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首页> 外文期刊>Digestive Diseases and Sciences >PYY Potently Inhibits Pancreatic Exocrine Secretion Mediated Through CCK-Secretin-Stimulated Pathways but Not 2-DG-Stimulated Pathways in Awake Rats
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PYY Potently Inhibits Pancreatic Exocrine Secretion Mediated Through CCK-Secretin-Stimulated Pathways but Not 2-DG-Stimulated Pathways in Awake Rats

机译:PYY强有力地抑制清醒大鼠中通过CCK-分泌素刺激途径介导的胰腺外分泌分泌,但不抑制2-DG刺激途径介导的胰腺分泌。

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摘要

Peptide YY (PYY) is an important modulator of stimulated pancreatic exocrine secretion. PYY acts proximal to the acinar cell but the exact site and mechanism of action are unknown. The aim of the present study is to determine the pathway through which PYY exerts its effect on the exocrine pancreas in awake rats under physiological condition. When pancreatic secretion was stimulated by graded doses of cholecystokinin (CCK) (14, 28, 58 pmol/kg/hr) with secretin (1.25, 2.5, 5.0 pmol/kg/hr) or CCK alone at 28 pmol/kg/hr, PYY 1-36 dose-dependently inhibited pancreatic secretory responses. Moreover, PYY1-36 at 50 pmol/kg/hr almost completely blocked the stimulation by CCK (P < 0.01). Although background infusion of PYY1-36 or PYY3-36 at 12.5 pmol/kg/hr inhibited basal pancreatic fluid and protein secretion, but both of them only partly inhibited the subsequent 2-DG stimulated pancreatic fluid and protein secretion. Furthermore, PYY1-36 at 50 pmol/kg/hr failed to inhibit 2-DG-stimulated pancreatic secretion. These results confirm that PY1-36 inhibits CCK-stimulated pancreatic secretion under all experimental conditions. However, in the awake, surgically recovered rat, PYY1-36 at both low and high doses failed to fully inhibit 2-DG-stimulated pancreatic secretion. Therefore, the site of PYY's inhibitory action on pancreatic secretion appears to be primarily on the CCK-stimulated pathway at a site proximal to the convergence of the CCK and 2-DG pathways.
机译:YY肽(PYY)是刺激的胰腺外分泌分泌的重要调节剂。 PYY作用于腺泡细胞近端,但确切的作用部位和作用机理尚不清楚。本研究的目的是确定在生理条件下PYY对清醒大鼠的外分泌胰腺发挥作用的途径。当通过逐步剂量的胆囊收缩素(CCK)(14、28、58 pmol / kg / hr)和分泌素(1.25、2.5、5.0 pmol / kg / hr)或单独的CCK以28 pmol / kg / hr刺激胰腺分泌时, PYY 1-36 剂量依赖性抑制胰腺分泌反应。此外,PYY1-36 在50 pmol / kg / hr时几乎完全阻断了CCK的刺激作用(P <0.01)。尽管以12.5 pmol / kg / hr的背景输注PYY1-36 或PYY3-36 可以抑制基础胰液和蛋白质分泌,但是它们都仅部分抑制了随后的2-DG刺激的胰腺液和蛋白质分泌。此外,以50 pmol / kg / hr的PYY1-36 不能抑制2-DG刺激的胰腺分泌。这些结果证实PY1-36 在所有实验条件下均能抑制CCK刺激的胰腺分泌。然而,在清醒的,经过手术恢复的大鼠中,低剂量和高剂量的PYY1-36 都不能完全抑制2-DG刺激的胰腺分泌。因此,PYY对胰腺分泌的抑制作用的部位似乎主要在CCK和2-DG途径趋同的近端的CCK刺激途径上。

著录项

  • 来源
    《Digestive Diseases and Sciences》 |2001年第1期|156-165|共10页
  • 作者单位

    Division of Gastroenterology and Hepatology Department of Medicine and Department of Cell Biology and Physiology University of PittsburghPittsburgh Veterans Affairs Medical Center;

    Division of Gastroenterology and Hepatology Department of Medicine and Department of Cell Biology and Physiology University of PittsburghPittsburgh Veterans Affairs Medical Center;

    Division of Gastroenterology and Hepatology Department of Medicine and Department of Cell Biology and Physiology University of PittsburghPittsburgh Veterans Affairs Medical Center;

    Division of Gastroenterology and Hepatology Department of Medicine and Department of Cell Biology and Physiology University of PittsburghPittsburgh Veterans Affairs Medical Center;

    Division of Gastroenterology and Hepatology Department of Medicine and Department of Cell Biology and Physiology University of PittsburghPittsburgh Veterans Affairs Medical Center;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Peptide YY; cholecystokinin; 2-deoxy-d-glucose; pancreatic secretion; rat;

    机译:肽YY;胆囊收缩素;2-脱氧-d-葡萄糖;胰腺分泌;大鼠;

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