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Consumption of kininogen in the submandibular salivary gland when activated by chorda stimulation

机译:软骨刺激刺激下颌下唾液腺激肽原的消耗

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摘要

1. A method is described for determination of kininogen 1 (substrate mainly for plasma kallikrein) and kininogen 2 (substrate for glandular kallikrein) independently in cat plasma.2. In anaesthetized cats the arterial inflow to, and venous outflow from, the submandibular salivary gland were isolated: a roller pump giving constant volume inflow was interposed in the arterial circuit.3. Venous blood was collected at rest, during and after stimulation of the chorda tympani, and its content of kininogens 1 and 2 were estimated. Kininogen 2 was reduced up to 60% by chorda stimulation, whereas the level of kininogen 1 was unchanged.4. On close arterial infusion of bradykinin or histamine in amounts which produce large vascular effects, including increased capillary permeability, the venous blood levels of both kininogens 1 and 2 were unchanged.5. It is concluded that the selective loss of kininogen 2 on chorda stimulation results from the release of kallikrein into the tissue spaces and reflects the extent of kinin formation within the gland.
机译:1.描述了一种在猫血浆中独立测定激肽原1(主要用于血浆激肽释放酶的底物)和激肽原2(用于腺激肽释放酶的底物)的方法。2。在麻醉的猫中,下颌下唾液腺的动脉流入和静脉流出被隔离:在动脉回路中插入了体积流量恒定的滚子泵。3。在静息鼓膜刺激期间和之后收集静息时的静脉血,并估计其激肽原1和2的含量。激肽原2降低了60%,而激肽原1的水平没有改变。4。在对动脉缓激肽或组胺进行紧密动脉输注时,产生的血管作用大,包括毛细血管通透性增加,激肽原1和2的静脉血水平不变。5。结论是激肽原2在软骨刺激上的选择性损失是由于激肽释放酶释放到组织空间中,反映了腺体内激肽形成的程度。

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