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血红蛋白零交联聚合物的研发,这类聚合物不会渗出,输注时也不会导致压力升高。

Development of zero-link polymers of hemoglobin, which do not extravasate and do not induce pressure increases upon infusion.

作者信息

Bucci Enrico, Kwansa Herman, Koehler Raymond C, Matheson Barbara

机构信息

Department of Biochemistry and Molecular Biology, University of Maryland Medical School, Baltimore, Maryland, USA.

出版信息

Artif Cells Blood Substit Immobil Biotechnol. 2007;35(1):11-8. doi: 10.1080/10731190600974277.

Abstract

Intramolecular crosslink of hemoglobin tetramers solved the problem of urine elimination and short intravascular retention time of cell free hemoglobin infusion. It also produced a family of crosslinked hemoglobins with P50 between 18 and 30 mmHg. However, it did not solve the problem of MAP increases in infused animals. It was proven that extravasation of hemoglobin into interstitial fluid was responsible for MAP increases. Extravasation and the MAP increase was avoided using a hemoglobin polymer with average size near 25 MDa. In spite of a very high oxygen affinity, this polymer delivered oxygen to tissues, producing either vasodilation or vasoconstriction according to oxygen needs. It was also proven that cell free hemoglobins are more efficient than red cells in delivering oxygen to tissues.

摘要

血红蛋白四聚体的分子内交联解决了无细胞血红蛋白输注后排尿问题及血管内保留时间短的问题。它还产生了一系列P50在18至30 mmHg之间的交联血红蛋白。然而,它并未解决输注动物中平均动脉压(MAP)升高的问题。已证实血红蛋白渗入组织间隙液是MAP升高的原因。使用平均大小接近25 MDa的血红蛋白聚合物可避免渗漏及MAP升高。尽管该聚合物具有非常高的氧亲和力,但它能根据组织对氧气的需求向组织输送氧气,从而引起血管舒张或收缩。还证实无细胞血红蛋白在向组织输送氧气方面比红细胞更有效。

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本文引用的文献

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Role of nitric oxide scavenging in vascular response to cell-free hemoglobin transfusion.一氧化氮清除在无细胞血红蛋白输血血管反应中的作用。
Am J Physiol Heart Circ Physiol. 2005 Sep;289(3):H1191-201. doi: 10.1152/ajpheart.00251.2005. Epub 2005 May 13.
5
Cell-free hemoglobin, oxygen off-load and vasoconstriction.游离血红蛋白、氧卸载与血管收缩
Anasthesiol Intensivmed Notfallmed Schmerzther. 2001 Nov;36 Suppl 2:S123-4. doi: 10.1055/s-2001-18180.
8
Effect of cross-linked hemoglobin transfusion on endothelial-dependent dilation in cat pial arterioles.
Am J Physiol. 1998 Oct;275(4):H1313-21. doi: 10.1152/ajpheart.1998.275.4.H1313.

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