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雷公藤、黄芪及其合剂对巨噬细胞J774活性的调节作用 被引量:1
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作者 贾泰元 《中国皮肤性病学杂志》 CAS 北大核心 1995年第4期195-196,共2页
应用雷公藤、黄芪及其合剂对J774巨噬细胞株活性的调节作用进行了实验研究。细胞与不同浓度的药液一起培养,结果显示雷公藤抑制、黄芪增强该细胞株的免疫活性。二者合用,增强作用比单用黄芪有所减弱。但与无药对照组比较仍有显著... 应用雷公藤、黄芪及其合剂对J774巨噬细胞株活性的调节作用进行了实验研究。细胞与不同浓度的药液一起培养,结果显示雷公藤抑制、黄芪增强该细胞株的免疫活性。二者合用,增强作用比单用黄芪有所减弱。但与无药对照组比较仍有显著增强作用(P<0.05)。作者认为它们是分别作用于不同的免疫活性细胞和(或)免疫环节而发挥其免疫调节作用的。 展开更多
关键词 雷公藤 黄芪 j774 巨噬细胞株
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多抗甲素A对鼠J774巨噬细胞免疫活性的增强作用
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作者 贾泰元 BenjaminH.S.Lau 《西安医科大学学报》 CSCD 1994年第4期349-351,共3页
对多抗甲素A对J774巨噬细胞活性的调节作用作了观察研究。细胞与多抗甲素A共同孵育,加酵母多糖作激发剂,在自动微量荧光分析仪下进行分析。结果显示多抗甲素能增强该细胞的免疫活性。500mg/L和1000mg/L为最佳浓度,增强效果分别达2.02倍... 对多抗甲素A对J774巨噬细胞活性的调节作用作了观察研究。细胞与多抗甲素A共同孵育,加酵母多糖作激发剂,在自动微量荧光分析仪下进行分析。结果显示多抗甲素能增强该细胞的免疫活性。500mg/L和1000mg/L为最佳浓度,增强效果分别达2.02倍和2.07倍。高于或低于该浓度,增强效果减弱,3000mg/L时,出现抑制效应。 展开更多
关键词 多抗甲素A 巨噬细胞 j774细胞系 酵母多糖
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Essential Gene(s) Targeted by Peptide Nucleic Acids Kills <i>Mycobacterium smegmatis</i>in Culture and in Infected Macrophages
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作者 Md. Ariful Islam Mst. Minara Khatun +1 位作者 Nammalwar Sriranganathan Stephen M. Boyle 《Advances in Infectious Diseases》 2021年第2期156-164,共9页
<em>Background:</em> Antisense peptide nucleic acids (PNAs) exhibit growth inhibitory effects on bacteria by inhibiting the expression of essential genes and could be promising therapeutic agents for treat... <em>Background:</em> Antisense peptide nucleic acids (PNAs) exhibit growth inhibitory effects on bacteria by inhibiting the expression of essential genes and could be promising therapeutic agents for treating bacterial infections. A study was carried out to determine the efficacy of several antisense PNAs in inhibiting extracellular and intracellular growth of <em>Mycobacterium smegmatis</em>. <em>Methods: </em>Six PNAs obtained from a commercial supplier were tested to evaluate the inhibitory effect on bacterial growth by inhibiting the expression of the following essential genes: <em>inhA </em>(a fatty acid elongase), <em>rpsL</em> (ribosomal S12 protein), <em>gyrA</em> (DNA gyrase), <em>pncA</em> (pyrazinamidase), <em>polA</em> (DNA polymerase I) and <em>rpoC</em> (RNA polymerase <em>β</em> subunit) of <em>M. smegmatis</em>. Each PNA was tested at 20 μM, 10 μM, 5 μM and 2.5 μM concentrations to determine whether they caused a dose dependent killing of <em>M. smegmatis</em> cultured in Middlebrook 7H9 broth or in a J774A.1 murine macrophage cell line.<em> Results:</em> In Middlebrook broth, the strong growth inhibitory effect against <em>M. smegmatis</em> was observed by PNAs targeting the <em>inhA </em>and <em>rpsL</em> genes at all four concentrations. The PNAs targeting the<em> pncA</em>, <em>polA</em> and<em> rpoC</em> genes were found to exhibit strong growth inhibition against <em>M. smegmatis</em> but only at 20 μM concentration. No growth inhibition of <em>M. smegmatis </em>was seen in pure culture when treated with PNAs targeting gyrA and a mismatch PNA targeting dnaG (DNA primase). All six PNAs showed killing of <em>M. smegmatis </em>in J774A.1 macrophage cell line that were statistically significant (p < 0.05). <em>Conclusion:</em> It may be concluded from this study that PNAs could be potential therapeutics for mycobacterial infections. 展开更多
关键词 Middlebrook 7H9 Broth Culture j774A.1 Murine Macrophage cell line Antisense Therapy Peptide Nucleic Acid cell Penetrating Peptide Mycobacterium
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