Effectiveness of the immunomodulatory extract of Kalanchoe pinnata against murine visceral leishmaniasis

被引:22
|
作者
Gomes, D. C. O. [1 ]
Muzitano, M. F. [3 ]
Costa, S. S. [2 ]
Rossi-Bergmann, B. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21949900 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Nucleo Pesquisas Prod Nat, BR-21949900 Rio De Janeiro, Brazil
[3] Univ Estadual Norte Fluminense, Ctr Biociencias & Biotecnol, Campos Dos Goytacazes, Brazil
关键词
visceral leishmaniasis; Kalanchoe pinnata; Leishmania chagasi; oral treatment; NITRIC-OXIDE; CUTANEOUS LEISHMANIASIS; MICE; MILTEFOSINE; METABOLISM; FLAVONOIDS; QUERCITRIN; RESISTANCE; QUERCETIN; INFECTION;
D O I
10.1017/S0031182009991405
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Previously, we described the protective action of the immunomodulatory extract of kalanchoe pinnata (Kp) in murine and human cutaneous leishmaniasis. In the present study, we investigated the effectiveness of Kp against visceral leishmaniasis, using the BALB/c mouse model of infection with Leishmania chagasi. Mice receiving oral daily doses of Kp (400 mg/kg) for 30 days displayed significantly reduced hepatic and splenie parasite burden, when compared with untreated animals. Protectiveness was accompanied by a reduction in parasite-specific IgG serum levels, and impaired capacity of spleen cells to produce IL-4, but not IFN-gamma and nitric oxide upon antigen recall in vitro. The reference drug Pentostam (72 mg/kg) given by the intro-peritoneal route on alternate days produced in anti-leishmanial effect similar to oral Kp. Our findings show that the oral efficacy of Kp, seen previously in murine cutaneous leishmaniasis, extends also to visceral leishmaniasis caused by L. chagasi, a difficult to treat and lethal disease of man.
引用
收藏
页码:613 / 618
页数:6
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