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大鼠肾乳头体外合成前列腺素。血管紧张素II的刺激机制。

Synthesis of prostaglandins by the rat renal papilla in vitro. Mechanism of stimulation by angiotensin II.

作者信息

Danon A, Chang L C, Sweetman B J, Nies A S, Oates J A

出版信息

Biochim Biophys Acta. 1975 Apr 18;388(1):71-83. doi: 10.1016/0005-2760(75)90063-6.

Abstract
  1. The biosynthesis of prostaglandins in the rat renal papilla was studied in a whole-cell preparation in vitro. Prostaglandins recovered from the incubation medium were identified by gas chromatography-mass spectrometry as prostaglandin E2 and prostaglandin F2alpha. Quantitative estimates of prostaglandin output were obtained by bioassay and confirmed by selected ion monitoring. 2. Prostaglandin biosynthesis was enhanced by exogenous arachidonic acid and also by triglyceride lipase, indicating that arachidonic acid released from papillary triglycerides is readily available for prostaglandin biosynthesis. 3. Angiotensin II (10--100 ng/ml) stimulated the biosynthesis of both prostaglandin E2 and prostaglandin F2alpha, thus increasing prostaglandin levels in both the incubation medium and the tissues. 4. The mechanism whereby angiotensin II stimulates prostaglandin biosynthesis was investigated using the isotope dilution technique. In the presence of [14-C]-arachidonic acid, angiotensin II stimulated the output of more prostaglandin that had a significantly lower specific activity than the controls. Angiotensin II therefore increased the availability of endogenous, non-labelled substrate for prostaglandin biosynthesis. This conclusion was supported by experiments in which enough arachidonic acid was added to make the kinetics of prostaglandin synthesis zero order. Under such conditions angiotensin II failed to cause any further increase in prostaglandin synthesis. 5. It is concluded that angiotensin II controls prostaglandin biosynthesis in the renal papilla by regulating the availability of free precursor. Possible mechanisms for increased levels of free arachidonic acid could be the activation of a tissue acyl hydrolase or decreased utilization of fatty acids.
摘要
  1. 在体外全细胞制剂中研究了大鼠肾乳头中前列腺素的生物合成。从孵育培养基中回收的前列腺素通过气相色谱 - 质谱法鉴定为前列腺素E2和前列腺素F2α。通过生物测定获得前列腺素产量的定量估计,并通过选择离子监测进行确认。2. 外源性花生四烯酸和甘油三酯脂肪酶均可增强前列腺素的生物合成,这表明从乳头甘油三酯释放的花生四烯酸易于用于前列腺素的生物合成。3. 血管紧张素II(10 - 100 ng/ml)刺激前列腺素E2和前列腺素F2α的生物合成,从而增加孵育培养基和组织中的前列腺素水平。4. 使用同位素稀释技术研究了血管紧张素II刺激前列腺素生物合成的机制。在存在[14 - C] - 花生四烯酸的情况下,血管紧张素II刺激产生的更多前列腺素的比活性明显低于对照组。因此,血管紧张素II增加了内源性非标记底物用于前列腺素生物合成的可用性。这一结论得到了实验的支持,在这些实验中加入了足够的花生四烯酸以使前列腺素合成动力学为零级。在这种情况下,血管紧张素II未能导致前列腺素合成进一步增加。5. 得出的结论是,血管紧张素II通过调节游离前体的可用性来控制肾乳头中前列腺素的生物合成。游离花生四烯酸水平升高的可能机制可能是组织酰基水解酶的激活或脂肪酸利用的减少。

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