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Effects of morphine during Mycobacterium tuberculosis H37Rv infection in mice

机译:吗啡在小鼠结核分枝杆菌H37Rv感染中的作用

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The effects of opiates in various infections are well known; however, very little is known about tuberculosis infection. Therefore, in the present study, we report for the first time, the effects of morphine curing murine tuberculosis. Mice were infected intravenously with Mycobacterium tuberculosis H37Rv, administered morphine (0.1-100 mg/kg subcutaneously on day 0 and day +15) and sacrificed on day +30 for CFU enumeration in lungs and spleen. Morphine exerted maximum suppression of infection at 5 mg/kg, and sometimes completes elimination of infection; naloxone, silica and aminoguanidine blocked the protective effect of morphine. In vitro, morphine lacked direct antimycobacterial activity up to 1 x 10(-4) M concentration, as assessed by radiometric BACTEC method. In macrophage model of infection, morphine showed maximal killing at 1 x 10(-7) M concentration, the activity was blocked by naloxone and aminoguanidine. These observations suggest that morphine exerts a dose-dependent effect in murine tuberculosis, the protective effect being naloxone-reversible and may involve macrophage-mediated protective mechanisms. These results may be helpful in developing new opioid-like chemical entities against tuberculosis infection. (C) 2007 Elsevier Inc. All rights reserved.
机译:阿片类药物在各种感染中的作用是众所周知的。然而,对结核感染的了解甚少。因此,在本研究中,我们首次报道了吗啡治疗鼠结核的效果。用结核分枝杆菌H37Rv静脉感染小鼠,在第0天和第+15天皮下注射吗啡(0.1-100mg / kg皮下注射),并在+30天处死小鼠以用于肺和脾中的CFU计数。吗啡在5 mg / kg时可最大程度地抑制感染,有时可完全消除感染。纳洛酮,二氧化硅和氨基胍阻断了吗啡的保护作用。在体外,吗啡缺乏高达1 x 10(-4)M浓度的直接抗分枝杆菌活性,通过放射BACTEC方法评估。在感染的巨噬细胞模型中,吗啡在1 x 10(-7)M浓度下显示出最大杀伤力,其活性被纳洛酮和氨基胍阻断。这些观察结果表明吗啡在鼠结核中发挥剂量依赖性作用,其保护作用是纳洛酮可逆的,并且可能涉及巨噬细胞介导的保护机制。这些结果可能有助于开发新的类阿片样化学实体以抵抗结核感染。 (C)2007 Elsevier Inc.保留所有权利。

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