PHYSIO B Kidney And Cardiovascular Flashcards

1
Q

How much of the human body is composed of water? How is it divided?

A

About 60% of the human body weight is water. Intracellular volume constitutes about 40%, extra cellular volume about 20% considering that 4% is plasma volume, and interstitial volume about 14%.

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2
Q

What is the Gibbs Donnan equilibrium?

A

It describes the unequal distribution of permeant charged particles on epithet side of a semipermeable membrane and this occurs when we have non permeant charged elements such as proteins. Proteins attract anions and consequently attract cations.

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3
Q

What are other main functions of the kidneys apart from producing urine?

A
  1. The excretion of metabolic products that arrive from the liver, muscles and other cells such as hormone metabolites, creatinine, drugs and other chemicals.
  2. homeostatic control and the balance of bodily fluids, such as the regulation of electrolyte balance, working with the lungs to maintain acid base balance.
  3. Production and secretion of some hormones, such as Renin important in blood pressure regulation, production of prostaglandins and kinins.
  4. Ability to perform gluconeogenesis, during fasting it accounts for 20/30% of glucose.
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4
Q

At what level are the kidneys located?

A

More or less at level T12 vertebra.

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5
Q

What is the anatomical structure of the medulla of the kidney?

A

It consists of renal pyramids alternating with renal columns which are inward extensions of the cortex. The end part of the renal pyramid is called Renal papilla which empties the urine in tubes. All these tubes will then join and form the Renal pelvis which once it exits the kidney is called ureter.

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6
Q

How does the blood supply to the kidney work?

A

The renal artery entering the renal hilus branches off the abdominal aorta. It then splits into interlobar artery which runs in between lobes. Moving up towards the cortex in branches off into the arcuate arteries which branches off the cortical radiated arteries. These small arteries in the cortex give off Afferent arterioles which feeds into the renal corpuscle therefore in the glomerulus. The afferent arterioles also give off the peritubular capillaries which then drain into the cortical radiated vein.

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7
Q

What is, anatomically speaking, the vasa recta in the kidney?

A

It is a peritubular capillary network but in the medulla.

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8
Q

What is the anatomical structure of the nephron and where does the filtrate later go?

A

The capsule around the glomerulus is called Bowmans capsule, then we have the PCT in the medulla and moving downward in the medulla we have the descending limb of the loop of Henle. Then we have the actual loop of Henle, followed by the ascending limb of the loop of Henle. Back in the medulla we have the DCT. The DCT dumps the filtrate in the Collecting duct. Once it gets to the renal papilla, specifically to the papillary duct the filtrate, now urine, dumps into tubes.

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9
Q

What is the anatomical structure of the renal corpuscle?

A

Feeding it is the afferent arteriole and draining it is the efferent arteriole. In afferent arterioles you have Juxtaglomerular cells which are pressure receptors and sense blood pressure changes. In close proximity we have a portion of the DCT called Macula densa. This apparatus and the JG cells are called the Juxtaglomerular Apparatus. The visceral layer of the bowmans capsul is in contact with the capillaries and it is made of Podocytes. The outer layer is made of simple squamous epithelium.

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10
Q

Why is the basement membrane in the renal corpuscle important?

A

It contains a middle layer called Lamina Densa made of type 4 collagen and laminins. Towards the epithelium above the lamina dense we have a layer of proteoglycans particularly Heparin sulfate, found also on the other side. Heparin sulfate is very negatively charged. This is relevant bc protein in the blood are also negatively charged so they repel each other. While positive molecules like electrolytes are attracted and can pass through easily.

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11
Q

Why are podocytes important in the renal corpuscle?

A

They make up the visceral layer of the bowman capsule. In between them there is a protein called Nephrin. The space between the podocytes is called the filtration slit. Nephrin only allow only molecules smaller that 9 nm to pass. The molecules that are able to pass are then going to go through the PCT.

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12
Q

What are mesangial cells?

A

They are phagocytose any unwanted molecule that passes through in the glomerulus. They also have contractile function that can modulate the amount of blood coming through. They have gap junction which connect them to JG cells.

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13
Q

How much fluid is filtrated in the glomerulus?

A

Every min about 1200 ml of plasma flowing through the glomerulus, only 625 ml per min are actually being filtrated. Only about 20% passes though the various barriers.

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14
Q

What composes the Net Filtration Pressure in the glomerulus?

A

It is composed of pressure forcing out minus the pressure fo forcing in. The first pressure is called GHP and pushes this out of the artery and into the bowman space, it si about 55 mmHg. Albumin tries to keep molecules in the blood and the pressure is called Colloy Osmotic P, an av 30 mmHg. The Capsular Hydrostatic P is exerted by the pressure buildup in the bowman space and tries to push back fluid out, 15 mmHg. NFP is about 10 mmHg and is proportional to the glomerular filtration rate.

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15
Q

What other factors, other than the NFR, are important for the GFR? What is the final formula of GFR?

A
  1. The surface area of the capsule. The more SA the higher GFR is and viceversa. Clinical ex. Diabetic nephropathy
  2. The permeability of the glomerulus. The more permeability the higher the GFR and viceversa. Clinical ex. Glomerulonephritis.

These two factors make up KF, which is filtration coefficient.

So GFR= NFP x KF

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16
Q

What is Osmolality?

A

It is the volume of particles per kg of solvent.

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17
Q

What is the name of the process that involves moving substances from the blood to the kidney tubule and viceversa ?

A

It is called Tubular secretion, active process requiring ATP.
The second is called Tubular reabsorption and can be active or passive.

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18
Q

What are sodium potassium ATPases?

A

They pump 3 Na out of the cell and bring in 2 K, this process requires ATP. Thus this means that inside the cells the concentration of K is high.

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19
Q

What is 2nd active transport and why is it relevant in the PCT?

A

A channel brings Na form the PCT inside the cell where na is low therefore it is passive. But the same channels also brings glucose in against the gradient but the entering Na aids this process.
Another example: Na goes in passively and helps to bring A.A inside.
This can also happen with lactate.

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20
Q

What happens after glucose, A.As or lactate go inside the cells from the PCT?

A

A transporter on the other side of the cells transports it out of the cell to the artery. The glucose, A.As or lactate are now back in the blood.

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21
Q

What is the mechanism of reabsorption of bicarbonate?

A

A transporter uses carbonic acid, formed by Carbonic anhydrase catalyzing H20 and CO2, which disassociates in protons so H+ and bicarbonate. Na enters the cell and helps to push the proton out, the proton and the bicarb and forms carbonic acid. The carbonic acid reacts with Carbonic anhydrase and produces CO2 and H2O which leaves. The bicarb made earlier is then pushed into the blood.

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22
Q

How is glucose reabsorbed in the PCT and how does it affect water?

A

Glucose is reabsorbed with Na+ and water follows by osmosi. It follows the sodium ions.

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23
Q

How are potassium, calcium and magnesium reabsorbed in the PCT?

A

They move in between the PCT cells, the process is called paracellular transport.

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24
Q

How are lipids reabsorbed in the PCT?

A

Ex.urea a Lipid soluble substance, can pass through the membrane and go in the blood stream.

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25
Q

How are small proteins reabsorbed in the PCT?

A

On the membrane of the cells they can get caught on receptors, they get pulled in by endocytosis. The proteins are then broken down by lysosomes. The constituent AA are moved to the blood stream.

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26
Q

Why are there 300 m OSM in the descending loop of H after all the ion reabsorption in the PCT?

A

Bc the same amount of water is also reabsorbed there for the proportion doesn’t actually change.

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27
Q

What happens to the osmolality as we descend in the renal medulla?Why?

A

It gets more hypertonic. This is due to the sodium potassium 2 chloride co-transporter which is found on the baso lateral cells of the ascending loop move the ions.

28
Q

How does water get reabsorbed in the descending loop of Henle?

A

Since there is a high concentration of ions outside to to the co transporter water is attracted and leaves the descending loop of Henle. The channels are called aquaporins type I and they are always open.

29
Q

What is the counter current multiplier mechanism?

A

It is the mechanism by which the ascending loop moves in the medullary interstitial space ions and as a consequence in the descending portion water move out in the medullary interstitial space.

30
Q

What is the osmolality of the filtrate before it goes into the ascending limb?

A

About 1200 m OSM which is very hypertonic compared to the osmolality before the descending limb.

31
Q

What is the osmolality of the filtrate after it leaves the ascending limb?

A

It is about 200 m OSM.

32
Q

What are the main functions of the vasa recta?

A

It helps to maintain the medullary interstitial gradient by preventing the rapid removal of sodium chloride and it provides oxygen and nutrients to the tissue cells.

33
Q

How much sodium and water is entering the DCT?

A

10% Na and 20% H2O

34
Q

What happens to the remaining sodium,chloride and calcium ions in the early portion of the DCT?

A

They get reabsorbed by a channel which symports them, about 5/6%. Low blood calcium levels can stimulate the parathyroid glands to release PTH, it stimulates the formation of protein kinase A that stimulates channels to absorb it to increase calcium levels.

35
Q

What does aldosterone do in the late portion of the DCT?

A

It leads to the production of proteins that allow sodium to enter the cells and then go in the blood stream. This allows also for potassium to enter the DCT to be eliminated.

36
Q

What is the difference between cortical nephrons and juxtamedullary nephrons?

A

Cortical nephrons have a short loop of Henle , no vasa recta and are responsible for most of the absorption.
Juxtamedullary nephrons have long loop of Henle, vasa recta.

37
Q

How much filtrate can a single nephron filter a day and how much filtrate is filtered in the two kidneys a day?

A

Each nephron filtrated about 0.1 ml of filtrate a day and the two kidneys about 180L.

38
Q

What is the renin angiotensin aldosterone system and how does it work?

A

If blood pressure and blood volume drops due to a hemorrhage for example, this causes a decrease GFR. This is a stimulus to release renin by Juxtaglomerular cells. Also if Na is low in the DCT macula densa cells can also stimulate renin. Renin activates angiotensinogen into angiotensin. The lung produces angiotensin converting enzyme, which transforms AT1 into AT2. AT2 constricts arterioles and increases BP. It also stimulates the adrenal glands to secrete aldosterone which tells the DCT to through out Na so water as a consequence. More water in the body means an increase in blood volume.

39
Q

What is the function of the intercalated A cell in the collecting ducts?

A

If the environment in the blood is low in PH, the cell exchanges H+ for K+, also NH3 is pumped out and combines with the excreted H+.

40
Q

What is the function of the intercalated B cell in the collecting ducts

A

If the environment in the blood is high in PH it does the opposite of the A cells, it brings Cl- in to balance PH out.

41
Q

How is cortisol removed from the cells in the collecting ducts?

A

Principal cells express enzyme 11 beta hydroxysteroid dehydrogenase which is responsible fo the removal.

42
Q

Where is the SA node located?

A

It is located in upper part of the RA right under the SVC.

43
Q

How does the SA node communicate with the LA?

A

Through the Bockmans bundle.

44
Q

How long does it take before the AV node sends the signal down the intraventricular septum? Why is it relevant and how does it happen?

A

It takes 0.15 seconds. It wants to give time to the atria to contract before the ventricles can contract. The AV node has less Gap junctions and a smaller dm fibers causing a decrease in conduction speed.

45
Q

How does a nodal cell depolarize?

A

It has these sorto of funny ion channels that let Na+ leak inside beginning the dep, later the T type channels are activated and allow Ca++ inside furthering the dep. Then L type II channels even more Ca++ start to flow in. At this point it goes up to approx +40 Mc.

46
Q

How does the depolarizer nodal cell communicate with the contractile cells? And what happens?

A

The gap junctions made of connexins allow for the positive ions in the nodal cell to move inside the contractile cell. The positive ions stimulate sodium channels allowing Na+ inside the contractile cell.

47
Q

What is excitation contraction coupling?

A

It relies on calcium induced calcium release. First an action potential is generated and transferred inside the cell which trigger the opening of L type Ca++ channels this allows Ca++ in the cell. The Ca++ opens the rynadine channels on the sarcoplasmic reticulum releasing even more Ca++. Then Ca++ binds to troponin and the contraction starts.

48
Q

What happens in the mid to late ventricular diastole?

A

Blood from the sup and inf vena cava and the p veins is accumulating in the atria and the blood is passively flowing into the L and R ventricles due to gravity. In the later part the SA node starts firing, causing the depolarization of the atria thus contracting pushing the last 20% of blood in the ventricles. This shows on the EKG as a P wave.

49
Q

What happens in the iso volumetric contraction/systole phase?

A

The myocardium starts to slowly depolarize and contract. The blood starts rising. The semilunar valves are still closed as the ventricular pressure is still less than the arterial pressure.

50
Q

What happens in the mid to late ventricular systole?

A

The pressure in the ventricle starts rising and reaches about 120 mmHg. Now then higher pressure causes the semilunar valves to open. In an EKG this represents the QRS complex.

51
Q

What happens in the iso volumetric relaxation phase?

A

The ventricles have ejected most of the blood out to be distributed. Pulmonary trunk and aortic pressure is now going to be heighten than ventricular pressure. The semilunar valves have shut. In a EKG this represents the T wave.

52
Q

What is cardiac output?

A

It is the product between the heart rate and the stroke volume. In other words the blood volume ejected per unit of time.

53
Q

What is the stroke volume?

A

It is the volume of blood that gets pumped out of the left ventricle with each heartbeat.

54
Q

What is poiseuilles equation and why is it relevant in hemodynamics?

A

R=8nL/πr^4. It is relevant to plug in in other formulas such as the flow= delta P/ R. Higher R the less blood flow we have. Viscosity and length are directly proportional to resistance. On the other hand resistance is inversely proportional to the fourth power of the radius.

55
Q

What is the carotid sinus reflex?

A

It is the dilation of the internal carotid artery after the ramification of the common carotid and external carotid artery. It is inveravate by afferent nerves an serves as a baroreceptor. It is sensitive to changes in pressure. When it senses a pressure increase the nerve afferent lead the activation of the vagal control.

56
Q

What is the brain bridge reflex?

A

It is a reflex mediated by baro receptors when there is a change in blood volume in the atria. When there is an increase in blood volume you would expect to lower the HR but the brain bridge reflex instead increases it but the SV and Q remain the same.

57
Q

What is endothelial mediated regulation?

A

It is vasodilation induced by nitric oxide. ACh stimulates NO synthesis which in the end creates cGMP which induces relaxation. This happens when longitudinal pressure increases.

58
Q

What are the two types of calcium channels important in heart contraction?

A

L type: L for long, prevails in the ventricles, have a higehr threshold, -30 mv, and has a more positive peak.

T type: T for transient, only in the SA node, important in the last part of diastolic depo, lower threshold of -50 mv.

59
Q

What are some different potassium channels important in heart contraction?

A

They are outward unlike Na or Ca, they are useful in the depolarization the membrane. Kv are voltage dependent. Ks for slow and Kr for rapid.

60
Q

What is a P wave and what is the following PR segment?

A

The P wave is caused by a flux of positive signal from the SA node to the AV node. This since it is moving toward the positive electrode gives a upward curvature. Following the P wave there is a flat segment referred to as PR segment which is caused by the retention of the signal by the AV node before sending it down to the ventricles.

61
Q

What is the Q wave?

A

The flow of positive charge is moving towards the negative electrode due to the position of the intraventricular septum therefore resulting in a downward deflection. It indicates septal depolarization.

62
Q

What is the R wave?

A

After the Q wave the signal move in the ventricles, since the LV is thicker the net vector is moving toward the positive electrode therefore causing a upward deflection. This is the R wave.

63
Q

What is the S wave?

A

The AP moves up into the two bundles pointing toward the negative electrode causing a negative deflection.

64
Q

What is the ST segment?

A

The entire ventricular myocardium is depolarized. It hasn’t begun to depolarize and there is no net movement of charges.

65
Q

What is the T wave?

A

The myocardium starts repolarizing from the base up, so towards the negative electrode. The depolarization is negative so negative plus negative is positive, that is why it is an upward deflection.