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On the endogenous mechanism of kinin release

II. Attempts at discriminating kininogens

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Summary

Sephadex G 200 chromatography of non-contacted human or bovine plasma reveals one peak of kininogen (LMW kininogen) which serves as substrate for both trypsin and contact kallikrein (= prekallikrein activated by Hageman Factor.)

  1. 2.

    Under special conditions (faster flow rate, protection with diisopropyl fluorophosphate and hexadimethrine bromide), a small kininogen fraction of higher molecular weight (HMW) occasionally preceded the LMW substrate. It appeared increased when the plasma was hemolytic whether contacted or not.

  2. 3.

    Native human plasma was subjected to DEAE sephadex chromatography using stepwise elution starting with relatively high salt concentration. The second peak called HMW-kininogen emerged together with the abrupt increase in ionic strength and contained 2.2 to 4.8 times less kinin than did the first. Both kininogens yielded kinin with purified contact kallikrein.

  3. 4.

    By analytical gel filtration of different HMW-kininogen preparations, molecular weights of about 100,000, 200,000 and 500,000 were estimated.

We conclude that HMW-kininogen is not represented by a distinct, individual molecule. It may be a polymer of the low molecular weight kininogen or an aggregate of it with other plasma constituents.

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Habermann, E., Jahrreiss, R. On the endogenous mechanism of kinin release. Naunyn-Schmiedebergs Arch. Pharmak. 269, 101–111 (1971). https://doi.org/10.1007/BF01422019

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