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作 者:涂自智[1] 彭小玲[1] 陈广文[1] 尤家騄[1]
机构地区:[1]湖南医科大学实验动物学部
出 处:《中国实验动物学报》1998年第1期12-18,共7页Acta Laboratorium Animalis Scientia Sinica
摘 要:白介素-2(IL-2)广泛用于治疗恶性肿瘤,由于大剂量可引起严重的低血压且机制不明,限制了其大剂量的使用。本研究用国产重组人白介素-2(rhIL-2)复制大鼠低血压模型并探讨其机制。24只wistar大鼠随机分成3组(每组n=8):正常对照组,IL-2实验组(rhIL-2)和氨基胍(AG)治疗组。结果显示:(1)IL-2可使大鼠提睾肌微动脉扩张及MAP下降,肺、肾、肝组织Evan′sBlue含量明显增加。(2)AG可使rhIL-2引起的低血压回升及微动脉缩小,肺组织Evan′sBlue含量明显下降。提示:rhIL-2引起低血压,可能与IL-2诱导NO产生,使血管扩张及通透性增加有关。? It was reported that hypotension induced by IL-2 in cancer therapy was associated with vascular leak syndrome.(VLS) or vascular dilatation mediated by nitric oxide (NO).This study aimed at investigating whether recombinant human IL-2(rhIL-2)could induce hypotension in rats and whether both VLS and NO were involved in hypotension induced by rhIL-2.24 wistar rats were randomly divided into 3 groups (1) control (NS),(2)rhIL-2,(3)rhIL-2 pluse aminoquanidine (AG).The results showed that:(1)In contrast to the control group,the arterioles were also dilated and MAP decreased significantly in rhIL-2 group.The content of Evan′s Blue was greatly increased in the tissue of lung,kidney and liver in rats at 180min.(2)In contrast to rhIL-2 group,MAP and the arterioles diameter were significantly ameliorated in rhIL-2+AG group.The content of Evan′s Blue in the tissue of lung was significantly reduced.Conclusion:Hypotension induced by rhIL-2 is attributed to both the dilatation of the arterioles and the increment of the vascular permeability and its mechanism may be related to the increment of inducible nitric oxide synthesis.
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