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失血性休克时异常的血红素-蛋白质模式。

Abnormal heme-protein patterns in hemorrhagic shock.

作者信息

Friedman-Mor Z, Chalon J, Gorstein F, Turndorf H, Chuba J V, Orkin L R

出版信息

J Trauma. 1978 Feb;18(2):104-7. doi: 10.1097/00005373-197802000-00005.

DOI:10.1097/00005373-197802000-00005
PMID:633416
Abstract

Allegedly toxic heme pigments have been described in the serum of animals bled to hemorrhagic shock (5,7). In addition, Sears et al. (9), and Braun et al. (1) have shown that the products derived from the degradation of hemoglobin following intravascular hemolysis were toxic (heme carried by hemopexin and albumin). The accumulation of metabolites, caused by the impeded circulation, degrades free hemoglobin into heme pigments and their concentration then reaches a level which exceeds the normal heme-carrying capacity of serum proteins. We have already demonstrated the presence of abnormal heme pigments in clinical cases of shock using scanning spectrophotometry (3). We have endeavored to identify these pigments by serum electrophoresis, and to relate the appearance of some of these compounds to mortality rates. There were no deaths associated with the presence of haptoglobin-hemoglobin alone in serum. As shock deepened and mortality rose, hemopexin-heme and methemalbumin appeared. The highest mortality rate (4 out of 5 cases) was found when both hemopexin-heme and methemalbumin were present. It appears, therefore, that the administration of serum proteins in shock may reduce the toxicity of the products of degradation formed in low-flow states.

摘要

据称,在因出血性休克而失血的动物血清中发现了具有毒性的血红素色素(5,7)。此外,西尔斯等人(9)以及布劳恩等人(1)已经表明,血管内溶血后血红蛋白降解产生的产物具有毒性(血红素结合蛋白和白蛋白携带的血红素)。循环受阻导致代谢产物积累,使游离血红蛋白降解为血红素色素,其浓度随后达到超过血清蛋白正常血红素携带能力的水平。我们已经使用扫描分光光度法在休克临床病例中证明了异常血红素色素的存在(3)。我们努力通过血清电泳来鉴定这些色素,并将其中一些化合物的出现与死亡率联系起来。血清中仅存在触珠蛋白 - 血红蛋白与死亡无关。随着休克加重和死亡率上升,出现了血红素结合蛋白 - 血红素和高铁血红蛋白。当血红素结合蛋白 - 血红素和高铁血红蛋白同时存在时,发现了最高死亡率(5例中有4例)。因此,似乎在休克时给予血清蛋白可能会降低低流量状态下形成的降解产物的毒性。

相似文献

1
Abnormal heme-protein patterns in hemorrhagic shock.失血性休克时异常的血红素-蛋白质模式。
J Trauma. 1978 Feb;18(2):104-7. doi: 10.1097/00005373-197802000-00005.
2
Tracheobronchial cytologic changes and abnormal serum heme pigments in hemorrhagic shock.失血性休克时气管支气管的细胞学变化及异常血清血红素色素
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3
Hemorrhagic shock: concept of toxic elements.失血性休克:毒性元素的概念
N Y State J Med. 1977 Dec;77(14):2217-9.
4
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Ann Biol Clin (Paris). 2003 May-Jun;61(3):332-6.
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Haptoglobin or Hemopexin Therapy Prevents Acute Adverse Effects of Resuscitation After Prolonged Storage of Red Cells.触珠蛋白或血红素结合蛋白疗法可预防长时间储存红细胞后复苏的急性不良反应。
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6
Transfer of heme from heme-albumin to hemopexin.血红素从血红素白蛋白向血红素结合蛋白的转移。
Biochim Biophys Acta. 1976 Sep 24;444(2):435-45. doi: 10.1016/0304-4165(76)90387-1.
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The role of RBC destruction in vascular regions with high turbulence on atherosclerosis.红细胞破坏在动脉粥样硬化中高湍流血管区域的作用。
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[Heme binding by the serum proteins of fish].[鱼类血清蛋白与血红素的结合]
Arch Exp Veterinarmed. 1979 Jan;33(1):21-6.
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Depletion of serum hemopexin in fulminant rhabdomyolysis. Evidence for an interaction of hemopexin with myoglobin-derived heme.暴发性横纹肌溶解症中血清血红素结合蛋白的消耗。血红素结合蛋白与肌红蛋白衍生血红素相互作用的证据。
Arch Neurol. 1978 Aug;35(8):547-8. doi: 10.1001/archneur.1978.00500320067016.
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Use of cysteine as a spectroscopic probe for determination of heme-scavenging capacity of serum proteins and whole human serum.使用半胱氨酸作为光谱探针测定血清蛋白和全人血清的血红素清除能力。
J Pharm Biomed Anal. 2019 Aug 5;172:311-319. doi: 10.1016/j.jpba.2019.05.013. Epub 2019 May 7.

引用本文的文献

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Cell-Free Hemoglobin in the Pathophysiology of Trauma: A Scoping Review.创伤病理生理学中的游离血红蛋白:一项范围综述
Crit Care Explor. 2024 Feb 12;6(2):e1052. doi: 10.1097/CCE.0000000000001052. eCollection 2024 Feb.
2
Hemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contenders.血红素结合蛋白和触珠蛋白:抵御血红蛋白所致血红素毒性的盟友而非竞争者。
Front Physiol. 2015 Jun 30;6:187. doi: 10.3389/fphys.2015.00187. eCollection 2015.
3
Methaemalbumin formation in sickle cell disease: effect on oxidative protein modification and HO-1 induction.
镰状细胞病中亚铁血红素白蛋白的形成:对氧化蛋白修饰和 HO-1 诱导的影响。
Br J Haematol. 2011 Aug;154(4):502-11. doi: 10.1111/j.1365-2141.2011.08738.x. Epub 2011 May 20.