Smooth Muscle Contraction

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Questions and Answers

What primarily determines whether a smooth muscle cell contracts or relaxes?

  • The absolute amount of negative input only.
  • The net input, considering both positive and negative influences. (correct)
  • The absolute amount of positive input only.
  • The presence of mechanically gated channels.

Which of the following is an example of electrical (electromechanical) regulation in smooth muscle?

  • The influence of paracrine agents.
  • Activation of ligand-gated channels by hormones.
  • Opening of voltage-gated calcium channels due to membrane depolarization. (correct)
  • The autonomic nervous system.

Depolarization in smooth muscle cells, leading to contraction, can be caused by:

  • Opening of voltage-gated $Ca^{2+}$ channels. (correct)
  • Increased activity of the sodium-potassium pump.
  • Influx of sodium ions through ligand-gated channels.
  • Activation of potassium leak channels.

What is the primary characteristic of 'slow wave potentials' in smooth muscle cells?

<p>They are cycles of subthreshold depolarization that may or may not lead to action potential. (D)</p> Signup and view all the answers

Which of the following is an example of pharmacomechanical regulation in smooth muscle?

<p>The influence of hormones binding to their receptors. (B)</p> Signup and view all the answers

In the context of smooth muscle regulation, what is the role of $IP_3$?

<p>It activates $IP_3$ receptors on the sarcoplasmic reticulum to release $Ca^{2+}$. (B)</p> Signup and view all the answers

How do neurotransmitters, hormones, and paracrine signals influence smooth muscle contraction?

<p>By altering the MLCK/MLCP ratio. (B)</p> Signup and view all the answers

A key difference between smooth muscle and skeletal muscle regulation is that in smooth muscle:

<p>The stimulus can be either stimulatory or inhibitory. (D)</p> Signup and view all the answers

What role does Myosin Light Chain Phosphatase (MLCP) play in smooth muscle contraction?

<p>It dephosphorylates myosin light chains, leading to relaxation (D)</p> Signup and view all the answers

Oscillating membrane potentials that regularly reach threshold are characteristic of:

<p>Pacemaker potentials (B)</p> Signup and view all the answers

What is the function of Nitric Oxide (NO) in smooth muscle regulation?

<p>It leads to smooth muscle relaxation. (C)</p> Signup and view all the answers

What is a primary characteristic of pharmacomechanical coupling?

<p>Contraction without changes in membrane potential (A)</p> Signup and view all the answers

How does increased intracellular calcium ($Ca^{2+}$) lead to smooth muscle contraction?

<p>By binding to calmodulin, which then activates myosin light chain kinase (MLCK). (A)</p> Signup and view all the answers

Which regulatory mechanisms are considered part of electrical (electromechanical) regulation in smooth muscle?

<p>Voltage-gated channel function and Mechanically gated channels (C)</p> Signup and view all the answers

What is the role of Rho-associated kinase (ROCK) in smooth muscle contraction?

<p>It inhibits myosin light chain phosphatase (MLCP) activity, increasing the level of phosphorylated myosin light chains. (A)</p> Signup and view all the answers

Which type of smooth muscle regulation is primarily involved when the Autonomic Nervous System affects smooth muscle contraction?

<p>Pharmacomechanical regulation (D)</p> Signup and view all the answers

In smooth muscle cells, what happens to membrane potential during electrochemical coupling?

<p>Contraction is accompanied by changes in membrane potential. (A)</p> Signup and view all the answers

How do pacemaker potentials lead to contraction in smooth muscle?

<p>They cause regular oscillations that reach threshold. (D)</p> Signup and view all the answers

How are calcium levels restored in the SR?

<p>The membrane channels automatically replenishes calcium (A)</p> Signup and view all the answers

Increased IP3 results in?

<p>Increased IP3-R in the SR (C)</p> Signup and view all the answers

Flashcards

Electrical (electromechanical) regulation

Regulation through electrical signals like mechanically-gated, voltage-gated and ligand-gated Ca2+ channels.

Pharmacomechanical regulation

Regulation via ligands binding to receptors, like autonomic nervous system, hormones and paracrine agents.

Depolarisation (Ca2+ entry)

Entry of Ca2+ into the cell due to opening of voltage gated channels, ligand gated channels or stretch activated channels

Slow wave potentials

A subthreshold 'slow wave' cycle, which can lead to contraction if threshold is reached.

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Pacemaker potentials

Oscillating potentials similar to cardiac action potentials that regularly reach threshold

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Pharmacomechanical Coupling

Contraction without changes in membrane potential; uses neurotransmitters, hormones & paracrine signals

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Smooth Muscle Regulation Signals

A group of signals including neurotransmitters, hormones, and paracrine signals that regulate smooth muscle.

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MLCK/MLCP Ratio

Smooth muscle contraction is altered by the ratio of Myosin Light Chain Kinase (MLCK) and Myosin Light Chain Phosphatase (MLCP).

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Smooth vs. Skeletal Muscle

Ways that smooth muscle differs from skeletal muscle, like stimulus is not always due to changes in membrane potential and stimulus doesn't always form a nerve.

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Study Notes

  • Smooth muscle regulation is complex, involving multiple organs with different functions and various mechanisms to regulate contraction.
  • Net input governs whether the cell contracts or relaxes, considering both positive and negative inputs.

Electrical (Electromechanical) Regulation

  • Regulation occurs through mechanically gated, voltage-gated, and ligand-gated Ca2+ channels.
  • Pacemaker and slow wave potentials also play a role.

Pharmacomechanical Regulation

  • Regulation occurs via ligand gated channels/receptors.
  • Regulation occurs via the Autonomic Nervous System.
  • Hormones and paracrine agents are also involved.

Depolarisation (Ca2+ Entry)

  • Depolarization and subsequent Ca2+ entry is caused by voltage gated Ca2+ channels.
  • Depolarization and subsequent Ca2+ entry is caused by ligand gated Ca2+ channels.
  • Depolarization and subsequent Ca2+ entry is caused by stretch activated channels.

Electrochemical Coupling

  • Contraction is accompanied by changes in the membrane potential.
  • Spontaneous opening/closing of ion channels influences muscle contraction.

Slow Wave Potentials

  • Slow wave potentials occur in a cycle of subthreshold waves.
  • Additional stimuli can cause the cell to reach threshold, resulting in contraction.
  • Intestines have slow waves and reach threshold when food initiates stretch receptors.

Pacemaker Potentials

  • Pacemaker potentials are the oscillating membrane potentials, similar to cardiac muscle.
  • Pacemaker potentials regularly reach threshold.
  • Phasic smooth muscles of the gut use this mechanism.

Pharmacomechanical Coupling

  • Contraction occurs without changes in membrane potential.
  • Neurotransmitters such as ACh and adrenaline are related to this.
  • Hormones like angiotensin II are related to this.
  • Paracrine signals like nitric oxide are related to this.

Neurotransmitters/Hormones/Paracrine Signals

  • IP3 release opens IP3 channels on the sarcoplasmic reticulum (SR), leading to the release of Ca2+.
  • Altered MLCK/MLCP ratio influences cross-bridge activity causing an increase.
  • Paracrine signals, including histamine, adrenaline, and nitric oxide, affect smooth muscle.

Smooth Muscle vs. Skeletal Muscle

  • Smooth muscle stimulus can be stimulatory or inhibitory, whereas skeletal muscle is usually only stimulatory.
  • Smooth muscle stimulus is not always a nerve unlike skeletal muscle.
  • Changes in membrane potential in smooth muscle are due to Ca2+ and not Na+.

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