumps with either saline, rat oxyntomodulin (0.47 nmol x kg(-1) x h[-1]), or glucagon (0.88 nmol x kg(-1) x h[-1]) for 7 days, and plasma hormone levels were measured. At death, intestinal dimensions and brush border uptake of D-glucose and L-proline were measured using an in vitro everted sleeve technique.RESULTSPlasma enteroglucagon and glucagon levels were increased 4- and 12-fold, respectively, but there were no effects on food intake, body weight, or intestinal dimensions. In contrast, oxyntomodulin and glucagon significantly stimulated total intestinal glucose uptake capacity by 44% and 53%, respectively, over controls. Oxyntomodulin most potently enhanced glucose uptake in the ileum (215%), whereas glucagon's greatest effect was in the jejunum (63%-85%). However, neither peptide affected proline uptake.CONCLUSIONSThese results support a new, specific action for oxyntomodulin in intestinal adaptation as a glucose uptake stimulator and confirm glucagon's role as a regulator of glucose uptake. (Gastroenterology 1997 Jun;112(6):1961-70)