胆管梗阻后大鼠血清AP、γ - gt、GlDH、GPT及蛋氨酸的活性。

H Putzki, B Reichert
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引用次数: 0

摘要

本研究探讨了AP、γ - gt、GlDH和GPT酶活性升高的病理机制。正如一些研究人员使用蛋白质合成抑制剂所证明的那样,已知AP的增加是由肝脏中重新合成蛋白质引起的。在这项研究中,雌性Wistar大鼠部分假手术,部分胆管阻塞。每组一半给予蛋白质合成抑制剂乙硫氨酸,在胆管梗阻24 h后,乙硫氨酸组测定血清酶活性:AP 216 +/- 80 U/l;γ - gt 4.5 +/- 1.9 U/l;GlDH 85 +/- 26 U/l;GPT 375 +/- 163 U/l。不含乙硫氨酸组的活性为:AP 459 +/- 69 U/l;γ - gt 4 +/- 0.9 U/l;GlDH 120 +/- 81 U/l;GPT 417 +/- 191 U/l。由于除AP外,添加和不添加蛋氨酸组之间的差异不显著,因此可以得出结论,在胆管梗阻早期至24 h内,γ - gt、GlDH和GPT活性的升高未显示出新生蛋白合成的影响。
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The serum activities of AP, gamma-GT, GlDH and GPT after bile duct obstruction and ethionine in the rat.

The increase of activity of the enzymes AP, Gamma-GT, GlDH and GPT was investigated in this study with regard to its pathomechanism. The increase of AP is known to be caused by a de novo-protein synthesis in the liver, as several investigators have demonstrated using protein synthesis inhibitors. In this study female Wistar rats were partly sham-operated, partly bile duct-obstructed. One half of each group received the protein synthesis inhibitor ethionine, 24 h after bile duct obstruction in the group with ethionine the following enzyme activities were measured in the serum: AP 216 +/- 80 U/l; gamma-GT 4.5 +/- 1.9 U/l; GlDH 85 +/- 26 U/l; GPT 375 +/- 163 U/l. In the group without ethionine the activities were: AP 459 +/- 69 U/l; gamma-GT 4 +/- 0.9 U/l; GlDH 120 +/- 81 U/l; GPT 417 +/- 191 U/l. Because the differences between the groups with and without ethionine were not significant with the exception of AP, it is concluded that in the early phase of bile duct obstruction up to 24 h no influence of de novo-protein synthesis can be demonstrated in the elevation of the activities of gamma-GT, GlDH and GPT.

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[7-ethoxycoumarin o-deethylase and fibrosis in chronic liver diseases]. [Effect of gastrointestinal hormones on duodenal motility in acute experiments]. Activities of APh, gamma-GT, GlDH and GPT and bile acid concentrations in serum after bile duct obstruction and cycloheximide in the rat. [Effects of pentagastrin and somatostatin on duodenal motility in chronic experiments]. [Sensitivity and specificity of alpha-1-antitrypsin and acid alpha-1-glycoprotein in colorectal carcinoma].
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