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Broccoli sprout extract induces detoxification-related gene expression and attenuates acute liver injury

机译:西兰花芽提取物诱导与排毒相关的基因表达并减轻急性肝损伤

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摘要

AIM: To investigate the effects of broccoli sprout extract (BSEx) on liver gene expression and acute liver injury in the rat.METHODS: First, the effects of BSEx on liver gene expression were examined. Male rats were divided into two groups. The Control group was fed the AIN-76 diet, and the BSEx group was fed the AIN-76 diet containing BSEx. After a 10-d feeding period, rats were sacrificed and their livers were used for DNA microarray and real-time reverse transcription-polymerase chain reaction (RT-PCR) analyses. Next, the effects of BSEx on acute liver injury were examined. In experiments using acute liver injury models, 1000 mg/kg acetaminophen (APAP) or 350 mg/kg D-galactosamine (D-GalN) was used to induce injury. These male rats were divided into four groups: Control, BSEx, Inducer (APAP or D-GalN), and Inducer+BSEx. The feeding regimens were identical for the two analyses. Twenty-four hours following APAP administration via p.o. or D-GalN administration via i.p., rats were sacrificed to determine serum aspartate transaminase (AST) and alanine transaminase (ALT) levels, hepatic glutathione (GSH) and thiobarbituric acid-reactive substances accumulation and glutathione-S-transferase (GST) activity.RESULTS: Microarray and real-time RT-PCR analyses revealed that BSEx upregulated the expression of genes related to detoxification and glutathione synthesis in normal rat liver. The levels of AST (70.91 ± 15.74 IU/mL vs 5614.41 ± 1997.83 IU/mL, P < 0.05) and ALT (11.78 ± 2.08 IU/mL vs 1297.71 ± 447.33 IU/mL, P < 0.05) were significantly suppressed in the APAP + BSEx group compared with the APAP group. The level of GSH (2.61 ± 0.75 nmol/g tissue vs 1.66 ± 0.59 nmol/g tissue, P < 0.05) and liver GST activity (93.19 ± 16.55 U/g tissue vs 51.90 ± 16.85 U/g tissue, P < 0.05) were significantly increased in the APAP + BSEx group compared with the APAP group. AST (4820.05 ± 3094.93 IU/mL vs 12465.63 ± 3223.97 IU/mL, P < 0.05) and ALT (1808.95 ± 1014.04 IU/mL vs 3936.46 ± 777.52 IU/mL, P < 0.05) levels were significantly suppressed in the D-GalN + BSEx group compared with the D-GalN group, but the levels of AST and ALT in the D-GalN + BSEx group were higher than those in the APAP + BSEx group. The level of GST activity was significantly increased in the D-GalN + BSEx group compared with the D-GalN group (98.04 ± 15.75 U/g tissue vs 53.15 ± 8.14 U/g tissue, P < 0.05).CONCLUSION: We demonstrated that BSEx protected the liver from various types of xenobiotic substances through induction of detoxification enzymes and glutathione synthesis.
机译:目的:研究西兰花芽提取物(BSEx)对大鼠肝脏基因表达和急性肝损伤的影响。方法:首先,研究BSEx对大鼠肝脏基因表达的影响。将雄性大鼠分为两组。对照组饲喂AIN-76日粮,而BSEx组饲喂含BSEx的AIN-76日粮。喂食10天后,处死大鼠,将其肝脏用于DNA微阵列和实时逆转录聚合酶链反应(RT-PCR)分析。接下来,检查了BSEx对急性肝损伤的影响。在使用急性肝损伤模型的实验中,使用1000 mg / kg对乙酰氨基酚(APAP)或350 mg / kg D-半乳糖胺(D-GalN)诱发损伤。将这些雄性大鼠分为四组:对照组,BSEx,诱导剂(APAP或D-GalN)和诱导剂+ BSEx。两次分析的喂养方案相同。经p.o施用APAP后二十四小时或通过腹膜内注射D-GalN,处死大鼠以确定血清天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)的水平,肝谷胱甘肽(GSH)和硫代巴比妥酸反应性物质的积累以及谷胱甘肽S-转移酶(GST)的活性。结果:微阵列和实时RT-PCR分析表明,BSEx上调了正常大鼠肝脏中与排毒和谷胱甘肽合成相关的基因的表达。在APAP中AST(70.91±15.74 IU / mL vs 5614.41±1997.83 IU / mL,P <0.05)和ALT(11.78±2.08 IU / mL vs 1297.71±447.33 IU / mL,P <0.05)被显着抑制+ BSEx组与APAP组相比。谷胱甘肽水平(2.61±0.75 nmol / g组织vs 1.66±0.59 nmol / g组织,P <0.05)和肝脏GST活性(93.19±16.55 U / g组织vs 51.90±16.85 U / g组织,P <0.05)与APAP组相比,APAP + BSEx组的显着增加。在D-GalN中,AST(4820.05±3094.93 IU / mL与12465.63±3223.97 IU / mL,P <0.05)和ALT(1808.95±1014.04 IU / mL与3936.46±777.52 IU / mL,P <0.05)水平在D-GalN中得到显着抑制+ BSEx组与D-GalN组相比,但D-GalN + BSEx组的AST和ALT水平高于APAP + BSEx组。与D-GalN组相比,D-GalN + BSEx组的GST活性水平显着增加(98.04±15.75 U / g组织vs 53.15±8.14 U / g组织,P <0.05)。结论:我们证明了BSEx通过诱导解毒酶和谷胱甘肽合成来保护肝脏免受各种异源物质的侵害。

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