禽营养与饲料 POULTRY NUTRITION AND FEED

饲粮中镉对蛋鸡的毒性效应研究

  • 张娟 ,
  • 李浪 ,
  • 刘光芒 ,
  • 王建萍 ,
  • 林燕 ,
  • 白世平 ,
  • 张克英 ,
  • 张军民 ,
  • 赵青余 ,
  • 吴彩梅
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  • 1. 四川农业大学动物营养研究所, 四川省农业部动物抗病营养与饲料重点实验室, 成都 611130;
    2. 中国农业科学院北京畜牧兽医研究所, 北京 100193
张娟(1994-),女,重庆万州人,硕士研究生,从事动物营养与饲料科学研究。E-mail:996022986@qq.com

收稿日期: 2019-12-10

  网络出版日期: 2020-06-16

基金资助

国家科技支撑计划项目(2014BAD13B05)

Toxic Effects of Dietary Cadmium on Laying Hens

  • ZHANG Juan ,
  • LI Lang ,
  • LIU Guangmang ,
  • WANG Jianping ,
  • LIN Yan ,
  • BAI Shiping ,
  • ZHANG Keying ,
  • ZHANG Junmin ,
  • ZHAO Qingyu ,
  • WU Caimei
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  • 1. Key Laboratory for Animal Disease-Resistance Nutrition and Feedstuffs of China Ministry of Agriculture and Sichuan Province, Institute of Animal Nutrition, Sichuan Agricultural University, Chengdu 611130, China;
    2. Institute of Animal Sciences of CAAS, Beijing 100193, China

Received date: 2019-12-10

  Online published: 2020-06-16

摘要

本试验旨在研究饲粮中镉对蛋鸡生产性能、蛋品质、抗氧化指标、血浆生化指标、组织病理改变的毒性效应。选取40周龄产蛋高峰期的健康罗曼粉壳蛋鸡150只,随机分为5组,每组3个重复,每个重复10只鸡。对照组饲喂基础饲粮,试验组饲喂在基础饲粮中分别添加10、30、50、70 mg/kg镉[实际添加物氧化镉(CdCl2·2.5H2O)]的试验饲粮。试验期8周,分为试验前期(1~4周)和试验后期(5~8周)。结果表明:1)与对照组相比,试验全期,10 mg/kg组平均日采食量升高,但差异不显著(P>0.05),30~70 mg/kg组随镉添加量的增加而降低,70 mg/kg组显著低于对照组(P<0.05);试验后期(5~8周)平均日采食量显著低于试验前期(1~4周)(P<0.05)。与对照组相比,试验全期,产蛋率随镉添加量的增加而降低,10、30 mg/kg组间差异不显著(P>0.05),50、70 mg/kg组显著降低(P<0.05)。2)与对照组相比,试验全期,10 mg/kg组蛋壳强度、蛋白高度升高,但差异不显著(P>0.05),30~70 mg/kg组随镉添加量的增加蛋壳强度显著降低(P<0.05),蛋白高度有降低趋势(P>0.05);试验后期(5~8周)哈夫单位显著低于试验前期(1~4周)(P<0.05)。3)肝脏、肾脏、卵巢中还原型谷胱甘肽(GSH)含量和总超氧化物歧化酶(T-SOD)活性随镉添加量的增加呈线性下降(P<0.05);与对照组相比,10 mg/kg组输卵管谷胱甘肽过氧化物酶(GSH-Px)、T-SOD活性和还原型谷胱甘肽(GSH)含量显著升高(P<0.05),但30~70 mg/kg组低于10 mg/kg组(P<0.05);10 mg/kg组卵巢丙二醛(MDA)含量降低(P>0.05),但30~70 mg/kg组显著高于10 mg/kg组(P<0.05)。4)与对照组相比,10 mg/kg组血浆甘油三酯(TG)含量显著升高(P<0.05),30~70 mg/kg组随镉添加量的增加而降低(P<0.05);血浆白蛋白(ALB)含量随镉添加量的增加呈线性降低(P<0.05);50、70 mg/kg组的血浆谷草转氨酶(AST)活性显著高于其他组(P<0.05)。5)与对照组相比,4个镉添加组的肝脏、肾脏、输卵管发生了不同程度的病理学改变;50、70 mg/kg组组织病理评分显著高于对照组和10~30 mg/kg组(P<0.05)。在本试验条件下,蛋鸡饲粮中10 mg/kg镉可提高蛋鸡采食量及蛋壳、蛋白品质,减轻输卵管氧化应激,但可引起肝脏、肾脏、输卵管发生一定程度病理改变,引起肝脏氧化应激和血液生化指标的改变。而蛋鸡饲粮中30、50、70 mg/kg镉降低了蛋鸡采食量、产蛋率和蛋品质,引起蛋鸡产生氧化应激和血液生化指标的改变,造成了肝脏、肾脏和输卵管病理改变。

本文引用格式

张娟 , 李浪 , 刘光芒 , 王建萍 , 林燕 , 白世平 , 张克英 , 张军民 , 赵青余 , 吴彩梅 . 饲粮中镉对蛋鸡的毒性效应研究[J]. 动物营养学报, 2020 , 32(6) : 2650 -2662 . DOI: 10.3969/j.issn.1006-267x.2020.06.024

Abstract

This experiment was conducted to investigate the toxic effects of dietary cadmium on performance, egg quality, antioxidant, plasma biochemical indicators and histopathology of laying hens. A total of 150 (40-week-old) healthy Lohmann pink-shell laying hens at the peak of egg production were randomly divided into 5 groups, 3 replicates in each group, 10 chickens per replicate: control group fed a basal diet, experimental groups fed the basal diet supplemented with 10, 30, 50 and 70 mg/kg cadmium (CdCl2·2.5H2O). The period of the experiment was 8 weeks, which included a pre-test period (1 to 4 weeks) and a post-test period (5 to 8 weeks). The results showed as follows: 1) compared with the control group, in the whole period of the test, the average daily feed intake (ADFI) in 10 mg/kg group enhanced, but the difference was not significant (P>0.05), and reduced with the increase of cadmium supplemental level in the 30 to 70 mg/kg groups, the ADFI in 70 mg/kg group was significantly lower than that in the control group (P<0.05); the ADFI in post-test period (5 to 8 weeks) was significantly lower than that in pre-test period (1 to 4 weeks) (P<0.05). Compared with the control group, the laying rate decreased with the increase of cadmium supplemental level, and there was no significant difference between the 10 and 30 mg/kg groups (P>0.05), and that in the 50 and 70 mg/kg groups had a significant decrease in the whole period of the test (P<0.05). 2) In the whole period of the test, compared with the control group, the shell intensity and albumin height in the 10 mg/kg group increased (P>0.05), the shell intensity significantly decreased with the increase of cadmium supplemental level (P<0.05) and the albumin height had a decreasing tendency in the 30 to 70 mg/kg groups (P>0.05). The huff unit in the post-test period (5 to 8 weeks) was significantly lower than that in pre-test period (1 to 4 weeks) (P<0.05). 3) The glutathione (GSH) content and total superoxide dismutase (T-SOD) activity in the liver, kidney and ovary decreased linearly with the increase of cadmium supplemental level (P<0.05). Compared with the control group, the activities of glutathion peroxidase (GSH-Px), T-SOD and GSH content in oviduct in the 10 mg/kg group significantly increased (P<0.05), furthermore, the 30 to 70 mg/kg groups was significantly lower than the 10 mg/kg group (P<0.05). The content of malonaldehyde (MDA) in ovaries in the 10 mg/kg group significantly decreased (P>0.05), and the 30 to 70 mg/kg groups were significantly higher than 10 mg/kg group (P<0.05). 4) Compared with the control group, the content of triglyceride (TG) in plasma in the 10 mg/kg group significantly increased (P<0.05), and the 30 to 70 mg/kg groups decreased with the increase of cadmium supplemental level (P<0.05). The plasma albumin (ALB) content decreased linearly with the increase of cadmium supplemental level (P>0.05). The plasma glutamic oxalacetic transaminase (AST) activity in the 50 mg/kg and 70 mg/kg groups were significantly higher than that in other groups (P<0.05). 5) Compared with the control group, the liver, kidney and oviduct in the four treatment groups adding cadmium had different pathological changes. The pathological score in 50 mg/kg 70 mg/kg groups were significantly higher than those in control group and 10 to 30 mg/kg groups (P<0.05). Therefore, under the conditions of the present experiment, 10 mg/kg dietary cadmium can enhance feed intake, eggshell and albumin quality, and alleviate oxidative stress of oviduct, however, it can cause pathological changes in the liver, kidney and oviduct to a certain extent, causing oxidative stress in the liver and changes in blood biochemical indexes. The 30 to 70 mg/kg cadmium reduce feed intake, egg production rate and egg quality, and resulting in oxidative stress and changes in blood biochemical indexes and pathological changes in liver, kidney and oviduct.

参考文献

[1] GODT J,SCHEIDIG F,GROSSE-SIESTRUP C,et al.The toxicity of cadmium and resulting hazards for human health[J].Journal of Occupational Medicine and Toxicology,2006,1:22.
[2] 孟君,赵耀光.火焰原子光谱法测定饲料和不同种类鸡蛋中的微量元素[J].粮食与饲料工业,2014,4(4):54-56,61.
[3] 朱建春,李荣华,张增强,等.陕西规模化猪场猪粪与饲料重金属含量研究[J].农业机械学报,2013,44(11):98-104.
[4] OLGUN O,BAHTIYARCA Y.Effects of dietary cadmium and boron supplementation on performance,eggshell quality and mineral concentrations of bone in laying hens[J].Biological Trace Element Research,2015,167(1):56-62.  
[5] LEACH R M,Jr,WANG K W L,BAKER D E.Cadmium and the food chain:the effect of dietary cadmium on tissue composition in chicks and laying hens[J].The Journal of Nutrition,1979,109(3):437-443.  
[6] 陈大伟,高玉时,唐修君,等.铅、镉联合暴露对蛋鸡生产性能、蛋品质及鸡蛋中微量元素含量的影响[J].动物营养学报,2014,26(6):1616-1623.
[7] OLGUN O.The effect of dietary cadmium supplementation on performance,egg quality,tibia biomechanical properties and eggshell and bone mineralisation in laying quails[J].Animal,2015,9(8):1298-1303.  
[8] 孙涛,代腊,唐飞江,等.饲料中镉对产蛋鸡生产性能、抗氧化功能及其体内残留的影响[J].畜牧兽医学报,2012,43(2):232-241.
[9] YANG S H,ZHANG Z W,HE J B,et al.Ovarian toxicity induced by dietary cadmium in hen[J].Biological Trace Element Research,2012,148(1):53-60.  
[10] WANG S,XU Z,YIN H,et al.Alleviation mechanisms of selenium on cadmium-spiked in chicken ovarian tissue:perspectives from autophagy and energy metabolism[J].Biological Trace Element Research,2018,186(2):521-528.  
[11] 吴彩梅,罗成,张娟,等.四川、山东、河北省鸡蛋中重金属Cd、Cr、Pb的溯源分析[J].四川农业大学学报,2018,36(4):535-541.
[12] 罗成.我国四川、山东、河北省蛋鸡配合饲料中镉、铬、铅污染程度评估[D]硕士学位论文.成都:四川农业大学.
[13] ZENG Q F,BAI P,WANG J P,et al.The response of meat ducks from 15 to 35 d of age to gossypol from cottonseed meal[J].Poultry Science,2015,94(6):1277-1286.  
[14] XIE T,BAI S P,ZHANG K Y,et al.Effects of Lonicera confusa and Astragali Radix extracts supplementation on egg production performance,egg quality,sensory evaluation,and antioxidative parameters of laying hens during the late laying period[J].Poultry Science,2019,98(10):4838-4847.  
[15] CZARNECKI G L,BAKER D H.Tolerance of the chick to excess dietary cadmium as influenced by dietary cysteine and by experimental infection with Eimeria acervulina[J].Journal of Animal Science,1982,54(5):983-988.  
[16] VODELA J K,LENZ S D,RENDEN J A,et al.Drinking water contaminants (arsenic,cadmium,lead,benzene,and trichloroethylene).2.Effects on reproductive performance,egg quality,and embryo toxicity in broiler breeders[J].Poultry Science,1997,76(11):1493-1500.  
[17] KORÉNEKOVA B,SKALICKÁ M,NAD P,et al.Effects of cadmium and zinc on the quality of quail's eggs.[J].Biological Trace Element Research,2007,116(1):103-109.  
[18] BAIN M M.Recent advances in the assessment of eggshell quality and their future application[J].World's Poultry Science Journal,2005,61(2):268-277.  
[19] RAHMAN M S,SASANAMI T,MORI M.Effects of cadmium administration on reproductive performance of Japanese quail (Coturnix japonica)[J].The Journal of Poultry Science,2007,44(1):92-97.  
[20] KAZANTZIS G.Cadmium,osteoporosis and calcium metabolism[J].Biometals,2004,17(5):493-498.  
[21] YANG J M,ARNUSH M,CHEN Q Y,et al.Cadmium-induced damage to primary cultures of rat Leydig cells[J].Reproductive Toxicology,2003,17(5):553-560.  
[22] LÓPEZ E,ARCE C,OSET-GASQUE M J,et al.Cadmium induces reactive oxygen species generation and lipid peroxidation in cortical neurons in culture[J].Free Radical Biology and Medicine,2006,40(6):940-951.  
[23] BERZINA N,MARKOVS J,ISAJEVS S,et al.Cadmium-induced enteropathy in domestic cocks:a biochemical and histological study after subchronic exposure[J].Basic & Clinical Pharmacology & Toxicology,2007,101(1):29-34.  
[24] 代腊,朱莎,孙涛,等.饲料中镉含量对蛋鸡生产性能及抗氧化功能的影响[J].中国畜牧杂志,2012,38(3):35-40.
[25] 孙涛,代腊,唐飞江,等.饲料中镉对产蛋鸡生产性能、抗氧化功能及其体内残留的影响[J].畜牧兽医学报,2012,43(2):232-241.
[26] LI J H,XING L,ZHANG R X.Effects of Se and Cd co-treatment on the morphology,oxidative stress,and ion concentrations in the ovaries of laying hens[J].Biological Trace Element Research,2018,183(1):156-163.  
[27] DAWEI C,PU J H,TANG X J,et al.Effects of exposure to lead and cadmium on the oxidative damage of livers in laying hens[J].Animal Husbandry and Feed Science,2014(5):249-253.
[28] LARREGLE E V,VARAS S M,OLIVEROS L B,et al.Lipid metabolism in liver of rat exposed to cadmium[J].Food and Chemical Toxicology,2008,46(5):1786-1792.  
[29] ABDELMOTTALEB S A,MOUSSA S,ALAAMER A,et al.Effect of zinc on the rheological properties of blood serum of cadmium treated rats[J].General Physiology and Biophysics,2016,35(3):71-75.
[30] SKOCZY?SKA A,WRÓBEL J,ANDRZEJAK R.Lead-cadmium interaction effect on the responsiveness of rat mesenteric vessels to norepinephrine and angiotensin Ⅱ[J].Toxicology,2001,162(3):157-170.  
[31] 黄纯波.饲粮镉对生长育肥猪的毒性效应及其组织蓄积规律研究[D].硕士学位论文.成都:四川农业大学,2017.
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