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作 者:王洪斌[1] 王劲[1] 郑钦岳[1] 李铁军[1] 李书桐[1] 陈海生[1]
机构地区:[1]第二军医大学药学院药理学教研室,第二军医大学药学系,西安空军医院,第二军医大学药学院植物化学教研室
出 处:《第二军医大学学报》1996年第2期150-153,共4页Academic Journal of Second Military Medical University
摘 要:本实验在建立DNA多聚酶α活性测定方法的基础上观察了商陆多糖I(PAP-I)对小鼠淋巴细胞增殖及淋巴细胞DNA多聚酶α活性的影响。采用[3H]-TdR掺入法和模板活化法([3H]-dTTP掺入法)分别检测PAP-I给药组及对照组小鼠淋巴细胞增殖能力和淋巴细胞DNA多聚酶α活性。体外实验发现PAP-I显著增强ConA诱导的小鼠脾淋巴细胞增殖及其DNA多聚酶α的活性;小鼠腹腔注射PAP-I(每周1次)对脾淋巴细胞DNA多聚酶α活性基本上无影响,但加入ConA(5μg/ml)刺激后,PAP-I10mg/kg剂量组DNA多聚酶α活性显著增强。结果提示PAP-I增强DNA多聚酶α活性可能是促进脾淋巴细胞增殖、增强免疫功能的机制之一。The purpose of the present study was to investigate the effect of Phytolacca acinosa polysaccharides(PAP-I) on DNA polymerase a activity of murine splenocytes and their proliferation.The activity of DNA polymerase a was measured by the method of [3H]-dTTP uptake by template DNA which was heated at 100℃for 5 min.The proliferation ability of murine splenocytes was tested by [3H]-TdR uptake by the splenocytes.The DNA polymerase a activity was found to be augmented by PAP-I at the dosage of 200μg/ml.In the same time,DNA synthesis of murine splenocytes was also increased. The DNA polymerase a activity from murine splencoytes,which were treated with ip PAP-I 5,10,50 mg/kg,was also measured in the present study.The results showed that PAP-I,10 mg/kg ip could significantly augment DNA polymerase a activity from murine splenocytes when the murine splenocytes were treated with Con A 5 μg/ml.DNA synthesis of murine splenocytes was also augmented by administration of PAP-I,10 mg/kg ip.These data indicate that enhancing effect of PAP-I on lymphocyte proliferation might be related with its augmenting effect on DNA polymerase a activity from murine splenocytes.
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