نتایج جستجو برای: glucantime and lymphocyte

تعداد نتایج: 16835454  

Journal: :iranian journal of public health 0
m mohajery aa shamsian m mahmoodi

background: various responses and different prognosis to specific treatment in different patients from one hand, and importance of ifn-γ producer cells on the other hand impressed us to study tc1. methods: the study was conducted in ghaem medical center and bu-ali research institute, mashhad university of medical sciences, iran from 2001 to 2002. lymphocytes of 36 patients were counted and cult...

Journal: :Dermatology research and practice 2016
Fariba Jaffary Mohammad Ali Nilforoushzadeh Amirhossein Siadat Elaheh Haftbaradaran Nazli Ansari Elham Ahmadi

Background. Cutaneous leishmaniasis is an endemic disease in Iran. Pentavalent antimonial drugs have been the first line of therapy in cutaneous leishmaniasis for many years. However, the cure rate of these agents is still not favorable. This study was carried out to compare the efficacies of intralesional glucantime with topical trichloroacetic acid 50% (TCA 50%) + glucantime and fractional ca...

2015
Elisangela Oliveira Freitas Dirlei Nico Marcus Vinícius Alves-Silva Alexandre Morrot Keith Clinch Gary B. Evans Peter C. Tyler Vern L. Schramm Clarisa B. Palatnik-de-Sousa Michael P Pollastri

BACKGROUND Immucillins ImmA (IA), ImmH (IH) and SerMe-ImmH (SMIH) are synthetic deazapurine nucleoside analogues that inhibit Leishmania (L.) infantum chagasi and Leishmania (L.) amazonensis multiplication in vitro without macrophage toxicity. Immucillins are compared to the Glucantime standard drug in the chemotherapy of Leishmania (L.) infantum chagasi infection in mice and hamsters. These ag...

Journal: :Revista da Sociedade Brasileira de Medicina Tropical 1992
E S Moreira J B Guerra M de L Petrillo-Peixoto

Growth inhibition in vitro tests were used to study the susceptibility to pentostam of different Leishmania strains involved in cutaneous and mucocutaneous leishmaniasis--one glucantime sensitive strain, three naturally glucantime resistant strains and one glucantime resistant line developed by in vitro drug exposure. Contrasting with the high degree of glucantime resistance, all strains were s...

Journal: :Revista do Instituto de Medicina Tropical de Sao Paulo 2011
Diana Copi Ayres Thiago Antonio Fedele Maria Cristina Marcucci Selma Giorgio

In this study we investigated the efficacy of hyperbaric oxygen (HBO) therapy, alone or combined with the pentavalent antimonial glucantime on Leishmania amazonensis infection. In parallel, the effect of Brazilian red propolis gel (propain) alone or combined with glucantime on L. amazonensis infection was evaluated. The inhibition of the infection in macrophages treated with glucantime in combi...

In this study we examined enhancement effects of Artemisinin plus Glucantime and shark cartilage extract, on promastigotes and amastigotes of L.infantum in in vitro condition.The toxicity of artemisinin, glucantime and shark cartilage extract on the L. infantum promastigotes and amastigote-infected macrophages was evaluated using MTT assay. The role of these drugs in inducing apoptosis in proma...

Journal: :Tropical medicine and parasitology : official organ of Deutsche Tropenmedizinische Gesellschaft and of Deutsche Gesellschaft fur Technische Zusammenarbeit 1992
A Fournet A A Barrios V Muñoz R Hocquemiller A Cavé

Plumbagin, 3,3'-biplumbagin and 8,8'-biplumbagin are naphthoquinones isolated by activity-directed fractionation from a Bolivian plant, Pera benensis, used in folk medicine as treatment of cutaneous leishmaniasis caused by Leishmania braziliensis. BALB/c mice were infected with L. mexicana or L. venezuelensis and treated 24 h after the parasitic infection with plumbagin (5 or 2.5 mg/kg/day), 3,...

Journal: :The Korean journal of parasitology 2006
Ghassem Solgi Amina Kariminia Khossor Abdi Majid Darabi Behnaz Ghareghozloo

For treating Leishmania major infection in BALB/c mice, we used thalidomide in conjunction with glucantime. Groups of mice were challenged with 510(3) metacyclic promastigotes of L. major subcutaneously. A week after the challenge, drug treatment was started and continued for 12 days. Thalidomide was orally administrated 30 mg/kg/day and glucantime was administrated intraperitoneally (200 mg/kg...

ژورنال: Hormozgan Medical Journal 2007
Bahmani, M, Salmanpoor, R,

Introduction: Cutaneous leishmaniasis is a parasitic disease caused by various Leishmaniasis species and can result in a disfiguring scar. Hence, effective treatment is mandatory for prevention of the disease sequellae. The goal of this study was assessment and comparison of intralesional Glucantime plus steroid with intralesional Glucantime in the treatment of cutaneous leishmaniasis. Method...

Journal: :Annals of the Academy of Medicine, Singapore 2008
Giti Sadeghian Hengameh Ziaei Masumeh Sadeghi

INTRODUCTION Antimonial compounds are regarded as the treatment of choice for cutaneous leishmaniasis (CL). Systemic administration of these drugs has some side effects including cardio toxicity and electrocardiogram (EKG) changes. The objective of our study was to evaluate EKG changes in the patients with CL treated with systemic glucantime. MATERIALS AND METHODS One hundred and thirty-one p...

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