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Smooth Muscles: Structure Function

by Thad Wilson, PhD
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    00:01 You can see smooth muscle is named because it’s non-striated appearance.

    00:07 Striations will be lines that occur.

    00:10 And when we went through the skeletal muscle, you noticed that there were varying components that you can see individual lines in the muscle itself.

    00:19 Why this occurs is because there are a number of different processes.

    00:24 Smooth muscle has a larger degree in which it can shorten.

    00:28 So a smooth muscle can shorten to a greater degree than skeletal muscle.

    00:34 They also have a large number of intermediate filaments that help maintain its structural integrity.

    00:40 They have thick filaments and thin filaments just like skeletal muscle.

    00:46 They also have these dense bodies and these dense bodies help maintain that structural relationship of thick and thin filaments.

    00:56 The other thing that’s different is they are mechanically coupled at least in the single unit or phasic smooth muscle via gap junctions.

    01:05 It can be seen here.

    01:08 Now, let’s talk through the various ways in which smooth muscle develop force as which there are a number.

    01:15 The first we’ll talk through is in this type of graph where we have force on the Y-axis and time on the X-axis.

    01:26 This is one type of force production in which force production is high almost all the time until you see a relaxation and then it returns back to a high amount of force.

    01:39 The good example for this are sphincters in which they are normally contracted and then relaxed for a very short period of time and contract again.

    01:51 Other types of smooth muscle work almost in the opposite way in which they are normally relaxed and then they have bursts of activity and then they go back to a relaxed state again.

    02:03 A good example of that is urinary bladder tissue in which it’s relaxed most of the time until one wants to urinate.

    02:12 Other types of smooth muscle have a partially contracted state almost all the time, and therefore, they have a tonic tone.

    02:22 They can constrict to a greater degree, but then will relax only a small amount.

    02:28 Good examples of these are blood vessels, where there always will be a tonic amount of vasoconstriction and then you can still vasoconstrict more, but there will be a tonic kind of contracted state.

    02:41 And then finally, we have very active type of smooth muscle and where there are lots of oscillations.

    02:48 These oscillations are oftentimes driven by such things as slow waves in the GI system.

    02:55 These can be phasically active and intestinal muscle is a great example in which you get waves of contraction and relaxation, contraction and relaxation, but the relative force is pretty low.

    03:09 So combining all of these together, you can see that smooth muscle has a wide range of functions and that’s probably why it’s present in so many different tissues because it could be contracted normally, partially contracted, phasically active, or normally relaxed.

    03:29 How do you get a muscle to contract in terms of smooth muscle? There are two primary ways.

    03:37 The first way is via causing an electrical potential across the membrane, which opens up calcium channels to cause calcium-induced calcium release.

    03:48 So calcium enters in through the cell from the extracellular fluid into the cell, which engages a calcium channel to release more calcium.

    03:58 So that’s done via an electrical mean.

    04:02 The other way to do it is by using a ligand or a particular substance to bind to a receptor.

    04:08 So good examples here are things like hormones and neurotransmitters that can bind to specific receptors to cause an enzymatic second messenger signal pathway to release calcium into the cell.

    04:23 So let’s go through those two in a little bit more detail.

    04:26 So let’s go through calcium-induced calcium release.

    04:30 Oftentimes, these L-type calcium channels are located in small invaginations in smooth muscle.

    04:36 These are located in close proximity to calcium-induced calcium release channels of the SR.

    04:43 SR is the sarcoplasmic reticulum.

    04:45 Therefore, once there’s a membrane potential change, these calcium channels open to allow little calcium influx into the cell.

    04:55 Once the small amount of calcium enters the cell, it activates this calcium-induced calcium release channel to spill out lots of calcium.

    05:05 So the calcium that comes into the cell isn’t really involved with the contraction to a great degree.

    05:11 The most of the contraction is induced from what is released from the SR.

    05:16 That can be seen here right below the caveolae.

    05:24 Now, a ligand-gated contraction, seen up here, can be done via again a hormone or a neurotransmitter activating let’s say a G-coupled protein receptor, and the example that we have here activates phospholipase C, which is an enzyme, and that converts a number of substances, but it creates IP3 and DAG, and it’s IP3 that then goes to the SR to bind to an IP3-gated channel to open up to allow calcium afflux into the cytosol.

    05:58 So both of these two mechanisms both involve calcium in the cytosol but how they get it out is via a different mechanism: one through calcium-induced calcium release and the other one through an enzymatic process involving phospholipase C and IP3.

    06:19 There are a number of calcium-binding proteins that are located in smooth muscle that help regulate its function.

    06:26 These smooth muscle-binding proteins will help activate to cause contraction to occur, as well as there are calcium-binding proteins that are there to help sequester calcium or to bind it up so it’s not in its free form.

    06:42 Graded contractions are a telltale sign of what smooth muscle does.

    06:48 You can have a little calcium release and get a little contraction or a lot of calcium release and get a lot of contraction.

    06:55 So it’s all graded by the amount of calcium release, whether it’s done via calcium-induced calcium release or whether it’s done via an IP3 mechanism.


    About the Lecture

    The lecture Smooth Muscles: Structure Function by Thad Wilson, PhD is from the course Musculoskeletal Physiology.


    Included Quiz Questions

    1. Sarcoplasmic reticulum
    2. Plasma membrane
    3. Caveolus
    4. Peroxisome

    Author of lecture Smooth Muscles: Structure Function

     Thad Wilson, PhD

    Thad Wilson, PhD


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