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裴凌鹏. 虾青素对四氯化碳致小鼠急性肝损伤保护作用[J]. 中国公共卫生, 2009, 25(5): 582-584. DOI: 10.11847/zgggws2009-25-05-39
引用本文: 裴凌鹏. 虾青素对四氯化碳致小鼠急性肝损伤保护作用[J]. 中国公共卫生, 2009, 25(5): 582-584. DOI: 10.11847/zgggws2009-25-05-39
PEI Ling-peng. Study on protective effects of astaxanthin on acute chemical liver injury in mice[J]. Chinese Journal of Public Health, 2009, 25(5): 582-584. DOI: 10.11847/zgggws2009-25-05-39
Citation: PEI Ling-peng. Study on protective effects of astaxanthin on acute chemical liver injury in mice[J]. Chinese Journal of Public Health, 2009, 25(5): 582-584. DOI: 10.11847/zgggws2009-25-05-39

虾青素对四氯化碳致小鼠急性肝损伤保护作用

Study on protective effects of astaxanthin on acute chemical liver injury in mice

  • 摘要: 目的研究虾青素对四氯化碳(CCl4)所致小鼠急性化学肝损伤的保护作用。方法雄性昆明种小鼠60只,随机分为正常对照组、急性化学性肝损伤模型组、联苯双酯(15 mg/kg)阳性对照组以及虾青素10,15,20 mg/kg剂量组,共6组。测定各组小鼠肝脏系数、血清中丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)活性与丙二醛(MDA)含量;测定肝组织中SOD、GSH-Px活性、MDA含量以及组织病理系数。结果虾青素3个剂量组小鼠血清SOD由低到高依次为(110.18±14.28),(138.09±17.81),(170.19±20.20)U/(mg pro);肝组织SOD由低到高依次为(141.52±28.29),(172.20±29.24),(200.12±33.42)U/(mg pro);与模型组血清(74.52±14.40)U/(mg pro)、肝组织(102.29±34.29)U/(mg pro)比较均明显升高(P<0.01)。虾青素3个剂量组小鼠血清GSH-Px活性由低到高次为(63.30±11.01),(72.40±10.77),(90.17±11.29)U/(mg pro);肝组织GSH-Px活性由低到高依次为(112.29±25.41),(142.96±24.13),(170.38±26.34)U/(mg pro);与模型组血清(60.13±10.28)U/(mg pro)、肝组织(110.69±24.26)U/(mg pro)比较均明显升高(P<0.01)。虾青素3个剂量组小鼠血清ALT由低到高依次为(99.29±5.27),(83.50±5.12),(68.12±5.12)U/L;血清AST活性由低到高依次为(80.49±4.28),(64.20±4.10),(52.21±4.42)U/L,与模型组血清ALT(108.02±15.06)U/L、血清AST活性(97.28±12.28)U/L比较明显降低;血清与肝组织MDA含量明显降低,差异均有统计学意义(P<0.01),并能不同程度地改善肝脏病理组织损伤。结论虾青素对CCl4所致急性化学性肝损伤具有预防性保护作用。

     

    Abstract: ObjectiveTo study the protective effects of astaxanthin against the acute chemical liver injury in mice and research its possible mechanism.MethodsSixty male Kunming mice were randomly distributed into control group, acute chemical liver injury model group, DDB group(15 mg/kg) and low,middle, high dose of astaxanthin groups(10, 15, 20 mg/kg).Deteunination and comparison were done for liver index, seaun alanine transaminase (ALT),aspartate transaminase (AST),superoxide dism utase (SOD),glutathione perioxidase (GSH-Px) activity, malondialdehyde (MDA)content, liver SOD,GSH-Px activity, MDA content and liver tissue pathology index.ResultsTreatment with different dose astaxanthin could significantly increase seaun and liver tissue SOD (model group: 74.52±14.40, 102.29±34.29; as taxanth in groups from low to high dose: 110.18±14.28, 141.52±28.29; 138.09±17.81, 172.20±29.24; 170.19±20.20, 200.12 ±33.42),GSH-Px activity (model group: 60.13±10.28, 110.69 ±24.26; astaxanthin groups from low to high dose: 63.30 ±11.01, 112.29±25.41; 72.40±10.77, 142.96±24.13; 90.17±11.29, 170.38±26.34) (P<0.01) and decrease seiwn ALT (model group: 108.02±5.06; astaxanthin groups from low to high dose: 99.29±5.27,83.50±5.12, 68.12±5.12), AST (model group: 97.28±12.28; astaxanthin groups from low to high dose: 80.49±28, 64.20±4.10, 52.21±4.42) (P<0.01) and MDA content in liver tissue(model group: 11.49±2.04, 12.66±2.01; astaxanthin groups from low to high dose: 10.15±1.12, 11.28±1.72; 9.71±1.26, 9.87±1.19; 8.21±1.38, 9.12±1.24)(P<0.01).Pathology index obser vations showed that astaxanthin could ameliorate the liver injury in different degree.ConclusionAs taxanthin showed protective effects on the acute chemical liver injury induce by CCl4 in mice.

     

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