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一种用于检测循环血液中血管加压素的灵敏且特异的检测方法。

A sensitive and specific assay for vasopressin in the circulating blood.

作者信息

Gilore N J, Vane J R

出版信息

Br J Pharmacol. 1970 Apr;38(4):633-52. doi: 10.1111/j.1476-5381.1970.tb09873.x.

DOI:10.1111/j.1476-5381.1970.tb09873.x
PMID:4392559
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1702591/
Abstract
  1. A search was made for an assay tissue with selective sensitivity to vasopressin. Of those smooth muscle preparations tested, the longitudinal muscle of the isolated rectum of the rabbit was the most satisfactory.2. The rabbit isolated rectum, bathed in Krebs solution, was contracted by acetylcholine, angiotensin II amide, bradykinin and 5-hydroxytryptamine. It was relaxed by vasopressin, oxytocin and the catecholamines.3. Vasopressin was active in concentrations of 4-100 muu./ml (0.01-0.25 ng/ml) and was 20-30 times more active than oxytocin. Bretylium had no effect on the relaxant action of vasopressin; nor did concentrations of alpha- and beta-adrenoceptor blocking agents sufficient to abolish the actions of catecholamines. Lignocaine reduced the sensitivity of the rabbit rectum to both vasopressin and oxytocin without altering the actions of adrenaline. High concentrations of either vasopressin or oxytocin desensitized the rabbit rectum to the actions of both hormones, without affecting the actions of adrenaline. It was concluded that vasopressin and oxytocin act on a common population of receptors different from those for catecholamines.4. Phentolamine, unlike other alpha-adrenoceptor antagonists, reduced the relaxant action of vasopressin on the rectum.5. When superfused with blood from an anaesthetized dog, the rabbit rectum maintained a higher tone than in Krebs solution; it retained its sensitivity to vasopressin. Pronethalol, administered intraluminally, reduced spontaneous movement and abolished the actions of low concentrations of catecholamines, thereby increasing the specificity of the assay. No other substance tested relaxed the rectum in concentrations likely to be found in blood.6. Vasopressin was stable in dog's blood; it survived passage through the pulmonary vascular bed; it had a half-life in the circulation of about 1 min.7. The half-life of vasopressin in the circulation may depend upon the duration of the infusion.
摘要
  1. 寻找一种对血管加压素有选择性敏感性的测定组织。在所测试的平滑肌制剂中,兔离体直肠的纵行肌最为理想。

  2. 置于 Krebs 溶液中的兔离体直肠,会被乙酰胆碱、血管紧张素 II 酰胺、缓激肽和 5 - 羟色胺收缩。它会被血管加压素、催产素和儿茶酚胺松弛。

  3. 血管加压素在浓度为 4 - 100 毫微单位/毫升(0.01 - 0.25 纳克/毫升)时具有活性,其活性比催产素高 20 - 30 倍。溴苄铵对血管加压素的松弛作用无影响;足以消除儿茶酚胺作用的α和β肾上腺素能受体阻断剂浓度也无影响。利多卡因降低了兔直肠对血管加压素和催产素的敏感性,而不改变肾上腺素的作用。高浓度的血管加压素或催产素会使兔直肠对两种激素的作用产生脱敏,而不影响肾上腺素的作用。由此得出结论,血管加压素和催产素作用于与儿茶酚胺不同的共同受体群体。

  4. 与其他α肾上腺素能拮抗剂不同,酚妥拉明降低了血管加压素对直肠的松弛作用。

  5. 当用麻醉犬的血液进行灌流时,兔直肠保持的张力比在 Krebs 溶液中更高;它对血管加压素仍保持敏感性。腔内给予普萘洛尔可减少自发运动并消除低浓度儿茶酚胺的作用,从而提高测定的特异性。所测试的其他物质在血液中可能存在的浓度下均未使直肠松弛。

  6. 血管加压素在犬血液中稳定;它在通过肺血管床后仍能留存;其在循环中的半衰期约为 1 分钟。

  7. 血管加压素在循环中的半衰期可能取决于输注持续时间。

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本文引用的文献

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The fate of the antidiuretic principle of postpituitary extracts in vivo and in vitro.垂体后叶提取物抗利尿原理在体内和体外的命运。
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