研究论文 RESEARCH PAPER

饲喂过瘤胃褪黑素对荷斯坦奶牛乳中褪黑素与其合成前体和代谢产物含量、褪黑素合成酶活性及生产性能的影响

  • 高伟星 ,
  • 马慧 ,
  • 杨敏娜 ,
  • 彭述宇 ,
  • 曲嘉晨 ,
  • 曲永利
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  • 1. 黑龙江八一农垦大学动物科技学院, 大庆 163319;
    2. 北京首农畜牧发展有限公司, 北京 100076
高伟星(1996-),男,陕西榆林人,硕士研究生,从事反刍动物营养研究。E-mail:1827976352@qq.com

收稿日期: 2022-01-08

  网络出版日期: 2022-07-14

基金资助

北京市科委课题(Z181100009318014);黑龙江省"百千万"工程(2021ZX12B03)

Effects of Feeding Rumen Protected Melatonin on Contents of Melatonin, Its Synthetic Precursors and Metabolites, Melatonin Synthase Activity in Milk and Performance of Holstein Dairy Cows

  • GAO Weixing ,
  • MA Hui ,
  • YANG Minna ,
  • PENG Shuyu ,
  • QU Jiachen ,
  • QU Yongli
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  • 1. College of Animal Science and Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China;
    2. Beijing Shounong Animal Husbandry Development Co., Ltd., Beijing 100076, China

Received date: 2022-01-08

  Online published: 2022-07-14

摘要

本试验旨在探究过瘤胃褪黑素(RPMT)对荷斯坦奶牛乳中褪黑素(MT)与其合成前体和代谢产物含量、MT合成酶活性及生产性能的影响。选取1~4胎次、泌乳天数在200 d以内的健康荷斯坦奶牛32头,随机分为4组,分别为对照组与试验Ⅰ、Ⅱ和Ⅲ组,每组8头。对照组饲喂正常全混合日粮(TMR),试验组在对照组饲粮的基础上分别添加140、160、180 mg/(头·d)RPMT,于每天14:00进行口腔投喂。试验期32 d,其中第0天为饲喂前1 d,第1~28天为饲喂期,第29~31天为停饲后3 d。试验组与对照组每日挤奶3次,分别在06:00、13:00和21:00。生产性能测定体系检测的乳样采样时间分别为第0、14、29天,MT含量及其他指标检测的乳样采样时间分别为第0、3、7、14、21、28、29、31天。结果表明:1)试验Ⅰ组06:00的乳脂率显著高于对照组与试验Ⅲ组(P<0.05),试验Ⅱ、Ⅲ组13:00的乳脂率显著高于对照组(P<0.05);试验Ⅱ、Ⅲ组13:00和21:00的乳糖率均显著高于对照组(P<0.05);同时,试验Ⅱ、Ⅲ组06:00和21:00的乳中体细胞数(SCC)均显著低于试验Ⅰ组(P<0.05),13:00的SCC显著低于对照组(P<0.05)。在06:00时,时间对乳糖率具有极显著影响(P<0.01),在13:00时,时间对乳脂率具有显著影响(P<0.05),组别与时间对乳糖率具有显著交互效应(P<0.05)。在21:00时,时间对上述指标均无显著影响(P>0.05),组别与时间也无显著交互效应(P>0.05)。2)试验Ⅲ组06:00、13:00和21:00的产奶量均极显著高于对照组与试验Ⅰ、Ⅱ组(06:00除外),但时间对产奶量无显著影响(P>0.05),组别与时间也无显著交互效应(P>0.05)。3)各试验组06:00、13:00和21:00的乳中谷胱甘肽过氧化物酶(GSH-Px)、超氧化物歧化酶(SOD)活性均极显著高于对照组(P<0.01),而试验Ⅲ组仅在21:00的乳中吲哚胺2,3-双加氧酶(IDO)活性显著高于对照组(P<0.05)和极显著高于试验Ⅰ组(P<0.01)。在06:00、13:00时,时间对乳中GSH-Px、SOD活性均具有极显著影响(P<0.01);在21:00时,时间对乳中GSH-Px、SOD及IDO活性均具有极显著影响(P<0.01),组别与时间对乳中IDO活性也具有极显著交互效应(P<0.01)。4)各组间06:00、13:00的乳中MT、6-羟基-褪黑素(6-OH-MT)含量及5-羟色胺-N-乙酰基转移酶(SNAT)、咖啡酸-O-甲基转移酶(COMT)及N-乙酰基-5-羟色胺-甲基转移酶(ASMT)活性均无显著差异(P>0.05),而试验组21:00的乳中MT、5-羟色胺(5-HT)、6-OH-MT含量及SNAT、COMT及ASMT活性均极显著高于对照组(P<0.01)。在06:00时,时间对乳中6-OH-MT含量具有极显著影响(P<0.01),在06:00与13:00时,时间对乳中SNAT活性具有显著影响(P<0.05);在21:00时,时间对乳中MT、5-HT、6-OH-MT含量和SNAT、COMT、ASMT活性均具有极显著影响(P<0.01),组别与时间对乳中MT、5-HT含量具有极显著交互效应(P<0.01),对乳中6-OH-MT含量及SNAT、COMT、ASMT活性均具有显著交互效应(P<0.05)。结果提示,给荷斯坦奶牛饲喂RPMT能够提升乳中乳脂率、乳糖率,同时RPMT饲喂量越大时,产奶量越高,SCC越低;给荷斯坦奶牛提供外源RPMT能够提高泌乳期奶牛抗氧化能力,增加乳中MT合成,同时乳中MT合成前体物5-HT与代谢产物6-OH-MT及MT合成酶活性会随着MT含量而变化,即MT合成与代谢具有同步性。

本文引用格式

高伟星 , 马慧 , 杨敏娜 , 彭述宇 , 曲嘉晨 , 曲永利 . 饲喂过瘤胃褪黑素对荷斯坦奶牛乳中褪黑素与其合成前体和代谢产物含量、褪黑素合成酶活性及生产性能的影响[J]. 动物营养学报, 2022 , 34(7) : 4438 -4451 . DOI: 10.3969/j.issn.1006-267x.2022.07.034

Abstract

This experiment was conducted to investigate the effects of rumen protected melatonin (RPMT) on contents of melatonin (MT), its synthetic precursors and metabolites, MT synthase activity in milk and performance of Holstein dairy cows. Thirty-two healthy Holstein dairy cows with 1 to 4 parities and lactation days less than 200 days were randomly divided into 4 groups, including control group, test groupⅠ, test group Ⅱ and test group Ⅲ, with 8 cows in each group. The control group was fed a normal total mixed diet (TMR), and the test groups were fed 140, 160 and 180 mg RPMT on the basis of the control group for one day one cow. Each additive was orally fed at 14:00 every day, respectively. The experiment lasted for 32 days, including the day 0 was one day before feeding, the days 1 to 28 was feeding period, and the days 29 to 31 was three days after stopping feeding. Milking 3 times a day, 06:00, 13:00 and 21:00, respectively. The sampling time of Dairy Herd Improvement (DHI) was 0, 14 and 29 days, and the sampling time of milk samples for MT content and other indexes was 0, 3, 7, 14, 21, 28, 29 and 31 days. The results showed as follows:1) the milk fat rate in test group Ⅰ at 06:00 was significantly higher than that in control group and test group Ⅲ (P<0.05); the lactose rate at 13:00 and 21:00 in test group Ⅱ and test group Ⅲ was significantly higher than that in control group (P<0.05), and the milk fat rate at 13:00 was significantly higher than that in control group (P<0.05). Meanwhile, milk somatic cell count (SCC) in test group Ⅱ and test group Ⅲ was significantly lower than that in test group Ⅰ at 06:00 and 21:00 (P<0.05) and that was significantly higher than that in the control group at 13:00 (P<0.05). At 06:00, time had extremely significant effect on lactose rate (P<0.01), at 13:00, milk fat rate had significant effect (P<0.05), group and time had significant interaction effect on lactose rate (P<0.05). At 21:00, time had no significant effect on the above indexes (P>0.05), and group and time had no significant interaction effect (P>0.05). 2) The milk yield in test group Ⅲ at 06:00, 13:00 and 21:00 was significantly higher than that in control group and test group Ⅰ and test group Ⅱ (except 06:00), but time had no significant effect on milk yield (P>0.05), and there was no significant interaction between group and time (P>0.05). 3) The activities of glutathione catalase (GSH-Px) and superoxide dismutase (SOD) in milk in experimental groups at 06:00, 13:00 and 21:00 were significantly higher than those in control group (P<0.01), while milk indoleamine 2, 3-dioxygenase (IDO) activity in test group Ⅲ at 21:00 was significantly higher than that in control group (P<0.05) and extremely significantly higher than that test group Ⅰ (P<0.01). At 06:00 and 13:00, time had extremely significant effects on GSH-Px and SOD activities in milk (P<0.01). At 21:00, time had extremely significant effects on the activities of GSH-Px, SOD and IDO in milk (P<0.01), group and time also had extremely significant interaction effects on the activities of IDO in milk (P<0.01). 4) At 06:00, 13:00, there were no significant differences in the contents of MT, 6-hydroxy-melatonin (6-OH-MT) and the activities of 5-hydroxytryptamine-N-acetyltransferase (SNAT), caffeine-o-methyl transferase (COMT) and N-acetyl-5-hydroxytryptamine-methyltransferase (ASMT) in milk among groups (P>0.05), while the contents of MT, 5-hydroxytryptamine (5-HT), 6-OH-MT and the activities of SNAT, COMT and ASMT in milk in test groups at 21:00 were significantly higher than those in control group (P<0.01). The content of 6-OH-MT in milk was significantly affected by time at 06:00 (P<0.01), and the SNAT activity was significantly affected by time at 06:00 and 13:00 (P<0.05). At 21:00, time had extremely significant effects on the contents of MT, 5-HT and 6-OH-MT and the activities of SNAT, COMT and ASMT (P<0.01), group and time had extremely significant interaction effects on the contents of MT and 5-HT in milk (P<0.01). There were significant interaction effects on 6-OH-MT content and activities of SNAT, COMT and ASMT in milk (P<0.05). The results indicate that RPMT feeding for Holstein dairy cows can improve milk fat rate and lactose rate in milk, and the higher the RPMT feeding amount is, the higher the milk yield is, the lower the SCC is. Providing exogenous RPMT to Holstein dairy cows during lactation can improve antioxidant capacity and increase MT synthesis in milk. Meanwhile, the contents of precursor of MT synthesis and 6-OH-MT metabolite and MT synthase activity in milk will change with MT content, that is, MT synthesis and metabolism have synchronization.

参考文献

[1] 朱根宝,于兰兰,刘亚.褪黑素调控动物生殖内分泌的研究进展[J].动物医学进展,2016,37(3):94-98. ZHU G B,YU L L,LIU Y.Progress on regulation of melatonin in animal reproductive endocrinology[J].Progress in Veterinary Medicine,2016,37(3):94-98.(in Chinese)
[2] CIPOLLA-NETO J,AMARAL F G,AFECHE S C,et al.Melatonin,energy metabolism,and obesity:a review[J].Journal of Pineal Research,2014,56(4):371-381.  
[3] 欧阳佳良.泌乳奶牛瘤胃内褪黑素的昼夜节律及其对瘤胃菌群结构的影响[D].硕士学位论文.扬州:扬州大学,2020:56. OUYANG J L.Diurnal variation of ruminal melatonin and the influence on rumen microorganisms in lactating cows[D].Master's Thesis.Yangzhou:Yangzhou University,2020:56.(in Chinese)
[4] 汪秀衡,刘垚,吴洁,等.褪黑素对昼夜节律和脂质代谢的影响[J].基础医学与临床,2020,40(6):838-841. WANG X H,LIU Y,WU J,et al.Effects of melatonin on circadian rhythm and lipid metabolism[J].Basic & Clinical Medicine,2020,40(6):838-841.(in Chinese)
[5] VAN MAANEN A,MEIJER A M,SMITS M G,et al.Classical conditioning for preserving the effects of short melatonin treatment in children with delayed sleep:a pilot study[J].Nature and Science of Sleep,2017,9:67-79.
[6] REITER R J,CALVO J R,KARBOWNIK M,et al.Melatonin and its relation to the immune system and inflammation[J].Annals of the New York Academy of Sciences,2000,917:376-386.
[7] 中华人民共和国卫生部,中国国家标准化管理委员会.保健食品中褪黑素含量的测定:GB/T 5009.170-2003[S].北京:中国标准出版社,2004. Ministry of Health of the PRC,Standardization Administration of the People's Republic of China.Determination of melatonin in health foods:GB/T 5009.170-2003[S].Beijing:Standards Press of China,2004.(in Chinese)
[8] HARDELAND R.Aging,melatonin,and the pro- and anti-inflammatory networks[J].International Journal of Molecular Sciences,2019,20(5):1223.
[9] JAWOREK J,LEJA-SZPAK A,BONIOR J,et al.Protective effect of melatonin and its precursor L-tryptophan on acute pancreatitis induced by caerulein overstimulation or ischemia/reperfusion[J].Journal of Pineal Research,2003,34(1):40-52.  
[10] MANNINO G,CARADONNA F,CRUCIATA I,et al.Melatonin reduces inflammatory response in human intestinal epithelial cells stimulated by interleukin-1β[J].Journal of Pineal Research,2019,67(3):e12598.
[11] YANG M H,SHI J M,TIAN J H,et al.Exogenous melatonin reduces somatic cell count of milk in Holstein cows[J].Scientific Reports,2017,7:43280.
[12] YAO S Y,WU H,MA H,et al.Effects of rumen bypass melatonin feeding (RBMF) on milk quality and mastitis of Holstein cows[J].PeerJ,2020,8:e9147.
[13] WU H,YAO S Y,WANG T K,et al.Effects of melatonin on dairy herd improvement (DHI) of Holstein cow with high SCS[J].Molecules,2021,26(4):834.
[14] GOMES P R L,MOTTA-TEIXEIRA L C,GALLO C C,et al.Maternal pineal melatonin in gestation and lactation physiology,and in fetal development and programming[J].General and Comparative Endocrinology,2021,300:113633.
[15] AVILÉS R,DELGADILLO J A,FLORES J A,et al.Melatonin administration during the dry period stimulates subsequent milk yield and weight gain of offspring in subtropical does kidding in summer[J].Journal of Dairy Science,2019,102(12):11536-11543.  
[16] MAURIZ J L,COLLADO P S,VENEROSO C,et al.A review of the molecular aspects of melatonin's anti-inflammatory actions:recent insights and new perspectives[J].Journal of Pineal Research,2013,54(1):1-14.  
[17] PENG X,CAI X L,LI J,et al.Effects of melatonin supplementation during pregnancy on reproductive performance,maternal-placental-fetal redox status,and placental mitochondrial function in a sow model[J].Antioxidants,2021,10(12):1867.
[18] BOUROUTZIKA E,CILIBERTI M G,CAROPRESE M,et al.Association of melatonin administration in pregnant ewes with growth,redox status and immunity of their offspring[J].Animals,2021,11(11):3161.
[19] TAN D X,HARDELAND R,MANCHESTER L C,et al.The changing biological roles of melatonin during evolution:from an antioxidant to signals of darkness,sexual selection and fitness[J].Biological Reviews of the Cambridge Philosophical Society,2010,85(3):607-623.
[20] MORTEZAEE K,POTES Y,MIRTAVOOS-MAHYARI H,et al.Boosting immune system against cancer by melatonin:a mechanistic viewpoint[J].Life Sciences,2019,238:116960.
[21] BOUROUTZIKA E,KOURETAS D,PAPADOPOULOS S,et al.Effects of melatonin administration to pregnant ewes under heat-stress conditions,in redox status and reproductive outcome[J].Antioxidants,2020,9(3):266.
[22] CHEN Y C,SHEEN J M,TIAO M M,et al.Roles of melatonin in fetal programming in compromised pregnancies[J].International Journal of Molecular Sciences,2013,14(3):5380-5401.  
[23] CARPENTIERI A,DÍAZ DE BARBOZA G,ARECO V,et al.New perspectives in melatonin uses[J].Pharmacological Research,2012,65(4):437-444.  
[24] GILL S S,TUTEJA N.Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants[J].Plant Physiology and Biochemistry,2010,48(12):909-930.  
[25] SUGISAWA H,ITOU T,SAKAI T.Promoting effect of colostrum on the phagocytic activity of bovine polymorphonuclear leukocytes in vitro[J].Biology of the Neonate,2001,79(2):140-144.  
[26] LEPILLER Q,SOULIER E,LI Q S,et al.Antiviral and immunoregulatory effects of indoleamine-2,3-dioxygenase in hepatitis C virus infection[J].Journal of Innate Immunity,2015,7(5):530-544.  
[27] WANG X X,SUN S Y,DONG Q Q,et al.Recent advances in the discovery of indoleamine 2,3-dioxygenase 1(IDO1) inhibitors[J].MedChemComm,2019,10(10):1740-1754.  
[28] TAN D X,REITER R J.An evolutionary view of melatonin synthesis and metabolism related to its biological functions in plants[J].Journal of Experimental Botany,2020,71(16):4677-4689.  
[29] STARCEVIC A,AKTHAR S,DUNLAP W C,et al.Enzymes of the shikimic acid pathway encoded in the genome of a basal metazoan,Nematostella vectensis,have microbial origins[J].Proceedings of the National Academy of Sciences of the United States of America,2008,105(7):2533-2537.  
[30] MCKINNEY J,KNAPPSKOG P M,HAAVIK J.Different properties of the central and peripheral forms of human tryptophan hydroxylase[J].Journal of Neurochemistry,2005,92(2):311-320.  
[31] LIU C H,JIANG X P,LIU G Q,et al.An ancient mutation in the TPH1 gene is consistent with the changes in mammalian reproductive rhythm[J].International Journal of Molecular Sciences,2019,20(23):6065.
[32] ZHOU W,YANG S,ZHANG Q,et al.Functional characterization of serotonin N-acetyltransferase genes (SNAT1/2) in melatonin biosynthesis of Hypericum perforatum[J].Frontiers in Plant Science,2021,12:781717.
[33] GAUDET S J,SLOMINSKI A,ETMINAN M,et al.Identification and characterization of two isozymic forms of arylamine N-acetyltransferase in Syrian hamster skin[J].Journal of Investigative Dermatology,1993,101(5):660-665.  
[34] TAN D X,HARDELAND R,BACK K,et al.On the significance of an alternate pathway of melatonin synthesis via 5-methoxytryptamine:comparisons across species[J].Journal of Pineal Research,2016,61(1):27-40.  
[35] 蔡安安,唐哲,刘平,等.环境友好合成褪黑素[J].长沙大学学报,2011,25(2):81-82. CAI A A,TANG Z,LIU P,et al.An environmental friendly synthesis of melatonin[J].Journal of Changsha University,2011,25(2):81-82.(in Chinese)
[36] BYEON Y,LEE H Y,LEE K,et al.Caffeic acid O-methyltransferase is involved in the synthesis of melatonin by methylating N-acetylserotonin in Arabidopsis[J].Journal of Pineal Research,2014,57(2):219-227.  
[37] LEE H Y,BYEON Y,LEE K,et al.Cloning of Arabidopsis serotonin N-acetyltransferase and its role with caffeic acid O-methyltransferase in the biosynthesis of melatonin in vitro despite their different subcellular localizations[J].Journal of Pineal Research,2014,57(4):418-426.  
[38] 杨明辉,史建民,陶景丽,等.外源褪黑素处理方式对荷斯坦奶牛体内褪黑素富集与代谢的影响[J].中国畜牧兽医,2017,44(9):2613-2620. YANG M H,SHI J M,TAO J L,et al.Effects of different melatonin injection ways on the enrichment and metabolism of blood melatonin in Holstein cows[J].China Animal Husbandry & Veterinary Medicine,2017,44(9):2613-2620.(in Chinese)
[39] MORERA-FUMERO A L,ABREU-GONZÁLEZ P,HENRY-BENÍTEZ M,et al.Chronotype as modulator of morning serum melatonin levels[J].Actas Espanolas de Psiquiatria,2013,41(3):149-153.
[40] CEINOS R M,CHANSARD M,REVEL F,et al.Analysis of adrenergic regulation of melatonin synthesis in Siberian hamster pineal emphasizes the role of HIOMT[J].Neuro-Signals,2004,13(6):308-317.  
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