Lectures

Global Effect of Sympathomimetic Drugs on the Vascular System

by Pravin Shukle, MD
(1)

Questions about the lecture
My Notes
  • Required.
Save Cancel
    Learning Material 2
    • PDF
      Slides Sympathomimetic Acivators and Effects ANS Pharmacology.pdf
    • PDF
      Download Lecture Overview
    Report mistake
    Transcript

    00:01 Now, when we take all of these together, we have to look at multiple innervation systems so that we can understand the overall effect.

    00:09 So in the vascular system, it is acted upon by alpha 1, alpha 2 and beta 2.

    00:15 So, let's take a look at each of these in this special circumstance.

    00:22 The alpha 1 agonists. The prototypical alpha 1 agonist is phenylephrine. It contracts smooth muscle in the splanchnic blood vessels, so that means the one that goes to the gut.

    00:35 And it increases blood pressure by incresing the total peripheral resistance.

    00:41 Now, one of the side effects of phenylephrine is reflex bradycardia.

    00:47 Now, I'm going to spend a little bit of time to explain this.

    00:52 We would think that an agonist of a sympathomimetic drug or a sympathomimetic system would cause a fast heart rate.

    00:59 But what we're talking about here is a very specific drug that is only acting on blood vessels, it's not acting on the heart. So the heart is free to respond however it wishes.

    01:11 When the heart senses that the blood pressure is higher, it will slow itself down, thinking that there's too much adrenaline around.

    01:20 Right. So that's why you get reflex bradycardia from phenylephrine.

    01:26 The other issue too is that the baroreceptors also have connections to the vagus nerve which innervates the heart, so the vagus nerve will actually slow down the heart as well. That's why phenylephrine causes the reflex bradycardia eventhough it's considered the sympathomimetic. And the reason why is cause it's an alpha 1 agonist.

    01:47 Okay. Does that sound like it make sense? Alright, let's move on.

    01:52 What about the alpha 2 agonist? The classical alpha 2 agonist is clonidine.

    02:01 Now, I just finished telling you that alpha 1 agonist will increase the blood pressure, and now I'm going to tell you that alpha 2 agonist are decreasing the blood pressure.

    02:11 Why is that happening? Well, let's take a look at the blood vessel itself.

    02:16 Yes, alpha 2 agonist cause vasoconstriction. And we sometimes use it topically in nasal sprays.

    02:24 So, clonidine for example, or other alpha 2 agonist can be sprayed up the nose when we're congested and it causes some mild constriction of the blood vessels. However, clonidine also crosses the blood brain barrier.

    02:38 And it accumulates in the brain. And now what it's doing is it's acting to reduce sympathetic outflow and blood pressure.

    02:46 Why? Well, if you have an excessive amount of adrenaline crossing through your system, and it's sensed by the brain, you know that the brain is saying "Uhh ohh, we're really in trouble. We need to reduce our sympathetic outflow." So, it's taking advantage of a feedback loop. That's why clonidine reduces blood pressure.

    03:04 Now, I should mention very quickly that clonidine is not our favourite form of blood pressure agent, I'm going to talk about it more in our hypertension lectures. The problem with clonidine is because it acts centrally, you can also get orthostatic drops when you stand up.

    03:22 Okay, let's go on to the beta 2 agonist. So, remember that the beta 2 receptor is in the lungs, right? There's two lungs, one heart, so beta 1 is heart, beta 2 is lungs.

    03:33 Albuterol, salbutamol. Salbutamol is better known as ventalin. There is going to be some vasodilation in the skeletal muscle with these drugs. But you have to usually take a very high dose in order to achieve that.

    03:47 There are maybe some reduction in blood pressure with the usage of ventalin.

    03:52 In general, I've never seen that in clinical practice.

    03:55 There is some vasodilations in the lungs as well. Cocaine is also an agonist.

    04:03 And remember that cocaine, when taken in the nose causes vasoconstriction.

    04:09 Cocaine, as crack cocaine, causes vasodilation, and that's why crack cocaine is absorbed so quickly, because where it's landing it's dilating the blood vessels and getting into the blood much more quickly.

    04:21 We are going to talk more about cocaine and crack in our toxicology lectures.

    04:27 So, let's talk about toxicity. With catecholamines, they rarely cause clinical problems as medications.

    04:36 It's quite rare because they're quite short lived. However, I do want you to go back and read up on "pheochromocytoma".

    04:42 It's a relatively rare kind of tumour of the adrenal gland. And it's best done if you read it on your own in a textbook.

    04:50 Dopamine. If you give excess amount of dopamine, you can sometimes cause digital ischemia and mesenteric ischemia.

    04:58 We kind of mentioned that in the case that I was talking about earlier where you risk losing fingers and you risk causing infarcts of the bowel with excess of levels of dopamine.

    05:09 And finally, amphetamines and cocaine which I've very briefly touched on and will cover later.


    About the Lecture

    The lecture Global Effect of Sympathomimetic Drugs on the Vascular System by Pravin Shukle, MD is from the course ANS - Pharmacology.


    Included Quiz Questions

    1. Phenylephrine
    2. Clonidine
    3. Intermediate dose dopamine
    4. Terbutaline
    5. Albuterol
    1. It acts centrally leading to a reduction in sympathetic outflow.
    2. It vasodilates in smooth muscle but vasoconstricts in mucosal blood vessels via activation of different adrenergic receptors.
    3. It only decreases blood pressure via orthostatic hypotension.
    4. It works by diverting blood flow to the splanchnic vessels leading to overall decrease in blood volume.
    5. It works via a reflex mechanism to decreased blood pressure.
    1. All of the answers would be expected.
    2. Increased blood pressure
    3. Contraction of smooth muscle in splanchnic vessels
    4. Reflex bradycardia
    5. Increased total peripheral resistance
    1. Mesenteric and digital ischemia
    2. Orthostatic hypotension
    3. Inadequate diastolic filling time
    4. Bronchoconstriction
    5. Reflex bradycardia

    Author of lecture Global Effect of Sympathomimetic Drugs on the Vascular System

     Pravin Shukle, MD

    Pravin Shukle, MD


    Customer reviews

    (1)
    5,0 of 5 stars
    5 Stars
    5
    4 Stars
    0
    3 Stars
    0
    2 Stars
    0
    1  Star
    0