首页> 中文期刊> 《畜牧与生物技术杂志(英文版)》 >Gas stunning with CO2 affected meat color, lipid peroxidation, oxidative stress, and gene expression of mitogen-activated protein kinases, glutathione S-transferases, and Cu/Zn-superoxide dismutase in the skeletal muscles of broilers

Gas stunning with CO2 affected meat color, lipid peroxidation, oxidative stress, and gene expression of mitogen-activated protein kinases, glutathione S-transferases, and Cu/Zn-superoxide dismutase in the skeletal muscles of broilers

         

摘要

Background:Meat color and lipid peroxidation are important traits related to meat quality.CO2 concentration is a critical factor that can affect meat quality in the commercial use of gas stunning (GS).However,the effect and mechanism of CO2 stunning on meat color and lipid peroxidation during long-term storage remain poorly studied.We aimed to study the effects of GS methods,especially CO2 concentration,on meat color and meat lipid peroxidation in broilers during long-term storage at 4 ℃ and to explore the potential mechanism of meat color change via lipid peroxidation and the inner lipid peroxide scavenging system.Methods:Eighteen broilers were sacrificed after exposure to one of the following gas mixtures for 90 s:40% CO2 + 21% O2 + 39% N2 (G40%),79% CO2 + 21% O2 (G79%),or no stunning (0% CO2,control).Meat color,serum variables,enzyme activities,and the gene expression of mitogen-activated protein kinase (MAPK),nuclear factor-erythroid 2-related factor 2 (Nrf2),glutathione S-transferase (GST) and superoxide dismutase (SOD) were determined.Results:The concentrations of serum triiodothyronine (-T-3,P =0.03) and the ratio of serum free triiodothyronine/free thyroxine (FT3/FT4,P < 0.01) were decreased,whereas levels of serum cortisol (P < 0.01) were increased in the 40% CO2 group compared with the control group.Additionally,the thiobarbituric acid-reactive substances (TOBARS) 3 d (P< 0.01) and TBARS 6 d (P=0.01) in breast meat and the TBARS 3 d in thigh meat (P< 0.01) were increased in the 40% CO2 group compared with the control group.Serum T3 was negatively correlated with TBARS6 d both in the breast and thigh meat (r=-0.63,P < 0.01 and r=-0.47,P=0.05 respectively).T3/T4 was negatively correlated with TBARS6 d in the breast meat and in the thigh meat (r=-0.57,P=0.01;and r=-0.53,P=0.03 respectively).Compared with the control group,Lightness (L*) 1 d (P =0.03) and L*9 d (P < 0.01) were increased,whereas total chromatic aberration (E*) 1 d (P =0.05) and E*3 d (P <0.01) were decreased in the breast meat of both the G40% and G79% groups.The values of yellowness (b*) 3 d (P=0.01),b*6 d (P< 0.01) and E*6 d (P< 0.01) in the thigh meat were lower in both the G40% and G79% groups than in the control group.In the breast muscle,the mRNA levels of c-Jun N-terminal kinase 2 UNK2,P =0.03),GSTT1 (P =0.04),and SOD1 (P =0.05) were decreased,and the mRNA levels ofJNK1 (P =0.07),Nrf2 (P =0.09),and GSTA3 (P =0.06) were slightly lower in both the G40% and G79% groups compared with the control group.However,among these genes,only the mRNA level of JNK1 was decreased in the G40% group compared with the control group and the G79% group (P =0.03) in the thigh muscle.Conclusions:Compared with the control group,meat color quality in the breast meat was decreased,and the expression of genes in the MAPK/Nrf2/ARE (antioxidant responsive element) antioxidant pathway in breast muscle was partly suppressed by GS of both 40% and 79% CO2.However,oxidative stress and meat lipid peroxidation during storage were aggravated by GS with 40% CO2 compared to GS with 79% CO2 and no GS.

著录项

  • 来源
    《畜牧与生物技术杂志(英文版)》 |2018年第3期|738-749|共12页
  • 作者单位

    Key Laboratory of Feed Biotechnology of Ministry of Agriculture & National, Engineering Research Center of Biological Feed, Feed Research Institute, Chinese Academy of Agricultural Sciences, No.12 Zhongguanchun South Street, Haidian District, Beijing 100081, China;

    College of Animal Science and Technology, Yangzhou University, No.48 Wenhui East Road, Yangzhou 225009, Jiangsu, China;

    Key Laboratory of Feed Biotechnology of Ministry of Agriculture & National, Engineering Research Center of Biological Feed, Feed Research Institute, Chinese Academy of Agricultural Sciences, No.12 Zhongguanchun South Street, Haidian District, Beijing 100081, China;

    Key Laboratory of Feed Biotechnology of Ministry of Agriculture & National, Engineering Research Center of Biological Feed, Feed Research Institute, Chinese Academy of Agricultural Sciences, No.12 Zhongguanchun South Street, Haidian District, Beijing 100081, China;

    Key Laboratory of Feed Biotechnology of Ministry of Agriculture & National, Engineering Research Center of Biological Feed, Feed Research Institute, Chinese Academy of Agricultural Sciences, No.12 Zhongguanchun South Street, Haidian District, Beijing 100081, China;

    College of Animal Science and Technology, Yangzhou University, No.48 Wenhui East Road, Yangzhou 225009, Jiangsu, China;

    College of Animal Science and Technology, Yangzhou University, No.48 Wenhui East Road, Yangzhou 225009, Jiangsu, China;

    Key Laboratory of Feed Biotechnology of Ministry of Agriculture & National, Engineering Research Center of Biological Feed, Feed Research Institute, Chinese Academy of Agricultural Sciences, No.12 Zhongguanchun South Street, Haidian District, Beijing 100081, China;

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