- •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
7.4. Regulation of water and salt metabolism and uropoiesis
Urine volume and ion content in it is regulated by the combined action of hormones and renal structural features. The daily urine volume is influenced by hormones aldosterone and vasopressin.
Aldosterone is a steroid hormone of the adrenal cortex. It belongs to mineralocorticoids. Aldosteron provides increased sodium reabsorption in the distal renal tubule by active transport. It is actively secreted by a significant decreasing of sodium concentration in blood plasma. Almost complete removal of sodium from the urine can occur in the case of very low concentrations of sodium in the blood plasma under the action of aldosterone. Increased sodium reabsorption leads to water retention in the body. Hypersecretion of aldosterone (hyperaldosteronism) results in sodium and water retention and leads to edema and hypertension, even heart failure. Insufficiency of aldosterone leads to a significant loss of sodium, chloride and water. The volume of blood plasma is decreased. In the kidneys, the processes of secretion of H+ and NH4+ are disturbed. It can lead to acidosis.
Vasopressin (antidiuretic hormone, ADH) is a peptide hormone synthesized in the hypothalamus and secreted from the neurohypophysis. It has a membrane mechanism of action. This mechanism is realized through the adenylatecyclase system in target cells. Vasopressin secretion increases with increasing osmotic pressure of blood plasma, for example, with an increase in salt intake or dehydration. Vasopressin causes peripheral vasoconstriction (arterioles), resulting in increased blood pressure. In the kidney, vasopressin increases the rate of water reabsorption. As a result, the relative concentrations of Na, C1, P and total N are increased. Vasopressin secretion increases with increasing osmotic pressure of blood plasma, for example, with an increase in salt intake or dehydration. It is believed that the action of vasopressin is associated with phosphorylation of proteins of apical membrane of the kidney, thus increasing its permeability. In the pituitary gland lesions, in the case of abnormal vasopressin secretion, diabetes insipidus is observed – a sharp increase in urine volume (4-5 liters) with a low specific gravity.
Parathhormone is parathyroid hormone of peptide nature (membrane mechanism of action via cAMP); it also affects the excretion of salts from the body. In the kidney, it increases the tubular reabsorption of Ca2+ and Mg2+, increases the excretion of K+, phosphate, HCO3 and decreases the excretion of H+ and NH4+. This is mainly due to reduced tubular reabsorption of phosphate. At the same time calcium concentration in plasma is increased. Hyposecretion of parathyroid hormone leads to the opposite phenomenon – an increase of phosphate in the blood plasma and to decrease the content of Ca2+ in the plasma.
Estradiol is a female sex hormone. It stimulates the synthesis of 1,25-dihydroxy vitamin D3; it increases the reabsorption of calcium and phosphorus in the kidney tubules.
Natriuretic factor (NFE, atrial natriuretic peptide (ANP), atriopeptin) is a peptide, which is formed in the cells of the atrium in the hypothalamus. This is hormone-like substance. Its targets are the cells of the distal renal tubules. It operates through guanilatcyclase messenger system, i.e. cGMP is its intracellular mediator. The result of the influence of NFE on tubular cells is a reduction of reabsorption of Na, i.e. natriuria develops.
The retention of a certain amount of water in the body is caused by adrenal hormones – aldosterone and cortisone. In this case, we have the retention of Na ions in the body and as a result – water retention. Hormone thyroxine leads to a decrease of the body weight due to enhanced excretion of water, mainly through the skin.
These mechanisms are controlled by the CNS. In the regulation of water metabolism diencephalon and gray tuber of the brain are involved. Excitation of the cerebral cortex leads to changes in the kidneys as a result of a direct transmission of the impulses along nerve pathways, or by bringing some of the endocrine glands, particularly the pituitary gland.
Disturbances of water balance in various pathological conditions may lead either to water retention in the body, or to a partial dehydration of tissues. If water retention in the tissues is of a chronic nature, it usually leads to development of various forms of edema (inflammatory, salt, and hunger).
Abnormal tissue dehydration is usually caused by increased excreation of water through the kidney (up to 15-20 liters of urine a day). This increased urination, accompanied by strong thirst, observed in diabetes insipidus. Patients, suffering from diabetes insipidus on the basis of lack of vasopressin, lose their ability to concentrate the primary urine; the urine becomes very dilute and has a low specific gravity. However, the restriction of drinking in this disease can lead to tissue dehydration incompatible with the life.
