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郝云涛, 刘睿, 珠娜, 刘欣然, 康家伟, 毛瑞雪, 麻慧娟, 张亭, 李勇. 核桃低聚肽对急性酒精中毒大鼠保护作用[J]. 中国公共卫生, 2021, 37(5): 840-844. DOI: 10.11847/zgggws1123401
引用本文: 郝云涛, 刘睿, 珠娜, 刘欣然, 康家伟, 毛瑞雪, 麻慧娟, 张亭, 李勇. 核桃低聚肽对急性酒精中毒大鼠保护作用[J]. 中国公共卫生, 2021, 37(5): 840-844. DOI: 10.11847/zgggws1123401
HAO Yun-tao, LIU Rui, ZHU Na, . Protective effect of walnut oligopeptides on acute alcoholism in rats[J]. Chinese Journal of Public Health, 2021, 37(5): 840-844. DOI: 10.11847/zgggws1123401
Citation: HAO Yun-tao, LIU Rui, ZHU Na, . Protective effect of walnut oligopeptides on acute alcoholism in rats[J]. Chinese Journal of Public Health, 2021, 37(5): 840-844. DOI: 10.11847/zgggws1123401

核桃低聚肽对急性酒精中毒大鼠保护作用

Protective effect of walnut oligopeptides on acute alcoholism in rats

  • 摘要:
      目的  探讨服用核桃低聚肽(WOPs)对急性酒精中毒大鼠的保护作用。
      方法  选用SPF级SD雄性大鼠,设立爬网实验、翻正实验、转棒实验及血乙醇浓度检测共四项独立实验,各实验均设立模型对照组、乳清蛋白组(0.44 g/kg·BW)及3个WOPs干预组(0.22 g/kg·BW、0.44 g/kg·BW、0.88 g/kg·BW),每组6~10只,共140只。30天连续灌胃后,50 % Vol.酒精按5.6 g/kg·BW乙醇剂量灌胃,建立大鼠急性酒精中毒模型(翻正实验为7 g/kg·BW),进行三项行为学实验并检测多时点血乙醇浓度。
      结果  相比模型对照及乳清蛋白组,WOPs高剂量组大鼠爬网时间显著增加(爬网时间平均秩次为8.83、8.33 vs 23.17)(P < 0.05),WOPs中、高剂量组大鼠翻正反射消失比率显著降低(30 %、30 % vs 80 %、80 %)(P < 0.05);相比模型对照组,WOPs中、高剂量组大鼠翻正反射消失的出现明显延迟(114.33 ± 50.50、128.33 ± 76.00 vs 35.75 ± 32.14 min)(P < 0.05),WOPs低、中、高剂量组大鼠翻正反射恢复时间明显缩短(369.25 ± 149.50、331.67 ± 86.05、344.64 ± 107.53 vs 711.25 ± 200.63 min)(P < 0.05),WOPs低剂量组大鼠在180 min时点血乙醇水平明显降低(3.84 ± 0.86 vs 5.51 ± 1.65 mg/mL)(P < 0.05),WOPs中、高剂量组大鼠在60、90、120、180 min时点血乙醇浓度均明显降低(3.65 ± 0.69、3.79 ± 0.74 vs 4.49 ± 0.96 mg/mL;3.96 ± 0.75、3.99 ± 0.64 vs 5.02 ± 1.06 mg/mL;3.83 ± 1.16、3.78 ± 0.87 vs 5.41 ± 1.27 mg/mL;3.22 ± 1.29、3.20 ± 1.31 vs 5.51 ± 1.65 mg/mL)(P < 0.05);相比乳清蛋白组,WOPs中、高剂量组大鼠翻正反射恢复时间明显缩短(331.67 ± 86.05、344.64 ± 107.53 vs 594.37 ± 198.06 min)(P < 0.05),WOPs中剂量组在180 min时点(3.22 ± 1.29 vs 4.94 ± 1.31 mg/mL)及WOPs高剂量组大鼠在120、180 min时点(3.78 ± 0.87 vs 5.06 ± 0.89 mg/mL、3.20 ± 1.31 vs 4.94 ± 1.31 mg/mL)血乙醇浓度明显降低(P < 0.05)。
      结论  WOPs可有效降低急性酒精中毒对机体的损害。

     

    Abstract:
      Objective  To investigate protective effect of walnut oligopeptides (WOPs) on acute alcoholism in rats.
      Methods  Totally 140 specific pathogen free male Sprague-Dawley (SD) rats were randomly assigned into 4 groups for climbing, loss of righting reflex, and rotating rod test and blood ethanol concentration measurement; the rats in each of the 4 groups were subdivided into a model control group (with double distilled water), whey protein group (0.44 g/kg·BW) and 3 WOPs intervention groups (0.22 g/kg·BW, 0.44 g/kg·BW, 0.88 g/kg·BW); all the treatments were conducted by intragastric administration once a day continuously for 30 days. After the 30-day administration, the acute alcoholism model of the rats was established by intragastric administration of 50% alcohol at the dosage of 5.6 g/kg·BW (at the dosage of 7 g/kg·BW for the rats of loss of righting reflex test group). Then, the three behavioral tests were carried out and blood ethanol concentrations were measured at multiple time points.
      Results  Compared to the rats of model control and whey protein group, the rats treated with high WOPs had a significantly increased climbing time (the average rank of crawling time: 23.17 vs. 8.83 and 8.33) (both P < 0.05). In comparison to those of the rats in model control group, significantly reduced ratio of righting reflex disappearance (30% and 30% vs. 80%) and prolonged time for the disappearance of righting reflex (114.33 ± 50.50 and 128.33 ± 76.00 vs. 35.75 ± 32.14 min) were observed in the rats with moderate and high WOPs treatment (all P < 0.05); the recovery time of righting reflex in the rats treated with low, moderate and high WOPs were significantly shortened (369.25 ± 149.50, 331.67 ± 86.05 and 344.64 ± 107.53 vs. 711.25 ± 200.63 min) (P < 0.05 for all); the blood ethanol concentration was significantly decreased in the rats with low WOPs at 180 minutes after the 50% alcohol treatment (3.84 ± 0.86 vs. 5.51 ± 1.65 mg/mL) (P < 0.05); and significantly decreased blood ethanol concentrations were detected in the rats treated with moderate and high WOPs groups at 60 minutes (3.65 ± 0.69 and 3.79 ± 0.74 vs. 4.49 ± 0.96 mg/mL), 90 minutes (3.96 ± 0.75 and 3.99 ± 0.64 vs. 5.02 ± 1.06 mg/mL), 120 minutes (3.83 ± 1.16 and 3.78 ± 0.87 vs. 5.41 ± 1.27 mg/mL), and 180 minutes (3.22 ± 1.29 and 3.20 ± 1.31 vs. 5.51 ± 1.65 mg/mL) after the 50% alcohol treatment (P < 0.05 for all). Compared with those in the rats of whey protein group, significantly shortened recovery time of righting reflex were observed in the rats with moderate and high WOPs treatment (331.67 ± 86.05 and 344.64 ± 107.53 vs. 594.37 ± 198.06 min) (both P < 0.05) and significantly reduced blood ethanol concentrations were detected in the rats with moderate WOPs treatment at 180 minutes (3.22 ± 1.29 vs. 4.94 ± 1.31 mg/mL) in the rats with high WOPs treatment at 120 minutes (3.78 ± 0.87 vs. 5.06 ± 0.89 mg/mL) and 180 minutes (3.20 ± 1.31 vs. 4.94 ± 1.31 mg/mL) after the 50% alcohol treatment (P < 0.05 for all).
      Conclusion  Oral intake of walnut oligopeptides can effectively reduce the damage of acute alcoholism in rats.

     

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