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胰抑制素样免疫反应性物质和胰岛素从灌注的猪胰腺中平行释放。

Pancreastatin-like immunoreactivity and insulin are released in parallel from the perfused porcine pancreas.

作者信息

Ostenson C G, Efendic S, Holst J J

机构信息

Department of Endocrinology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Endocrinology. 1989 Jun;124(6):2986-90. doi: 10.1210/endo-124-6-2986.

Abstract

Pancreastatin, a peptide isolated from the porcine pancreas, suppresses insulin release from pancreatic islets of the rat. Pancreastatin immunoreactivity has been localized to islet B and D cells in the porcine pancreas. We have developed a RIA for this peptide, using rabbit anti-porcine pancreastatin antibodies and 125I-Tyr-pancreastatin. Isolated pig pancreata were perfused with a nonrecirculating bicarbonate buffer solution containing 4% Dextran and 0.1% Albumin. Glucose (11 mmol/liter) induced a biphasic release of pancreastatin-like immunoreactivity (PLI). Electrical stimulation of the vagus nerves (8 Hz), as well as perfusion with acetyl choline (10(-6) mol/liter) in the presence of 5.5 mmol/liter glucose, also evoked prompt PLI responses. Furthermore, truncated GLP-1 (proglucagon 78-107; 10(-9) mol/liter) induced PLI release. All tested stimuli also elicited insulin secretion. To investigate whether the PLI measured could be ascribed to secretion of the low molecular weight pancreastatin (Mr 5,100) or to a possible precursor such as chromogranin A (Mr approximately 75,000), perfusates containing PLI were subjected to gel filtration on an Ultropac G3000SW column. All of the PLI was recovered at the elution position of the pancreastatin marker. In conclusion, PLI and insulin are released in parallel from the perfused porcine pancreas, exposed to stimuli known to affect insulin release.

摘要

胰抑制素是从猪胰腺中分离出的一种肽,它能抑制大鼠胰岛释放胰岛素。胰抑制素免疫反应活性已定位在猪胰腺的胰岛B细胞和D细胞中。我们利用兔抗猪胰抑制素抗体和125I-酪氨酸-胰抑制素开发了一种针对该肽的放射免疫分析法。将分离的猪胰腺用含有4%葡聚糖和0.1%白蛋白的非循环碳酸氢盐缓冲溶液灌注。葡萄糖(11毫摩尔/升)诱导了胰抑制素样免疫反应活性(PLI)的双相释放。迷走神经电刺激(8赫兹)以及在5.5毫摩尔/升葡萄糖存在下用乙酰胆碱(10^(-6)摩尔/升)灌注,也能迅速引发PLI反应。此外,截短的胰高血糖素样肽-1(胰高血糖素原78 - 107;10^(-9)摩尔/升)诱导了PLI释放。所有测试的刺激也都引发了胰岛素分泌。为了研究测得的PLI是否可归因于低分子量胰抑制素(分子量5100)的分泌或可能的前体如嗜铬粒蛋白A(分子量约75000),将含有PLI的灌注液在Ultropac G3000SW柱上进行凝胶过滤。所有的PLI都在胰抑制素标志物的洗脱位置回收。总之,在受到已知影响胰岛素释放的刺激时,PLI和胰岛素从灌注的猪胰腺中平行释放。

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引用本文的文献

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