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一种预防输血期间恰加斯病传播的策略。

A strategy for the prevention of the transmission of Chagas' disease during blood transfusion.

作者信息

Hammond D J, Croft S L, Hogg J, Gutteridge W E

出版信息

Acta Trop. 1986 Dec;43(4):367-78.

PMID:2882664
Abstract

Our strategy for preventing the transmission of Chagas' disease during blood transfusion is discussed. In addition, the possibility that the Peru, Sonya, Tulahuen and Y strains of Trypanosoma cruzi show varying sensitivities to a series of amphiphilic cationic drugs in vitro at 4 degrees C was investigated using a microscope lysis test. All 21 drugs tested at a concentration of 10(-3) M lysed Sonya bloodstream trypomastigotes, but Peru, Tulahuen and Y strains were affected by 17, 17 and 11 drugs, respectively. All four strains were most sensitive to the acridines; acranil, aminacrine and mepacrine. Although some variation was seen in their responses to certain drugs, no one strain was particularly insensitive to the series as a whole. The effects of gentian violet, maprotiline and mepacrine on the infectivity of Sonya trypomastigotes following incubation at 4 degrees C for 24 h were evaluated. Mepacrine, at a concentration of 2.5 X 10(-4) M greatly decreased the viability of trypomastigotes, while 10(-3) M concentrations of both maprotiline, mepacrine, and gentian violet (at low parasite densities only) apparently abolished all infectivity. Although the compounds we tested did not show a significant improvement over gentian violet, the compound currently used in some blood banks, other existing amphiphilic cationic drugs could be of use in preventing the transmission of Chagas' disease during blood transfusion.

摘要

本文讨论了我们在输血过程中预防恰加斯病传播的策略。此外,使用显微镜裂解试验研究了克氏锥虫的秘鲁株、索尼娅株、图拉亨株和Y株在4℃体外对一系列两亲性阳离子药物的敏感性差异。在浓度为10(-3)M时测试的所有21种药物均能裂解索尼娅株血液中的锥鞭毛体,但秘鲁株、图拉亨株和Y株分别受到17种、17种和11种药物的影响。所有四个菌株对吖啶类药物最为敏感,如吖啶黄、氨基吖啶和米帕林。尽管它们对某些药物的反应存在一些差异,但没有一个菌株对整个系列药物特别不敏感。评估了结晶紫、马普替林和米帕林在4℃孵育24小时后对索尼娅锥鞭毛体感染性的影响。浓度为2.5×10(-4)M的米帕林可显著降低锥鞭毛体的活力,而浓度为10(-3)M的马普替林、米帕林和结晶紫(仅在低寄生虫密度下)显然可消除所有感染性。尽管我们测试的化合物与目前一些血库使用的结晶紫相比没有显著改善,但其他现有的两亲性阳离子药物可能有助于预防输血过程中恰加斯病的传播。

相似文献

1
A strategy for the prevention of the transmission of Chagas' disease during blood transfusion.一种预防输血期间恰加斯病传播的策略。
Acta Trop. 1986 Dec;43(4):367-78.
2
Screening of drugs for rapid activity against Trypanosoma cruzi trypomastigotes in vitro.
Trop Med Parasitol. 1988 Jun;39(2):145-8.
3
Trypanosoma cruzi: possible control of parasite transmission by blood transfusion using amphiphilic cationic drugs.
Exp Parasitol. 1985 Aug;60(1):32-42. doi: 10.1016/s0014-4894(85)80020-5.
4
[Post-transfusion Chagas' disease].[输血后恰加斯病]
Rev Hosp Clin Fac Med Sao Paulo. 1988 May-Jun;43(3):135-7.
5
[The chemotherapy of Chagas disease].[恰加斯病的化疗]
Medicina (B Aires). 1999;59 Suppl 2:147-65.
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[Chagas' disease and blood transfusion: trypanocidal activity of maprotiline hydrochloride and gentian violet].[恰加斯病与输血:盐酸马普替林和龙胆紫的杀锥虫活性]
Medicina (B Aires). 1988;48(3):265-8.
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[Evaluation of the eventual activity of cyclosporin A in preventing the transmission, by blood transfusion, of Trypanosoma cruzi infection].
Rev Hosp Clin Fac Med Sao Paulo. 1997 Jul-Aug;52(4):195-6.
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Field evaluation of four novel enzyme immunoassays for Chagas' disease in Venezuela blood banks: comparison of assays using fixed-epimastigotes, fixed-trypomastigotes or trypomastigote excreted-secreted antigens from two Trypanosoma cruzi strains.委内瑞拉血库中用于查加斯病的四种新型酶免疫测定法的现场评估:使用来自两种克氏锥虫菌株的固定型前鞭毛体、固定型锥鞭毛体或锥鞭毛体排泄-分泌抗原的测定法比较
Transfus Med. 2006 Dec;16(6):419-31. doi: 10.1111/j.1365-3148.2006.00703.x.
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Potential use of WR6026 as prophylaxis against transfusion-transmitted American trypanosomiasis.WR6026作为预防输血传播的美洲锥虫病的潜在用途。
Antimicrob Agents Chemother. 1996 Mar;40(3):613-5. doi: 10.1128/AAC.40.3.613.
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A primary screen for drugs to prevent transmission of Chagas's disease during blood transfusion.用于筛选预防输血过程中恰加斯病传播药物的初步筛选。
Trans R Soc Trop Med Hyg. 1982;76(5):633-5. doi: 10.1016/0035-9203(82)90228-0.

引用本文的文献

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Efficient technique for screening drugs for activity against Trypanosoma cruzi using parasites expressing beta-galactosidase.利用表达β-半乳糖苷酶的寄生虫筛选抗克氏锥虫活性药物的高效技术。
Antimicrob Agents Chemother. 1996 Nov;40(11):2592-7. doi: 10.1128/AAC.40.11.2592.