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how does smooth muscle contract

by Paolo Berge Published 2 years ago Updated 2 years ago
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Full Answer

What are the steps of smooth muscle contraction?

the 4 steps of the contraction cycle:

  • ATP Hydrolysis.
  • Cross bridge attachment.
  • Power stroke.
  • Cross bridge detachment. Step 1: ATP Hydrolysis.

Can smooth muscle be contracted voluntarily?

Smooth muscle differs from skeletal muscle in a variety of ways, perhaps the most important being its ability to be contracted and controlled involuntarily. The nervous system can use smooth muscle to tightly regulate many of the body's subsystems for life with no thought from the user.

What are facts about smooth muscle?

Smooth muscle facts for kids. Smooth muscle is an involuntary non-striated muscle. It is divided into two subgroups; the single-unit (unitary) and multiunit smooth muscle. Within single-unit cells, the whole bundle or sheet contracts as a syncytium. Smooth muscle cells are found in the walls of hollow organs, including the stomach, intestines ...

Which muscle has the ability to contract?

The smooth muscle is a muscle tissue in which the contractile fibrils are not highly ordered, occurring in the gut and other internal organs and not under voluntary control. The smooth muscle is what helps push and contract your food so you can digest it. It is located in places like the intestines and stomach.

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What are the steps of smooth muscle contraction?

Steps involved in smooth muscle cell contraction:Depolarization of membrane or hormone/neurotransmitter activation.L-type voltage-gated calcium channels open.Calcium-induced calcium release from the SR.Increased intracellular calcium.Calmodulin binds calcium.Myosin light chain kinase activation.More items...

How is smooth muscle contraction different from skeletal muscle contraction?

The main difference between skeletal and smooth muscle contraction is that skeletal muscle contraction occurs through the binding of calcium to troponin, whereas smooth muscle contraction occurs through the binding of calcium to calmodulin.

What are the factors that trigger contraction in smooth muscles?

The triggers for smooth muscle contraction include hormones, neural stimulation by the ANS, and local factors. In certain locations, such as the walls of visceral organs, stretching the muscle can trigger its contraction (the stress-relaxation response).

Why is the contraction strength of smooth muscle?

Why is the contraction strength of smooth muscle relatively independent of its resting length? It gets nearly all of its Ca2+ from the extracellular fluid. It does not have intercalated discs.

How does smooth muscle contraction differ from skeletal muscle contraction quizlet?

How does smooth muscle differ from skeletal muscle? Smooth muscle has fewer sarcoplasmic reticulum. Smooth muscle lacks T tubules. Smooth muscle thick filaments have myosin heads along the entire length.

What is a major difference between skeletal muscle and smooth muscle?

Skeletal muscle fibers are cylindrical, multinucleated, striated, and under voluntary control. Smooth muscle cells are spindle shaped, have a single, centrally located nucleus, and lack striations.

What is the difference between smooth and skeletal muscle Brainly?

Answer: Smooth muscles are not under conscious control while skeletal muscles are under conscious control. Smooth muscles can be found within the walls of the internal organs like the stomach and the uterus while skeletal muscles are found in the biceps of the arm, the chest, and other muscles that can be moved.

How does smooth muscle compared to skeletal muscle quizlet?

Smooth muscles have more sarcoplasmic reticulum than skeletal muscles. Smooth muscle is under involuntary control while skeletal muscle is under voluntary control. Calcium binds to the regulatory protein, calmodulin, in smooth muscle while calcium binds to troponin in skeletal muscle.

What causes smooth muscle contractions?

Smooth muscle contractions are initiated by an increase in intracellular Ca2+ concentration that can occur by intracellular release of Ca2+ from the sarcoplasmic reticulum or by influx of Ca2+ from the extracellular fluid.

What is the main determinant of smooth muscle contraction?

The principal determinant of smooth muscle contraction is the intracellular free Ca2 + concentration, and phosphorylation of myosin light chain (MLC) by activated myosin light chain kinase (MLCK) in response to increased Ca 2 + is the main pathway by which vasoconstrictor stimuli induce crossbridge cycling of myosin and actin filaments. A secondary pathway for vascular smooth muscle contraction that is not directly dependent on Ca 2 + concentration, but rather mediating Ca 2 + sensitization, is the RhoA/Rho kinase pathway. In response to contractile stimuli, the small GTPase RhoA activates its downstream effector Rho kinase which, in turn, promotes contraction via myosin light chain phosphatase (MLCP) inhibition. RhoA/Rho kinase-mediated MLCP inhibition occurs mainly by phosphorylation and inhibition of MYPT1, the regulatory subunit of MLCP, or by CPI-17-mediated inhibition of the catalytic subunit of MLCP. In this review, we describe the molecular mechanisms underlying the pivotal role exerted by Rho kinase on vascular smooth muscle contraction and discuss the main regulatory pathways for its activity.

How does acetylcholine affect smooth muscle contraction?

Smooth muscle contraction, induced by acetylcholine through the muscarinic M3 receptor, starts with the release of Ca2+ from intracellular stores. Ca 2+ binds calmodulin that is complexed with myosin light chain kinase. This leads to activation of the kinase and subsequent phosphorylation of regulatory myosin light-chain at serine-19. Phosphorylation enables the onset of the ATPase cycle and sets in train the paddling of myosin-heads along an actin filament (a cycle of repeatedly binding, ratcheting, and letting go, sliding the thick filament over the thin filament). Reducing the intracellular free Ca 2+ concentration inactivates the kinase but does not necessarily stop smooth muscle contraction since the myosin light chain remains phosphorylated. Dephosphorylation of the myosin light chain occurs through the myosin-regulatory light-chain phosphatase which is composed of a regulatory subunit PPP1R12A, also known as MYPT-1 or M 110, and a catalytic subunit PPP1CC. PPP1R12A serves two purposes: it attaches the phosphatase to myosin, adjacent to the substrate, and it renders it highly selective for the myosin-regulatory light chain. The main outcome of the interaction of PPP1R12A with PPP1CC is the formation of an extended acidic groove, well adapted to accommodate the basic N-terminal sequence of myosin-regulatory light chain and making it much less attractive for other substrates ( Figure 2-49) ( Terrak et al., 2004 ).

What is the function of myosin and actin?

Myosin may be viewed to serve as an “engine” for smooth muscle contraction where as the actin cytoskeleton may function as a “transmission system” in smooth muscle. The actin cytoskeleton in smooth muscle also undergoes restructuring upon activation with growth factors or the ECM, which controls smooth muscle cell proliferation and migration.

How does actin cytoskeleton reorganization work?

Actin cytoskeletal reorganization facilitates smooth muscle contraction by promoting force transmission between the contractile unit and the extracellular matrix (ECM), and by enhancing intercellular mechanical transduction. Myosin may be viewed to serve as an “engine” for smooth muscle contraction whereas the actin cytoskeleton may function as ...

How does the colon work?

The colon works slowly, taking an average of 65 hours to transfer contents from the cecum to the rectum. However, transit can be much slower, without causing any symptoms. Disturbances of colonic motility and sensation, which primarily manifest as constipation, diarrhea, and abdominal discomfort in patients with disorders of function (e.g., irritable bowel syndrome; IBS) are major reasons for physician visits. These common disorders can be debilitating and last for years. In addition, colonic sensorimotor dysfunctions also occur in organic disorders such as inflammatory bowel disease.

Does smooth muscle increase cardiac output?

Venous smooth muscle contraction will decrease venous capacitance and thus increase cardiac output (Fig. 3 ). Arteriolar vasoconstriction occurs in the splanchnic circulation. The resulting decrease in its postcapillary pressure will cause translocation of blood out of the splanchnic bed and into the central veins, which again will contribute to the increased cardiac output ( Fig. 3) ( Barcroft and Samaan, 1935 ). Both decreased venous capacitance secondary to venous vasoconstriction and increased venous blood volume secondary to splanchnic arteriolar vasoconstriction are mediated by the sympathetic nervous system through the activation of vascular α-adrenoceptors.

How does smooth muscle work?

A person does not need to think about their blood pressure for it to adapt to increasing oxygen demands from exercise. The nervous system instead uses hormones, neurotransmitters, and other receptors to control smooth muscle spontaneously.

What is the function of smooth muscle?

The primary function of smooth muscle is contraction . Smooth muscle consists of two types: single-unit and multi-unit. Single-unit smooth muscle consists of multiple cells connected through connexins that can become stimulated in a synchronous pattern from only one synaptic input. Connexins allow for cell-to-cell communication between groups of single-unit smooth muscle cells. This intercellular communication allows ions and molecules to diffuse between cells giving rise to calcium waves. This unique property of single-unit smooth muscle allows for synchronous contraction to occur.[6]  Multi-unit smooth muscle differs from single-unit in that each smooth-muscle cell receives its own synaptic input, allowing for the multi-unit smooth muscle to have much finer control.

How does smooth muscle affect fertility?

In the genital system, smooth muscle is often a focus regarding its role in childbirth. Smooth muscle lines the uterus, which creates the contractile force during childbirth. Many pharmaceuticals exist specifically to help enhance smooth muscle contraction at the time of birth. While this may not represent an actual pathology, it is crucial to recognize that physicians can use a knowledge of smooth muscle physiology to prevent pathologies from occurring. In males, fertility is also a function of the contractions of smooth muscle in the epididymis and vas deferens. Without the contractile nature of smooth muscle, spermatozoa would never be able to assist in fertilization; this becomes important because of the apparent lack of information on the possible pathologic effects of smooth muscle and infertility. For example, many medications that are frequently used by males impact smooth muscle contractility and, therefore, may also affect fertility. Examples include nonsteroidal anti-inflammatory drugs, phosphodiesterase (PDE) inhibitors, nitrates, adrenergic receptor antagonists and agonists, psychotropic drugs, anticholinergic drugs, calcium antagonists, and ace inhibitors. [13]

How does calcium affect smooth muscle contraction?

Smooth muscle contraction depends on calcium influx. Calcium increases within the smooth muscle cell through two different processes. First, depolarization, hormones, or neurotransmitters cause calcium to enter the cell through L-type channels located in the caveolae of the membrane. Intracellular calcium then stimulates the release of calcium from the sarcoplasmic reticulum (SR) by way of ryanodine receptors and IP3; this process is referred to as calcium-induced calcium release.[7]  Unlike skeletal muscle, smooth muscle calcium release from the sarcoplasmic reticulum does not physically couple to the ryanodine receptor. Once calcium has entered the cell, it is free to bind calmodulin, which transforms into activated calmodulin. Calmodulin then activates the enzyme myosin light chain kinase (MLCK), MLCK then phosphorylates a regulatory light chain on myosin. Once phosphorylation has occurred, a conformational change takes place in the myosin head; this increases myosin ATPase activity, which promotes interaction between the myosin head and actin. Cross-bridge cycling then occurs, generating tension. The tension generated is relative to the amount of calcium concentration within the cell. ATPase activity is much lower in smooth muscle than it is in skeletal muscle. This factor leads to a much slower cycling speed of smooth muscle. However, the more extended period of contraction leads to a potentially greater force of contraction in smooth muscle. Smooth muscle contraction is enhanced even further through the use of connexins. Connexins allow for intercellular communication by allowing calcium and other molecules to flow to neighboring smooth muscle cells. This action allows for rapid communication between cells and a smooth contraction pattern.

What is the role of smooth muscle in asthma?

Smooth muscle also plays an essential role in the disease process throughout the body. The use of bronchodilators to relax airway smooth muscle is an important and life-saving treatment in asthmatics.[1]  Likewise, medications like metoclopramide can stimulate and promote gastric emptying by increasing smooth muscle signaling. Perhaps one of the most well-known uses of medical therapy and smooth muscle is the use of nitrates in the treatment of ischemic heart disease.[2]  Research showed that nitrates, in combination with ace inhibitors, can improve patient mortality.[3]  The uniquely significant impact that smooth muscle has throughout the body makes it an important topic for medical professionals to understand as many treatments at their core rely on modifying the signaling pathways that affect smooth muscle.

Why is smooth muscle important?

Smooth muscle derives from both mesoderm and neural crest cells; this is because smooth muscle contributes to many different tissues throughout the body. One unique feature of neural crest cells is that their migration occurs during embryological development. For this reason, numerous tissues throughout the body originate from neural crest cells. Neural crest cells play a vital role in the development of smooth muscle throughout the body, specifically in the regulation of blood vessels.

What is smooth muscle?

At a cellular level, smooth muscle functions as an involuntary non-striated muscle. Smooth muscle contains thick and thin filaments that do not arrange into sarcomeres, resulting in a non-striated pattern. On microscopic examination, it appears homogenous. Smooth muscle cytoplasm contains large amounts of actin and myosin. Actin and myosin act as the main proteins involved in muscle contraction. Actin filaments attach to dense bodies spread throughout the cell. Dense bodies can be observed under an electron microscope and appear dark. Another important structure is the calcium-containing sarcoplasmic reticulum, which aids in sustaining contraction. The shape of smooth muscle is fusiform, which is round in the center and tapering at each end. Smooth muscle can tense and relax but has greater elastic properties than striated muscle. This quality is important in organ systems like the urinary bladder, where the preservation of contractile tone is a necessity.

How does smooth muscle contract?

Like all muscle tissue, the function of smooth muscle is to contract. The image above shows how the actin and myosin fibers shorten, effectively shrinking the cell. However, there are some important differences in how the smooth muscle contracts, compared to other types of muscle. In skeletal muscle, a signal from the somatic nervous system traverses to the muscle, where it stimulates organelles in the muscle cell to release calcium. The calcium causes a protein to detach from actin , and myosin quickly binds to the opening on actin. Since there was always available ATP, the myosin uses it to quickly contract the cell.

What is smooth muscle?

Smooth muscle is a type of muscle tissue which is used by various systems to apply pressure to vessels and organs. Smooth muscle is composed of sheets or strands of smooth muscle cells. These cells have fibers of actin and myosin which run through the cell and are supported by a framework of other proteins. Smooth muscle contracts under certain stimuli as ATP is freed for use by the myosin. The amount of ATP released depends on the intensity of the stimuli, allowing smooth muscle to have a graded contraction as opposed to the “on-or-off” contraction of skeletal muscle.

What is the staircase arrangement of actin and myosin?

As seen in the image below, the actin and myosin filaments in smooth muscle are arranged in a stacked pattern across the cell. This “staircase” arrangement of actin and myosin is much different than the structure in skeletal and cardiac muscle. The actin filaments (red lines) in smooth muscle run from one side of the cell to the other, ...

Why is it important that the rest of the sheet of cells respond to a contraction?

B is correct. When a contraction happens in a smooth muscle tissue , it is important that the rest of the sheet of cells respond. The gap junctions found between cells allow for the passage of the nerve impulse or chemical signal which started the contraction. This ensures that many cells contract at once, producing the desired effect for the organism.

Why is smooth muscle adapted to many areas of the body?

This specialized function of contracting for long periods and hold that force is why smooth muscle has been adapted to many areas of the body. Smooth muscle lines many parts of the circulatory system, digestive system, and is even responsible for raising the hairs on your arm.

What is the ATP released by myosin?

Smooth muscle contracts under certain stimuli as ATP is freed for use by the myosin. The amount of ATP released depends on the intensity of the stimuli , allowing smooth muscle to have a graded contraction as opposed to the “on-or-off” contraction of skeletal muscle.

Why is smooth muscle important?

Smooth muscle, because of its ability to contract and hold , is used for many function in many places of the body. Besides those listed above, smooth muscle is also responsible for contracting the irises, raising the small hairs on your arm, contracting the many sphincters in your body, and even moving fluids through organs by applying pressure to them. While smooth muscle doesn’t contract or release as quickly as skeletal or cardiac muscle, it is much more useful for providing consistent, elastic tension.

Is smooth muscle contracts slowly and automatically?

Smooth muscle tissue, unlike striated muscle, contracts slowly and automatically. It constitutes much of the musculature of internal organs and the digestive system.

Does smooth muscle have slow contractions?

In general, smooth muscles contract more slowly than do skeletal muscle fibers and maintain the contraction for longer periods of time. Smooth muscles can be divided into phasic muscles which contract more rapidly and tonic muscles which contract slowly and maintain tension for long periods of time.

Which muscle tissue has slow contractions?

Smooth muscle cannot be controlled consciously and thus acts involuntarily. The non-striated (smooth) muscle cell is spindle-shaped and has one central nucleus. Smooth muscle contracts slowly and rhythmically.

Is smooth muscle slow to contract?

In general, smooth muscles contract more slowly than do skeletal muscle fibers and maintain the contraction for longer periods of time. Smooth muscles can be divided into phasic muscles which contract more rapidly and tonic muscles which contract slowly and maintain tension for long periods of time.

What receptor causes constriction of smooth muscle?

Alpha-1 and alpha-2 receptors function to cause vasoconstriction by contracting vascular smooth muscle cells leading to systemic hypertension. Beta-2 receptors also respond to sympathetic stimulation but produce a vasodilatory effect and which will lead to systemic hypotension.

How do you stimulate smooth muscle?

Smooth muscle can be stimulated by pacesetter cells, by the autonomic nervous system, by hormones, spontaneously, or by stretching. The fibers in some smooth muscle have latch-bridges, cross-bridges that cycle slowly without the need for ATP; these muscles can maintain low-level contractions for long periods.

Does smooth muscle contract automatically?

Smooth muscle tissue, unlike striated muscle, contracts slowly and automatically. It constitutes much of the musculature of internal organs and the digestive system.

How do smooth muscle cells work?

Smooth muscle cells can undergo hyperplasia, mitotically dividing to produce new cells. The smooth cells are nonstriated, but their sarcoplasm is filled with actin and myosin, along with dense bodies in the sarcolemma to anchor the thin filaments and a network of intermediate filaments involved in pulling the sarcolemma toward the fiber’s middle, shortening it in the process. Ca ++ ions trigger contraction when they are released from SR and enter through opened voltage-gated calcium channels. Smooth muscle contraction is initiated when the Ca ++ binds to intracellular calmodulin, which then activates an enzyme called myosin kinase that phosphorylates myosin heads so they can form the cross-bridges with actin and then pull on the thin filaments. Smooth muscle can be stimulated by pacesetter cells , by the autonomic nervous system, by hormones, spontaneously, or by stretching. The fibers in some smooth muscle have latch-bridges, cross-bridges that cycle slowly without the need for ATP; these muscles can maintain low-level contractions for long periods. Single-unit smooth muscle tissue contains gap junctions to synchronize membrane depolarization and contractions so that the muscle contracts as a single unit. Single-unit smooth muscle in the walls of the viscera, called visceral muscle, has a stress-relaxation response that permits muscle to stretch, contract, and relax as the organ expands. Multiunit smooth muscle cells do not possess gap junctions, and contraction does not spread from one cell to the next.

Does smooth muscle increase in size?

Similar to skeletal and cardiac muscle cells, smooth muscle can undergo hypertrophy to increase in size. Unlike other muscle, smooth muscle can also divide to produce more cells, a process called hyperplasia. This can most evidently be observed in the uterus at puberty, which responds to increased estrogen levels by producing more uterine smooth muscle fibers, and greatly increases the size of the myometrium.

How Does Ach Cause Smooth Muscle Relaxation?

Smooth muscle relaxation is caused by the release of acetylcholine (ACh) from the presynaptic neuron. ACh binds to muscarinic receptors on the postsynaptic cell and causes an increase in cyclic adenosine monophosphate (cAMP) levels. This increase in cAMP levels leads to smooth muscle relaxation.

How Does Ach Affect Smooth Muscle Contraction?

Channels open as a result of interactions with, causing ion flow to depolarize muscle cells by promoting cell division. Muscle contraction occurs as a result of depolarization, similar to how skeletal muscle does.

Does Acetylcholine Cause Muscle Relaxation Or Contraction?

There is no one definitive answer to this question. Acetylcholine is a neurotransmitter that can have different effects on muscles depending on the type of receptor that is activated. In general, activation of muscarinic receptors tends to cause muscle relaxation, while activation of nicotinic receptors tends to cause muscle contraction.

Does Acetylcholine Increase Smooth Muscle Contraction

Muscarinic acetylcholine receptors are classified as muscarinic and are a class of metabotropic receptors that regulate muscarinic cholinergic receptors. Acetylcholine, the main neurotransmitter in muscarinic cholinergic receptors, depolarizes various smooth muscles and initiates contraction.

Effect Of Atropine On Smooth Muscle

The effects of amino acid atropine, both at lower and higher concentrations, can be felt on cavernosal smooth muscle at lower doses and at higher concentrations.

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