Excitation contraction coupling in smooth muscle. Excitation Contraction Coupling 2018-12-22

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Smooth muscle

excitation contraction coupling in smooth muscle

The heart derives energy from aerobic metabolism via many different types of nutrients. Structure of t-tubules in adult cardiomyocytes isolated from healthy rat left and from rat receiving heterotopically transplanted heart for four weeks right. For example, cyclic nucleotides can relax arterial smooth muscle without reductions in crossbridge phosphorylation, a process termed force suppression. Each of these heavy chains contains the head domain, while the tails take on a morphology, holding the two heavy chains together imagine two snakes wrapped around each other, such as in a. It is found primarily in nervous and muscular tissue.

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Smooth muscle

excitation contraction coupling in smooth muscle

Contraction is initiated by a calcium-regulated phosphorylation of myosin, rather than a calcium-activated troponin system. The caveolae are often close to sarcoplasmic reticulum or mitochondria, and have been proposed to organize signaling molecules in the membrane. Berlin, Springer, 1996; Chapter 46, Table 46. From , it also can be seen that in rat ureter, cooling produced a significantly greater effect on the duration of the Ca 2+ transient at its peak level compared with guinea pig ureter five to eight times versus two to three times, respectively. The ratio of to is between 2:1 and 10:1 in smooth muscle.

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Smooth muscle

excitation contraction coupling in smooth muscle

The action potentials of both species were markedly altered by cooling, but in different ways. Force generation of the contractile elements: the cross-bridging cycle. The series elastic element has no anatomic counterpart, and it reflects the tendency of the muscle to develop tension before actual shortening occurs. Neuromuscular junctions are more difficult to identify than in skeletal muscle. Exp Cell Res 251: 92—101, 1999.


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Excitation

excitation contraction coupling in smooth muscle

Together, myosin and actin form myofibrils, the repeating molecular structure of sarcomeres. Recurring Ca 2+ release-uptake cycles provide the basis for periodic elevations of cytosolic Ca 2+ concentration and contractions of myocytes, hence for the orderly beating of the heart. Similarly to skeletal muscle, the influx of sodium ions causes an initial depolarization; however, in cardiac muscle, the influx of calcium ions sustains the depolarization so that it lasts longer. Crossbridge cycling causes contraction of myosin and actin complexes, in turn causing increased tension along the entire chains of tensile structures, ultimately resulting in contraction of the entire smooth muscle tissue. The influence of temperature on smooth muscle force production has been reported for several smooth muscles , and as mentioned above the effects of decreasing temperature have been reported to potentiate or inhibit force.

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Excitation Contraction Coupling in Skeletal and Smooth Muscle Flashcards

excitation contraction coupling in smooth muscle

In turn, this would tend to increase force production. The linear leakage current was subtracted from the overall membrane current. Lactate, created from lactic acid fermentation, accounts for the anaerobic component of cardiac metabolism. Contractility and calcium transients have only recently been examined as a potential mechanism for inducing heart failure in a subset of patients with cardiac atrophy. Agonist stimulation of smooth muscle contractility involves integration of many signal-transducing events from the plasma membrane to myofilaments in the cytoplasm.

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On the Mechanisms Whereby Temperature Affects Excitation

excitation contraction coupling in smooth muscle

The close proximity of the RyR2 to the T tubule enables each L-type Ca 2+ channel to activate 4 to 6 RyR2s and generate a Ca 2+ spark. In a similar manner, the myosin head possesses stored energy, which is released when the myosin heads bind to actin and swivel. The Rhoa and Rac portion of the signaling pathway provides a calcium-independent way to regulate resistance tone. Ionic currents in single smooth muscle cells from the ureter of the guinea-pig. The minimum concentration of free Ca required to evoke contraction in skinned muscle cells was 1-2 × 10 -7 m and the maximum contraction was produced at 10 -5 m.

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Cardiac Muscle Tissue

excitation contraction coupling in smooth muscle

The produced pyruvate can then be burned aerobically in the citric acid cycle also known as the tricarboxylic acid cycle or Krebs cycle , liberating a significant amount of energy. We can use the data obtained in this study to understand the effects of cooling to increase maximal force in the rat and decrease it in the guinea pig, as follows. However, there is surprisingly little definitive information concerning the fundamental mechanisms underlying the effect of cooling, which vary substantially between different smooth muscles. Electrical Activity The changes found with cooling on electrical activity, go some way, but not entirely, to explaining the effects seen on force. Evidence for multiple sources of calcium for activation of the contractile mechanism of guinea-pig taenia coli on stimulation with carbachol. Roles of Ca 2+ and Na + in the inward current and action potentials of guinea pig ureteral myocytes Am.

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Smooth muscle

excitation contraction coupling in smooth muscle

Effects of Cooling on Contraction Cooling produced a reduction in the amplitude of the contraction of the guinea pig ureter, but an increase in the rat ureter. Extracellular Ca ++ directly activates smooth muscle actin, whereas the sarcoplasmic reticulum is the primary source of Ca ++ in skeletal muscle. A jump from 22 to 32°C on the parameters of the phasic contraction of the rat ureter. Upper and lower left panels from rabbit portal vein and lower right from chicken amnion. As mentioned above the kinetics of the Ca 2+ rise were also little altered by cooling. The intermediate filaments are connected to other intermediate filaments via dense bodies, which eventually are attached to also called focal adhesions in the of the smooth muscle cell, called the.

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