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甘丙肽和生长抑素对大鼠P物质诱导的气道黏液分泌的抑制作用。

Galanin and somatostatin inhibition of substance P-induced airway mucus secretion in the rat.

作者信息

Wagner U, Fehmann H C, Bredenbröker D, Yu F, Barth P J, von Wichert P

机构信息

Department of Internal Medicine, Philipps-University of Marburg, Germany.

出版信息

Neuropeptides. 1995 Jan;28(1):59-64. doi: 10.1016/0143-4179(95)90075-6.

Abstract

Substance P is present in several neurons innervating the lung. Tachykinin receptors are expressed on submucosal gland cells. Substance P is known to be a potent stimulator of airway mucus secretion. In the present study we characterized the effects of galanin and somatostatin on basal and substance P-induced mucus secretion. The stimulatory effect of substance P was concentration-dependent (100 pmol/l: 112%, 1 nmol/l: 120%, 10 nmol/l: 153%, 100 nmol/l: 223%, 1 mumol/l: 275%, 10 mumol/l: 172%) and was inhibited by galanin and somatostatin (1 mumol/l substance P: 277%; 1 mumol/l substance P + 1 mumol/l somatostatin: 190%, p < 0.01; 1 mumol/l substance P + 1 mumol/l galanin: 206%, p < 0.05). In the presence of lower concentrations of substance P 1 mumol/l somatostatin and 1 mumol/l galanin did not modify mucus secretion. Lower concentrations of galanin and somatostatin did not significantly change mucus secretion stimulated by 1 mumol/l substance P. Both, galanin and somatostatin at 1 mumol/l left basal airway mucus secretion unaltered. These data suggest that mucus secretion into airways is regulated by a complex network of peptidergic stimulators and inhibitors including substance P, somatostatin and galanin.

摘要

P物质存在于支配肺部的多个神经元中。速激肽受体在黏膜下腺细胞上表达。已知P物质是气道黏液分泌的强效刺激物。在本研究中,我们表征了甘丙肽和生长抑素对基础和P物质诱导的黏液分泌的影响。P物质的刺激作用呈浓度依赖性(100 pmol/L:112%,1 nmol/L:120%,10 nmol/L:153%,100 nmol/L:223%,1 μmol/L:275%,10 μmol/L:172%),并被甘丙肽和生长抑素抑制(1 μmol/L P物质:277%;1 μmol/L P物质 + 1 μmol/L生长抑素:190%,p < 0.01;1 μmol/L P物质 + 1 μmol/L甘丙肽:206%,p < 0.05)。在较低浓度的P物质存在下,1 μmol/L生长抑素和1 μmol/L甘丙肽不会改变黏液分泌。较低浓度的甘丙肽和生长抑素不会显著改变由1 μmol/L P物质刺激引起的黏液分泌。1 μmol/L的甘丙肽和生长抑素均未改变基础气道黏液分泌。这些数据表明,气道黏液分泌受包括P物质、生长抑素和甘丙肽在内的肽能刺激物和抑制剂的复杂网络调节。

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