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肺炎球菌诱导的家兔血小板减少症。

Pneumococcus-induced thrombocytopenia in rabbits.

作者信息

Goldblum S E, Simon T L, Thilsted J P, Babcock T L

出版信息

J Lab Clin Med. 1985 Sep;106(3):298-307.

PMID:4031631
Abstract

Thrombocytopenia without other hemostatic changes is the most common coagulopathy associated with sepsis. We studied pneumococcus (PNC)-induced hemostatic changes, including thrombocytopenia, in rabbits. Nonviable PNC or saline solution was injected into rabbits preinfused with chromium 51-labeled platelets or iodine 125-fibrinogen. Blood was serially obtained for determination of platelet counts, 51Cr activity or 125I activity, and fibrinogen and fibrin degradation products. Lung, liver, and spleen tissues were counted for 51Cr or 125I activities per gram of wet tissue. PNC-challenged animals displayed profound thrombocytopenia from 0.5 to 48 hours with the mean nadir (-80% relative to the baseline) at 3 hours and a significantly (P less than 0.025) shortened 51Cr-platelet survival of 1.45 +/- 0.71 days vs. 2.72 +/- 1.09 days for saline-injected controls. Circulating fibrinogen level increased, whereas 125I-fibrinogen survival was unchanged (2.6 +/- 0.5 days in PNC-challenged vs. 2.8 +/- 1.0 days in saline-injected). No increased tissue deposition of either 51Cr-labeled platelets or 125I-fibrinogen was found. Rabbits infused with either serum, plasma, or saline solution after each was incubated with PNC all developed significant thrombocytopenia of less than 1 hour duration with maximal mean decreases relative to the baseline of -76% (P less than 0.001), -65% (P less than 0.0005), and -84% (P less than 0.0005), respectively. Inactivation of serum or plasma complement before PNC incubation or heat treatment after PNC incubation in serum or saline solution did not alter the thrombocytopenia. The thrombocytopenia-promoting activity was also trypsin resistant, did not require the presence of serum, plasma, or PNC capsular polysaccharide for its in vitro generation, and had a mol wt of 100,000 to 300,000. Therefore, PNC-induced thrombocytopenia, in the absence of other hemostatic changes, may be explained on the basis of the direct action of a PNC-derived substance(s) on circulating platelets.

摘要

血小板减少而无其他止血变化是与脓毒症相关的最常见凝血病。我们研究了肺炎球菌(PNC)诱导的家兔止血变化,包括血小板减少。将无活力的PNC或盐溶液注入预先注入51铬标记血小板或125碘纤维蛋白原的家兔体内。连续采集血液以测定血小板计数、51铬活性或125碘活性以及纤维蛋白原和纤维蛋白降解产物。对肺、肝和脾组织进行计数,以测定每克湿组织的51铬或125碘活性。受PNC攻击的动物在0.5至48小时内出现严重血小板减少,3小时时平均最低点(相对于基线降低80%),51铬标记血小板存活时间显著缩短(1.45±0.71天,而注入盐水的对照组为2.72±1.09天,P<0.025)。循环纤维蛋白原水平升高,而125碘纤维蛋白原存活时间未改变(受PNC攻击组为2.6±0.5天,注入盐水组为2.8±1.0天)。未发现51铬标记血小板或125碘纤维蛋白原的组织沉积增加。将血清、血浆或盐溶液与PNC孵育后注入家兔,所有家兔均出现持续时间少于1小时的显著血小板减少,相对于基线的最大平均降低分别为-76%(P<0.001)、-65%(P<0.0005)和-84%(P<0.0005)。在PNC孵育前使血清或血浆补体失活或在PNC与血清或盐溶液孵育后进行热处理均未改变血小板减少情况。促进血小板减少的活性也具有抗胰蛋白酶性,其体外产生不需要血清、血浆或PNC荚膜多糖的存在,分子量为100000至300000。因此,在无其他止血变化的情况下,PNC诱导的血小板减少可能是基于PNC衍生物质对循环血小板的直接作用来解释。

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