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作 者:雷林生[1] 王庆彪[1] 孙莉莎[1] 杨淑琴[1]
机构地区:[1]第一军医大学药理学教研室
出 处:《中药药理与临床》1998年第2期16-18,共3页Pharmacology and Clinics of Chinese Materia Medica
基 金:国家自然科学基金
摘 要:小鼠脾细胞体外培养3h即可检测到IL1αmRNA的表达,4h达到高峰,5h后降至不能检出的水平。TNFαmRNA在4h开始出现,4.5h时达到高峰,5.5h后逐渐消失。在培养开始时分别加入灵芝多糖GLB75、10、20、40μg/ml,4h及4.5h分别检测IL1α及IL1αmRNA的表达情况。结果GLB7能促进IL1α及IL1αmRNA的表达,对IL1αmRNA的表达提高率分别为7.6%、67.3%、105.0%、143.1%;对TNFαmRNA的表达提高率分别为9.9%、33.9%、45.9%、75.8%。8h后GLB7对培养上清中IL1活性的提高率分别为1.4%、3.0%、6.7%、8.1%;12h后对培养上清中TNFα活性的提高率分别为3.0%、14.1%、28.2%、35.7%。结果说明灵芝多糖GLB7能通过促进小鼠脾细胞原代培养时IL1α及TNFαmRNA的表达从而促进IL1及TNFα的合成与分泌。Interleukin1(IL1)α mRNA expression could be detected in murine splenocytes after 3h incubation,it reached the peak level at 4h and then declined to be undetected after 5h incubation.TNF(Tumor Necrosis Factor)α mRNA expression occured after 4h incubation,reached the peak level at 4.5h and disappeared gradually after 5.5h.Ganoderma polysaccharide (GLB7) in different final concentrations(5,10,20,40μg/ml) was added into the cultures at the beginning of incubation and then,the amount of mRNA expressions for IL1α and TNFα was determined after 4h and 4.5h respectively.It was found that GLB7 could promote the mRNA expressions for both IL1α and TNFα,the increase rates of mRNA expression for IL1α were 7.6%,67.3%,105.0% and 143.1%,and were for TNFα 9.9%,33.9%,45.9% and 75.8% respectively.After 8h incubation,GLB7 could increase the activity of IL1 in the supernatants by 1.4%,3.0%,6.7% and 8.1%,and raise the activity of TNFα by 3.0%,14.1%,28.2% and 35.7% after 12h incubation respectively.It is suggested that the enhancement effects of Ganoderma polysaccharide on the production and secretion of IL1 and TNFα in primary murine splenocyte culture are due to promoting of the mRNA expressions for IL1α and TNFα respectively.
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