- General overview of the RAAS system: Cells and hormones
- Renin production in the kidneys
- Activating angiotensin 2
- Angiotensin 2 raises blood pressure
- Aldosterone raises blood pressure and lowers potassium
- Aldosterone removes acid from the blood
- ADH secretion
- ADH effects on blood pressure
- Aldosterone and ADH
Learn the important cells and hormones that are working together to control your blood pressure! The Renin-Angiotensin-Aldosterone System (RAAS) is a crucial mechanism for blood pressure control in the body. Learn how juxtaglomerular cells in the kidneys release renin in response to low blood pressure, triggering a cascade of hormones that ultimately raise blood pressure. Rishi is a pediatric infectious disease physician and works at Khan Academy. Created by Rishi Desai.
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- @3:57When the Macula Densa cells in the distal convoluted tubule sense a LOW sodium concentration, it triggers renin production to raise blood pressure. If this is the case, why do people who have a large intake of sodium have high blood pressure? It seems like the system would drive blood pressure down.(37 votes)
- Excess dietary sodium in the body fluids causes increased retention of water because water will move by osmosis to regions of high salt levels. Water retention increases the blood volume and so increases blood pressure. Cells in the atria of the heart react to this increase in distension by producing atrial natriuretic factor which inhibits sodium reabsorption in the kidneys and increases the filtration rate in order to try and remove the excess sodium.(54 votes)
- Is renin a hormone or a enzyme? because in the video he one time said it was an enzyme but than said it was a hormone(9 votes)
- Enzymes are those molecules whose role is to catalyze a reaction: in this case renin is just cleaving a piece of angiotensinogen so it's an enzyme.
Hormones are molecules that have a receptor in a cell, and when they bind it the cell starts (or stops) an activity as response.
So renin is an enzyme and starts the conversion of angiotensinogen to angiotensin II, while angiotensin II is an hormone and induces in the target cells the responses shown in the video.
Note that angiotensin II induces the release of ADH and aldosterone that are also hormones theirselves.(24 votes)
- Why do we need higher blood pressure?(4 votes)
- If your blood pressure is low some of the organs cant get enough out of the blood.
the brain is the best example, it really needs a good blood pressure to function properly.
For example; if you have been lying down for some time and suddenly stand up you can easily become dizzy, that is because of low blood pressure.
So if you have been bleeding your blood pressure drops.
Or if you are dehydrated your blood pressure drops.
Then the body tries to get the blood pressure back up to normal.(12 votes)
- At 4 minutes of video, you said that the macula densa cells have an especial hability to detect/sense the level of Sodium and this trigger the release of renin. But the macula densa cells have the same ability to sense a decrease or increase in the chloride concentration as well, so can we expect release of renin when your chloride blood concentration augment?(4 votes)
- You are right, macula densa cells are chemoreceptors specific for detection of sodium as well as chloride in blood. This is due to the fact that the cells have two types of protein channels: Na+/H+ antiporter and Na+/2Cl-/K+ co-transporter. If there is a low sodium concentration in the blood, then the cells cannot import enough sodium to keep the cell volume constant and the cells shrink; this causes JuxtaGlomerular cells (mechanoreceptors that sense cell shrinkage) to release renin. If there is a decrease in chloride as well as sodium concentration (low sodium chloride in the blood), then the cells shrink faster (two channels are involved), and you can expect release of renin. However, if for some reason sodium is present when there is a deficit in chloride only, then the cell volume may not necessarily decrease as long as the Na+/H+ antiporter imports enough sodium to keep the cell volume constant. I hope this helps.(6 votes)
- How does the retention of water in the kidneys pursuant to ADH and Angiotensin II increase the stroke volume of the heart? Retention of water would seem to reduce volume systemically and leave the heart with less preload ability if anything.(2 votes)
- The retention of water occurs in the collecting duct, where ADH triggers the insertion of aquaporins into the renal epithelial cell membrane where the urine is forming. Aquaporin insertion into the membrane allows water to flow out of the urine (filtrate), through the renal cells, and into the blood. Water will flow in this direction because the renal medullary interstitial space is hyperosmotic, thus drawing water into the interstitial space, and then into the blood. This hypertonicity is created via the countercurrent multiplier system in the loop of Henle and the presence of urea in the medullary interstitium.(5 votes)
- Low BP --> Low fluid flow through glomerulus --> Low fluid through nephron --> "a lot of salt being reabsorbed." I don't follow this logic. How would less fluid through the nephron lead to more salt reabsorption?(4 votes)
- Your body is trying to compensate for the low BP in the body. Therefore by trying to reabsorb Na, it tries to increase water reabsorption (water follows Na), consequently increases BP.(4 votes)
- At4:37, Rishi mentions that the Macula Densa cells are not sensing a lot of salt because blood pressure is low. How are these two related? How does having low blood pressure decrease salt levels?(3 votes)
- Often, when Na is low in blood it also means that there isn't a lot of water (volume) in your blood, and when there is low volume in the blood it consequently causes a low blood pressure. Just imagine your body having 5L of blood, now it only has 3L to work with so therefore the BP will be lower with 3L of blood.(4 votes)
- Is there a reason the RAAS is so long. Why didn't the Juxta Glomerular cells simply evolve to produce angiotensin 2 directly. Is it for some sort of delayed reaction?(2 votes)
- Think of it as a bunch of checkpoints. The body is constantly making sure that it really wants to get rid of its water because water is sooooo important. You'll also notice that there are a lot of negative inhibitor mechanisms, so if the body loses a lot of water unexpectedly (maybe you vomit), all it needs is one checkpoint to be a little off for the body to say "hold it! keep the water! something's wrong!"(3 votes)
what is the difference in functions between aldosterone and ADH ?(1 vote)
- Aldosterone has many functions but basically increases sodium and water reabsorption and causes potassium loss. This leads to elevated blood pressure but sodium is typically normal. ADH preferentially causes water reabsorption and as a result leads to low body sodium. It also may increase blood pressure by acting directly to increase blood vessel constriction.(5 votes)
- How does an increase in water volume in the kidney lead to an increase in blood pressure?(2 votes)
- What we measure and think of as "blood pressure" is the amount of force pushing out on the walls of the large arteries. When the kidneys retain water volume, that doesn't stay in the kidneys - it goes out in the blood, through the veins, and adds to the circulating volume of the blood. Arteries and veins are stretchy tubes, and when you push more fluid into a stretchy tube it applies more force to the wall of the tube. This is how we can measure an increase in blood volume as an increase in blood pressure.(3 votes)
The body has a really, really cool way of controlling blood pressure. And you'll hear about this RAAS system, and RAAS stands for Renin-Angiotensin, R-A A- Aldosterone System. So let's go through this RAAS system, kind of as an overview, just looking at where things start from and where things go, in terms of cells and hormones. So those are the two things I want to try to distinguish between. So this RAAS system, R-A-A-S, begins with a set of cells. So I'm going to draw all of my cells as little blue houses like that. And the hormones that they release are going to be orange messengers. So I'm going to draw a little messenger. This will be my little person. And so the person is the hormone and the blue house is the cell. Now, the key cell in the RAAS system is juxtaglomerular cell. It's a JG cell. And these juxtaglomerular cells are actually in the kidney, but they're in a specific location. They're actually in blood vessels. And if you look closely, these JG cells are nothing more than very special smooth muscle cells. So if you look in the blood vessel they're actually just like smooth muscle cells. I'm going to write smooth muscle just to remind you. This is just a reminder of where they are. And of course, these are in the kidney. So here's my little kidney. It may not look like a kidney but that's what it's supposed to be. So the juxtaglomerular cells are releasing a hormone called renin. And when would they do that? Well, renin is eventually-- we'll see when-- eventually going to help us raise blood pressure. So if the juxtaglomerular cells, if these guys, notice that blood pressure is low, that would be a trigger for releasing renin. That's the first trigger. So, low blood pressure. Very good. Now, that's not the only trigger. There are actually three triggers in total. So let me write out two and three, and let's go through what they are. So the second trigger is a neighboring cell. So this neighboring cell is actually a sympathetic nerve cell. And we know that sympathetic nerve cells fire whenever something big is going on. So for example, let's say you're running away from a bear, or let's say you're trying to win a fight, or let's say you're in a car accident and you're bleeding. Any sort of major, major stressor is going to cause these nerve cells to start firing. And when they fire, that JG cell starts releasing renin. So the second trigger would be sympathetics. I'll just write sympathetics. Or maybe sympathetic nerves. Now, if these are your neighboring cells, these little sympathetic nerve cells, because they literally end right on the JG cells, then a little ways away-- still the kidney of course-- but still a little ways away, not touching the JG cells, would be the macula densa cells. Now stay with me for this. These macula densa cells are also in the kidney. And actually they're specifically in the distal tubule of the nephron. So remember, the distal convoluted tubule. They're there. And their interesting ability is the ability to sense sodium. And when you have low blood pressure, not a lot of blood is moving through that glomerulus, and so not a lot of fluid is moving through the nephron as a result. And a lot of the salt is being reabsorbed. So by the time it gets to the distal convoluted tubule, the macula densa cells, they're kind of tasting or sensing the fluid that goes by. And they say, there's not a lot of salt here. And they put two and two together and they realize that the reason there's not a lot of salt is that blood pressure is low. So when they don't sense much salt they say, hey JG cells, wake up, do something about this. Raise blood pressure for us. And so they send a message over in the form of prostaglandins. So prostaglandins are kind of local messengers. Unlike renin, which is kind of a long distance messenger, prostaglandins act locally. And actually, lots and lots of cells in our body use prostaglandins to send local messages. So that's what they do. So the third trigger, just to summarize it, would be low salt in the distal convoluted tubule. And you know, specifically, that it's the macula densa cells that pick up on this. OK. So these are the three major triggers for renin release. And, now this is all happening in the kidney, right? That's where all this action is occurring. But you know there are other organs involved in blood pressure control as well. And the one that is next on our list is the liver cell. So liver cells are actually-- here we go, a little house for cells-- are also making a hormone of their own. And it's going to meet up with renin in a second. And it's called angiotensinogen. And angiotensinogen is like a sleep-walker. If you were to zoom in on its face it would be asleep. And so, I'm going to draw it that way. It's there and it's moving around the body but it's not active, and that's the key thing. It's not active. But it meets renin. And renin literally chops off a big hunk of angiotensinogen. And if that doesn't wake you, I don't know what would. So angiotensinogen becomes angiotensin I after meeting renin. So renin is an enzyme that cuts a big chunk of this angiotensinogen protein away and angiotensin I is the result. And if you were to zoom in on this guy's face, it would be awake. Maybe even a little smile. So angiotensin I now floats through blood vessels. And of course blood vessels have cells lining them. So let's draw a little house. So little cells, and these are the endothelial cells. These are the cells that are lining the blood vessel on the inside. And classically, we used to think that this is almost always happening in the lungs. But more and more, we're realizing that it definitely does happen in the lungs but it's in other places as well, other vessels as well. And so endothelial cells, in a number of parts of our body, including the lungs, are able to convert angiotensin I into angiotensin II. So angiotensin II is formed. And this is also, of course, a hormone. So I'll draw it as a little person. And angiotensin II is happy as a clam, because angiotensin II has lots of activity. A very, very active hormone. It does all sorts of things. And I'm going to draw them in for you now. So angiotensin II will go out to a number of different places. I'm going to draw four arrowheads here. One, two, and then two in the middle here. Three, let's do four. As it goes to four places. And four different cell types are affected by angiotensin II. Now keep in mind at the beginning of all this, we're trying to raise blood pressure. So just keep that thought in your head. So four different cell types are affected and here is the fourth. So the first one over here is smooth muscle cells in the blood vessels. And this is blood vessels all over the body, not just in the kidney, but this is smooth muscle cells all over the body, are going to contract. They're going to constrict down and they're going to cause increased resistance. Because you remember that as the blood vessels constrict, vasoconstrict, that will increase resistance. OK. So that's one effect. Now in a different cell type altogether, in the kidney cells, you actually have the ability-- the angiotensin II actually makes these kidney cells hold on to more water. So you have more volume. It actually helps the kidney hold on to more water. And more volume, think about in terms of stroke volume, is going to increase stroke volume. So you've got increased resistance, and now increased stroke volume. So those are two cell types that angiotensin II will act on. It also acts on a couple of glands. I'm going to try to draw for you the pituitary gland. And this pituitary gland is sitting at the base of the brain. And this gland is called that because it secretes hormones, as well. So it's actually sending off messengers, as well. So here's a little hormone again in orange. Remember, all our hormones are orange. And this one is called ADH. ADH, or antidiuretic hormone. And that ADH does some of the same stuff, at the end of the day, that angiotensin II will do, in that it will increase resistance of blood vessels. And it will actually, also, increase volume by making the kidney hold onto more water. Now, the fourth cell type is going to be the adrenal gland. So the adrenal gland is here. And this adrenal is called ad-renal because it's sitting on top of the kidney, which is the adrenal. This adrenal gland is also making a hormone, because it's a gland, and that hormone is going to act right there. And this is their little messenger, and this is called aldosterone. So you've got aldosterone and ADH that are also acting on some of the same cells. And I should rephrase that. Not exactly the same cells, but the same organs as the angiotensin II. So here, aldosterone is going to act on kidney cells to increase volume. And ADH is going to act on, as I said before, the kidney and smooth muscle. So let me scroll up and show you now, from the top, some interesting things I want to point out. So we've got, at the very top, all of the action, you'll remember, started in our kidneys, right? It started in the kidney, or the macula densa cell, and our JG cell, and even our nerve endings were in the kidneys. And one of the key target organs down here is, of course, the kidneys. So things are starting in the kidney and also ending in the kidney. Now you'll say, well, what about the smooth muscle cells and that, all over the body? And you're absolutely right. It does also affect smooth muscle in other parts of the body. But I just want to point out the fact that the kidney is a major player in this game. Now that's one point. The other point is that when people talk about the renin-angiotensin-aldosterone system, they're talking about certain pathways. And they're specifically talking about, for example, this arrow right here, this hormone obviously. And they're talking about this angiotensinogen and they're talking about angiotensin I. And they're also referring to angiotensin II, and all of its targets. So they're going to talk about angiotensin II affecting the smooth muscle, and the two glands, the pituitary, as well as the adrenal gland, and its effect on the kidney. So they're really referring to all of those things. So they want to make sure you remember that it's affecting four, at least four, target cell types. And finally, that aldosterone down here has a huge effect on the kidney, as well. So these are the important points to take away from this overview, that there are many different hormones involved-- and I've tried to keep them color coded all in orange to make sure we keep track of them-- and the fact that the kidney is a major player in blood pressure control.