- •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
11.1. Respiratory function of blood. Buffer systems of blood
Blood plays a crucial role in maintaining the acid-base balance, the change of which can lead to pathological conditions or death of the organism. Therefore, in the body, there are special systems that prevent change in pH of the blood and other body fluids in the formation of acidic and alkaline substances or high water inflow. This is the role of individual physiological systems (respiratory, excretory) and buffer systems. The latter are very fast (within seconds), respond to changes in the concentration of H + and OH- in aqueous solutions and are urgent regulators of acid-base status in the tissues of the body.
Buffer systems are mixtures of a weak acid and its soluble salts, two salts, or proteins that are able to prevent the change of pH of body fluids. Effect of buffer systems is directed to binding excess H+ or OH- in the environment and the maintenance of constant pH. Weakly dissociated substances or water are formed under the influence of the buffer system. The main buffer systems of blood are bicarbonate, protein (hemoglobin) and phosphate. There are also the acetate and ammonium buffer systems.
Bicarbonate buffer system is powerful and very manageable system of the blood and extracellular fluid. It accounts for about 10% of the total buffer capacity of the blood. Bicarbonate system is a conjugate acid-base pair consisting of a molecule of carbonic acid H2CO3, acting as a proton donor, and bicarbonate ion HCO3- performing the role of a proton acceptor:
СО2 + Н2О ↔ Н2СО3 ↔ Н+ + НСО3-
The true concentration of undissociated Н2СО3 molecules in the blood is low and is directly dependent on the concentration of dissolved CO2. At normal blood pH (7,4), the concentration of bicarbonate ions HCO3- in plasma exceeds the CO2 concentration in about 20 times. Bicarbonate buffer system is functioning as an effective regulator of pH = 7,4. The mechanism of action of this system is characterized by the secretion of relatively large amounts of blood acidic substances. Protons H + react with bicarbonate ions HCO3-. This leads to the formation of weakly dissociated Н2СО3. The following decrease in the concentration of Н2СО3 is achieved as a result of the accelerated release of CO2 through the lungs as a result of hyperventilation. If the amount of bases in the blood is increased, they interact with weak carbonic acid; and bicarbonate ions and water are formed. This does not occur to any appreciable changes in pH. In addition, to maintain normal relations between the components of the buffer system in this case, the physiological mechanisms of regulation of acid-base balance are involved. There is retention of a certain amount of CO2 in the blood plasma as a result of lungs hypoventilation. Bicarbonate system is closely connected to hemoglobin system.
Phosphate buffer system is a conjugate acid-base pair consisting of an ion Н2РО4- (proton donor, acts as acid) and ion НРО42- (proton acceptor plays the role of salt). Phosphate buffer system is only 1% of the buffer capacity of blood. In other tissues, this system is one of the key. Phosphate buffer system is capable to influence on pH changes from 6,1 to 7,7 and can provide a capacity of intracellular fluid, the pH of which is within the limits of 6,9-7,4. In the blood, the maximum capacity of phosphate buffer is near 7.2. Organic phosphates also have buffer properties, but their buffer capacity is weaker than the inorganic phosphate buffer.
Protein buffer system is less important for maintaining acid-base balance in blood plasma than the other buffers. Proteins form a buffer system due to the presence of acid-base groups in the molecules of proteins: a protein-Н+ (acid, proton donor) and protein (conjugate base, the acceptor of protons). The protein buffer system of blood plasma is effective in the pH range of 7,2-7,4.
Hemoglobin buffer system is the most powerful buffer system of blood, accounting for 75% of the buffer capacity. Participation of hemoglobin in the regulation of blood pH is due to its role in the transport of oxygen and carbon dioxide. At oxygen saturation hemoglobin become more stronger acid (ННbО2). Hemoglobin, giving oxygen, turns into a very weak organic acid (ННb).
Hemoglobin buffer system consists of non-ionized hemoglobin ННb (a weak organic acid, proton donor) and potassium salt of hemoglobin КНb (conjugate base, the acceptor of protons). In the same way oxyhemoglobin buffer system can be considered. The system of hemoglobin and oxyhemoglobin are exist as a coherent whole. Buffering properties of hemoglobin are due to the ability of acid reacting compounds interact with potassium salt of hemoglobin:
KHb + Н2СО3 =>КНСО3 + ННb.
This ensures maintaining of blood pH within physiologically acceptable values, despite the flow of large amounts of CO2 and other metabolic products of acidic nature in venous blood. Hemoglobin (ННb), entering into the capillaries of the lungs, is converted into oxyhemoglobin (ННbО2), which leads to an acidification of the blood, the displacement of Н2СО3 from bicarbonate and a decrease in alkali reserve of blood.
Respiratory function of the blood. An important function of blood is its ability to carry oxygen to the tissues and CO2 from the tissues to the lungs. Agent performing this function is hemoglobin. Hemoglobin is able to absorb O2 at relatively high concentration of it in the air and can easily give it at lower partial pressure of O2:
Нb + О2 ↔ НbО.
Therefore, blood in the pulmonary capillary is saturated with O2, while in tissue capillaries, where the partial pressure of its greatly decreased, there is a reverse process - the return of blood oxygen to the tissues.
Forming in tissues during oxidative processes CO2 is subjected to removal from the body. Ensuring of such gas exchange is carried out by several body systems.
The most important are: external, or pulmonary, respiration, providing directed diffusion of gases through alveolar-capillary walls in the lungs and gas exchange between outside air and blood; respiratory function of blood, depending on the capacity of plasma to dissolve and the ability of hemoglobin reversibly bind oxygen and carbon dioxide; transport function of the cardiovascular system (blood flow), ensuring the transfer of blood gases from the lungs to the tissues and back; function of enzyme systems, providing the exchange of gases between the blood and tissue cells, i.e., tissue respiration.
The diffusion of gases of blood realizes through the cells membranes in a concentration gradient. Due to this process in the alveoli of the lungs at the end of inspiration there is the alignment of the partial pressures of gases in alveolar air and blood. Exchange with atmospheric air during expiration and inspiration again leads to differences in the concentration of gases in alveolar air and blood, and therefore the diffusion of oxygen into the blood and carbon dioxide from the blood occure.
Most of the O2 and CO2 is transferred into the bound with hemoglobin in the form of HbO2 and HbCO2 molecules. The maximum amount of oxygen, bounding by blood at full saturation of hemoglobin with oxygen, is called oxygen capacity of blood. Normally, its value varies between 16,0-24,0% vol. and depends on the content of hemoglobin in the blood, 1 g of which can bind 1,34 ml of oxygen (Hüfner number).
The binding of oxygen by hemoglobin is reversible process, dependent on oxygen partial pressure in the blood, as well as other factors, such as the pH of the blood.
CO2 produced in the tissues, passes into the blood capillaries, and then diffuses into the erythrocytes, where under the influence of carbonic anhydrase turns into carbonic acid which dissociates into H+ and НСО3-. НСО3- ions partly diffuse into the blood plasma, forming sodium bicarbonate. It enters to the lungs with the blood flow (as НСО3- ions contained in red blood cells) and forms CO2, which diffuses into the alveoli. About 80% of the total amount of CO2 is transferred from tissues to the lungs in the form of bicarbonate, 10% - in the form of freely dissolved carbon dioxide and 10% - in the form of carboxyhemoglobin. Carboxyhemoglobin dissociates in the pulmonary capillaries on hemoglobin and free CO2 that is removed with the expired air. Release of CO2 from the complex with hemoglobin contributes the transformation of the latter in oxyhemoglobin, which, having expressed acidic properties is able to convert bicarbonate into carbonic acid, which dissociates to form molecules of water and CO2.
With low blood saturation by oxygen hypoxemia is developed, which is accompanied by development of hypoxia, i.e., insufficient supply of oxygen to tissues. Severe forms of hypoxemia can cause complete cessation of oxygen supply to tissues, whereas anoxia is developed, in these cases loss of consciousness occurs, which can result in death.
Pathology of the gas exchange is associated with infringement of transport of gases between the lungs and body cells and observed at a decrease of the gas capacity of the blood due to insufficiency or changes of hemoglobin, and manifested in the form of anemic hypoxia. In anemia oxygen capacity of blood is decreased in proportion to the decrease of concentration of hemoglobin. Decreasing of hemoglobin concentration in anemia limits the transport of carbon dioxide from the tissues to the lungs in the form of carboxyhemoglobin.
Violation of oxygen transport by blood also occurs in the pathology of hemoglobin, such as sickle cell anemia, inactivation of hemoglobin molecules by converting it to methemoglobin, for example, in cases of poisoning by nitrates (methemoglobinemia) or carboxyhemoglobin (CO poisoning).
Disturbances of gas exchange by reducing the volume velocity of blood flow in capillaries occur in heart failure, circulatory failure (including the collapse, shock), local disturbances - during vasospasm, and others. When there is blood stagnation the concentration of reduced hemoglobin is increased. In heart failure, this phenomenon is especially expressed in the capillaries of the distant from the heart parts of the body, where blood flow is slowed down more that clinically is manifesteded by acrocyanosis. Primary disturbance of gas exchange at the cellular level is mainly observed during influence of poisons that block the respiratory enzymes. As a result, cells lose the ability to utilize oxygen, and acute tissue hypoxia is developed, which leads to structural disorganization of the subcellular and cellular elements, up to necrosis. Vitamin deficiency, such as lack of vitamins B2, PP, which are coenzymes of respiratory enzymes, can lead to disruption of cellular respiration.
