首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Evidence that inhibitory factor extracted from bovine retractor penis is nitrite whose acid-activated derivative is stabilized nitric oxide.
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Evidence that inhibitory factor extracted from bovine retractor penis is nitrite whose acid-activated derivative is stabilized nitric oxide.

机译:从牛牵开器阴茎中提取的抑制因子是亚硝酸盐的证据其酸活化衍生物是稳定的一氧化氮。

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摘要

1. Unactivated extracts of bovine retractor penis (BRP) contains 3-7 microM nitrite. Acid-activation of these extracts at pH 2 for 10 min followed by neutralization generates the active form of inhibitory factor (IF; assayed by its vasodilator action on rabbit aorta), and is associated with partial loss of nitrite. 2. Increasing the time of acid-activation at pH 2 from 10 to 60 min with intermittent vortex mixing generates greater vasodilator activity and increases nitrite loss. 3. When acid-activated and neutralized extracts are incubated at 37 degrees C or 30 min or boiled for 5 min, vasodilator activity is lost and nitrite content increased. Reactivation of these samples at pH 2 for 10 min followed by neutralization leads to partial recoveries of vasodilator activity with loss in nitrite content. 4. Addition of sodium nitrite to BRP extracts increases acid-activatable vasodilator activity pro rata. 5. Acid-activation of aqueous sodium nitrite solutions results in less loss of nitrite and generation of less vasodilator activity than BRP extracts. Vasodilatation is only transient and is rapidly abolished on neutralization, whereas responses to acid-activated BRP extracts are more prolonged and activity is stable on ice. 6. Bovine aortic endothelial cells yield vasodilator activity that is indistinguishable from that isolated from BRP. It is activated by acid, stable on ice, abolished by boiling or by haemoglobin, and appears to be due to the generation of nitric oxide (NO) from nitrite.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.牛牵开器阴茎(BRP)的未活化提取物含有3-7 microM亚硝酸盐。这些提取物在pH 2下酸活化10分钟,然后中和,产生活性形式的抑制因子(IF;通过其对兔主动脉的血管扩张作用进行测定),并与亚硝酸盐的部分损失有关。 2.在间歇涡流混合下,将pH 2的酸活化时间从10分钟增加到60分钟会产生更大的血管舒张活性,并增加亚硝酸盐的损失。 3.将酸活化和中和的提取物在37摄氏度或30分钟下孵育或煮沸5分钟后,血管舒张活性会下降,亚硝酸盐含量会增加。将这些样品在pH 2下重新活化10分钟,然后中和会导致血管扩张活性部分恢复,亚硝酸盐含量降低。 4.在BRP提取物中添加亚硝酸钠可按比例增加酸激活性血管舒张剂的活性。 5.与BRP提取物相比,亚硝酸钠水溶液的酸活化可减少亚硝酸盐的损失,并产生较少的血管扩张活性。血管舒张只是短暂的,在中和后迅速消失,而对酸活化的BRP提取物的反应则更长,并且在冰上的活性稳定。 6.牛主动脉内皮细胞产生的血管扩张活性与从BRP分离出的血管扩张活性没有区别。它被酸激活,在冰上稳定,被沸腾或血红蛋白消除,似乎是由于亚硝酸盐产生的一氧化氮(NO)(摘要截断为250个字)。

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