- •Биологическая химия
- •060101 – Лечебное дело
- •Часть II
- •Contents
- •Cholesterol
- •I. Theoretical part
- •1. Lipids metabolism
- •1.1. Classification of lipids
- •2. Glycolipids (basically glycosphingolipids).
- •Galactosyl ceramide
- •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
The role of the liver in the metabolism of proteins and amino acids
The liver plays an important role in the metabolism of proteins. The greatest amount of protein is synthesized in the muscles. But in terms of 1 g of the mass their amount in the liver is more than in the muscles. Here, not only proteins of hepatocytes are produced, but also a large amount of secreted proteins that are required to meet the needs of the organism as a whole. Most of the blood plasma proteins are synthesized in the liver. The most important of them is albumin, which synthesis is 25% from the total formation of proteins in the liver and 50% - from the amount of secreted proteins.
In the synthesis of albumin mRNA translation occurs on the polyribosomes of rough endoplasmic reticulum. Albumin synthesis is regulated by the transcription rate of mRNA and tRNA availability. With a decrease of oncotic pressure of plasma albumin synthesis is increased. Albumin synthesis is also dependent on income of amino acids, especially tryptophan.
In patients with large carcinoid synthesis of albumin can decrease significantly, as the tumor cells use tryptophan to serotonin synthesis. 75-90% of α-globulins and 50% of β-globulins are synthesized by hepatocytes. γ-Globulins are produced by Kupffer cells.
12.2. Choleresis. Pigment metabolism. Types of jaundice
Bile is produced by the liver cells – hepatocytes. Choleresis is the synthesis and secretion of bile by hepatocytes; the secretion of water by epithelial cells of bile ducts; reabsorption of water as it moves through the ducts of bile; excretion by hepatocytes of organic and inorganic components. In the day the person is secreted from 250 to 1000 ml of bile. Choleresis occurs continuously. After the meal, secretion of bile is enhanced reflexively after 3-12 min, and one of the stimuli that affect the acceleration of the process is the bile itself.
Cleavage products, toxic compounds and drugs are excreted with the bile. Bile acids emulsify fats, allowing absorption of fatty acids, cholesterol, vitamins B, K, E, and calcium salts in the small intestine. Bile creates favorable conditions for digestion in the small intestine, improves digestion of proteins and carbohydrates, facilitates the absorption of their cleavage products, stimulates the motility of the small intestine, prevents putrefaction in the intestines, providing an antimicrobial effect, and stimulates the secretion of pancreatic juice and bile formation function of the liver.
The components of bile are bile acids, bile pigments, cholesterol, phospholipids, fatty acids, sodium, potassium, calcium, chlorine, phosphatidylcholine and water. Bile contains enzymes, vitamins, urea, uric acid, amino acids and other useless to the body compounds. Many substances, including drugs are excreted with bile. Substances secreted in the bile are divided into two groups:
- substances associated with proteins in plasma (e.g. hormones). They cannot penetrate the kidney filter and are excreted in bile;
- substances which are insoluble in water (cholesterol, steroids). In the liver they join with glucuronic acid and pass into a water-soluble state, after this they are excreted through the kidneys.
Cholesterol exists in a dissolved state in the complex with bile salts and phosphatidylcholine. With a lack of bile acids cholesterol precipitates, and the stones can be formed. Intensive formation of stones is marked in bile stasis and infection.
Bile pigments (bilirubin is the main) do not take part in digestion. Their secretion by the liver is only excretory process.
Bile removes from the body many drugs, toxins, and inorganic substances - compounds of copper, zinc and mercury.
The production of bile is controlled by nerve and humoral mechanisms. Increased level of bile components in blood stimulate choleresis. Hormones have significant impact on choleresis. Vasopressin, ACTH, and insulin stimulate it. The pineal gland hormone also stimulates secretion of bile, as a result of its direct effect on the liver parenchyma. Choleresis process is most closely associated with the cleavage of the hemoglobin in the tissues and the formation of bile pigments.
Pigment metabolism. Heme is the prosthetic group of hemoglobin and hemin enzymes; about 80% of the body’s heme is in hemoglobin. With the destruction of red blood cell hemoglobin is released. Its cleavege occurs in the liver, spleen and bone marrow. The degradation of the hemoglobin in the liver begins with α-methine linkage between rings I and II of the porphyrin ring. This process is catalyzed by NADPH- containing oxidase and leads to the formation of green pigment verdoglobin. Then verdoglobin spontaneously decomposes, iron and globin protein are released and one of the bile pigments – biliverdin - is formed. The formed biliverdin is enzymatically reduced to the main bile pigment bilirubin in the liver.
