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落地生根对一例皮肤利什曼病患者的毒理学分析及疗效

Toxicological analysis and effectiveness of oral Kalanchoe pinnata on a human case of cutaneous leishmaniasis.

作者信息

Torres-Santos E C, Da Silva S A G, Costa S S, Santos A P P T, Almeida A P, Rossi-Bergmann B

机构信息

Instituto de Biofísica Carlos Chagas Filho.

出版信息

Phytother Res. 2003 Aug;17(7):801-3. doi: 10.1002/ptr.1242.

Abstract

Leishmaniasis is an extremely difficult disease to treat. Previously, it was shown that oral Kalanchoe pinnata (Kp) leaf extract is strongly effective against murine leishmaniasis. Here, it is shown that the serum levels of alanine-aminotransferase (ALT), aspartate-aminotransferase (AST), urea and alkaline phosphatase were unchanged in mice orally treated with supraoptimal Kp doses for 30 days, indicating the absence of chronic toxicity to the liver, heart or kidney. Additionally, evidence is presented that human leishmaniasis may also be controlled with oral Kp. A 36-year-old man with an active cutaneous leishmaniasis was orally treated with 30 g wet weight of Kp leaves/day for 14 days. During the Kp treatment, the lesion stopped growing and slightly decreased. No adverse reactions or toxicity was observed. This study reports for the first time that Kalanchoe pinnata contains substances potentially active and safe for the oral treatment of human cutaneous leishmaniasis.

摘要

利什曼病是一种极难治疗的疾病。此前有研究表明,口服落地生根(Kp)叶提取物对小鼠利什曼病有显著疗效。在此研究中发现,用超最佳剂量的Kp对小鼠进行30天口服治疗后,其血清中的丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、尿素和碱性磷酸酶水平未发生变化,这表明对肝脏、心脏或肾脏不存在慢性毒性。此外,有证据表明口服Kp也可能控制人类利什曼病。一名36岁的皮肤利什曼病患者,每天口服30克湿重的Kp叶,持续14天。在Kp治疗期间,病灶停止生长并略有缩小。未观察到不良反应或毒性。本研究首次报道,落地生根含有对人类皮肤利什曼病口服治疗具有潜在活性且安全的物质。

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