首页|期刊导航|黑龙江畜牧兽医|甘草查尔酮A改善黄曲霉毒素B1诱导的雏鸡肝脏脂质代谢异常的作用研究

甘草查尔酮A改善黄曲霉毒素B1诱导的雏鸡肝脏脂质代谢异常的作用研究OA

Study on the effect of licochalcone A on improving aflatoxin B1 induced abnormal liver lipid metabolism in chicks

中文摘要英文摘要

为探究甘草查尔酮 A(Licochalcone A,Lico A)对黄曲霉毒素 B1(aflatoxin B1,AFB1)诱导的雏鸡肝脏脂质代谢异常的影响,试验将 80 只 1 日龄爱拔益加公鸡适应性饲喂 3 d 后随机分为 4 组,每组 20 只,分别为对照组、Lico A(按饲料重量 50 mg/kg)组、AFB1(按饲料重量 2 mg/kg)组、AFB1(按饲料重量 2 mg/kg)+Lico A(按饲料重量 50 mg/kg)组,连续饲喂 21 d 后测量生长性能指标、血脂指标,雏鸡处死后采集肝脏组织进行油红 O 染色、转录组学分析及脂代谢相关蛋白表达的检测.结果表明:与对照组相比,AFB1 组平均日增重显著降低(P<0.05);与 AFB1 组相比,AFB1+Lico A 组平均日增重显著升高(P<0.05).对照组与 Lico A 组中均无红色脂滴沉积,AFB1 组中脂滴着色较深且体积较大,AFB1+Lico A 组脂滴着色变浅,脂滴数量与体积均减小.与对照组相比,AFB1 组三酰甘油(TG)、总胆固醇(T-CHO)、高密度脂蛋白总胆固醇(HDL-C)和低密度脂蛋白总胆固醇(LDL-C)质量浓度均极显著升高(P<0.01);与AFB1 组相比,AFB1+Lico A 组 TG、T-CHO、LDL-C 质量浓度显著降低(P<0.05),HDL-C 质量浓度极显著降低(P<0.01).与对照组相比,AFB1 组脂代谢相关基因 PPARA、PPARGC1A 基因表达量极显著上调(P<0.01),脂代谢通路发生改变;AFB1 组肝脏中脂肪氧化相关蛋白过氧化物酶体增殖受体 γ 辅激活因子 α(PGC-1α)和过氧化物酶体增殖物激活受体 α(PPARα)的相对表达显著升高(P<0.05),脂肪酸合成相关蛋白 3-羟基 3-甲基戊二酰辅酶 A 还原酶(HMGCR)、胆固醇调节元件结合转录因子 1(SREBP1)和脂肪酸合成酶(FAS)的相对表达量极显著降低(P<0.01).与AFB1 组相比,AFB1+Lico A 组FAS 相对表达量显著降低(P<0.05).说明Lico A 通过改善AFB1 所致雏鸡肝脏的脂肪代谢紊乱及调节脂代谢关键通路等多重途径,从而缓解 AFB1 诱导的雏鸡肝脏脂质损伤.

In order to investigate the effect of licochalcone A(Lico A)on abnormal liver lipid metabolism induced by aflatoxin B1(AFB1)in chicks,80 one-day-old Arbor Acres roosters were adaptively fed for 3 days and then randomly divided into four groups(20 each group):the control group,Lico A group(50 mg/kg by feed weight),AFB1 group(2 mg/kg by feed weight),and Lico A(50 mg/kg by feed weight)+AFB1(2 mg/kg by feed weight)group.The chicks were fed continuously for 21 days.At the end of the experiment,growth performance indicators and blood lipid indicators were measured.After the chicks were sacrificed,liver tissues were collected for oil red O staining,transcriptomic analysis,and detection of lipid metabolism-related protein expression.The results showed that compared with the control group,the average daily weight gain in AFB1 group was significantly decreased(P<0.05).Compared with the AFB1 group,the average daily weight in Lico A+AFB1 group was extremely significantly increased(P<0.01).No red lipid droplet deposits were observed in the control group and Lico A group,while in AFB1 group,lipid droplets were deeply stained and larger in size.In Lico A+AFB1 group,lipid droplet staining became lighter,and both the number and volume of lipid droplets decreased.Compared with the control group,the mass concentrations of triglycerides(TG),total cholesterol(T-CHO),high-density lipoprotein cholesterol(HDL-C),and low-density lipoprotein cholesterol(LDL-C)in the serum of AFB1 group were extremely significantly increased(P<0.01).Compared with AFB1 group,the mass concentrations of TG,T-CHO,LDL-C in Lico A+AFB1 group were significantly decreased(P<0.05),the mass concentration of HDL-C was extremely significantly decreased(P<0.01).Compared with the control group,the expression levels of lipid metabolism-related genes PPARA and PPARGC1A were extremely significantly upregulated in AFB1 group(P<0.01),and lipid metabolism pathways were altered,the relative expressions of fatty acid oxidation-related proteins peroxisome proliferator-activated receptor gamma coactivator 1-α(PGC-1α)and peroxisome proliferator-activated receptor α(PPARα)in the liver was significantly increased in the AFB1 group(P<0.05),while the relative expression of fatty acid synthesis-related proteins 3-hydroxy-3-methylglutaryl coenzyme A reductase(HMGCR),sterol regulatory element-binding transcription factor 1(SREBP1),and fatty acid synthase(FAS)was extremely significantly decreased(P<0.01).Compared with AFB1 group,the relative expression of FAS in Lico A+AFB1 group was significantly decreased(P<0.05).It indicated that Lico A alleviates AFB1-induced liver lipid damage in chicks through multiple pathways,such as improving the lipid metabolism disorder in the liver caused by AFB1 and regulating key lipid metabolism signaling pathways.

于晓庆;张杰兴;杨淞雅;魏翔建;刘冰雪;龙文渊;邓旭明;吕红明

黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319吉林大学 动物医学学院人畜共患病研究所,长春 130001黑龙江八一农垦大学 动物科技学院,黑龙江 大庆 163319

农业科技

雏鸡黄曲霉毒素B1甘草查尔酮A肝脏脂质代谢

chicksaflatoxin B1licochalcone Aliverlipid metabolism

《黑龙江畜牧兽医》 2026 (6)

17-23,7

国家自然科学基金青年项目(32202862)黑龙江省自然科学基金优秀青年项目(YQ2021C028)黑龙江八一农垦大学三纵科研支持计划青创人才项目(ZRCQC202305)

10.13881/j.cnki.hljxmsy.2025.06.0026

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