11实验十一酮体的生成和利用.doc

实验十一 酮体的生成和利用【实验目的】了解酮体的生成部位及掌握测定酮体生成与利用的方法。【实验原理】在肝脏线粒体中，脂肪酸经-氧化生成的过量乙酰辅酶A缩合成酮体。酮体包括乙酰乙酸、-羟丁酸和丙酮三种化合物。肝脏不能利用酮体，只有在肝外组织，尤其是心脏和骨骼肌中，酮体可以转变为乙酰辅酶A而被氧化利用。本实验以丁酸为基质，与肝匀浆一起保温，然后测定肝匀浆液中酮体的生成量。另外，在肝脏和肌肉组织共存的情况下，再测定酮体的生成量。在这两种不同条件下，由酮体含量的差别我们可以理解以上的理论。本实验主要测定的是丙酮的含量。酮体测定的原理：在碱性溶液中碘可将丙酮氧化成为碘仿。以硫代硫酸钠滴定剩余的碘，可以计算所消耗的碘，由此也就可以计算出酮体（以丙酮为代表）的含量。反应式如下：CH3COCH3十3I2十4NaOH CHI3十CH3COONa十3NaI十3H2OI2十2Na2S2O3 Na2S4O6十2NaI【实验材料】1. 实验器材试管；移液管；锥形瓶；滴定管及架。2. 实验试剂(1) 0.1% 淀粉液。(2) 0.9% NaCl溶液。(3) 15% 三氯乙酸。(4) 10 NaOH溶液。(5) 10 HCl溶液。(6) 0.5mol/L丁酸溶液：取5ml丁酸溶于100ml 0.5mol/L NaOH中。(7) 0.1mol/L碘液：I2 12.5g和KI 25g加水溶解，稀释至刻度1L，用0.1mol/L Na2S2O3标定。(8) 0.02mol/L Na2S2O3: 24.82g Na2S2O35H2O和400mg无水Na2CO3溶于1L刚煮沸的水中，配成0.1mol/L溶液，用0.1mol/L KIO3标定。临用时将标定Na2S2O3溶液稀释成0.02mol/L。【实验操作】1.标本的制备：将兔致死，取出肝脏，用0.9% NaCl洗去污血，放滤纸上，吸去表面的水分，称取肝组织5g置研钵中，加少许0.9% NaCl至总体积为10ml，制成肝组织匀浆。另外再取后腿肌肉 5g，按上述方法和比例，制成肌组织匀浆。2.保温和沉淀蛋白质：取试管3只，编号，按下表操作：管号试剂 ABC肝组织匀浆2.0 ml2.0 ml预先煮沸的肝组织匀浆2.0 mlpH 7.6的磷酸盐缓冲液4.0 ml4.0 ml4.0 ml正丁酸2.0 ml2.0 ml2.0 ml43水浴保温60分钟肌组织匀浆4.0 ml预先煮沸的肌组织匀浆4.0 ml4.0 ml43水浴保温60分钟15%三氯醋酸3.0 ml3.0 ml3.0 ml摇匀后，用滤纸过滤，将滤液分别收集在3支试管中,为无蛋白滤液。3.酮体的测定取锥形瓶3只，按下述编号顺序操作： 编 号试 剂123无蛋白滤液5.0 ml5.0 ml5.0 ml0.1mol/L I2-KI3.0 ml3.0 ml3.0 ml10% NaOH3.0 ml3.0 ml3.0 ml摇匀，静置10分钟，向各管中加入10% HCl 3ml,加1%淀粉液1滴呈兰色，分别用0.02mol/L Na2S2O3滴定至溶液呈亮绿色为止。【实验结果与计算】肝脏生成的酮体量（mmol/g）=(CA)Na2S2O3的摩尔数1/6肌肉利用的酮体量（mmol/g）=(CB)Na2S2O3的摩尔数1/6A: 滴定样品1消耗的Na2S2O3 ml数。B: 滴定样品2消耗的Na2S2O3 ml数。C: 滴定样品3消耗的Na2S2O3 ml数。【思考题】为什么只有在肝外组织，酮体才可以被氧化利用？Experiment 11 Production and Degradation of Ketone Bodies【Purpose】Understand the production organs and master the method used for production and degradation of ketone bodies measurement.【Principle】Within the mitochondria of liver, the excess acetyl-CoA produced during fatty acid -oxidation is converted to acetoacetate, -hydroxybutyrate, and acetone, this group of molecules is called the ketone bodies. Liver can not use ketone bodies as an energy source. Only in several tissues out of liver, most notably cardiac and skeletal muscle, ketone bodies are converted to acetyl-CoA, the acetyl-CoA is then oxidated to generate energy .We use butyric acid as initial stuff in this experiment, the butyric acid is heated with the liver plasm, and then measure the content of ketone bodies in liver plasm. Moreover, measure the content of ketone bodies under the condition of coexistence of liver plasm and skeletal muscle in reaction system. We can comprehend the above theories from the difference of the ketone bodies content under the two different conditions. We determine the content of acetone in this experiment.The ketone bodies measurement principle is shown below: In alkaline aqua the iodine can oxidize acetone to become iodoform , titrate the remainder iodine in the reaction system with hyposulphite, we can calculate the consumption of iodine according to the result of hyposulphite titration, we can also calculate the content of ketone bodies (take acetone as to represent) according to the titration result.The equation of Reaction is as follows:CH3COCH3十3I2十4NaOH CHI3十CH3COONa十3NaI十3H2OI2十2Na2S2O3 Na2S4O6十2NaI【Materials】1. Apparatus:Tubes, Pipets, Flasks Burettes and burette support.2. Reagents:(1) 0.1% aqua of starch.(2) 0.9% aqua of NaCl.(3) 15% trichlorine acetic acid.(4) 10% aqua of NaOH.(5) 10% aqua of HCl.(6) 0.5mol/L butyric acid: Dissolve 5ml butyric acid in 100ml 0.5mol/L NaOH.7 0.1mol/L aqua of iodine: Dissolve I2 12.5g and KI 25g in distilled water, dilute the solution to 1L, demarcate the solution with 0.1mol/L Na2S2O3.8 0.02 mol/L Na2S2O3: Dissolve 24.82 g Na2S2O3 5 H2O and 400 mg anhydrous Na2CO3 in 1L fresh boiled water to get 0.1 mol/L solution, demarcate the solution with 0.1 mol/L KIO3. Dilute the solution to 0.02 mol/L just before using.【Procedures】1. Preparation of the specimen:Execute the rabbit, take out the liver, scour off the blood with 0.9% NaCl, put the liver on filter paper to suck away the surface humidity, weigh 5 g of the liver organize, place it into the mortar, add a few 0.9% NaCl to total volume 10 ml. Then take 5 g muscle of rear leg, make it into the liver organization plasm according to above- mentioned method and comparisons.2. Heat preservation and precipitation of the protein:Take three tubes, number the tubes and operate as the table followed：Tube No.ReagentABCThe liver organization plasm 2.0 ml2.0 mlThe liver organizationn plasm that boiled in advance 2.0 mlPhosphoric acid salt buffer liquid of pH7.64.0 ml4.0 ml4.0 mlorthobutyric acid2.0 ml2.0 ml2.0 mlHeat preservation at 43 water bath for 60 minutes.The muscle organization plasm4.0 mlThe muscle organization plasm that boiled in advance4.0 ml4.0 mlHeat preservation at 43 water bath for 60 minutes.15% trichlorine acetic acid3.0 ml3.0 ml3.0 mlFilter with the filter paper after shaking evenly, collect the filtrate respectively in 3 tubes, then we get the filtrate without protein.3. Determination of the ketone bodies Take 3 flasks, operate as below-mentioned serial number in proper order: Flask NoReagent123Filtrate without protein5.0 ml5.0 ml5.0 ml0.1mol/L I2-KI3.0 ml3.0 ml3.0 ml10% NaOH3.0 ml3.0 ml3.0 mlPlace Statically for 10 minutes after shaking evenly, add 10% HCl 3ml to each tube, and add one drop of 1% starch liquid to each tube, then we can see the solution presents the color of orchid, titrate with 0.02mol/L Na2S2O3 until the solution presents the color of bright green respectively.【Result and calculation】Ketone bodies produced in liver( mmol/g)=(CA)Moore content of the Na2S2O3 1/6Ketone bodies consumed in muscle ( mmol/g)=(CB)Moore content of the Na2S2O3 1/6A: volume of the Na2S2O