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Central Nervous System Agents Used as Trypanosoma cruzi Infection Chemotherapy: Phenothiazines and Related Compounds

机译:用作克氏锥虫感染化学疗法的中枢神经系统药物:吩噻嗪和相关化合物

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Phenothiazines and related compounds are tricyclic drugs used in psychiatric treatments as antidepressant, anxiolytic and antipsychotic They accumulate in brain, provoking dopamine receptors blockade, They also have antiemetic and antihistaminic effects and many biological activities.WHO promotes the development of a single treatment for African Trypanosomiasis, Chagas'disease and Leishmaniasis, The features of the organisms that produce these diseases, the knowledge of their biology and the sequenced of the three parasites genomes, provide the basis for identifying common metabolic pathways that can provide new drug targets.Such target must be characteristic of these parasites, but absent or altered in the mammalian host. The trypanothione reductase, enzyme of the redox defense system, present in these tripanosomatides has been widely identified as a drug target It is irreversibly inhibited by peroxidase / H2O2 / phenothiazine systems depending on the phenothiazine structure and concentration,We have studied the effect of some phenothiazines and related compounds upon the Trypanosoma cruzi, causative agent of Chagas'disease. The drugs currently used for treatment have high toxicity and frequently parasites appear resistant to them.Phenothiazines produced trypanothione reductase inhibition and other trypanocidal effects upon T, cruzi such as anticalmodulin action, disruption of mitochondria and cell membrane disorganization. This tricyclic drugs were also effective in treatment of different T cruzi strains infected mice, since they modified the natural evolution of the infection; cardiac function and survival of infected and treated animals were not different from non-infected. Phenothiazines and related compounds are promising trypanocidal agents for treatment of Chagas'disease.
机译:吩噻嗪和相关化合物是用于精神病治疗的三环药物,作为抗抑郁药,抗焦虑药和抗精神病药,它们在脑中积累,引起多巴胺受体阻滞,还具有止吐,抗组胺作用和许多生物学活性。WHO促进了非洲锥虫病单一治疗方法的发展。 ,查加斯病和利什曼病,产生这些疾病的生物的特征,其生物学知识和三种寄生虫基因组的序列,为鉴定可以提供新药物靶标的常见代谢途径提供了基础。这些寄生虫的特征,但在哺乳动物宿主中不存在或改变。这些三甲胞嘧啶中存在的氧化还原防御系统酶锥虫二烯还原酶已被广泛鉴定为药物靶标。过氧化物酶/ H2O2 /吩噻嗪系统根据吩噻嗪的结构和浓度不可逆地抑制它。我们研究了某些吩噻嗪的作用以及恰加斯氏锥虫病(锥虫锥虫)的相关化合物。目前用于治疗的药物具有很高的毒性,并且寄生虫经常对它们产生抵抗力。由于三环药物改变了感染的自然演变,因此它还可以有效治疗不同的T克鲁兹菌株感染的小鼠。被感染和治疗的动物的心脏功能和存活率与未感染的动物没有区别。吩噻嗪和相关化合物是治疗查加斯病的有前途的杀锥虫剂。

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