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木脂素对醋酸铅染毒小鼠生精功能影响
引用本文:沈楠, 王艳春, 范红艳, 李治伟, 路倩, 王燕, 刘师兵, 齐玲, 任旷. 木脂素对醋酸铅染毒小鼠生精功能影响[J]. 中国公共卫生, 2015, 31(3): 321-323. DOI: 10.11847/zgggws2015-31-03-20
作者姓名:沈楠  王艳春  范红艳  李治伟  路倩  王燕  刘师兵  齐玲  任旷
作者单位:1.吉林医药学院药理学教研室, 吉林 吉林 132013;2.湖南中医药高等专科学校
基金项目:国家自然科学基金(81201671);吉林省教育厅基金(2010254;2013359)
摘    要:目的探讨木脂素对醋酸铅染毒小鼠生精功能的影响及其作用机制。方法将昆明种雄性小鼠60只随机分为对照组、模型组、阳性对照组、木脂素组, 除对照组外, 其余3组小鼠均腹腔注射醋酸铅(40 mg/kg), 连续 10 d, 建立雄性小鼠生精障碍模型;造模后第2 d开始, 阳性对照组小鼠腹腔注射绒毛膜促性腺激素(500 IU/kg), 木脂素组小鼠给予木脂素(200 mg/kg)灌胃, 对照组及模型组小鼠灌胃等量生理盐水, 连续30 d;末次给药24 h后, 处死小鼠, 取睾丸和附睾, 检测睾丸组织超氧化物歧化酶(SOD)、乳酸脱氢酶(LDH)、三磷酸腺苷(ATP)酶含量。比较各组小鼠精子存活率。苏木精-伊红染色观察睾丸组织形态。结果与对照组比较, 模型组小鼠精子活率[(53.2±1.3)%]降低, LDH、SOD、Mg2+、Ca2+-ATP酶活性[分别为(0.18±0.03)U/gprot、(16.80±2.23)U/mgprot、(31.03±4.87)、(8.12±1.24) μmolPi/(mgprot·hour)]降低, 差异有统计学意义(P<0.01);与模型组比较, 木脂素组小鼠精子活率[(68.7±2.2)%]升高;LDH、SOD、Mg2+、Ca2+-ATP酶活性[分别为(0.23±0.09) U/gprot、(23.01±3.86) U/mgprot、(64.21±10.49)、(17.20±5.18) μmolPi/(mgprot·hour)]升高, 差异有统计学意义(P<0.05)。结论木脂素对醋酸铅所致生精障碍小鼠的生殖功能具有一定保护作用, 其机制可能与抗氧化损伤有关。

关 键 词:木脂素  醋酸铅  抗氧化损伤  生精功能
收稿时间:2014-10-24

Effects of lignans on spermatogenesis in mice exposed to lead acetate
SHEN Nan, WANG Yan-chun, FAN Hong-yan.et al, . Effects of lignans on spermatogenesis in mice exposed to lead acetate[J]. Chinese Journal of Public Health, 2015, 31(3): 321-323. DOI: 10.11847/zgggws2015-31-03-20
Authors:SHEN Nan  WANG Yan-chun  FAN Hong-yan.et al
Affiliation:1.Department of Pharmacology, School of Basic Medical Sciences, Jilin Medical College, Jilin, Jilin Province 132013, China
Abstract:ObjectiveTo study effects of lignan on spermatogenesis and its mechanism in mice with lead acetate exposure.MethodsSixty Kunming male mice were randomly divided into a control group,model group,positive drug group,and lignans group.Except for those in the control group,all the mice were injected lead acetate for 10 days at the dosage of 40 mg·kg-1·d-1 to establish spermatogenesis disorder model; two days after lead acetate injection,the mice in positive drug group were treated with human chorionic gonadotropin(500 IU·kg-1·d-1) via intraperitoneal injection and those in lignans group were given lignans(200 mg·kg-1·d-1) via gavage; the mice in the control group and model group were given normal saline; the experiment lasted for 30 days.Twenty-four hours after the last treatment,all the mice were sacrificed and testis and epididymis of the mice were sampled.Superoxide dismutase(SOD),lactate dehydrogenase(LDH),Mg2+ ATP enzyme and Ca2+ ATP enzyme in testicular tissue were detected and sperm viability was compared between the groups and the morphology of testicular tissue were observed with hematoxylin-eosin staining.ResultsCompared with the control group,sperm motility was reduced; SOD,Mg2+ ATPase and Ca2+ ATPase contents were decreased; and LDH level was increased for the mice of the model group(P<0.05,P<0.01).Compared with the model group,sperm motility was increased,the level of SOD was increased,and that of LDH was decreased in the mice of lignans group(P<0.05,P<0.01).ConclusionLignans could protect spermatogenesis from lead acetate-induced damages in mice and the mechanism of the effect may related to anti-oxidativation of lignans.
Keywords:lignans  lead acetate  oxidative damage  spermatogenesis
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