安徽医药
安徽醫藥
안휘의약
ANHUI MEDICAL AND PHARMACEUTICAL JOURNAL
2014年
11期
2044-2047,2048
,共5页
冯玉杰%徐羊阳%张龙%王国琛%王玉峰%杨津兰%王华
馮玉傑%徐羊暘%張龍%王國琛%王玉峰%楊津蘭%王華
풍옥걸%서양양%장룡%왕국침%왕옥봉%양진란%왕화
乙醇/毒性%N-乙酰半胱氨酸/药理学%睾丸损伤%小鼠
乙醇/毒性%N-乙酰半胱氨痠/藥理學%睪汍損傷%小鼠
을순/독성%N-을선반광안산/약이학%고환손상%소서
ethanol/toxicity%N-acetylcysteine/pharmacology%testicular injury%mouse
目的:在成功建立乙醇诱导小鼠睾丸损伤模型的基础上,该研究主要探讨N-乙酰半胱氨酸( NAC)对急性乙醇暴露致小鼠睾丸损伤的保护作用。方法该研究由2个实验组成。实验1:28只雄性小鼠被随机分成4组,对照组和乙醇(1、3、6 g· kg-1)处理组;实验2:24只雄性小鼠被随机分成4组,对照组、乙醇组、NAC组和NAC+乙醇组。2个实验均于乙醇处理后24 h剖杀小鼠,取睾丸称重,各组小鼠睾丸用MDF液固定,制作石蜡切片,以备后续睾丸HE染色和免疫组织化学检测。结果3和6 g·kg-1乙醇暴露明显引起小鼠睾丸内多核巨细胞并向管腔内生殖细胞脱落等组织病理学改变;1和3 g·kg-1乙醇暴露明显抑制小鼠睾丸生殖细胞增殖;NAC明显保护3 g·kg-1乙醇暴露所致小鼠睾丸病理学损伤,显著减轻3 g·kg-1乙醇暴露对小鼠睾丸细胞增殖的抑制作用。结论 NAC明显保护乙醇急性暴露对小鼠睾丸组织病理学损伤。
目的:在成功建立乙醇誘導小鼠睪汍損傷模型的基礎上,該研究主要探討N-乙酰半胱氨痠( NAC)對急性乙醇暴露緻小鼠睪汍損傷的保護作用。方法該研究由2箇實驗組成。實驗1:28隻雄性小鼠被隨機分成4組,對照組和乙醇(1、3、6 g· kg-1)處理組;實驗2:24隻雄性小鼠被隨機分成4組,對照組、乙醇組、NAC組和NAC+乙醇組。2箇實驗均于乙醇處理後24 h剖殺小鼠,取睪汍稱重,各組小鼠睪汍用MDF液固定,製作石蠟切片,以備後續睪汍HE染色和免疫組織化學檢測。結果3和6 g·kg-1乙醇暴露明顯引起小鼠睪汍內多覈巨細胞併嚮管腔內生殖細胞脫落等組織病理學改變;1和3 g·kg-1乙醇暴露明顯抑製小鼠睪汍生殖細胞增殖;NAC明顯保護3 g·kg-1乙醇暴露所緻小鼠睪汍病理學損傷,顯著減輕3 g·kg-1乙醇暴露對小鼠睪汍細胞增殖的抑製作用。結論 NAC明顯保護乙醇急性暴露對小鼠睪汍組織病理學損傷。
목적:재성공건립을순유도소서고환손상모형적기출상,해연구주요탐토N-을선반광안산( NAC)대급성을순폭로치소서고환손상적보호작용。방법해연구유2개실험조성。실험1:28지웅성소서피수궤분성4조,대조조화을순(1、3、6 g· kg-1)처리조;실험2:24지웅성소서피수궤분성4조,대조조、을순조、NAC조화NAC+을순조。2개실험균우을순처리후24 h부살소서,취고환칭중,각조소서고환용MDF액고정,제작석사절편,이비후속고환HE염색화면역조직화학검측。결과3화6 g·kg-1을순폭로명현인기소서고환내다핵거세포병향관강내생식세포탈락등조직병이학개변;1화3 g·kg-1을순폭로명현억제소서고환생식세포증식;NAC명현보호3 g·kg-1을순폭로소치소서고환병이학손상,현저감경3 g·kg-1을순폭로대소서고환세포증식적억제작용。결론 NAC명현보호을순급성폭로대소서고환조직병이학손상。
Objective To investigate the protective role of N-acetylcysteine on acute ethanol-induced testicular damage,based on an established mouse model of ethanol-induced testicular injury. Methods The current study included two separate experiments. Experi-ment 1,twenty-eight male mice were assigned into four groups,control group and three ethanol-treated groups. All male mice except for controls received ethanol (1,3 and 6 g·kg-1,i. g. ) administration. Experiment 2,twenty-four male mice were assigned into four groups,control,NAC,ethanol,and NAC+ethanol groups. Male mice in NAC +ethanol group were pretreated with NAC ( 100 mg · kg-1 ,i. p. ) at 12 h and 0. 5 h before ethanol (3 g·kg-1 ,i. g. ) and then received a dose of NAC (100 mg·kg-1 ,i. p. ) at 12 h af-ter ethanol treatment. Other mice except for control (either saline) and NAC group were injected with ethanol (3 g·kg-1,i. g. ). All male mice were sacrificed at 24 h after ethanol treatment. Mouse testes were weighed and collected for HE staining and immunohisto-chemical detection. Results Acute ethanol (3,6 g·kg-1 ) exposure markedly caused multinucleated giant cells and sloughing of germ cells in testicular seminiferous tubules. Acute ethanol (1,3 g·kg-1 ) exposure obviously inhibited germ cell proliferation in mouse testes. NAC protects against acute ethanol-induced testicular histopathological damages and inhibition of germ cell proliferation. Conclu-sions N-acetylcysteine protects against acute ethanol-induced testicular histopathological damage in mouse.