smooth muscle structure and function Flashcards

1
Q

Provide examples of smooth muscles and their function in different organs

A

Phasic: rhythmic; seen in sphincters, esophagus, urinary blader

Tonic: continuous activity; respiratory airways and blood vessels

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2
Q

Describe single vs mutli unit smooth muscle

A

Multi-unit: muscle cells behave as individuals. These are usually involved in finer movements, such as lens and ciliary function in the eye, and in arrector pili of the skin

Single unit: muscle cells act as a group; this relies on gap junctions! This allows for coordinated contraction. This is seen in the smooth muscle of the GI tract in peristaltic contractions

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3
Q

Contraction is regulated by ___ filaments

A

thick

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4
Q

Describe caveoli

A

Invaginations of the sarcolemma that are open to the extracellular space; they’re thought to allow for expansion of the cell membrane.

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5
Q

What thin filaments are present in smooth muscle?

A

Actin and tropomyosin, no troponin

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6
Q

Describe the organization of thick and thin filaments in smooth muscle

A

Small groups of thick filaments are surrounded by many thin filaments to form a contractile unit.

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7
Q

What are dense bodies? Where are they found? What connects them to each other?

A

Sites of attachment for thin filaments; they’re found in the sarcolemma and in the cytoplasm; intermediate filaments such as desmin and vimentin

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8
Q

What junction type mechanically connects muscle cells

A

Adherens junctions

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9
Q

Describe the role of different pathways and factors in the initiation and regulation of
smooth muscle contraction

A

Can be controlled by autonomic control, circling hormones, electronic coupling, locally generated signaling molecules, or intrinsic electrical activity

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10
Q

Describe the steps leading to cross-bridge cycling in smooth muscle

A

-Calcium binds to calmodulin

-Calcium-calmodulin activates MLCK

-MLCK phosphorylates myosin

-Myosin can attach to actin

-ADP AND PI dissociate from the myosin head and contraction can happen

-ATP binds the myosin head, releasing actin and relaxing the muscle

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11
Q

Describe myosin phosphatase

A

Myosin phosphatase removes the phosphate from the myosin, releasing actin filaments and stopping contraction

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12
Q

Describe pharmacomechanical coupling and its physiological significance

A

Impacts contraction without changing membrane potential; this is usually receptor specific and may or may not use calcium

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13
Q

Give examples of ligands capable of calcium mediated pharamcomechanical coupling

A

Examples capable of this include norepinephrine, angiotensin, and vasopressin

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14
Q

Describe calcium mediated pharmacomechanical coupling

A

Activation of phospholipase C, forming IP3 and DAG. IP3 increases calcium cytosolic concentration, which can increase contraction. Store-activate channels will be activated to bring extracellular calcium into the sarcoplasmic reticulum, and SERCA will remove calcium from the cytosol to maintain the decrease and increase of calcium needed for contraction.

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15
Q

Describe how cAMP regulates pharmacomechanical coupling

A

-Lowering MLCLK activity: cAMP is decreased, lowering MLCK phosphorylation and thus its activity. This leads to muscle relaxation. Ligand examples include norepinephrine, adenosine, and b2 agonists

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16
Q

Describe how NO regulates pharmacomechanical coupling

A

Raising MP activity: release of NO activates guanylate cyclase which increases cGMP. The increase of cGMP increases MP activity, which leads to relaxation of the muscle. Viagra blocks this.

17
Q

less myosin phosphatase indicates ___ contraction

A

more

18
Q

NO leads to ___ of muscle

A

relaxation

19
Q

cAMP leads to ___ of muscle

A

contraction