Insulinotropic action of bombesin-like peptides mediated by gastrin-releasing peptide receptors in steers.
Insulinotropic action of bombesin-like peptides mediated by gastrin-releasing peptide receptors in steers.
复制标题
牛体内胃泌素释放肽受体介导的铃蟾肽样肽的促胰岛素作用。
DOI:
10.2527/jas.2015-9495
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发表时间:
2016
影响因子:
3.3
通讯作者:
H. Kuwayama
中科院分区:
文献类型:
--
作者:
H. Zhao;G. Yao;S. Yannaing;S. Thanthan;H. Kuwayama
The present study characterizes the receptor that mediates the insulinotropic action of bombesin-like peptides (BLP) in ruminants. Eight Holstein steers were randomly and intravenously injected with synthetic bovine gastrin-releasing peptide (GRP; 0.9 nmol/kg BW), neuromedin B (NMB; 0.9 nmol/kg BW), or neuromedin C (NMC; 0.9 nmol/kg BW), each alone or combined with the antagonist of GRP receptors N-acetyl-GRP-OCHCH (N-GRP-EE; 22.5 nmol/kg BW) or the antagonist of GH secretagogue receptor type 1a (GHS-R1a) [D-Lys]-GHRP-6 (21.5 nmol/kg BW). Blood samples were collected at -10, 0 (just before injection), 5, 10, 15, 20, 30, 45, 60, 75, and 90 min relative to injection time. Levels of injected peptides, insulin, and glucose in plasma were analyzed. Results showed that the peak of insulin levels was seen at 5 min after injection of NMC or GRP. Plasma glucose was observed in 2 phases; a significant rise followed a remarkable fall after NMC or GRP administration compared with injection of the vehicle ( < 0.05). On a same molar basis, effects of GRP on insulin and glucose were more potent than those of NMC ( < 0.05). The NMC-induced changes of insulin and glucose were completely blocked by N-GRP-EE, but [D-Lys]-GHRP-6 did not block any of these changes. Administration of NMB or N-GRP-EE alone did not change the circulating levels of insulin or glucose during any of the sampling time points ( > 0.05). These results indicated that the insulinotropic action of BLP is mediated by GRP receptors but not through a ghrelin/GHS-R1a pathway and that BLP may be involved in the regulation of glucose homeostasis in ruminants.
影响因子:
7.7
作者:
Y. Date;M. Nakazato;S. Hashiguchi;K. Dezaki;M. S. Mondal;H. Hosoda;M. Kojima;K. Kangawa;T. Arima
通讯作者:
Y. Date;M. Nakazato;S. Hashiguchi;K. Dezaki;M. S. Mondal;H. Hosoda;M. Kojima;K. Kangawa;T. Arima