配合饲料替代杂鱼对中华绒螯蟹生长发育、体成分及脂肪酸组成的影响

通过分别投喂配合饲料和天然杂鱼,研究配合饲料替代杂鱼对中华绒螯蟹生长发育、体成分及脂肪酸组成的影响。试验池塘设在上海市崇明县水产技术推广站特色水产养殖基地,每种饵料设3个平行。试验时间为2010年4月至11月,养殖结束后统计各试验组的存活率、体质量、产量,并随机取样测定各试验组雌雄蟹的肝胰腺指数、性腺指数、出肉率,同时测定肝胰腺、性腺和肌肉中水分、总脂、粗蛋白含量及脂肪酸组成。结果显示,杂鱼组和配合饲料组蟹的存活率、体质量、肝胰腺指数、性腺指数、出肉率等指标均无显著差异(P>0.05);杂鱼组雌雄蟹肝胰腺及雄蟹肌肉中水分含量极显著高于配合饲料组(P<0.01);杂鱼组雌雄蟹肝胰腺、性腺及雌蟹肌肉中总脂含量均显著低于配合饲料组(P<0.05);杂鱼组雌雄蟹肝胰腺中粗蛋白含量均显著高于配合饲料组(P<0.05),但杂鱼组雌蟹卵巢中粗蛋白含量极显著低于配合饲料组(P<0.01)。配合饲料组雌蟹肝胰腺游离脂肪酸含量显著高于杂鱼组(P<0.05),磷脂含量杂鱼组显著高于配合饲料组(P<0.05);配合饲料组雌蟹卵巢和肌肉甘油三酯含量均显著高于杂鱼组(P<0.05或P<0.01),游离脂肪酸和磷脂含量则杂鱼组显著高于配合饲料组(P<0.05或P<0.01);雌蟹肌肉中胆固醇含量配合饲料组极显著高于杂鱼组(P<0.01)。两组饵料雄蟹肝胰腺各脂类组成无显著差异;精巢中甘油三酯及游离脂肪酸含量为杂鱼组显著高于配合饲料组(P<0.01),磷脂含量为杂鱼组显著低于配合饲料组(P<0.05);雄蟹肌肉胆固醇含量配合饲料组显著低于杂鱼组(P<0.05)。杂鱼组雄蟹肝胰腺和肌肉中LOA含量极显著或显著低于配合饲料组(P<0.01或P<0.05),而杂鱼组雄蟹肌肉中ARA含量显著高于配合饲料组(P<0.05);杂鱼组雌蟹卵巢中LNA、ARA和DHA的含量极显著或显著低于配合饲料组(P<0.01或P<0.05)。研究结果表明,适宜的配合饲料替代杂鱼全程养殖中华绒螯蟹成蟹对其生长发育无显著负面影响,而对其体成分组成及脂肪酸组成有一定影响。     

低分子壳聚糖对罗非鱼的肝脂代谢和饲料利用效率的影响研究

为研究低分子壳聚糖 (SMW Chitosan)对罗非鱼 (Tilapia)肝脏脂肪代谢和饲料利用率的影响效果 ,实验采用单因子浓度梯度法饲养罗非鱼 (体重 1 8 96± 1 2 4g)。 3个月后测定结果表明 ,对照组罗非鱼的肝体比明显高于实验组 ,0 5 0 %低分子壳聚糖实验组罗非鱼的肝体比最小 ;实验组罗非鱼的肝脂含量均显著低于对照组 ,其中含 0 5 0 %低分子壳聚糖组罗非鱼的肝脂含量比对照组下降了2 8 2 4 %;0 5 0 %低分子壳聚糖实验组的饲料系数比对照组下降 2 4 1 0 %。壳聚糖对罗非鱼的特殊增长率也有显著性影响。实验表明 ,一定剂量的低分子壳聚糖能有效促进罗非鱼的肝脂代谢 ,提高罗非鱼的饲料利用能力。     

饲料牛磺酸对尼罗罗非鱼生长、体成分及组织游离氨基酸含量的影响

本文探讨了饲料牛磺酸水平对尼罗罗非鱼幼鱼生长性能、体成分及游离氨基酸含量的影响。选用体重为5.89±0.03g的罗非鱼300尾,随机分为5个处理组,每个处理3个重复,每个重复20尾。在基础饲料中分别添加0、0.4%、0.8%、1.2%、1.6%的牛磺酸,配制成5种试验料,分别饲喂不同处理组的罗非鱼,饲养周期为56d。结果表明： 0.8%牛磺酸组罗非鱼增重率最高,且显著高于0%和1.6%组(P<0.05);饲料牛磺酸水平(0.4%-1.2%)显著提高了罗非鱼摄食率、肝脏指数和内脏指数,显著降低了饲料系数(P<0.05)。随着饲料牛磺酸水平的提高,鱼体粗蛋白质和粗脂肪含量随之升高,鱼体水分和粗灰分含量随之降低(P<0.05);以增重率为指标,通过二次曲线回归分析得出罗非鱼饲料牛磺酸最适需要量为0.75%。罗非鱼血清、肝脏、肌肉和全鱼中牛磺酸含量与饲料牛磺酸含量存在正相关关系,且牛磺酸添加组血清、肝脏、肌肉和全鱼牛磺酸含量显著高于对照组相(P<0.05)。罗非鱼肝脏和肌肉中游离氨基酸含量随饲料牛磺酸含量的增加均呈逐渐下降的趋势,且牛磺酸添加组肝脏和肌肉中游离氨基酸含量显著低于对照组(P<0.05)。     

茯苓多糖对中华鳖非特异性免疫功能的免疫调节作用

研究了口服茯苓多糖对中华鳖(Trionyxsinensis)非特异性免疫功能的影响。试验共分3个组,在基础饲料中添加20·0mg/kg茯苓多糖作为试验组,添加500·0mg/kg酵母细胞壁作为免疫刺激剂对照组,以投喂基础饲料作为空白对照组。连续投喂28d后,测定中华鳖血液中白细胞的吞噬活性、血清溶菌活力和补体活性。结果表明:在中华鳖饲料中添加茯苓多糖和酵母细胞壁能显著提高中华鳖白细胞的吞噬活性(t检验,P<0·05),而2个试验组之间中华鳖血液中白细胞的吞噬活性没有显著差异(t检验,P>0·05);2个试验组中华鳖血清中补体C3和C4的活性与对照组之间呈显著差异(t检验,P<0·05),而试验组之间无显著性差异(t检验,P>0·05)。本研究结果说明在中华鳖饵料中添加茯苓多糖和酵母细胞壁对中华鳖的非特异性免疫功能有增强作用。     

饲喂不同水平虫草培养残基对中华绒螯蟹营养品质的影响

在基础饲料中分别添加0.25%、0.5%、1.0%、2.0%、4.0%、8.0%、16.0%的蛹虫草培养残基(简称虫草基),以基础饲料为对照,饲喂规格为(4.0±1.0)g的中华绒螯蟹75 d,测定中华绒螯蟹(Eriocheir sinensis)常规营养成分、肌肉与血清氨基酸及肝胰腺脂肪酸含量,研究虫草基对中华绒螯蟹营养品质的影响。结果显示:(1)虫草基对中华绒螯蟹水分和蛋白含量无影响(P>0.05),0.5%和1.0%添加组的全蟹、肌肉、肝胰腺粗脂肪含量显著高于对照组(P<0.05)。(2)适量添加虫草基可增加中华绒螯蟹肌肉游离氨基酸含量,0.5%～2.0%的添加组显著高于对照组(P<0.05),但对氨基酸组成及主要呈味氨基酸含量影响不显著(P>0.05);1.0%和16.0%添加组中华绒螯蟹血清氨基酸和主要呈味氨基酸含量明显提高(P<0.05)。(3)虫草基的添加可提高肝胰腺不饱和脂肪酸及必需脂肪酸含量,且1.0%添加组显著高于对照组(P<0.05)。饲料中添加适量的虫草基可提高中华绒螯蟹肌肉与血清的游离氨基酸、血清必需氨基酸、肝胰腺不饱和脂肪酸和必需脂肪酸含量,从而改善中华绒螯蟹营养品质。     

水体盐度与饲料脂肪含量对尼罗罗非鱼生长、营养组成和肉质的影响

为研究水体盐度和饲料脂肪含量对尼罗罗非鱼生长、营养组成和肉质的影响,本实验设置0、8和16共3个盐度梯度,每个梯度分别投喂中脂(6%)和高脂(12%)饲料,投喂初始体质量为(5.0±0.2) g的尼罗罗非鱼8周,并测定生长性能、血清生化指标、肌肉营养成分和肉质相关指标。结果显示,在中脂饲料投喂下,与对照组(盐度为0)和高盐组(盐度为16)相比,中盐组(盐度为8)的尼罗罗非鱼具有最大终末体质量、躯壳比、脂体比、肌肉蛋白质含量、肌肉氨基酸和乳酸含量和总产肉率,但其饲料系数、脏体比、肝体比和肌肉p H值显著降低;而中脂高盐组的尼罗罗非鱼其饲料系数、肥满度、脏体比、肝体比、全鱼总脂、肝脏甘油三酯、血糖、血清乳酸和血清甘油三酯含量、血清谷草转氨酶活性较高,但全鱼和肌肉水分、全鱼灰分、产肉率和肌肉离心失水率降低。在高脂饲料投喂下,随着盐度的上升,其终末体质量、成活率和脂体比降低,但饲料系数、脏体比、肝体比和肥满度增大。其中,高脂中盐组尼罗罗非鱼的肌肉蛋白以及氨基酸含量显著降低,而高脂高盐组的全鱼灰分、肝脏甘油三酯、血糖、谷草转氨酶活性、肌肉总脂、肌肉甘油三酯和磷脂含量显著提高,但全鱼总脂、肝糖原、产肉率、肌肉离心失水率和pH值显著降低。而不论在淡水还是盐水养殖情况下,与中脂饲料组相比,高脂饲料组尼罗罗非鱼均显示出更高的脂肪积累量和肌肉乳酸含量,以及更低的成活率和产肉率。尤其在高盐度水体中,高脂饲料对尼罗罗非鱼肌肉脂肪和乳酸积累的促进作用和对成活率、饲料系数和产肉率的负面作用尤为明显。研究表明,在中脂饲料投喂下,适宜的盐度(盐度8)可以促进尼罗罗非鱼的生长并提高肌肉品质,然而,在高盐度水体中使用高脂饲料对尼罗罗非鱼的生长与肉质则有较大的负面影响。     

低聚木糖对奥尼罗非鱼幼鱼生长、体成分和消化酶活力的影响

研究了在(27.0±1)℃条件下,饲料中添加不同水平的低聚木糖(0.015%、0.030%、0.045%、0.060%)对初始体重为(6.29±0.94)g的奥尼罗非鱼(Oreochromis niloticus×O.aureus)幼鱼生长、饲料转化率、体成分和消化酶活性的影响。共设5个试验组,每组设3个重复,每个水族箱内随机放幼鱼12尾,投喂率为6%,自然光周期,循环过滤水系统饲养8周。结果显示:添加0.030%低聚木糖组的特定生长率显著高于对照组(P<0.05);0.030%和0.045%低聚木糖组的饲料转化率显著高于对照组(P<0.05),两组之间差异不显著。奥尼罗非鱼幼鱼全鱼的水分、灰分、粗蛋白和粗脂肪含量在试验组间差异不显著(P>0.05);各组样本中的肝胰脏蛋白酶和肠蛋白酶活力均呈先上升后下降的趋势,0.030%组的最高,添加低聚木糖组与对照组之间差异显著(P<0.05);肠淀粉酶和脂肪酶活力在分别在0.030%与0.045%组最高,各组之间差异显著(P<0.05);肝胰脏淀粉酶和脂肪酶活力在各组之间差异不显著(P>0.05)。低聚木糖添加量(x)与特定生长率(y)之间存在关系:y=-256.34x2+16.716x+3.6479(R2=0.9266),低聚木糖添加量在0.033%左右时,可以提高幼鱼的消化酶活力和饲料转化率,从而较好促进奥尼罗非鱼幼鱼的生长,对鱼体的营养成分则没有影响。     

家蝇蛆粉替代鱼粉对凡纳滨对虾生长、抗氧化和免疫指标的影响

设计6种等氮等能的试验饲料,以评价不同比例的家蝇蛆粉替代鱼粉对凡纳滨对虾幼虾生长性能、抗氧化以及非特异性免疫指标的影响。选用960尾体质量为(0.56±0.03)g的凡纳滨对虾随机分为6组,分别投喂用家蝇蛆粉替代鱼粉的6种饲料,替代比例(等蛋白替代)分别为0、20%、40%、60%、80%和100%,记为G0、G20、G40、G60、G80和G100。45 d的养殖试验结果显示,G20~G60组凡纳滨对虾的增重率(WGR)与对照组相比差异不显著(P>0.05),G80、G100组WGR显著降低(P<0.05)。除G40组外,各替代组凡纳滨对虾的特定生长率(SGR)均显著低于对照组(P<0.05)。G100组摄食量(FI)显著低于其它各组(P<0.05)。当替代水平不超过60%时,家蝇蛆粉对凡纳滨对虾的饲料系数(FCR)、蛋白质效率(PER)、蛋白质沉积率(PPV)和肝胰指数(HSI)影响不显著(P>0.05);随替代水平的继续增加,FCR和HSI显著升高,PER和PPV显著降低(P<0.05)。替代组对虾肥满度(CF)和存活率(SR)均不同程度的高于对照组,但差异不显著(P>0.05)。随家蝇蛆粉替代水平的增加,全虾粗蛋白、钙(Ca)和总磷(P)含量显著升高(P<0.05),粗脂肪含量显著降低(P<0.05),干物质和灰分含量差异不显著(P>0.05)。各替代组对虾血清和肝胰腺超氧化物歧化酶(SOD)活性、血清丙二醛(MDA)含量与对照组相比差异不显著(P>0.05),G80和G100组肝胰腺MDA含量显著高于对照组(P<0.05)。血清酚氧化酶(PO)活性随家蝇蛆粉替代量的增加而显著降低,其中G20组显著高于其它各组(P<0.05)。肝胰腺碱性磷酸酶(AKP)活性随添加量的增加而显著降低(P<0.05)。家蝇蛆粉替代鱼粉对凡纳滨对虾的血细胞总数(THC)、血清一氧化氮(NO)含量、AKP活性和肝胰腺PO活性、NO含量影响不显著(P>0.05)。     

脆化专用饲料对罗非鱼生长和肌肉品质的影响

为考察脆化饲料对罗非鱼(Tilapia)生长和肌肉品质的影响,实验分别以配合饲料(对照组)、脆化饲料(试验组)喂养体质量为(115.30±23.69)g的罗非鱼99 d。结果显示:配合饲料组和脆化饲料组罗非鱼的增重率分别为185.25%、94.96%;饲料系数为1.87、2.94;肥满度为15.23、12.50;肌肉粗蛋白含量为19.40%、18.26%;粗脂肪含量为0.75%、1.32%;胶原蛋白为2.03、2.91;肌原纤维耐折力为33.93μm、64.84μm;滴水损失为2.59%、1.82%。与对照组相比,在生长方面,脆化饲料组罗非鱼增重率、肥满度显著降低,饲料系数显著增加(P<0.05);在肌肉品质方面,肌肉的粗蛋白含量和滴水损失显著降低,而粗脂肪含量、胶原蛋白含量和肌原纤维耐折力显著提高(P<0.05)。结果表明,脆化饲料在一定程度上改善了罗非鱼的肌肉品质。     

饲料中蛋白水平对三疣梭子蟹雌体生长、卵巢发育和生化组成的影响

本研究配制蛋白水平分别为32.16%、36.13%、39.59%和41.24%的等脂等能配合饲料(分别记为饲料1~4),对初始体重为(10.98±0.28) g的三疣梭子蟹(Portunus trituberculatus)雌体进行池塘养殖120 d,以探究饲料蛋白水平对三疣梭子蟹雌体生长、卵巢发育和生化组成的影响。结果显示,饲料蛋白水平对池塘养殖条件下雌体的生长无显著影响。饲料3组雌体的卵巢指数和总可食率均最高(P<0.05)。饲料4组卵巢中粗蛋白含量最高(P<0.05),3组和4组的肝胰腺粗蛋白含量显著高于1组和2组(P<0.05),而肌肉中的粗蛋白含量则在1组和3组中较高(P<0.05)。卵巢中的总脂含量随着饲料蛋白水平的增加呈上升趋势(P<0.05),肝胰腺和肌肉中总脂含量均在饲料1组中最高,而饲料2组中最低(P<0.05)。饲料1组和3组肌肉中的总必需氨基酸(∑EAA)和总非必需氨基酸(∑NEAA)均显著高于另外两组(P<0.05)。综上所述,在本实验条件下,三疣梭子蟹雌体育肥饲料中适宜的蛋白水平约为40.16%。研究表明,适宜的饲料蛋白水平可以提高三疣梭子蟹的卵巢发育和肌肉的营养品质。     

不同蛋白能量比饲料对草鱼幼鱼消化酶活性的影响

以鱼粉和豆粕为蛋白源,鱼油和豆油等比例混合油为脂肪源,共配制4个蛋白水平(20%、25%、30%、35%),每一蛋白水平设4个脂肪水平(4.5%、8%、11.5%、15%),共16组饲料。每组设3个重复,在水温23~29℃下,连续投喂初始体重为(16.84±0.28)g的草鱼(Ctenopharyngodon idellus)10周,研究不同蛋白能量比饲料对草鱼幼鱼消化酶活性的影响。结果显示:肠道蛋白酶的活性随着饲料蛋白含量的升高而显著升高(P<0.05),饲料蛋白水平在20%~30%时,饲料中的脂肪水平对蛋白酶活性影响不显著(P>0.05),蛋白水平在35%时,高脂肪抑制了蛋白酶活性,肝胰脏的蛋白酶变化规律类似于肠道;肠道和肝胰脏淀粉酶活性在饲料蛋白含量相同的情况下,随着脂肪含量的升高呈现显著的下降趋势(P<0.05),但饲料中蛋白(30%,35%)和脂肪(8%,11.5%,15%)含量较高时,淀粉酶活性较稳定;肠道和肝胰脏的脂肪酶活性在饲料蛋白含量相同的情况下,随着脂肪含量的升高,呈显著上升的趋势(P<0.05),但在蛋白含量(30%,35%)和脂肪含量(8%、11.5%,15%)的6个试验组之间差异不显著(P>0.05);在脂肪含量分别为4.5%、8%和11.5%时,饲料的蛋白含量对肠道的脂肪酶活性无显著性影响(P>0.05),当脂肪含量为15%时,随着蛋白含量的升高,肠道的脂肪酶活性显著降低(P<0.05)。结果表明,草鱼饲料中蛋白含量为30%和脂肪为8%(即蛋白能量比21.7 mg/kJ)的试验组草鱼获得较高的消化酶活性。     

蚯蚓粉替代鱼粉对大鳞副泥鳅生长、肌肉成分、血清生化指标及免疫性能的影响

以初始体重为(3.86±0.23)g的大鳞副泥鳅(Paramisgurnus dabryanus)为试验对象,研究蚯蚓(Eisenia foetida)粉替代鱼粉对其生长、肌肉成分、血清生化指标及免疫性能的影响。以0代替鱼粉为对照组,用蚯蚓粉替代25%、50%、75%、100%的鱼粉配制成5组等氮等能饲料,在网箱中进行10周的养殖试验。结果显示,饲料中的蚯蚓粉替代鱼粉对大鳞副泥鳅的存活率无显著影响;随着替代水平的升高,饲料系数、增重率升高(P0.05),肥满度、肝体比降低(P0.05)。各组间脾体比、特定生长率均无显著性差异;75%和100%替代组肌肉粗脂肪含量显著高于对照组(P0.05),100%替代组粗蛋白和水分含量显著低于对照组(P0.05)。随着饲料中蚯蚓粉水平的上升,鱼体肌肉蛋白质的精氨酸、胱氨酸、天门冬氨酸含量升高(P0.05),脯氨酸、组氨酸、蛋氨酸、苏氨酸、苯丙氨酸含量显著降低(P0.05);各组间血清谷丙转氨酶活力、高密度脂蛋白胆固醇含量、脂肪酶和淀粉酶活性均无显著性差异(P0.05)。随着代替水平的上升,血清甘油三酯和总胆固醇含量显著升高(P0.05),谷草转氨酶显著降低(P0.05);随着替代水平的继续上升,肝胰脏过氧化氢酶、谷胱甘肽过氧化物酶、溶菌酶活力下降,肝胰脏丙二醛含量、碱性磷酸酶活力、攻毒后的发病率和死亡率上升。各组间的肝胰脏总超氧化物歧化酶活力和总抗氧化能力均无显著性差异(P0.05)。研究表明,本实验条件下,蚯蚓粉可部分替代(22%)饲料鱼粉而不影响大鳞副泥鳅的生长和存活,且能提高鱼体肌肉成分,有效预防肝胰脏损伤和过氧化,但显著降低了鱼类免疫性能(P0.05)。     

不同蛋白质和脂肪水平对细鳞鲑幼鱼生长和肌肉氨基酸含量的影响

本研究旨在探讨不同蛋白质和脂肪水平对细鳞鲑(Brachymystax lenok)幼鱼生长、体成分以及肌肉氨基酸含量的影响。采用蛋白质水平为40%、45%、50%和55%,脂肪水平为8%和16%,共8组实验饲料。在水温为(16±0.2)℃的循环流水水族箱系统内进行为期10周的养殖试验。采用常规生化分析方法对该鱼肌肉营养学组成及含量进行测定分析。研究结果表明,不同蛋白和脂肪水平对细鳞鲑幼鱼增重率、特定生长率、肥满度和肝体比等均有显著影响(P0.05)。随着蛋白水平增加,增重率、特定生长率、肥满度和肝体比率先升高后降低,其肌肉粗蛋白含量也随之显著升高(P0.05),而对粗脂肪和粗灰分不存在显著影响;随着脂肪水平增加,其肌肉粗脂肪含量也随之显著提高(P0.05),而对水分、粗蛋白和灰分含量不存在显著影响。肌肉中共测定出17种氨基酸(除色氨酸),不同蛋白和脂肪水平对氨基酸总量(WTAA)和必需氨基酸的构成比例(WEAA/WTAA)不存在显著影响。综合生长性能与氨基酸模式的实验结果,本研究认为细鳞鲑幼鱼最适蛋白质和脂肪水平分别为50%和8%,适宜蛋能比为29.36 g/MJ。     

不同脂肪源饲料对中华绒螯蟹幼蟹生长、消化酶活力和脂肪酸组成的影响

选用初始体重为(2.15±0.10)g的中华绒螯蟹(Eriocheir sinensis)雄性幼蟹,随机分为5组(每组12只幼蟹),饲喂100%鱼油组(简称F1组)、100%豆油组(F2组)、100%亚麻油组(F3组)、50%鱼油+50%豆油组(F4组)、50%鱼油+50%亚麻油组(F5组)不同脂肪源配制的5种等氮等能饲料。实验蟹单个体养殖,实验周期为112 d。结果表明,F5组体重、增重率和特定生长率都显著高于其他饲料组(P0.05),各组的蜕壳间隔和肝胰腺指数没有显著差异(P0.05)。肝胰腺组织消化酶活力测定结果表明,F1组幼蟹肝胰腺的类胰蛋白酶活力显著高于其他各组(P0.05);F3组的胃蛋白酶活力显著高于其他各组(P0.05);F1组、F2组和F4组的脂肪酶活力显著高于其他两组(P0.05);各组的淀粉酶活力差异不显著(P0.05)。脂肪酸测定结果表明,肝胰腺和肌肉中的亚油酸(LOA)(C18:2n-6)、亚麻酸(LNA)(C18:3n-3)、EPA(C20:5n-3)和DHA(C22:6n-3)等主要脂肪酸含量与饲料脂肪酸组成呈正相关关系,F1组的高度不饱和脂肪酸(HUFA)含量显著高于其余各组(P0.05),F2组的LOA含量显著高于其余各组(P0.05),F3组的LNA含量显著高于其余各组(P0.05)。本研究结果表明,以50%的豆油或亚麻油替代鱼油能促进中华绒螯蟹幼蟹的生长,但可能使幼蟹的成活率降低。以豆油或亚麻油替代鱼油会影响幼蟹胰蛋白酶、胃蛋白酶和脂肪酶的活力和肝胰腺、肌肉脂肪酸组成。     

消化酶活力在千年笛鲷幼鱼不同消化器官中的比较研究

测定和比较了千年笛鲷(Lutjanussebae)幼鱼不同消化器官的消化酶活性。结果表明,蛋白酶比活力为:肠>胃>肝胰脏(P<0·01);淀粉酶比活力为:肠>肝胰脏>胃(P<0·01);脂肪酶比活力为:肠>肝胰脏>胃,胃和肝胰脏间差异不显著(P>0·05),但二者和肠之间差异极显著(P<0·01)。千年笛鲷幼鱼肠道对食物的整体消化能力始终较强,肝胰脏和胃是消化食物的辅助器官。     

Effect of dietary oxidized fish oil on growth performance,body composition,antioxidant defence mechanism and liver histology of juvenile largemouth bass Micropterus salmoides

Four isonitrogenous and isolipidic diets containing fresh fish oil (peroxide value, POV: 11.5 meq kg^?1, diet FR) and three degrees of oxidized fish oil (POV: 132, 277 and 555 meq kg^?1, diet OX₁₃₂, OX₂₇₇ and OX₅₅₅, respectively) were formulated to investigate the effects of dietary oxidized fish oil on growth performance, body composition, antioxidant defence mechanism and liver histology of juvenile largemouth bass. After a 12‐week feeding trail, a proportion of approximately 9% of Micropterus salmoides showed inflammation and haemorrhage at the base of dorsal, pectoral and tail fin in both groups OX₂₇₇ and OX₅₅₅. Fish fed oxidized oil diets obtained significantly higher (P < 0.05) weight gain and specific growth rate because of their remarkable higher feed intakes, compared with the fresh oil receiving group. The analysis of biometric parameters and body composition indicated significant differences (P < 0.05) in various test diets. The activities of hepatic catalase and superoxide dismutase were significantly stimulated (P < 0.05) by oxidized oil ingestion. Hepatic glutathione peroxidase, glutathione reductase and glutathione‐S‐transferase activities were significantly higher (P < 0.05), and liver glutathione content was markedly lower (P < 0.05) in group OX₅₅₅ than the other treatments. Oxidized oil consumption resulted in marked depletion (P < 0.05) of vitamin E concentration in plasma, liver and muscle tissue, increased plasma and muscle malondialdehyde content along with decreased haematocrit value. Histological examinations indicated that hepatocytes with lipid vacuoles and nuclear migration were shown in groups OX₂₇₇ and OX₅₅₅. The overall results in this study suggested that an increased oxidative stress in M. salmoides fed oxidized lipid may account for their stimulated hepatic antioxidant defences, vitamin E depletion in plasma and certain tissues, and pathological changes. The detrimental effect of oxidation products on fish health and the unexpectedly enhanced feed intake of oxidized feeds in M. salmoides underline the importance that cares should be taken to minimize dietary oxidation products to the greatest extent possible.     

Dietary high level of vitamin premix can eliminate oxidized fish oil–induced oxidative damage and loss of reducing capacity in juvenile largemouth bass (Micropterus salmoides)

Utilizing a 2 × 2 factorial design, four experimental diets (diet LVFF, low‐vitamin premix + fresh fish oil; diet LVOF, low‐vitamin premix + oxidized oil; diet HVFF, high‐vitamin premix + fresh oil; diet HVOF, high‐vitamin premix + oxidized oil) were formulated to investigate the protective role of high level of vitamin premix against the deleterious effects of highly oxidized fish oil (peroxide value, POV: 450 meq kg^?1) consumption in juvenile largemouth bass. After a 10‐week feeding trial, survival rates of all treatments were 100%. Neither vitamin premix level nor oil type affected feed intake, growth performance or feed utilization, although treatment HVFF obtained the highest weight gain and specific growth rate, and the lowest feed conversion ratio. Hepatosomatic and viscerosomatic index increased while intraperitoneal fat ratio decreased with rancid oil reception, and they did not benefit from increasing vitamin premix supply. However, dietary high level of vitamin premix ameliorated the decreased whole‐blood haemoglobin content and increased plasma low‐ and high‐density lipoprotein cholesterol levels induced by oxidized oil reception. Whole‐body and liver composition were sensitive to dietary oil oxidation, and vitamin premix addition eliminated the decreased whole‐body lipid content challenged by rancid oil consumption. Hepatic superoxide dismutase activity was stimulated by dietary oil oxidation and increment of vitamin premix abrogated this effect. Dietary oxidized oil inclusion resulted in increased malondialdehyde contents and decreased vitamin E concentrations both in the liver and muscle, and vitamin premix supplementation ameliorated these effects. In conclusion, the results in this study suggested that the well‐ingested oxidized oil could induce severe oxidative damage and loss of reducing capacity in largemouth bass, and dietary high level of vitamin premix could alleviate these effects. This practice is recommended in intensive aquaculture practice in tropical or subtropical regions where oils are susceptible to lipid peroxidation under unsatisfactory storage.     

Iron catalyzed oxidation of trout diets and its effect on the growth and physiological response of rainbow trout

Two experiments were conducted to determine 1) the effect of iron supplementation and the quality of fish oils on dietary lipid peroxidation and 2) the concurrent effects of diet rancidity and iron overload on the growth and physiological response of rainbow trout. Semi-purified diets supplemented with graded levels of iron (0–6250 mg/kg diet as ferrous sulphate) were fed to trout for 12–36 weeks. The malonaldehyde (MA) concentration of the test diets increased as the iron levels in the diets increased indicating that iron catalyzed lipid oxidation was occurring. However, when ethoxyquin was added to the oils, the increase in dietary MA level was significantly reduced. Fish oils with an initial high peroxide value were more susceptible to iron-catalyzed lipid oxidation. The concurrent effects of diet rancidity and iron overload (greater than 86 mg/kg) led to the development of unique histopathological signs, poor growth and high mortalities in the trout. In contrast, when diet rancidity was low (less than 10 µg MA/g diet), the toxic level of dietary iron was greater than 1380 mg/kg diet. The concentration of iron in trout tissues, and the hematocrit and hemoglobin concentrations increased as dietary iron levels increased and were not affected by the degree of diet rancidity.     

Effects of ferulic acid on growth performance,immunity and antioxidant status in genetically improved farmed tilapia (Oreochromis niloticus) fed oxidized fish oil

A study was conducted to characterize the effects of dietary oxidized fish oil on the growth performance, immunity and antioxidant status of genetically improved farmed tilapia (Oreochromis niloticus) and to determine the role of ferulic acid on the oxidative damage induced by the oxidized fish oil. The tilapia (13.73 ± 0.31 g) were fed four experimental diets containing untreated (peroxide value, POV: 2.2 meq/kg) and highly oxidized (POV: 120.6 meq/kg) fish oil either with or without ferulic acid (0 or 400 mg/kg) supplementation for 12 weeks. From the results, the oxidized fish oil treatments increased antioxidant enzyme activities and MDA values but decreased the weight gain and the immunological parameters in tilapia. Meanwhile, the serum biochemical indices were significantly affected by the oxidized fish oil. Besides, the addition of ferulic acid partially counteracted the free radical‐induced damage and improved the health status of tilapia. In conclusion, the oxidized fish oil may induce oxidative stress, destroy liver, dysregulate lipid metabolism as well as reduce non‐specific immunity, and eventually result in growth inhibition of tilapia. The ferulic acid supplementation partially offset the negative effects of the oxidized fish oil on tilapia.