Final Q&A 80-119 Flashcards

1
Q
  1. Notion of “blood system”. Main blood functions.
A

———Notion of “blood system”
blood system – a repository blood (which excluded of the total blood flow in blood depots).
1- Peripheral blood located in vessels
2-Blood-forming organs – red bone marrow, spleen, lymph nodes
3-Hemoclastic organs – red bone marrow, spleen, lymph nodes, liver
4-neurohumoral regulation apparatus (mechanisms)
——–Main blood functions.
1. Transport ; of various substance necessary for vital activity of organs and tissuesО2, СО2 nutrients, hormones, proteins, electrolytes, enzymes
2- Respiratory – transport of О2 from the lungs to tissues and СО2 from tissues to lungs.
3-Nutritive – transport of basic nutrients from digestive organs to body tissues.
4-Excretory – transport of intermediate and final products of metabolism (urea, uric acid, ammonia .) and water excesses to organs of their excretion (kidneys, lungs, sweat glands, intestine).
5-Regulatory or humoral – delivery of the hormones, peptides, ions and other substances having regulatory effects on different target cells.
6-Thermoregulatory –blood transports heat from more heated bodies to less heated ones and to bodies of heat transfer, to maintaining its temperature constancy.
7-Protective – participation in immunity (implementing humoral specific and non-specific protection mechanisms) as well as blood coagulation and arrest of bleeding
8-homeostatic function, that is maintenance of internal medium constancy (acid-base balance, water-electrolytic balance and other types of exchange).
this is the main function of the blood

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2
Q
  1. Peripheral blood. Total amount of blood. Circulating blood volume and its calculating.
A

– Peripheral blood : is the one that is in blood vessels and depots. Its main parts: plasma and formed elements
-Formed elements :-1. Erythrocytes (red blood cells) = 4.5–5.51012 pieces/liter.
-2. Leukocytes = 4–9
109 /liter. -3. Platelets =
-plasma composition :
1. Water (90-92 %).
2. Inorganic compounds. For example, ions and their salts.
3.Organic compounds. For example, organic acids, proteins, etc.
——.Total amount of blood.:
The total amount of blood (circulating and deposited) in the body of an adult human is 6-8% of body weight
—–
the notion of circulating blood volume is used ( CBV ; mass of blood ). CBV is a hemodynamic indicator which represents the total volume of blood that is contained in functioning blood vessels. Сalculating of referenceСalculating of reference CBV: CBV = M*K
М – body weight (kg),
k – coefficient that is equal 70 for men and 60 for women.
CBV, despite its name, does not differentiate blood, which is located in the depot from those one which circulates in vessels, it’s a total blood

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3
Q
  1. Hematocrit. Serum and its clinical importance.
A

— hematocrit : its the relationship between plasma and formed elements , A hematocrit is the volume of blood that falls on the share of formed elements. It equals 40-45% and shows the amount of formed elements of the total mass of blood.

———Serum and its clinical importance. :
Blood, devoid of formed elements is called plasma. Plasma without fibrinogen is serum, the main clinical value of which is determined by the presence of antibodies in it.

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4
Q
  1. Values of a general blood test. Basic parameters of biochemical blood test.
A

—–general blood test ( common parameters )
Hematocrit = 40-45%
Erythrocytes (male) = 4.0-5.5·1012/l
Erythrocytes (female) = 3.7-4.9·1012/l
Leukocytes = 4.0-9.0·109/l
Platelets = 180-320·109/l
Hemoglobin, Hb (male) = 130-170 g/l
Hemoglobin, Hb (female) = 120-150 g/l
Erythrocyte sedimentation rate, ESR (male) = 1-10 mm/h
Erythrocyte sedimentation rate, ESR (female) = 2-15 mm/h

-----Basic parameters of biochemical blood tests
Water =900-920 g/l
Total protein Proteins in fractions:=65-85 g/l
1. Albumins=35-50 g/l
2. Globulins=20-30 g/l
– α1- globulins=1-3g/l
– α2- globulins=5-9g/l
– β- globulins=6-9g/l
– γ- globulins=8-13g/l
3. Fibrinogen=2-4g/l
Total  bilirubin =8.5-20.5 мkmol/L
VLDL = 0.2-1.5 mmol/L
LDL =<4.5 mmol/L
HDL=>1.0 mmol/L
Triglycerides (lipids)=0.45-2.5 mmol/L
Glucose =3.3-5.5 mmol/L
Sodium+=135-150 mmol/L
Potassium+=3.5-5.0 mmol/L
Free calcium2+=1.15-1.3 mmol/L
Magnesium2+=0.7-1.2 mmol/L
Chlorine–=95-110 mmol/L
Hydrogen сarbonate–=20-30 mmol/L
Protein anions–=15-20 mmol/L
Total calcium =2.25-2.75 mmol/L
Free (nonheme) iron=12-32 mcmol/l
Copper=11-24 mcmol/l
 Phosphorus=1-2 mmol/L
Ammonia=7-30 mcmol/l (up to 40 mcmol/l)
Residual nitrogen =14-28 mmol/L
Uric acid=0.15-0.5 mmol/L
Creatinine=40-110 mcmol/l
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5
Q
  1. Osmotic pressure, colloid-osmotic pressure. Iso-, hypo- and hypertonic solutions. Physiological solutions
A

——–Osmotic pressure
is the force with which a dissolved substance holds or attracts water , creates conditions for transmembrane transport of all other substances; nutrient substances , – inside cells, metabolism products – out, and formed mainly from ions
Osmotic pressure of blood of 7.3-7.6
its function :
1 water-salt metabolism in the body ensures implementation of all other substances exchange,
2 formation of membrane potentials and the course of excitable processes
3 homeostasis maintenance.
——-oncotic (colloid) pressure : formed by proteins (it is much lower – 1/200 of osmotic pressure). its 30 mm Hg
——–
-Isoosmotic solutions used in clinic are called physiological solutions. These are various solutions: 0.9% NaCl, Ringer’s solution, Ringer-Lock’s solution, Tyrode’s solution etc.
-hypotonic solutions :Solutions having a lower osmotic pressure than that of plasma ,They cause an increase in cells size. This is a result of water passage from a solution into a cell
-hypertonic solutions : Solutions having high osmotic pressure

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6
Q
  1. Specific functions of electrolytes.
A
  • Sodium (Nа+). Its content is more than any others, that is why it creates osmotic pressure.
  • Potassium (К+), Magnesium (Мg2+). As well as Са2+, these two ions are not of decisive importance in regulation of plasma osmotic pressure, as their concentration is low. Unlike Са2+ and Nа+ increase of К+ and Мg2+ decrease excitability, causing hyperpolarization of the membrane.
  • Hydrocarbonate anion (НСО3–). Its specific function is participation in blood pH regulation. An increase in the content of this ion causes alkalosis of blood, increasing of pH. Lack of НСО3– – leads to acidosis
  • Chlorine (Сl–). Chlorine is the most indifferent ion for the organism. Cl– concentration is a non-rigid constant, its content can verify widely without significant effect on vital functions. Therefore, changing Сl– contents turns out to be a “goodly” mechanism for maintaining electroneutrality of plasma (see Gamble rule
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7
Q
  1. Blood total calcium, hyper- and hypocalcemia
A

—-normal content of Са2+ in plasma is not too large, that is why even small changes in its concentration can significantly affect these functions. And expressed change in concentration of this ion (less than 1.15 and more than 3.27 mmol/L) can be life-threatening. An organism “will agree” to any regulatory changes to maintain the concentration of Са2+ in the homeostatic ranges. The main depot of Са2+ in a body is the skeletal system

----- hypercalcemia :
effects on 
1-CNS : irritablity and anxiety , paresthesia's ,seizures , laryngospasm ,bronchospasm 
2-CVS : heart failure
3-MSK: Muscles cramps 
----- hypocalcemia :
effects on 
1-CNS :decreases ability to concentrate , increased sleep requirement 
2-CVS : arrhythmias , bradycardia 
3-MSK: Muscles weakness
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8
Q
  1. Hydrocarbonate anion and its role in blood pH regulation.
A

Hydrocarbonate anion (НСО3–). Its specific function is participation in blood pH regulation. An increase in the content of this ion causes alkalosis of blood, increasing of pH. Lack of НСО3– – leads to acidosis.

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9
Q
  1. Gamble rule and its clinical relevance.
A
  • Gamble rule. Plasma is always electrically neutral, the total charge of cations and anions is equal to 0.
  • Plasma electrical neutrality is a rigid constant of homeostasis, only in this case it is possible to maintain normal water-salt balance. This fact has an important clinical relevance.
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10
Q
  1. Blood pH and its regulation (three main organism’s systems). Acidosis and alkalosis
A
- the three main mechanasim is 
1 - homeostasis or chemical buffer 
2- lung 
3- kidney 
------------ Acidosis and alkalosis
In the norm blood рН = 7.35-7.47. More often an average value is named – 7.37. рН of venous blood is 0.02 lower than that of arterial blood. Acidosis – рН is lower than 7.35. Alkalosis – рН is more than 7.47. Acidosis and alkalosis are an immediate risk of loss of life. And рН equal to 6.8 and 7.8 is fatal.
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11
Q
  1. Types of blood proteins and their common functions. Oncotic blood pressure.
A

—— Proteins make 65-85 g/l (6-8 %). They are presented by
albumins (35-50 g/l or 3-5 %)
– α1- globulins
– α2- globulins
– β- globulins
– γ- globulins
globulins (20-30 g/l or 2‑3 %)
fibrinogen (2-4 g/l or 0,2-0,4 %).
Blood plasma proteins perform a variety of functions:
1) ensure oncotic pressure;
2) regulate water homeostasis;
3) perform a nutritional function;
4) take part in transport of numerous substances;
5) ensure immune homeostasis;
6) determine blood viscosity and coagulation;
7) maintain acid-base balance (protein buffer).
———-Oncotic blood pressure. :
Oncotic blood pressure – part of osmotic pressure created by plasma proteins. Its value is 25-30 mm Hg , brought about mainly by albumins. Albumins possess a small size, therefore, a large surface area; they are able to attract intensively water. Oncotic pressure plays an important role in regulating water distribution between plasma and tissues.

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12
Q
  1. Blood proteins specific functions.
A

—— they are 3
albumins
globulins
fibrinogen

-1- Albumins : low molecular weight proteins of small size, they make about a half of all plasma proteins Lat. albumen – protein . As they are numerous
and this protein on 80% defines plasma oncotic pressure.
Albumins are synthesized in the liver.

-2-(Lat. globulus – ball) – are larger than albumins. Their several fractions are distinguished: alpha ‑, beta- and gamma-globulins
they are formed in the liver, bone marrow, spleen and lymph nodes
function : . A specific function of globulins is transport. Globulin molecules on their surface have active centers with the help of which biochemical or electrostatic bond with substances that are transported is carried out.

α-globulins transport hormones, vitamins, minerals, lipids. For example, a variant of alpha-globulin, binding glucose, is called glycoproteids. About 60% of all plasma glucose circulates in the composition of glycoproteids

β-globulins are involved in transport of phospholipids, cholesterol, steroid hormones, cations of metals. For example, transferrin serves as an agent of copper and iron for the synthesis of red blood cells.

γ-globulins are known as antibodies or immunoglobulins which have five classes: JgA, JgG, JgM, JgD, JgE. They are able to bind with foreign proteins, membrane structures of pathological microorganisms,

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13
Q
  1. Erythrocytes. Hemoglobin. Its physiological and pathological compounds.
A

—- Erythrocytes :
-Erythrocytes (red blood cells) are the most numerous formed elements of blood. The blood of males normally contains it is non-rigid homeostatic constant.
-Human erythrocytes are devoid of nucleus their cytoplasm is filled with hemoglobin They have predominantly the form of a bi-concave disk Erythrocytes of this form are called normocytes
- A special form of erythrocytes results in increase in its surface that improves its basic function – respiratory function.
—– Hemoglobin. :
Hemoglobin (Hb) is a special protein that performs
1) respiratory function and 2) maintains blood pH
In men blood contains in average 130-170 g/l in women – 120 -150 g/l.
—— Its physiological and pathological compounds.
– physiological :
1 - oxyhemoglobin (НbО2). = is transport of oxygen and carbon dioxide.
Hemoglobin which bound О2,
- deoxyhemoglobin or reduced hemoglobin (H+Нb). = Hemoglobin which gave away О2
3- carbhemoglobin (НbCО2). = Hemoglobin, coupled with СО2 Connection of hemoglobin with СО2 takes place in capillaries of body tissues. This connection is unstable as well. In the form of this compound 20% of CO2 is transported.
4- myoglobin = located In skeletal and cardiac muscle and its muscle hemoglobin , It plays an important role in supplying oxygen to the working muscles; it can be seen as a depot of O2 in muscles.
5-6 - In a fetus mainly (80%) fetal hemoglobin (HbF) is contained. It has a higher ability to bind oxygen, it has greater affinity to О2 and it gives it away harder. After birth HbF is almost completely replaced by adult hemoglobin (HbA). In erythrocytes of an adult HbA makes 95-98%.
-Pathological:
1)CarboxyHb - HbCO
2) MethaHb -MtHb

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14
Q
  1. Carboxyhaemoglobin. First aid after carbon monoxide poisoning. Methaemoglobin.
A

—— carboxyhaemoglobin. its path logical compound of hemoglobin
Normally it does not exist, because there is no CO in atmosphere. HbCO is a stabile compound ,
–Hemoglobin is blocked in it by carbon monoxide and is not capable of transferring oxygen. The affinity of hemoglobin to carbon monoxide is higher than its affinity to oxygen and carbon dioxide, so even a small amount of carbon monoxide in the air is dangerous for life. At this not concentration of carbon monoxide but duration
Even extremely low levels of CO in the air, but with prolonged inhalation of it, such as during sleep, can be lethal.

Carbon monoxide poisoning very often arise in drivers at their long stay in a closed garage with an working car engine. Another common source of CO are woody smoke and fumes
feature of Carbon monoxide poisoning
A feature of carbon monoxide is that it has no smell, so poisoning develops without being noticed. Often the victim is understand of his poisoning, when myorelaxing action (relaxation of skeletal muscles) of CO is manifested

– First Aid
The victim must be taken to “fresh air”. But this is not enough , you can using an oxygenous pillow If it is not available – make artificial ventilation «mouth-to-mouth». At this air will be forced into the victim’s lungs under higher pressure. The partial
pressure of О2 in such air turns out to be larger than normal,
. Due to this some CO get out from compound with hemoglobin. Later, the victim should be taken to the hospital.

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15
Q
  1. Color indicator. Hemolysis and its types.
A

——- Color indicator
-The content of hemoglobin in erythrocytes is judged by the colour indicator (CI)
the formula : CI = Hb * 3 / first three figures of Er amount
CI – colour indicator;
Hb – amount of hemoglobin, g/l;
Er – amount of erythrocytes (first three figures).
For example, in norm Hb=166g/l, and Er=5∙1012 /l. Then
CI = 166 * 3 / 510 = 0.98,
In norm CI = 0.75-1.0 or more. Such erythrocytes are - normochromatic erythrocytes.
If CI is less than 0.7, these erythrocytes are - hypochromatic erythrocytes.
When CI is more than 1.1, they speak about - hyperchromatic erythrocytes.

—— Hemolysis and its types.
- Hemolysis : its destruction of the erythrocytes membrane and hemoglobin going out to the blood plasma,At this plasma turns red and becomes transparent “laky blood”.
-types :
1-Osmotic hemolysis:Osmotic hemolysis is possible only in laboratory , as in a whole organism blood under no circumstances can reach such a low hypotonicity

2-Biological hemolysis:It occurs when some substances of animal and vegetable origin (bites of snakes, insects, mushroom poisoning) enter the blood stream.

3-Chemical hemolysis:may be caused by chloroform, ether, solutions of acids and alkali,

4-Temperature (or thermal hemolysis) :occurs at blood freezing/unfreezing as a result of erythrocytes membrane destruction by ice crystals.

5-Mechanical hemolysis : occurs at strong mechanical impacts on blood, for example, while shaking the ampoule with blood,

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16
Q
  1. Erythrocyte sedimentation rate. Suspension stability of blood and its mechanism. Laboratory clinical importance of its determination.
A
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17
Q
  1. General information on digestion. Nutrients groups, their examples.
A

—- Digestion is the process during which food physicaly changes and particularly enzymaticallybreaks down to its elementary constituents (monomers) and is absorbed
——–Nutrients groups, their examples.
1- proteins :
- in the polymer :polypeptides
- in the Oligomer : Peptides
- in the Monomer : Amino acids
2- Fat :
- in the polymer :Triglycerides
- in the Oligomer : -
- in the Monomer : Glycerol and fatty acids
3-Carbohydrate :
- in the polymer :Starch, cellulose, etc.
- in the Oligomer : Sucrose, maltose, etc.
- in the Monomer : Glucose, fructose

18
Q
  1. The concept of digestion enzyme, its difference from hormone. Examples.
A
  • —- - An enzyme is a biological catalyst, connecting with a molecule of another substance with a view to its rendering into an active state.
  • Enzymes are secreted very diverse (not necessarily secretory) cells.
  • Enzymes of the digestive system are secreted into the cavity of this system. As the cavity of the digestive system opens into the external environment (by its oral and anal orifices), enzymes are excreted out. Therefore, glands of the digestive system are called exocrine glands. The enzymes of the digestive system are substances causing breaking down food polymers to monomers (which means to such active state that they can be absorbed).
  • —its difference from hormone. Examples.
  • Enzyme : enzyme is a biological catalyst and is almost always a protein. It speeds up the rate of a specific chemical reaction in the cell. EX; Lipases
  • hormones’ : Hormones are chemical substances that act like messenger molecules in the body. After being made in one part of the body, they travel to other parts of the body Ex: (insulin) formed in the pancreas
19
Q
  1. Some main types of digestion. Parietal digestion, its advantages..
A

-1-Autolytic digestion.
-2-Intracellular digestion.
-3-Cavitary digestion.
-4-Parietal digestion : Parietal digestion is carried out by enzymes fixed on intestinal microvilli
—–Advantage of Parietal digestion
1- Economy of enzymes.
2-. High intensity of breakdown.
3- High intensity of absorption
4- . Bactericidal property.

20
Q
  1. Digestion in the oral cavity.
A
  • Composition of saliva
    -1- Water – more than 99%.
    -2- Dry residue which is divide into :
    1- Inorganic substances : ions, bases (mainly hydrocarbonates)
    2- Organic compounds : mainly enzymes
    —– Key enzymes in saliva :
    1- amylase : Amylase breaks down polymers of sugars to disaccharides – maltose and sucrose.
    2- maltase : Maltase breaks down maltose to glucose.
    —-
  • The quantity of saliva is up to 2.0 liters per 24 hours, salivary pH is weakly alkaline which is betwenen 6.2-7.6 PH
    -As food in the mouth stays a few tens of seconds, digestion under the action of salivary enzymes occurs mainly in the stomach.
21
Q
  1. Gastric glands, composition of gastric juice and its enzymes functions.
A

——Gastric glands
- we have 4 types of cells in the stomach
1-Mucocytes (mucoid cells). They secrete mucous especially abundant in the pyloric part
2-Parietal glandulocytes (oxyntic cells). They form HCl and are located everywhere except the pyloric part
3-(chief) glandulocytes (principal cells). They form pepsin and are mainly located in the fundus of the stomach.
4-G-cells – endocryne cells. They produce gastrin.
——composition of gastric juice and its enzymes functions. :
- The quantity of gastric juice is up to 2,0 liters per 24 hours.
its composed of 4 substance
1- water
2-HCL
3-Mucus
4-Enzymes :
4.1-Pepsin, its inactive form – pepsinogen;&raquo_space; For proteins
4.2-Gastricsin, a variety of pepsin; For proteins
4.3-Chemosin (rennin) For proteins
4.4-Gelatinase; for conjunctive tissue
4.5-Lipase for fat

22
Q
  1. Significance of HCI.
A
  • Gastric juice is the most acidic body medium about 1-2 PH
    – function of HCL :
    1- It denaturants proteins., Denaturation is a protein’s loss of its :
  • quaternary
  • tertiary
  • and secondary structure.
    At this amino acid sequences in a protein do not change. The protein does not lose its polymeric structure, therefore denaturation is not breakdown
    2-. It creates an acidic medium and activates pepsinogen :
    Pepsin is secreted in an inactive form of pepsinogen in order not to break down stomach own mucosa in absence of food
    Activation of pepsinogen occurs under the action of hydrochloric acid. pH of HCl – 1.0, gastric pH is – 1.5 – 2.0, pH of gastric contents is 2.0 and more.
    3- It has a bactericidal action.
    4-It performs regulatory functions : its creates optimal acidic environment for the help the pepsin work properly
23
Q
  1. Gastric functions (major and minor).
A

-. The function of the stomach can be divided into
1- major function:
1.1 Deposition of food.
1.2 Forming a food bolus – chymus.
1.3 Food portioning.
1.4 Primary break downing of nutrients, mainly proteins.
1.5 Regulatory function.

2- minor function:

  1. 1 Digestion.
  2. 2 Absorption.
  3. 3 Hematopoietic.
  4. 4 Regulation of blood pH.
24
Q
  1. Composition of pancreatic juice, its enzymes and their functions. usefulness
A
  1. Organic compounds – the most significant of which are enzymes.
  2. Inorganic substances – ions, bases (mainly hydrocarbonates).
  3. Water
    - - The quantity of pancreatic juice is up to 2.0 liters per 24 hours; its pH is 7.8-8.4. That means that pancreatic juice medium is alkaline, it is the most alkaline fluid in the body.
    - —- Enzyme :
  4. Proteases.
    - Trypsin and its inactive form trypsinogen.
    - Chymotrypsin and chemotrypsinogen.
    - Carboxypeptidases, elastases, phospholipases and their inactive forms procarboxypeptidases, proelastases, prophospholipases.
    - Nucleases, ribonucleases and others.
    - Enterokinase.
  5. Lipases.
  6. Amylase, maltase.
    - - In the absence of food most proteases are secreted in an inactive form to prevent self-digestion of intestinal mucosa
    - - At food a particularly large quantity of enterokinase secretes, which triggers a chain of proteases’ activation:
    - enterokinaze → trypsinogen → trypsin → chemotrypsinogen → chymotrypsin → other proteases → carboxypeptidase, elastase, phospholipase.
    - –Basic pancreatic proteases are trypsin and chymotrypsin, which break down internal peptide linkages
    - Lipases break down fats.
    - Amylase and maltase break down carbohydrates. Amylase of the pancreas is much more active than salivary amylase and is called α-amylase. It can break down polysaccharides not only into disaccharide but even into monosaccharides
    - -NB!-Enzymes on fats and on carbohydrates are secreted directly in their active form because even in the absence of food they cannot damage the mucosa.
25
Q
  1. Functions of the bile.
A
  1. It emulsifies fats.
    -Emulsification is passage of fat into a state of microscopic droplets Thus the surface area dramatically increases, thus increasing the contact area with the lipases and speed of fat breakdown.
    -But emulsification is not breaking down; during emulsification fat does not lose its polymeric structure of triglycerides.
  2. It neutralizes acidic gastric juice reaction. Pancreatic enzymes are active only in an alkaline medium.
  3. It dissolves fat hydrolysis products.
  4. It promotes their absorption.
  5. It activates enzyme of the pancreas and the intestines.
    Not only enterokinase but the bile as well activates pancreatic enzymes.
  6. It stimulates motor and secretory activity of the intestines.
  7. It activates bile-forming (choleresis) and bile secretion (cholekinesis).
  8. It has a bacteriostatic effect
  9. It facilitates absorption of fat-soluble vitamins.
26
Q
  1. Digestion in the small intestine and the large intestine. Classification of colonic microflora, usefulness of symbiotic one.
A

— -small intestine : food enters the small intestine, which length is up to 5 m. Digestion in the small intestine does not fundamentally differ from that in the duodenum. Everything is digested. That is why we do not discuss it in detail.
-large intestine: The final part of the digestive tract is the colon. Only 5% of digestion takes place in the large intestine. Here mainly water absorption takes place. Complete breaking down of food is due to enzymes which passed with the chymus from previous digestive parts. Here food left-over contains a large number of toxic products which have not undergone absorption in the upper intestine
—-Classification of colonic microflora,
1- Symbiontic:
1.1Lactic,
1.2bifidum bacteria,
1.3 bacteroids
-Symbiosis is a mutually beneficial coexistence, close collaboration, joint vital activity of two different species of living creatures.
2-Potentially pathogenic:
2.1 Escherichia coli,
2.2 streptococci,
2.3 staphylococci,
2.4 sporeforming anaerobes
—-usefulness of symbiotic one.
1- It suppresses potentially pathogenic microflora
2-It immunizes the microorganism
3-It digests cellulose
4-It produces vitamin K

27
Q
  1. Theories of hunger and thirst. Neural and humoral mechanisms of their both formations. True thirst hunger and false thirst and hunger
A

—— humoral and neural
-Hunger describes those sensations that promote attainment of minimal energy needs while thirst represents sensations that promote attainment of minimal hydration needs
– we can describes what if the body rich in energy or poor in energy or full only by looking at the hormon
level in the body bcs these hormons will send a signal to the part in the brain that’s reasonable for detramaining that we are hungry or not which is the ( hypothalamus )
—-there is 3 hormones’ will be produced to control the hunger and thirst.
- glucose :
1- in rich of energy body the will release a hormon that called insulin
for storing the rich amount of the glucose and block the receptor of the hypothalamus therefor inhibiting the body of taking more energy bcs is already rich in energy
2- in the poor of energy body the insulin will not be produced , so there is nothing will block the receptor of the hypothalamus and inhibit the hunger
-lipids
1-in rich of energy body the will release a hormon that called leptin
for storing the rich amount of the glucose and block the receptor of the hypothalamus therefor inhibiting the body of taking more energy bcs is already rich in energy
2-in the poor of energy body the leptin will not be produced , so there is nothing will block the receptor of the hypothalamus and inhibit the hunger
-Ghrelin (stomach hormon or hunger hormon )
1- its only produced with small amounts in stomach when the stomach is empty
to send a signal to the hypothalamus that’s the body poor in energy

28
Q
  1. Blood groups. ABO-system. Method of blood groups determination.
A

—Blood - system
-according only 2 types of major agglutinogens there are 2 classification if blood exist
-ABO blood groups - Rhesus (RH) blood groups
- this system includes 2 types of antigens A and B which called agglutinogens
- according to the presence of A and B antigen on the membrane of erythrocytes there are 4 groups of human blood exist
1- Group A ( about 41% of people) only type A antigen is present
2- group B ( about 9% of people) only type B antigen is present
3- group AB ( about 3% of people) both A and B antigen are present
4 - group O ( about 47 % of people) both A and B are absent .
—-ABO-system
- agglutinins it’s antibodies that located in the plasma of erythrocytes, these antibodies are antagonists to the red cells agglutinogens
- there are 2 types of agglutinins
1- Anti-A ( or alpha ) agglutinins
2- Anti-B ( or beta ) agglutinins
—-Method of blood groups determination.:
-chemicals :

29
Q
  1. Agglutination. The rules of blood transfusion.
A

—Agglutination.
- agglutinogens are specific kind of antigens which are located on the membrane of RBC And according to which blood group exist .
-according only 2 types of major agglutinogens there are 2 classification if blood exist
-ABO blood groups
- Rhesus (RH) blood groups
- this system includes 2 types of antigens A and B which called agglutinogens
- according to the presence of A and B antigen on the membrane of erythrocytes there are 4 groups of human blood exist
1- Group A ( about 41% of people) only type A antigen is present
2- group B ( about 9% of people) only type B antigen is present
3- group AB ( about 3% of people) both
A and B antigen are present
4 - group O ( about 47 % of people) both A and B are absent .
—-The rules of blood transfusion.
-Rules
- for transfusion if self-titled blood group we should follow these statements
1- donor blood should be same named group with that of recipient
2- the Hb content of donor blood must be not less then 90%
3- the donor blood should be free from diseases
4-donor blood should be fresh not frozen
5- pretransfusion test must be done
— indications for transfusion such as :
1- blood diseases such as leukaemia
2- poisoning , by carbon monoxied , snakes poisons
3- shocks
–Pretransfusion test :
- for safe blood transfusion , the following tests must be done
1- blood typing : the test which making with standard serum to determine the group of blood which are going to transfuse
2- crossmatching : it is the way which health care provider tests the patients blood against a donor blood ,to make sure that fully compatible
- to do this test , the donor red blood cells are combined with recipient blood serum
3- biological test : transfusion of 10ml of donor blood looking for no reaction of recipient, before transfused the whole blood volume

30
Q
  1. Landsteiner’s rule. Ottenberg’s principles.
A

– -Landstenier found that there some special substances in the blood
- agglutinogens ( antigen )And -agglutinins ( antibody )
He took a note of this substances may induce clumping of red blood cells when red cells of another blood are added
- individual forms immune antibodies to blood group antigen he do not possess
- precisely , substances present on the membrane of erythrocytes are similar to blood group antigen, as well as the constant production to plasma of antibodies to blood group antigen they do not possess are realises
-By simple way :
One blood group must not have self-titled agglutinins and agglutinogens
—-Ottenberg’s principles.
- we can transfer different- titled blood group during in emergency situations only ( outside the condition of an inpatient clinic ) by ottenberg principal:
— according to this principle
1- Donor O blood group is compatible for recipient O and all other blood groups
2-Donor gr A it’s compatible for recipient gr A and gr AB
3- Donor gr B ots compatible for recipient gr B and AB
4 - for recipient gr AB its compatible donor may be with any blood group
— generally blood transfusion should not be more then 0,5 L in any case it’s can’t be transfused more then 0,5 L of donor

31
Q
  1. Hazards of blood transfusion and their symptoms.
A

–Hazard blood types are 4 types :
1- reaction due to different-tilted blood transfusion
2- reaction due to massive blood transfusion
3- reaction due faulty technics during blood transfusion
4- transmission of infection
–symptoms:
- different-tilted blood transfusion leads to agglutination of the following donor red blood cells followed by their hemolysis and results to following things :
1- sever pain elsewhere in the body (mainly in chest )
2- hemolytic jaundice ( its genetic disorder of the red blood cell membrane)
3- dyspnea ( shortness of breath)
4- fever
5- hypotension

32
Q
  1. Rh-system. Haemolytic Disease of the New Borns and another reasons of Rh-conflict
A

— Rh-system. :
this system of agglutinogens firstly present in the red blood cells of Rhesus monkeys and also in human red blood cells
- there is 40 antigen and along with C- , D- and E- antigen
- antigen D has the strongest antigenic effect so if D-antigen is present so the RH factor is positive (+)
- is D antigen is absent then Rh factor is negative (-)
— during the blood transfusion to the Rh-factor there may be 3 cases possible
1- of the donor has positive RH then it can only transferred to a positive recipient Rh factor
2- if the donor has Rh negative ( no Rh factor ) so it can be transferred to Rh negative recipient
3- if the donor has negative RH it can be transferred to a positive Rh recipient
—Haemolytic Disease of the New Borns
Rh- incompatibility may cause Erythroblastosis fetalis (HDN)
- if Rh- lady marry Rh+ man , baby may have Rh+ fetal RBC the first pregnancy will pass normally because the blood of the mother and the baby will not mix , however during Childbearing the Rh+ of the fetus will will got into the mother blood , and antibody against them will develop in her organism , during the next pregnancy the antibody will enter through the placentae of fetal and cues death ,
- for preventing this disease the health provider should give the mother Anti-Rh antibody called Anti-Rh gamma globuin
— another reasons of Rh-conflict :
If a Rh negative individual receives blood from a Rh positive person.

33
Q
  1. Hemostasis. Thrombocytic clotting, its mechanism and steps.
A

— Hemostasis
The physiological process of stopping blood from flowing out of blood vessels by changing blood from a liquid to a gel, forming a blood clot.
— Thrombocytic clotting its mechanism and steps.
Thrombocytic clotting realizes due to platelet factors which are contained in thrombocytes (platelets).
- the main platelet factors:
-thromboplastin (No3)
-antiheparin(No4)
-fibrinogen(No5)
-thrombostenin(No6)
-serotonin(No10)
-factor of thrombocytic aggregation (No11)
–Stages:
1 - Vasospasm is constriction of vessels that causes decrease in blood flow to the injured area. Happens due to factor no. 10 - Serotonin.
Note: even vasospasm may stop bleeding that’s mean some time no need to go through all the steps

2- platelet adhesion
Happens due to factor no. 3( thromboplastin) and 4 ( antiheparin)
in the endothelium. Factor 3 has three active biochemical centers.
Two of them bind to sub-endothelian collagen fibers due to Willibrant factor.
This lasts 3-10 sec. After this occurs platelets activation.
- platelet activation
Happens in presence of factor no. 5 – Thrombocytic fibrinogen
Activation of platelet is associated with the appearance of high concentration of ADP from ATP.
ADP is released from active platelets, as well as from damaged endothelium, which induces the next phase – aggregation.

3- platelet aggregation (platelet plug formation)
Happens in presence of factor no. 11 – Platelet aggregation factor.
It begins almost simultaneously with adhesion and consists of twisting the platelets and adhering them to the site of damage.

4-retraction of a platelet thrombus
Happens in presence of factor no.6 – Thrombostenin. Retraction is the compaction and fastening of a blood clot on a damaged vessel.
It is carried out under the influence of thrombostenin of platelets, due to the active reduction of their actin-myosin complex. Results of platelet coagulation is formation of platelet thromb. It is not strongly fixed on vessel, so it may be flown away. Since, the thromb flows away plasmic coagulation is followed
.

34
Q
  1. Plasmic coagulation, its phases and a scheme. Plasmic coagulation factors.
A

—Plasmic coagulation:
It helps to stop bleeding from high pressure vessels (arteries).
—its phases and a scheme. :
»> Draw the scheme
-There are 3 main phases of plasmic coagulation, but 2 more supplementary (pre- and post-) phases are also exist.
- / PRE-PHASE
1. The formation of prothrombinase.
2. The formation of thrombin.
3. The formation of fibrin.
- / POST–PHASE
—Plasmic coagulation factors. :
I – Fibrinogen
II – Prothrombin
III – Thromboplastin (tissue factor)
IV – Ca2+
V – Proaccelerin (labile factor),
VI – Accelerin (active factor)
VII – Proconverting (stable factor)
VIII – Antihaemophilic globulin A
IX – Antihaemophilic globulin B (Christmas factor)
X – Autothrombin (Stuart prower factor)
XI – Antihaemophilic globulin C
XII – Hageman factor (glass factor, contact factor)
XIII – Fibrinase (Fibrin stabilizing factor, Laki-Lorand factor)
XIV– Prekallikerin (Fletcher factor)

35
Q
  1. The formation of prothrombinase, thrombin, fibrin. Fibrinolysis.
A

— The formation of prothrombinase :
-During this phase the active enzyme complex, prothrombinase is formed, which will further activate prothrombin.
It proceeds by two pathways:
-1-EXTERNAL
-2- INTERNAL
The formation of prothrombinase is only possible by both of the pathway went to the utmost
1- INTERNAL pathway
Factor XII (hageman factor, contact factor ) is typically activated. It is called as “contact” because, it works only when a physical external influence (e.g. injury) happens.
Factor XII sets off a series of cascade proteins activation reactions that in turn activates factor XI(Antihaemophilic globulin C)
then factor IX( Antihaemophilic globulin B (Christmas factor) )
and then X (Autothrombin (Stuart prower factor)
2- EXTERNAL pathway
It is initiated by tissue damage.
Then factor III is released from the membrane of damaged cells of the vessel and surrounding tissues.
Factor III (tissue factor) goes on to activate factor VII.( Proconverting (stable factor))
- Finally, factor VIII (Antihaemophilic globulin A)
combines with factor IX( Antihaemophilic globulin B (Christmas factor) ) to form an enzyme complex
that activates factor X, ( Autothrombin (Stuart prower factor) leading to the common pathway.
- Factor VII Proconverting (stable factor) a goes on to activate factor X into factor Xa.
-Xa further forms as prothrombinase

—thrombin :
- The appearance of prothrombinase results into the starting of the next phase of coagulation – the formation of thrombin from prothrombin in the presence of calcium ions (Ca2+).
- If prothrombinase is formed, organism “understands” that the vessel has been damaged. Therefore, the subsequent phases proceed quickly.
- Thrombin formation process lasts 2-5 s.
— fibrin :
-In the third phase – the formation of fibrin from fibrinogen. Initially, soluble fibrin monomer is formed under the influence of thrombin. Thrombin also activates the fibrin-stabilizing factor (XIII). Then, with the participation of calcium ions, a soluble fibrin polymer is formed, which is then converted by the fibrin-stabilizing factor into an insoluble fibrin polymer. In such a fibrin network, blood cells, in particular erythrocytes, settle and a red blood clot forms, which clots the wound
—Fibrinolysis.( post phase ) :
- Includes the processes of fibrinolysis and vessels recanalization.
Cause the normal condition of vessel is its passability of blood the thromb finally must be removed. This realises by process of restoration of damaged vessel by lysis of fibrin. It is lengthy process which lasts for somewhere 10 days or more.
-They may call this process as the post-phase but need to understand that it is not a process of coagulation. Coagulation finishes by appearance of secondary fibrin thromb.

36
Q
  1. Exogenic factors of blood coagulation increasing and decreasing.
A

— increasing :
1. Vitamin K: with the presence of vitamin K only majority of plasmic factors are synthesised in liver. Vitamin K containing drugs increases plasmic factor synthesis. And the result is increased coagulation
2. Calcium: calcium is one of the plasmic factor (IV).
Calcium is widely contained in many drugs. Applying them, you should always take into account its great (!!!) influence on increasing of blood coagulation and a risk of thrombosis
3.Hypoxia, hypercapnia, acidosis and temperature increase:
all this processes and changes realize during physical stress, and any physical stress is a risk of vessels damage.

  • – decreasing :
    1. Heparin and Plasmin: strong anticoagulant drugs.
    2. Antibiotics: increases danger of microcirculatory haemorrhage.
    3. Aspirin: also increases danger of microcirculatory haemorrhage.
    4. Hirudin : obtained from leechs.
    5. Decrease in temperature: because of less activity of enzymes.
    6. Alkalosis: the same reason.
37
Q
  1. Urine content. Features of the structure and blood supply of a nephron
A

—————Urine content
- Urine is liquid by-product of metabolism produced by kidneys
- its primarily consist of water (91-96% ) with a lot of different
- non organic
- organic Components
—Organic components of Urine ? g/L
-Urea :25-30
-Uric acid : 0.5 - 0.8
-Creatinine :1.0 - 1.5
-orgainc sulphate
- Amino acid - trace amount
- Urobilinogen
-Nitrogen : 0.3 -1.2
—non-Organic components of Urine ? g/L
-Chloride 10-15
-Sulphate 1-2
- Calcium 0.1 - 0.3
-Sodium 3-5
- Potassium 0,8 -1.3
-inorgainc phosphate 0.8-1.3
- Ammonia 0,7-0,8
——–Features of the structure and blood supply of a nephron
—Types of Nephrons And there function :
1-Cortical
- they comprise 85-86 % of the nephrons in the kidneys
- its plays a major role in excretion of waste products in dissolved form in the urine
2- Juxta-medullary
- they comprise 14-15% of the nephrons in the kidney
-not take a part in urine formation and play a major role in regulatory mechanism of blood pressure changes
—parts of Nephron:
1-Malphigian corpuscle , Glomerulus , bowmans cup
2- Proximal convulated Tubule (PCT)
3-loop of henle
4-Distal comvulated tubule ( DCT )
— collecting duct ( not part of the nephron )
—blood supply of a nephron :
-artery :
1-interlubular artery - afferent arteriole
- Vine :
1-interlubular vine - venule

38
Q
  1. The theory of urine formation. Glomerular filtration.
A
  • — - Glomerular filtration is the passive transport of plasma with its dissolved small solutes from glomerular capillaries into Bowmans capsule and further to proximal convulated tubule
  • the resultant is fluid is known as glomerular filtrate or ultra filtrate or primary urine

-this process of filtration occurs in Malpighian corpuscle
Bowman capsule and glomerular together constitute the malphigian corpuscle

-1- Bowman’s capsule
- its the initial dilated part of nephron
- its forms the filtration membrane
- it has two layers : visceral and parietal
— the space between visceral and parietal layer is called bowmen space , here the glomerular filtrate enter and continues into PCT

-2- Glomerulus
: its formed by invagination of a tuft of capillaries into the bowmans capsule, it has an extremely thin membrane and is made up of 3 layers
-layer 1 : padocytes cells , Visceral Epithelium covering the capillaries, its not continuous, its gives series of process called pedicels interdigiting upon capillary surface to form : filtration slits ( lacuna ) along the capillary wall
-layer 2 : besment membrane
-layer 3 : endothelial cells , the endothelial layer of glomerular capillaries is fenestrated with pores of 100 nm , ( this feature allow the plasma filtration with retention of plasma protein and blood cells

——What are the forces that causing Filtration ?
1- glomerular hydrostatic pressure: its constitute. Filtration force driving fluid out of the glomerular capillaries and into bowmans capsule

2- Ultrafiltrate hydrostatic pressure: hydrostatic pressure of ultrafiltrate in the bowmans capsule , it opposes filtration

3- glomerular oncotic pressure: colloidal osmotic pressure of the plasma in the glomerular capillaries bringing fluid into glomerular capillaries

—- Formula :
- Filtrate pressure (pf) = glomerular hydrostatic pressure (P h/g) — Ultrafiltrate hydrostatic pressure ( P h/u ) — glomerular oncotic pressure ( P onc. )

  • Pf = P h/g — P h/u — P onc

If we put norm values of these
Pf = 70-20-30= 20 mmhg

39
Q
  1. The theory of urine formation. Reabsorption in kidneys.
A
  • Reabsorption : means the transport of solutes and water from tubular lumen into peritubular capillaries.
  • kidney uses active and passive kinds of transport for the process of reabsorption

1- Passive transport : in the passive transport substances move across the cell membrane without any energy expenditure by the cell due to some gradience presence , and these gradience is :
1- Diffusion : is a passive process by which molecules move from areas of high concentration to area of low contraction
- and it consist of 2 types :

1- simple diffusion : is movement if substance from region of higher concentration to region of lower concentration, ions utilize ionic channels to cross the cell membrane, some channels are continuously open while other are gates Ex/ diffusion mechanism is available for sodium ion to pass through the tight junction of PCT cells in association with chloride ions
2- Facilitated diffusion : it is a carrier mediated process that enables molecules that are too large to flow though membrane channels by simple diffusion, facilitated diffusion of glucose

2-Osmosis : flow of solvent water across a selectivity permeable membrane from a region of lower solute concentration to higher solute concentration, by this water follows the sodium ions

3- filtration : it occurs due to the presence of hydrostatic gradient , the pressure of the primary urine is slightly higher than that one of blood in capillaries of PCT

4- Electrostatic diffusion : cations attract to negatively charged ions and vice versa

—2 Active transport: in active transport substance are transported against their chemical and electrical gradient , this form of transport requires energy in form of ATP
- active transport consist of 2 types
1- Primary active transport: they directly use energy obtained from hydrolysis of ATP , Ex sodium- potassium pump

2- secondary active transport: secondary active transport uses the energy stored by primary active transport to drive across the membrane some other substance
- sodium ion is transporting by primary active transport, but its transposing in sodium- potassium pump is able only in the situation of its connecting in triads with one molecule of glucose and one aminos acid , so in this case glucose and amino acid went by secondary active transport

–How the substance are reabsorbed ?
all substances including harmful ones are reabsorbed passively
- there are active forms of transport for the return of the substance useful for the body from primary urine
-the only substance thats reabsorbs only passively is water

40
Q
  1. The theory of urine formation. Secretion in nephrons
A
  • secretion : refers to the transport of solutes form peritubular capillaries into tubular lumen , it is an active process
  • Substances secreted back from capillaries to final urine are (protons, non-volatile acids , potassium ions , toxins , some drugs like penicillin as well as hydronium ions , bile salts oxalates , urates ,)
  • after secretion final urine is formed which then passes to collecting duct and further to renal pelvis , urtere and urinary bladder