Detection of artemisinin effect on macrophage inducible nitric oxide gene expression in macrophage infected with Leishmania donovani.

无鞭毛体 U937电池 巨噬细胞 杜氏利什曼原虫 利什曼原虫 青蒿素 生物 一氧化氮合酶 一氧化氮 墨西哥利什曼原虫 川地163 分子生物学 药理学 微生物学 利什曼病 免疫学 细胞凋亡 内脏利什曼病 生物化学 体外 恶性疟原虫 寄生虫寄主 疟疾 万维网 计算机科学 内分泌学
作者
Suhair Dakhil Neamah,Hayder Z. Ali,Mohammad M. F. Al-Halbosiy
出处
期刊:PubMed 卷期号:68 (2): 331-338
标识
DOI:10.17420/ap6802.439
摘要

Leishmaniosis is a parasitic infection spreads to humans by sand flies. Over 20 different species of Leishmania are responsible for the disease, which infect over 14 million people around the world. Chemotherapy is one of the most effective treatments for leishmaniosis, however it is restricted by the high cost and/or toxicity. In this study, the possible effect of artemisinin (ART) was detected on intracellular amastigotes of Iraqi strain of Leishmania donovani in ex vivo condition in U937 macrophage cell line. Gene expression of inducible nitric oxide synthase (iNOS) in U937 macrophage was investigated, before and after treatment with artemisinin. Kinetic result by real-time PCR demonstrated that the iNOS expression folding reached the maximum at concentration of 500 μM after 24 hours, at 750 μM after 48 hours and at 1000 μM after 72 hours, which was 56, 11, and 6, respectively. The copy number of iNOS gene expression was also significantly higher in treated infected U937 cells compared to both non-treated-infected cells and intact macrophages, under different concentration of ART along the three times of follow-up. Moreover, stained macrophages with fluorescent DAPI proved that the percentage of intracellular infective amastigotes was decreased to the minimum in treated U937 cells, in comparison to non-treated cells. The minimal amastigote-invasion percentage was recorded at 1000 μM, which was 26%, 27%, 21% compared to 61%, 87%, 75% in untreated cells after 24, 48, 72 hours respectively. These findings demonstrated ART positive efficacy against iNOS expression and this compound can be further studied as novel therapeutic rather than toxic available chemotherapies.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
2秒前
4秒前
4秒前
rui发布了新的文献求助10
4秒前
慕青应助范星宇采纳,获得10
5秒前
bling发布了新的文献求助10
6秒前
华仔应助月落西山采纳,获得10
6秒前
酸菜炖粉条完成签到,获得积分10
7秒前
7秒前
7秒前
思源应助是真的采纳,获得10
7秒前
高家琚发布了新的文献求助20
7秒前
共享精神应助慕冰蝶采纳,获得10
8秒前
jopaul完成签到,获得积分10
8秒前
AryaZzz完成签到 ,获得积分10
9秒前
大模型应助13081466750采纳,获得10
9秒前
AryaZzz完成签到 ,获得积分10
9秒前
夜信完成签到,获得积分10
9秒前
蔡晓华发布了新的文献求助10
9秒前
小绵羊完成签到,获得积分20
9秒前
tb168tb完成签到,获得积分10
11秒前
zihaoz发布了新的文献求助10
11秒前
过时的傲玉完成签到 ,获得积分10
11秒前
次次实验次次成完成签到,获得积分10
11秒前
bkagyin应助wm采纳,获得10
12秒前
等待的鱼完成签到,获得积分10
12秒前
枫落完成签到,获得积分10
13秒前
啸西风完成签到,获得积分10
14秒前
Reader完成签到 ,获得积分10
14秒前
搞怪冷之完成签到 ,获得积分10
15秒前
rui完成签到,获得积分10
16秒前
16秒前
maybe完成签到,获得积分10
16秒前
16秒前
huazhangchina完成签到,获得积分10
16秒前
Merci完成签到,获得积分10
19秒前
泡菜汤味豆腐完成签到,获得积分10
19秒前
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Introduction to Helicopter and Tiltrotor Flight Simulation, Second Edition 2500
Developing Genetic Editing Tools for Lysobacter 2000
卤化钙钛矿人工突触的研究 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Malcolm Fraser : a biography 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6512685
求助须知:如何正确求助?哪些是违规求助? 8306136
关于积分的说明 17744249
捐赠科研通 5614594
什么是DOI,文献DOI怎么找? 2923820
邀请新用户注册赠送积分活动 1901060
关于科研通互助平台的介绍 1762776