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硫利达嗪对多重耐药结核分枝杆菌临床分离株呼吸作用的抑制:在新诊断结核病初始治疗中的潜在用途

Inhibition of the respiration of multi-drug resistant clinical isolates of Mycobacterium tuberculosis by thioridazine: potential use for initial therapy of freshly diagnosed tuberculosis.

作者信息

Amaral L, Kristiansen J E, Abebe L S, Millett W

机构信息

Department of Pathology and Clinical Laboratories, Bronx-Lebanon Hospital Center, New York, USA.

出版信息

J Antimicrob Chemother. 1996 Dec;38(6):1049-53. doi: 10.1093/jac/38.6.1049.

Abstract

Chlorpromazine and thioridazine are phenothiazines employed in the treatment of psychosis. These agents inhibited the respiration of clinical isolates of Mycobacterium tuberculosis resistant to streptomycin, rifampin, isoniazid, ethambutol and/or pyrazinamid, all first line drugs. Since any adverse reaction to thioridazine is generally less severe than to chlorpromazine, the possibility is attractive that thioridazine may have a potential in the initial management of patients with newly diagnosed tuberculosis with an as yet undetermined antibiotic susceptibility profile.

摘要

氯丙嗪和硫利达嗪是用于治疗精神病的吩噻嗪类药物。这些药物抑制了对链霉素、利福平、异烟肼、乙胺丁醇和/或吡嗪酰胺(所有一线药物)耐药的结核分枝杆菌临床分离株的呼吸。由于硫利达嗪的任何不良反应通常比氯丙嗪轻,因此硫利达嗪在新诊断的抗生素敏感性尚未确定的结核病患者的初始治疗中可能具有潜力,这一可能性很有吸引力。

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