S N Taheri, H Mahmoudvand, J Ghasemian Yadegari, S Pourhossein, L Masoori
{"title":"黄芪提取物体内外抗皮肤利什曼病的实验研究。","authors":"S N Taheri, H Mahmoudvand, J Ghasemian Yadegari, S Pourhossein, L Masoori","doi":"10.32592/ARI.2024.79.5.929","DOIUrl":null,"url":null,"abstract":"<p><p>Given the distinctive characteristics of <i>Astragalus</i> in the treatment of diseases and the strengthening of the immune system, for the first time, this study represents the first attempt to study the <i>in vitro</i> and <i>in vivo</i> leishmanicidal effects of chloroform extract of <i>A. ecbatanus</i> (AECE) on <i>Leishmania major</i>. The <i>in vitro</i> activity was determined against <i>L. major</i> (MHOM/AF/88/KK27). In addition, the effect of AECE on the generation of nitric oxide (NO) and the rate of macrophage infectivity was evaluated. The, antileishmanial effects of topical administration of AECE at 10 and 20 mg/kg were evaluated <i>In vivo</i> on cutaneous leishmaniasis in mice. The 50% inhibitory concentration (IC<sub>50</sub>) index of AECE and amphotericin B for promastigotes was found to be 76.3 and 2.78 μg/mL, respectively. The number of amastigotes exhibited a dose-dependent decline following treatment with AECE. The IC<sub>50</sub> and 50% cytotoxic concentration (CC<sub>50</sub>) for AECE were 39.4 and 408.3 µg/ml, respectively. The extract was observed to induce the creation of NO while simultaneously reducing the level of macrophage infection. Following a four-week course of AECE therapy, the lesions of CL were observed to have healed in the infected mice. Additionally, the number of the amastigote forms of <i>Leishmania</i> in the CL lesions was significantly reduced following AECE therapy in infected mice (p<0.05). These findings demonstrate the considerable inhibitory and eliminatory effects of AECE on <i>Leishmania</i> <i>in vivo</i> and <i>in vitro</i>. Even though we have identified some cellular mechanisms of action for AECE, e.g. reducing the infectivity rate and the induction of NO production against <i>Leishmania</i> parasites, further experiments are essential to identify the specific mechanisms of action, assess safety, and determine its ability in animals and human subjects.</p>","PeriodicalId":8311,"journal":{"name":"Archives of Razi Institute","volume":"79 5","pages":"929-934"},"PeriodicalIF":0.0000,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12018737/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>In Vitro</i> and <i>In Vivo</i> Effects of <i>Astragalus Ecbatanus</i> Extract against Cutaneous Leishmaniasis.\",\"authors\":\"S N Taheri, H Mahmoudvand, J Ghasemian Yadegari, S Pourhossein, L Masoori\",\"doi\":\"10.32592/ARI.2024.79.5.929\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Given the distinctive characteristics of <i>Astragalus</i> in the treatment of diseases and the strengthening of the immune system, for the first time, this study represents the first attempt to study the <i>in vitro</i> and <i>in vivo</i> leishmanicidal effects of chloroform extract of <i>A. ecbatanus</i> (AECE) on <i>Leishmania major</i>. The <i>in vitro</i> activity was determined against <i>L. major</i> (MHOM/AF/88/KK27). In addition, the effect of AECE on the generation of nitric oxide (NO) and the rate of macrophage infectivity was evaluated. The, antileishmanial effects of topical administration of AECE at 10 and 20 mg/kg were evaluated <i>In vivo</i> on cutaneous leishmaniasis in mice. The 50% inhibitory concentration (IC<sub>50</sub>) index of AECE and amphotericin B for promastigotes was found to be 76.3 and 2.78 μg/mL, respectively. The number of amastigotes exhibited a dose-dependent decline following treatment with AECE. The IC<sub>50</sub> and 50% cytotoxic concentration (CC<sub>50</sub>) for AECE were 39.4 and 408.3 µg/ml, respectively. The extract was observed to induce the creation of NO while simultaneously reducing the level of macrophage infection. Following a four-week course of AECE therapy, the lesions of CL were observed to have healed in the infected mice. Additionally, the number of the amastigote forms of <i>Leishmania</i> in the CL lesions was significantly reduced following AECE therapy in infected mice (p<0.05). These findings demonstrate the considerable inhibitory and eliminatory effects of AECE on <i>Leishmania</i> <i>in vivo</i> and <i>in vitro</i>. 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引用次数: 0
摘要
鉴于黄芪在治疗疾病和增强免疫系统方面的独特特点,本研究首次尝试研究了A. ecbatanus (AECE)氯仿提取物对大利什曼原虫的体内外杀灭作用。测定其对L. major (MHOM/AF/88/KK27)的体外活性。并观察AECE对大鼠一氧化氮(NO)生成及巨噬细胞侵染率的影响。在小鼠体内研究了外用AECE 10和20 mg/kg对皮肤利什曼病的抗利什曼病作用。AECE和两性霉素B对promastigotes的50%抑制浓度(IC50)指数分别为76.3和2.78 μg/mL。在AECE治疗后,无尾线虫的数量呈剂量依赖性下降。AECE的IC50和50%细胞毒浓度(CC50)分别为39.4和408.3µg/ml。观察该提取物在诱导NO生成的同时降低巨噬细胞感染水平。经过4周的AECE治疗,观察到感染小鼠的CL病变已经愈合。此外,在感染小鼠(体内和体外的利什曼原虫)的AECE治疗后,CL病变中利什曼原虫的无鞭毛体形式的数量显着减少。尽管我们已经确定了AECE的一些细胞作用机制,例如降低传染性和诱导NO产生对抗利什曼原虫,但需要进一步的实验来确定具体的作用机制,评估安全性,并确定其在动物和人类试验中的能力。
In Vitro and In Vivo Effects of Astragalus Ecbatanus Extract against Cutaneous Leishmaniasis.
Given the distinctive characteristics of Astragalus in the treatment of diseases and the strengthening of the immune system, for the first time, this study represents the first attempt to study the in vitro and in vivo leishmanicidal effects of chloroform extract of A. ecbatanus (AECE) on Leishmania major. The in vitro activity was determined against L. major (MHOM/AF/88/KK27). In addition, the effect of AECE on the generation of nitric oxide (NO) and the rate of macrophage infectivity was evaluated. The, antileishmanial effects of topical administration of AECE at 10 and 20 mg/kg were evaluated In vivo on cutaneous leishmaniasis in mice. The 50% inhibitory concentration (IC50) index of AECE and amphotericin B for promastigotes was found to be 76.3 and 2.78 μg/mL, respectively. The number of amastigotes exhibited a dose-dependent decline following treatment with AECE. The IC50 and 50% cytotoxic concentration (CC50) for AECE were 39.4 and 408.3 µg/ml, respectively. The extract was observed to induce the creation of NO while simultaneously reducing the level of macrophage infection. Following a four-week course of AECE therapy, the lesions of CL were observed to have healed in the infected mice. Additionally, the number of the amastigote forms of Leishmania in the CL lesions was significantly reduced following AECE therapy in infected mice (p<0.05). These findings demonstrate the considerable inhibitory and eliminatory effects of AECE on Leishmaniain vivo and in vitro. Even though we have identified some cellular mechanisms of action for AECE, e.g. reducing the infectivity rate and the induction of NO production against Leishmania parasites, further experiments are essential to identify the specific mechanisms of action, assess safety, and determine its ability in animals and human subjects.