- •Биологическая химия
- •060101 – Лечебное дело
- •Часть II
- •Contents
- •I. Theoretical part
- •1. Lipids metabolism
- •1.1. Classification of lipids
- •2. Glycolipids (basically glycosphingolipids).
- •Galactosyl ceramide
- •Cholesterol
- •1.2. Digestion and absorption of fats
- •Lipolysis of triglycerides in adipose tissue
- •1.3. Fatty acids oxidation
- •2. Transport of fa inside mitochondrion.
- •3 Ketocyl CoA tyolase Palmitic acid preformed rest Palmityl-CoA Acetyl-CoA
- •Oxidation of unsaturated fatty acids
- •Violations of fatty acids oxidation
- •Acetyl-CoA metabolism
- •1.4. Lipogenesis
- •Regulation of fatty acids synthesis and break down
- •1.5. Metabolism of phospholipids
- •1.6. Essencial fatty acids. Eicosanoids
- •1.7. Cholesterol metabolism
- •Distribution and functions of cholesterol
- •Cholesterol biosynthesis
- •1. Conversion of active acetate into mevalonic acid.
- •2. Squalene formation from mevalonic acid.
- •Regulation of cholesterol synthesis
- •Cholesterol esters metabolism
- •Synthesis of bile acids
- •1.8. Regulation of lipid metabolism
- •1.9. Violations of lipid metabolism
- •Violation of fats adsorption processes:
- •Test questions
- •2. Proteins metabolism
- •2.1. Pathways of proteins degradation
- •2. Digestion of proteins.
- •The selectivity of peptidases
- •2.2. Amino acids metabolism
- •The reactions of amino groups
- •Intramolecular deamination.
- •Reactions of the carboxyl group
- •2. Aminoacyladenylate formation.
- •2.3. Ammonia neutralization in the body
- •Storage and transport of ammonia
- •Fumarate pyruvate aspartate
- •2.4. Violations of nitrogen metabolism
- •2.5. Metabolism of individual amino acids
- •2. Metabolism of sulfur amino acids.
- •3. Metabolism of branched chain amino acids.
- •Leu, Ile, Val α-keto acids acyl-CoA derivatives
- •4. Metabolism of dicarboxylic amino acids
- •5. Metabolism of diaminomonocarboxylic acids.
- •6. Metabolism of phenylalanine and tyrosine.
- •7. Metabolism of tryptophan.
- •2.6. Metabolism of conjugated proteins. Chromoproteins metabolism
- •The degradation of hemoglobin in the tissues (the formation of bile pigments)
- •The hemoglobin biosynthesis
- •2.7. Nucleoproteins metabolism
- •Adenine hypoxanthine; guanine xanthine
- •The synthesis of pyrimidine nucleotides u, c, t
- •I nosine-5'-phosphate Xantosine-5'-phosphate
- •The synthesis of deoxyribonucleotides
- •Test questions
- •3. Template biosynthesis
- •3.1. Biosynthesis of nucleic acids
- •3.1.1. Dna biosynthesis (replication)
- •Synthesis of dna in the rna template
- •3.1.2. Rna biosynthesis
- •Rna synthesis in rna template
- •3.2. Protein biosynthesis
- •The properties of the genetic code
- •Preparatory stage of protein synthesis
- •3.2.1. Translation
- •1. Initiation.
- •2. Elongation.
- •3.2.2. Post-translational modification of proteins
- •Transport of synthesized proteins through membranes
- •3.2.3. Regulation of protein biosynthesis
- •3.3. Genetic engineering
- •Test questions
- •4. Hormones, nomenclature, classification
- •Test questions
- •5. Metabolic processes interaction
- •In the organism
- •Protein and carbohydrate metabolisms interconnection
- •Protein and lipid metabolisms interconnection
- •Carbohydrate and lipid metabolisms interconnection
- •Levels of homeostasis regulation
- •Changes in metabolism during starvation
- •Test questions
- •6. Mineral and water and salt metabolism
- •6.1. Water in the human body
- •6.2. Salt metabolism
- •7. Renal biochemistry. The role of the kidneys in the regulation of water and salt metabolism
- •7.1. Excretory function of the kidneys
- •7.2. Homeostatic function of the kidneys
- •7.3. Metabolic functions of the kidneys
- •7.4. Regulation of water and salt metabolism and uropoiesis
- •Test Questions
- •8. Biochemistry of nervous tissue
- •8.1. Features of metabolism of nervous tissue
- •8.2. Mechanism of nerve impulses conduction
- •Cholinergic synapses
- •Test Questions
- •9. Biochemistry of muscle tissue
- •9.1. Chemical composition of muscle tissue
- •Sources of energy for muscle work
- •9.2. Mechanism of muscle contraction and its regulation
- •9.3. Biochemical changes in muscles within pathology
- •Test Questions
- •10. Biochemistry of extracellular matrix
- •10.1. Structure of extracellular matrix
- •Collagens.
- •Fibril-forming collagens
- •Collagen, forming a tela
- •10.2. Features of metabolism of extracellular matrix Catabolism of extracellular matrix proteins
- •Reparation of damage of the extracellular matrix in norm
- •Biochemical changes of connective tissue with aging
- •The lesions of connective tissue
- •11. Blood biochemistry
- •11.1. Respiratory function of blood. Buffer systems of blood
- •11.2. Blood coagulation system. Changes in pathology
- •Extrinsic and intrinsic pathways of blood clotting
- •Test Questions
- •12. Liver biochemistry
- •12.1. Main functions of the liver
- •The role of the liver in the metabolism of carbohydrates
- •The role of liver in lipid metabolism
- •The role of the liver in the metabolism of proteins and amino acids
- •12.2. Choleresis. Pigment metabolism. Types of jaundice
- •The cleavage of hemoglobin: hemoglobinverdoglobinbiliverdinbilirubin.
- •12.3. Detoxifying liver function
- •Test Questions
- •13. Regulation of calcium and phosphorus metabolism
- •14. Bone biochemistry
- •Test Questions
- •II. Laboratory workshop Laboratory work 1. Lipid metabolism
- •Hydrolysis of milk fat by lipase
- •Test Questions
- •Laboratory work 2. Phospholipids. Cholesterol
- •4.1. Schiff reaction.
- •4.2. Salkowski reaction.
- •4.3. Lieberman-Burchard reaction.
- •Preparation of solutions of cholesterol for the calibration curve
- •Test Questions
- •Laboratory work 3. Digestion of proteins. Determination of acids of gastric contents
- •Experiment 2. Qualitative determination of free hydrochloric acid in gastric juice using indicator congo red.
- •Results of the determination of gastric acidity
- •Test Questions
- •Laboratory work 4. The end products of nitrogen metabolism
- •Test Questions
- •Laboratory work 5. Hormones
- •2.1. Biuretic reaction.
- •2.2. Millon’s reaction.
- •2.4. Geller’s test.
- •3. Qualitative reaction to thyroxine.
- •4. Qualitative reactions to the 11-dehydro-17-oxykortikosteron (cortisone).
- •4.1. The reaction with phenylhydrazine sulfate.
- •4.2. The reaction with Fehling's reagent.
- •Test Questions
- •Laboratory work 6. Mineral and water and salt metabolism
- •1.1. Determination the pH of saliva.
- •1.2. Detection of phosphates in saliva.
- •2.1. Qualitative detection of chlorides in the urine.
- •2.2. Detection of calcium in the urine.
- •2.3. Detection of phosphates in the urine.
- •The composition of mixtures for the calibration curve
- •Test Questions
- •Laboratory work 7. Urine biochemistry
- •3.1. Qualitative detection and quantitative determination of protein in the urine.
- •3.1.1. The test by boiling in weak acid environment.
- •3.1.2. The test by boiling in an acid medium in the presence of saturated sodium chloride solution.
- •3.1.3. Geller’s test.
- •3.1.4. The test with sulfosalicylic acid.
- •3.1.5. Quantitative determination of protein in the urine by the method of dilution (Brandberg - Roberts - Stolnikov method).
- •Determination of protein in the urine using dilution method
- •3.2. Semi-quantitative method for determining glucose and ketone bodies in urine using test strips.
- •3.3. Detection of blood pigments in the urine by boiling with alkali (Geller’s test).
- •Test Questions
- •Laboratory 8. Blood biochemistry
- •1. Buffer properties of blood serum.
- •2. Quantitative determination of total protein in serum according to biuretic reaction.
- •The composition of mixtures for the ployying of the calibration curve
- •3. Determination of calcium in serum by the method of de Waard.
- •Test Questions
- •Laboratory work 9. Detection of bile pigments in urine
- •Test Questions
- •Laboratory work 10. Biochemistry of bone and connective tissue
- •1. Preparation of extracts of bone and teeth tissues.
- •Test Questions
- •Bibliography
- •Biochemistry
- •In Two Parts Part II
- •392008, Г. Тамбов, ул. Советская, 190г
1.2. Digestion and absorption of fats
The daily requirement for fats is 50-100 g. They provide up to 50% of an organism's energy requirements.
Digestion of fats occurs in thin intestines. In the duodenum there is a neutralisation of hydrochloric acid of gastric juice got to the intestine with food by the bicarbonates contained in pancreatic and intestinal juice. Bubbles of carbon dioxide excreted thus promote agitating of food mass. There is fat emulsification, basically by the salts ofbile acids which get to a duodenum with bile. Bile contains basically cholic, deoxycholic and chenodeoxycholic acids. Usually they are conjugated with glycine or taurine.
Pancreas secretes inactive prolipase. Its transformation into active lipase occurs with the participation of bile acids and protein of pancreatic juice colipase. Colipase joins lipase and makes its resistant to trypsin influence, and also promotes connection of lipase with micelles. Lipases рН optimum is 8-9, in the presence of bile it shifts to 6.
Lipase is absorbed on the surface of micelles and hydrolyzes an ester group in triacylglycerine. Main degradation products are 2-monoglycerides and fatty acids.
Fatty acids with a short carbon chain and glycerin are well soluble in water. They are absorbed in intestine and move to blood of portal vein, and then into the liver. The absorption of fatty acids with the long carbon chain and of monoglycerides happens with the assistance of bile from micelles. Fatty acids and monoglycerides are absorbed, and salts of bile acids remain in an intestine lumen. Their basic part is absorbed by blood in ileum, enters the liver and then is excreted with bile. This process is called enterohepatic circulation. During the day it occurs 6-8 times.
In cells of an intestinal wall epithelium there is a lipids resynthesis. It is carried out in two ways.
The first is β-monoglyceride pathway. Fatty acids form their active form - acyl-CoA. Then there is an acylation of β-monoglyceride. Reactions are catalyzed by the enzymetic complex triglyceridesynthetase.
The second is α-glycerophosphate pathway. Glycerine is phosphorylated. The donor of the phosphoric acid residue is ATP. Then α-glycerophosphate interacts with acyl-CoA.
If mainly fatty acids enter into cells, synthesis of lipids goes along α-glycerophosphate pathway, if fatty acids with β - monoglycerides - then β-monoglyceride pathway.
Lipids are practically insoluble in water and in organism fluids. Therefore special mechanisms are necessary for their transport.
Transport of lipids is provided by special particles - lipoproteins. They have spherical form. Their superficial part is formed by phospholipids and proteins (apolipoproteins). Phospholipids are oriented with the hydrophilic ends outside. Hydrophobic ends are “solved” in the lipid phase inside particles. Intrinsic lipid phase contains basically triacilglycerins and cholesterol ethers (fig. 1).
Lipoproteins (LP) differ in composition and contents of lipids and proteins. They density increases with increasing of protein content. LP can be separated by centrifugation. They also differ by the electrophoretic mobility. There are divided into:
- chylomicrons (CM) (diameter - 0,1-5 microns);
- very-low density lipoproteins (VLDL);
- low-density lipoproteins (LDL):
- high-density lipoproteins(HDL).
Fig. 1. Structure of lipoprotein
Lipoproteins are formed in cells of mucosa of intestine (chylomicrons and VLDL), in blood plasma (LDL and HDL), in hepatocytes (VLDL and HDL). Chylomicrons and VLDL serve basically for transport of fats along the bloodstream, and LDL and HDL - for cholesterol transport. The fats synthesised in cells of intestine, are included mainly in CM. CM enter the lymphatic system and then into the general blood stream.
In about 1-2 hours after intake of fatty meal we observe alimentary hyperlipemia. This is a physiological phenomenon when the concentration of triglycerides in blood rises, and CM appears in it. Its peak is observed in 4-6 hours, and after 10-12 hours the number of triglycerides comes to norm. CM disappear from blood.
Triglycerides of CM are hydrolyzed on the surface of endothelium capillars of adipose tissue under the action of the enzyme lipoprotein lipase. Fatty acids and glycerine are formed. Glycerine is transported into liver where it can be used for synthesis of fats. The most of fatty acids penetrates into tissues. In adipose tissue they are deposited in the form of fats, in a cardiac muscle and working skeletal muscles they are used as an energy source. Residual chylomicrons are captured by liver cells.
