- •Introduction into biochemistry
- •General properties
- •Classification of proteins
- •Simple Proteins – representatives, properties and role
- •Globulins [g]
- •Histones (h) h are basic non value proteins. Localized in nucleus with mol. Mass (mm) 10000-20000 d. They contain of 30% diaminomonocarboxylic acids and have positive charge. Their iep is equal 10.
- •Table 1 “The properties of globular simple proteins”
- •Conjugated proteins
- •Table 2 Composition of the free (transport) lipoproteins in plasma of human
- •True gp Proteoglycans
- •Table 3 Chemical nature of glycosaminoglycans
- •Nucleoproteins (np)
- •Mononucleotides
- •Table 4 The composition and names of nucleosides, nucleotides and their phosphoric derivatives
- •Structure of dna Primary st. Of dna is a spirally one polynucleotides chain (pnc), the disposition of nucleotides in which determine all hereditary properties of organism.
- •Structure of rna
- •Enzymes
- •Mechanism of enzyme action
- •Factors influencing on enzyme activity
- •Enzyme inhibition
- •Classification of enzymes
- •III. Hydrolases
- •Bioenergetics
- •Table 6 Redox potential (rp)
- •Inhibition of oxidative phosphorylation.
- •The types of oxidation
- •Peroxidase’s type
- •Vitamins
- •Vitamin b12
- •Ascorbic acid (vitamin c)
- •Rutin, vitamin p (permeability) – bioflavonoids, capillaris’s strengthening
- •Fat soluble vitamins
- •Deficiency diseases
- •Vitamin k
- •Carbohydrates metabolism. Digestion and absorption of carbohydrates. Intermediate metabolism of carbohydrates
- •Carbohydrates metabolism. Intermediate and final stages of carbohydrates metabolism
- •Lipids of food, their importance, digestion, absorption. Micelles and chylomicrons. The role of intestinal wall, liver, lungs and adipose tissue in lipid metabolism
- •Lipids metabolism. Lipoproteins, their composition and role. The pathways of usage of glycerol and free fatty acids in cells
- •“Pathologic chemistry of lipid’s metabolism”
- •The intermediate Metabolism of Simple Proteins (part 1): the conversion of amino acids in tissues. The formation and usage of Creatine. The decarboxylation of amino acids, the role of biogenic amines
- •Simple proteins metabolism. The pathways of formation and detoxification of ammonia
- •Conjugated proteins metabolism
- •Biochemistry of liver
- •Classification of hormones
- •General properties of hormones
- •Hormones of epiphysis Melatonin
- •Hypothalamic hormones
- •Vasopressin (antidiuretic hormone)
- •Oxytocin
- •Hormones of hypophysis
- •Hormones of pancreas
- •Hormones of adrenal glands
- •Sexual hormones are formed in gonads.
- •Estrogens
- •If the pregnancy beginns so development of embryo occurs; if the pregnancy doesn’t occur so degeneration of yellow body proceeds and mensis beginns again Androgens
- •Biochemistry of blood plasma
- •Table 10 a main biochemical indices in the blood plasma (serum)
- •Functions and diagnostic importance of some fractions of proteins Table 11 Biologic and clinic importance of blood serum proteins
- •Blood clotting system
- •Blood dissolution system
- •Complement system
- •Inorganic constituents of blood plasma. Water-mineral metabolism. Acidosis and alkalosis
- •Acidosis and alkalosis Table 12 Acidosis and alkalosis
- •Water metabolism
- •Biochemistry of erythrocytes
- •Metabolism in erythrocytes
- •The physiological and pathological derivatives of hemoglobin and their spectra of taking up
- •Biochemistry of white blood cells
- •Biochemistry of kidneys
- •Normal and pathologic constituents of urine. Urine analysis – its clinical significance Composition of normal urine
- •Physical examination
- •I. Volume
- •The term polyuria implies an increased volume of urine
- •II. Colour
- •III. Specific Gravity
- •Clinical significance
- •IV. Acidity and pH
- •Clinical Significance
- •V. Odor
- •Causes of abnormal odor
- •VI. Turbidity
- •Types of turbidities
- •Inorganic constituents
- •Chlorides
- •Clinical significance
- •Organic constituents
- •Clinical significance
- •II. Ammonia
- •Clinical significance
- •Increase
- •Uric acid
- •Clinical significance
- •Clinical aspect
- •Creatinine and creatine
- •Oxalic Acid
- •Clinical significance
- •Aminoacids
- •Aminoacidurias
- •Proteins
- •Proteinuria
- •Abnormal constituents
Carbohydrates metabolism. Digestion and absorption of carbohydrates. Intermediate metabolism of carbohydrates
The role of carbohydrates
The ration of proteins, lipids and carbohydrates in food should be 1:1:4, i.e. must be supplied through the diet 400-500g of carbohydrates or 124g per 1000kcal a day.it is desirable that disaccharides made up 25% from this quantity. Overeating of carbohydrates results in obesity and atherosclerosis.
The role of carbohydrates:
Energetical function: 99% of carbohydrates is used for energy production. The oxidation of 1g of glucose gives 17,2kj (4,1kcal) of energy;
Structural role: formation of GAG, glycoproteins, and other compounds (nucleic acids, nucleoproteins, glycolipids, nucleosidedi and triphosphates, coenzymes, glucuronic acid);
reserve function: glycogen is a storage of glucose
signal role: receptors and some hormones contain carbohydrates. Carbohydrates stipulate antigenicity of tissues
food fibers promotes the retention of water in intestine and formation of feces.
The diet riched by food fibers decreases possibility of appearance of diverticulitis, cancer of large intestine, heart-vessel diseases and diabetes mellitus. Cellulose favourably acts on function of large intestine. Pitch and pectins decrease the level of cholesterol in blood. Perhaps it is due to the binding of bile acids and cholesterol. Pitch and pectins stop evacuation od acydchym from gaster, decrease level of glucose in blood.
The digestion of carbohydrates
The digestion of the starch and glycogen of food beginns in mouth under action of salivary amylase. Gaster doesn’t contain glycosidases, but food undergoes the cleavage under influence of salivary amylase. The action of amylase continues in small intestine. Some other enzymes take part in digestion of starch and glycogen of food, e.g. pancreatic amylase:
(C6H10O5)n + (H2O)n (Maltose)n
maltose is broken up to 2 glucoses in small intestine under action of maltase (intestinal enzyme)
Lactose is broken up to beta-galactose and glucose in small intestine under action of lactase (intestinal enzyme)
Sucrose is hydrolyzed under action of intestinal sucrase to fructose and glucose:
The digestion of nucleic acids gives pentoses
Table 7 The absorption of monosaccharides
Lumen of intestine |
Wall of intestine |
Portal vein |
|
Na-Glucose transporter (act. tr.)
Galactose Glucose
GLUT (facilitated diffusion) Fructose
----------simple diffusion |
GLUT (Facilitated diffusion)
Galactose Glucose Fructose
Pentoses
All monosaccharides ↓ liver ↓ glucose ↓ blood circulation
|
The conversion of glucose in tissues. Glucostatic function of liver
The following tissues and organs use glucose particularly intensive:
nervous tissue because glucose is only source of energy
muscles (for production of energy fro contraction)
wall of intestine (absorption demands the energy)
kidneys (formation of urine is energy dependent process)
adrenal glands (energy is necessary for synthesis of hormones)
erythrocytes
adipose tissue (glucose is necessary as source of glycerol)
mammary glands, particularly in lactation (glucose is necessary for lactose formation)
65% of glucose is oxidized; 30% of glucose is used for liponeogenesis; 5% of glucose is used on glycogen formation.
Glucostatic function of liver: is provided by 3 processes:
glycogenogenesis (formation of glycogen)
glycogenolysis (cleavage of glycogen)
gluconeogenesis (formation of glucose from intermediates).
Increase of glucose in blood causes increase of glycogenogenesis. Decrease of glucose in blood causes glycogenolysis and gluconeogenesis.
The normal level of glucose in blood is 3.4-6.1mM/L and liver regulates concentration of glucose in blood
Glycogenogenesis 2/5 of glycogen is stored in liver. 1/5 of glycogen is formed in muscles and other organs and tissues. Glycogen is a reserve of glucose. It is a high molecular compound and therefore doesn’t increase osmotic pressure in cells. This process is complex and consists of following stages:
ATP ADP UTP PP UDP
Glucose------------ Glucose-6-ph---------UDP-glucose -------- (C6H10O5)n+1
Glycogenolysis 1) Phosphorolysis; 2) hydrolysis
Phosphorolysis occurs in different tissues:
Phosphorylase
(C6H10O5)n ---------------------- (C6H10O5)n-1 + Gl-1-Ph
+H3PO4 ↓ Gl-6-ph-ase
oxidation←Gl-6-Ph----------glucose (in liver)
Hydrolysis of glycogen occurs in liver only:
γ-amylase
(C6H10O5)n ----------------------- (C6H10O5)n-1 + Glucose
+HOH
Anaerobic glycolysis and its energetic value
1) Glucose+ATPglucose-6-phosphate+ADP (glucokinase)
2) glucose-6-phosphate↔fructose-6-phosphate
3) fructose-6-phosphate+ATP fructose-1,6-diphosphate+ADP (fructokinase)
4) fructose-1,6-diphosphate↔phosphoglyceraldehyde(PGA)+ dioxyacetone phosphate (DOAP) (aldolase)
5) 2PGA+2NAD+2H3PO4↔2(1,3diphosphoglycerate)
6) 2(1,3diphosphoglycerate)+2ADP↔2ATP+2(3-phosphoglycerate) (substrate phosphorylation)
7) 2(3-phosphoglycerate) ↔ 2(2-phosphoglycerate)
8) 2(2-phosphoglycerate) ↔ 2(phosphoenolpyruvate)+2H2O (enolase)
9) 2(phosphoenolpyruvate) +2ADP2(pyruvic acid)+2ATP (pyruvate kinase)
10) 2(pyruvic acid) +2NADH2 ↔ 2 lactic acid +2NAD (lactate dehydrogenase)
Energetic value of anaerobic glycolysis:
If glycolysis beginns from glucose 2 ATP is used for formation of glucose-6-phosphate and fructose-1,6-diphosphate. Glycolysis gives 4 ATP, hence 2 ATP is remained. If glycolysis beginns from gl-6-Ph formed in glycogenolysis 1 ATP is used for formation of fructose-1,6-diphosphate, hence 3ATP is remained.
The importance of glycolysis:
glycolysis is a source of energy in some organs and tissues, e.g. in erythrocytes, lens, retina
this process is emergency pathway because it provides by energy in hypoxia and anoxia, e.g. in mountains, intoxication, anemia, diseases of heart, lungs, and vessels, hard work.
Some intermediates of glycolysis are used for synthetic processes, e.g. phosphotrioses, pyruvic acid, lactic acid cab be used on formation of glucose (gluconeogenesis), liponeogenesis and synthesis of unessential amino acids
