Lecture 9 - smooth muscle & EC coupling Flashcards

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1
Q

Decribe the structure/characteristics of a smooth muscle cell

A
  • spindle/ rod shaped
  • uninucleated
  • no strations
  • able to proliferate throughout lifetime, unlike skeletal muscle
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2
Q

How is smooth muscle classified?

A
  • classfied by its** patterns of activity**
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3
Q

What are the 2 most common forms of classification of smooth muscle?

A
  1. rhythmic smooth muscle
  2. tonic smooth muscle
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4
Q

Describe **rhythmic smooth muscle **

ie phasic smooth muscle & eg

A
  • active/contracting for discrete/short periods at a time
    * phasic smooth muscle spends a fair amount of time in a relaxed state, contracting only from time to time
  • EG - smooth muscle of the** bladder **only contracts a few times a day & the GIT sm contracts a few times an hour
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5
Q

Describe **tonic smooth muscle **

A
  • tonically active smooth muscle remains contracted for most of the time & only relaxes briefly
  • EG - the lower oesophageal sphincter which controls the entry of food into stomach, remains contracted all day long to prevent food going back up …
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6
Q

In what other way are smooth muscle classified?

A
  • based on whether the smooth muscle cells in an organ function together as ‘one’ muscle or whether each muscle cell is independent/acts on it’s own
  • ie single unit or multi unit smooth muscle
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7
Q

Describe multi unit smooth muscle

+ example

A
  • the smooth muscle cells in an organ all behave independently of each other - ie each cell contracts & relaxes on it’s own
  • has** fewer gap junctions** than the other types of smooth muscle - since it acts on it’s own- there is no need for electrically communicating to other cells
  • EG - tonically active smooth muscle - eg vascular smooth muscle
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8
Q

Describe **single unit/visceral **smooth muscle

A
  • all the smooth muscle cells in an organ behave as** one unit ** - multiple fibres contract as a unit or in some cases are self excitable
  • they have lots of gap junctions - to allow cells to communicate with eachother electrically - when one cell depolarises, they all do
  • eg smooth muscle found in the walls of hollow organs eg smooth muscle in the GIT
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9
Q

What is a dense body?

A

thin filaments that are anchored to cytoplasmic stuctures

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10
Q

What controls smooth muscle?

A
  • The autonomic system
  • hormonal secretions
  • spontaneous electrical activity - ie pacemaker cells
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11
Q

Whats the difference between thin & thick filaments in skeletal vs smooth muscle?

A
  • smooth muscle contains** thick myosin filaments & thin actin filaments **
  • instead of the troponin protein on actin in skeletal muscle, it contains calmodulin which binds to Ca2+
  • actin and myosin** loosely arranged** in the cell & held by dense bodies - unlike sarcomeres in skeletal muscle
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12
Q

Describe the sequence of events of ‘cross bridge cycling’ in smooth muscle

A
  • increase in intracellular Ca2+
  • Ca2+ binds to calmodulin
  • Calmodulin then binds to the **myosin light chain kinase enzyme ** (MLCK)
  • MLCK is activated & it uses ATP to phosphorylate myosin light chains on myosin head
  • myosin ATPase enzyme hydrolyses ATP-ADP
  • phosphorylated myosins bind to actin - cross bridge
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13
Q

How can the cross bridge cycling in smooth muscle cells be intervened by drugs?

ie what ways ?

A
  • through a Ca2+ channel blocker which will reduce the intracellular Ca2+
    *
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14
Q

How can certain drugs increase intracellular Ca2+ in smooth muscles?

A
  • they increase intracellular Ca2+ by agonists activating G protein coupled receptors and hence using the PLC pathway to generate IP3 & DAG which causes a release of stored intracellular Ca+ in the SR
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15
Q

what are the 2 different sources of cytosolic Ca2+?

A
  • from the sarcoplasmic reticulum (Ca2+ stored here)
  • extracellular Ca2+ that enters via voltage channels
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16
Q

Why does smooth muscle **have a much slower shortening velocity **in comparision to straited skeletal muscle?

A

smooth muscle myosin has a** low rate of ATP splitting** (breaking up - adp & pi)

17
Q

What ion is involved in the rising phase of an action potential of smooth muscle?

A
  • Ca2+ - influx of Ca2+ through open calcium channels
18
Q

How do some smooth muscle cells generate action potentials in the absence of any external input?

A
  • due to the presence of **pacemaker cells **
  • they generate pace maker potentials (graded potentials) that reach threshold & cause the membrane to depolarise
19
Q

In comparison to skeletal muscle (that use an NMJ), what do smooth muscles have instead?

A
  • instead of an NMJ, smooth muscle cells are innervated by many autonomic neurons & a number of smooth muscle cells may be influenced by neurotransmitters that are released from the varicosities on these neurons
  • the neurotransmitters released can have inhibitory or excitatory effects on the smoth muscle
20
Q

Compare smooth muscle contraction w/ skeletal muscle contraction

A
21
Q

What is** rhokinase pathway**?

A
  • this pathway** modulates the level of phosphorylation** of the myosin light chain kinase
  • it mainly acts through inhibition of myosin phosphatase and contributes to
22
Q

what is the difference between skeletal muscle SR and smooth muscle SR?

A
  • skeletal muscles have an organised SR & T tubules
  • Smooth muscles dont have an organised SR and T tubules
23
Q

What channel does EET activate?

note that EET is an EDHF produced by endothelium

A
  • EET activates a transient receptor channel eg TRPV4 in the sarcolemma of smooth muscle
24
Q

what does the activation of the TRPV4 channel lead to?

A
  • it leads to an influx of calcium which opens the ryanodine channels in the sarcoplasmic reticulum
25
Q

after the influx of Ca2+, what channel is activated & what happens?

A
  • the large influx / sparks of Ca2+ activate a large conductance K+ channel in the sarcolemma and the smooth muscle cell becomes hyperpolarised
  • hyperpolarisation in turn decreases basal Ca2+ influx and therefore **decreases intracellular Ca2+ and hence relaxes the smooth muscle **