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五步蛇毒对小鼠免疫功能的影响
引用本文:宋天麟,周马林,蒙怡,李亚兰,陶慧娟,廖明,班建东,张学荣.五步蛇毒对小鼠免疫功能的影响[J].蛇志,2021(1):1-4.
作者姓名:宋天麟  周马林  蒙怡  李亚兰  陶慧娟  廖明  班建东  张学荣
作者单位:广西医科大学
基金项目:国家自然科学基金资助项目(编号:81360078,81860344)。
摘    要:目的探索五步蛇毒对正常小鼠免疫功能的影响。方法将KM小鼠随机分为5组,分别为空白组、五步蛇毒安全范围内低剂量组(30 mg/kg)、五步蛇毒安全范围内中剂量组(60 mg/kg)、五步蛇毒安全范围内高剂量组(120 mg/kg)(以下简称五步蛇毒低、中、高剂量组)以及西洋参组(30 mg/kg),每组10只。各组小鼠每日定时灌胃1次,连续14天。观察小鼠的呼吸、精神状态等生命体征。取小鼠脾脏和胸腺组织称重后,计算小鼠脾脏、胸腺指数;制备脾细胞悬液,采用CCK-8法检测小鼠脾淋巴细胞增殖率,碳粒廓清法检测小鼠吞噬系数α,中性红法检测小鼠腹腔巨噬细胞吞噬率;同时采用二硝基氟苯诱导小鼠迟发型变态反应,检测小鼠耳廓肿胀度。结果小鼠的吞噬系数α在五步蛇毒高剂量组最高(5.56±0.46),高于其余四组,差异均有统计学意义(均P<0.05)。小鼠腹腔巨噬细胞吞噬率(%)在五步蛇毒中剂量组和西洋参组中较高,分别为(119.07±19.31)%、(124.79±24.93)%,差异有统计学意义(均P<0.05)。小鼠的B淋巴细胞增殖率(%)在五步蛇毒中剂量组和西洋参组中较高,分别为(105.95±14.59)%、(108.14±10.58)%,差异有统计学意义(均P<0.05)。小鼠的T淋巴细胞增殖率(%)在五步蛇毒中、高剂量组中较高,分别为(119.30±20.07)%、(110.85±23.13)%,差异有统计学意义(均P<0.05)。与空白组比较,五步蛇毒中、高剂量组和西洋参组均能显著提高小鼠的耳廓肿胀度,差异有统计学意义(均P<0.05)。与空白组比较,五步蛇毒各剂量组和西洋参组均能显著提高小鼠脾脏指数(均P<0.05)。与空白组比较,各实验组胸腺指数均无明显差异(均P>0.05)。结论口服低于120 mg/kg的五步蛇毒对正常小鼠的免疫功能具有一定的增强作用。

关 键 词:五步蛇毒  细胞免疫  体液免疫  非特异性免疫

Immune Effects of the Deinagkistrodon Acutus Venom in Mice
SONG Tian-lin,ZHOU Ma-lin,MENG Yi,LI Ya-lan,TAO Hui-juan,LIAO Ming,BAN Jian-dong,ZHANG Xue-rong.Immune Effects of the Deinagkistrodon Acutus Venom in Mice[J].Journal of Snake,2021(1):1-4.
Authors:SONG Tian-lin  ZHOU Ma-lin  MENG Yi  LI Ya-lan  TAO Hui-juan  LIAO Ming  BAN Jian-dong  ZHANG Xue-rong
Institution:(Guangxi Medical University,Nanning City,Guangxi Zhuang Autonomous Region,530021,China)
Abstract:Objective To explore the effects of the Deinagkistrodon acutus venom on the immune function in normal mice.Methods The KM mice were randomly divided into 5 groups:blank group,low-dose group(30 mg/kg)within the safety range of Deinagkistrodon acutus venom,medium-dose group(60 mg/kg)within the safety range of Deinagkistrodon acutus venom,high-dose group(120 mg/kg)within the safety range of Deinagkistrodon acutus venom(hereinafter referred to as low,medium-and high-dose groups of Deinagkistrodon acutus venom)and American ginseng group(30 mg/kg),10 mice in each group.Gave the medicine once a day at regular intervals for 14 days.The vital signs such as respiration and mental state were observed.Took spleen and thymus tissues,calculate spleen and thymus index after weighing;prepared spleen cell suspension,used CCK-8 method to detect lymphocytes proliferation rate;carbon particle clearance method to detect mouse phagocytic coefficientα;the mouse peritoneal macrophage phagocytosis was detected by neutral red assay;dinitrofluorobenzene(DNFB)was used to induce delayed type hypersensitivity in mice and detected the auricle swelling of mice.Results The phagocytic coefficientαof mice in high-dose Agkistrodon acutus venom group was the highest(5.56±0.46),and the differences were statistically significant(all P<0.05).The phagocytosis rate(%)of mice were higher in the medium-dose group and the American ginseng group,which respectively were(119.07±19.31)%and(124.79±24.93)%,the differences were statistically significant(P<0.05).The B lymphocyte proliferation rate(%)of mice were higher in the medium-dose group of and the American ginseng group,which respectively were(105.95±14.59)%and(108.14±10.58)%,the differences were statistically significant(P<0.05).The T lymphocyte proliferation rate(%)of mice were higher in the medium-dose and high-dose groups,which respectively were(119.30±20.07)%and(110.85±23.13)%,the differences were statistically significant(P<0.05).Compared with the blank group,the medium-dose and high-dose groups and the American ginseng group could significantly improve the auricle swelling degree of mice,the differences were statistically significant(P<0.05).Compared with blank group,each experimental group could significantly increase the spleen index of mice(P<0.05).Compared with blank group,there was no significant difference in the thymus index of each experimental group(P>0.05).Conclusion Oral administration of the Deinagkistrodon acutus venom lower than 120 mg/kg has a certain enhancement effect on the immune function in normal mice.
Keywords:Deinagkistrodon acutus venom  Cellular immunity  Humoral immunity  Nonspecific immunity
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