13. Smooth muscle, excitation and contraction Flashcards

1
Q

Where is smooth muscle found

A

Walls of hollow organs eg gastrointestinal tract, bladder, ureters, uterus, blood vessels, respiratory tract, around hair follicles, iris and cilliary body

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2
Q

2 types of contraction
Why is contraction slower than skeletal

A

Tonic= sustained, slow contraction

Phasic= rapid contraction and relaxation

Because myosin heads breakdown atp much slower, low ATP ase activity

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3
Q

Morphology of the smooth muscle cells

A

Spindle/ fusiform shape
Smaller than skeletal muscle
Actin and myosin filaments BUT NO STRAITIONS
NOT organised into sarcomeres
Central 1 nucleus
Less developed SR
No myofibrils

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4
Q

What increases the surface area of smooth muscles

A

small invaginations called caveolae

(involved in regulation of intracellular Ca2+ conc)

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5
Q

Do they have Z lines?

A

No
Actin filaments bind to DENSE BODIES

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6
Q

They have actin, myosin, tropomyosin

What are the regulatory proteins (eqv to troponin)

A

Calmodulin and caldesmon

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7
Q

Differences btw the 2 types of smooth muscle

A

Single unit:Not all cells are innervated by ANS- only modulating effect. They can self excite spontaneously.
Linked by GAP JUNCTIONS

Multiunit: Each cell is innervated by the ANS

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8
Q

Where can you find unitary smooth muscle

A

gastrointestinal tract, bladder, uterus, and ureter

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9
Q

Where can you find multi unit smooth muscle

A

Large arteries and airways
Cillilary body and iris
Vas deferns
pilomotor muscles (hair)

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10
Q

Which type has pacemaker potential

A

Single unit

The frequency of slow waves sets a characteristic pattern of
action potentials within an organ, which then determines the frequency of contractions

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11
Q

Physiological properties of smooth muscle

A

Excitability

Conductivity

Contractility

Elongation

Plasticity= smoothly change length while maintain steady force of contraction

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12
Q

What is the membrane potential of smooth muscle

A

-45 to -60mV

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13
Q

Where is the major sources of Ca2+

A

Extracellular fluid

Sarcoplasmic reticulum

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14
Q

What is the role of calcium ions in the regukation of smooth muscle contraction

A
  • C\2+ binds to calmodulin- complex results in activation of myosin light chain kinase
  • MLCK phosphorylates light chains of myosin leading to activation of myosin ATPase
  • Myosin ATPase breaks down ATP and release energy for contraction and increase affinity between actin and myosin
  • Ca2+/ calmodulin complex also increases affinity of acitn and myosin therefore promotes CROSS BRIDGES
  • Caldesmon = functional analogue to troponin
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15
Q

How is the cytoskeleton of smooth muscles organized and what are their properties

A

Dense bodies and intermediate filaments where actin and myosin attach

It has multidirectional spatial arrangement of cytoskeleton filaments so contraction is transmitted in all directions

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16
Q

Force velocity relationship compared to skeletal muscle

A

Maximal force is similar with both

But max shortening velocity of smooth muscles is 100 times lower

17
Q

Passive tension in smooth muscles

A

They exhibit more resustance to stetch due to network of connective tissue that reisst overextension

18
Q

Influence of contraction of smooth muscle compared to skeletal

A

skeletal= impulses

smooth= various stimuli

19
Q

Regulation of smooth muscle contraction (stimuli)

A
  1. Automaticity phenomenon in single-unit type of smooth muscles.
  2. Stimuli coming from the autonomic nervous system.
  3. Hormones that reach smooth muscles through the blood:
    epinephrin, vaposresin, oxytocin.
  4. Local humoral factors like: serotonin, endothelins, angotensin II,
    prostaglandins, NO, or changes in pO2, pCO2, or concentration of H+, K+
  5. Mechanical stretching in single-unite type of smooth muscles.
  6. Changes in the temperature.
20
Q

How does the conc of Ca2+ in cytoplasm increase

A
  1. Enters from extracellular space through voltage gated/ ligand gated channels
  2. Mechanically when sudden muscle stretching causes ca2+ channels open
  3. Release from SR mediated by IP3
  4. By calcium channels that open when Ca 2+ ions are depleted in SR.
21
Q

How is calcium ions released from SR

Pharmaco mechanical coupling

A

Mediated by second messenger, IP3

  1. IP3 generated by breakdown of membrane phospholipid (PIP2) by the PLC.
  2. PLC is activated by Gq receptor when neurotransmitter/hormone such as Epinephrine,
    Norepinephrine, Angiotensin II, or Endothelin binds to it
  3. IP3 activation leads to opening of specific
    Ca2+ channels expressed of the surface of SR
22
Q

How is calcium ions released from SR

Calcium induced calcium release

A

Induced by entry of Ca 2+ ions
through Ca 2+ channels on the cell membrane.

23
Q

How does smooth muscle relax

A

Ca2+ conc decreases by calcium pumps pumping it out into extracellular fluid or SR
SLOWER ACTING THAN SKELETAL so lasts a couple of seconds

Myosin phosphatase activated which dephosphorylates light chains of myosin head separating myosin from actin

THEREFORE TIME FOR RELAXATION DEPENDS ON CONC OF MYOSIN PHOSPHATASE

24
Q

is contraction/relaxation slow or fast in smooth muscles

A

Contraction and
relaxation are very slow processes,
because the myosin heads break down
ATP very slowly.

Due to the slow rate of ATP breakdown
in smooth muscle, no signs of fatigue
are observed during prolonged
contraction.

Moreover, they can perform very long
(in duration) tonic contractions with
high tension while very low energy is
used.

25
Q

WHat is cross bridge latching

A

When myosin heads are already dephosphorylated BUT still attached to actin = can do long tonic contractions

No energy is used = no ATP breaksown

26
Q
A