In skeletal muscle

In higher animals, large percentages of the terminal cisternae of cardiac muscle are not associated with t-tubules at all. For SR of this type, Ca release must occur by a different mechanism from that found in skeletal muscle. In this case, it appears that Ca leaking through sarcolemmal Ca channels can trigger the release of even more Ca from the SR. This latter process is called Ca -induced Ca release (abbreviated CICR). 

Lnczak-Szcznrek, A., and Flisinska-Bojanowska, A., 1977. Effect of high-protein diet on glycolytic processes in skeletal muscles of exercising rats. Journal of Physiology and Pharmacology 48 119—126. 

Hardie DG, Sakamoto K (2006) AMPK a key sensor of fuel and energy status in skeletal muscle. Physiology (Bethesda) 21 48-60... 

DICR (depolarization-induced Ca2+ release) is Ca2+ release triggered by depolarization of the sarcolemma. In skeletal muscle, conformational change in the voltage sensor (a 1S subunit of the dihydropyridine receptor) in the T-tubule is directly transmitted to the... 

NFAT proteins are expressed in skeletal, cardiac, and smooth muscle and play important roles in the regulation of the development and differentiation of these tissues. In skeletal muscle, NFAT isoforms are expressed at different stages of development and regulate progression from early muscle cell precursors to mature myocytes. NFAT proteins have also been shown to control the expression of the myosin heavy chain and positively regulate muscle growth [1, 2]. 

The subtypes of nAChR that are not found in skeletal muscle are collectively referred to as neuronal nAChRs . 

Parvalbumin is a cytosolic protein expressed mainly in skeletal muscles and brain. 

Tissue-Specific Expression. In the adult rodent, PPARy is expressed in brown and white adipose tissue, and at lower levels in intestine, retina, skeletal muscle, and lymphoid organs. In human, PPARy is most abundantly expressed in white adipose tissue and at lower levels in skeletal muscle, the heart, and liver, but not in lymphoid tissues, although PPARy has been identified in macrophages in human atheromas. 

Ryanodine leads to contracture of mammalian skeletal muscle, whereas it causes negative inotropism in cardiac muscle. This apparent opposite effects are due to difference in the Ca2+ extruding activity the released Ca2+ remains within cytoplasm in skeletal muscle because of low Ca2+ extruding activity, whereas the increased cytoplasmic Ca2+ is rapidly excluded out of the cytoplasm in cardiac muscle via Na+ -Ca2+ -exchange. 

S100A1 is the most abundant in the myocardium but is also expressed in brain and other tissues. S100A1 was found to stimulate Ca2+-induced Ca2+-release (CICR) in skeletal muscle terminal cisternae. In the presence of nanomolar Ca2+-concentrations, S100A1 binds to the ryanodine receptor increasing its channel open probability, and was shown to enhance SR Ca2+-release and contractile performance. Several animal models (over expressing S100A1 or S100A1-deficient mice) have... 

These cascades of reactions need time in the range of seconds synaptic transmission through GPCRs is slow. All further postsynaptic changes depend on the type of postsynaptic cell. For example activation of 32-adrenoceptors causes in the heart an increase of the rate and force of contraction in skeletal muscle glycogenolysis and tremor in smooth muscle relaxation in bronchial glands secretion and in sympathetic nerve terminals an increase in transmitter release. 

The skeletal muscle relaxants are contraindicated in patients with known hypersensitivity. Baclofen is contraindicated in skeletal muscle spasms caused by rheumatic disorders. Carisoprodol is contraindicated in patients with a known hypersensitivity to meprobamate. Cyclobenzaprine is contraindicated in patients with a recent myocardial infarction, cardiac conduction disorders, and hyperthyroidism, hi addition, cyclobenzaprine is contraindicated within 14 days of the administration of a monoamine oxidase inhibitor. Oral dantrolene is contraindicated in patients with active hepatic disease and muscle spasm caused by rheumatic disorders and during lactation. See Chapter 30 for information on diazepam. 

The structure of the contractile apparatus of smooth muscle at the next higher level is also characteristically different from other muscles. The concentrations of actin and myosin in smooth muscle are about three times higher for actin and four times lower for myosin than in skeletal muscle. Correspondingly, in smooth muscle the ratio of the numbers of moles of actin to moles of myosin, and the ratio of the number of actin filaments to those of myosin filaments, are about 12 times larger than for other muscles. Thus, the arrangements of the two sets of filaments are bound to be quite different just on the basis of numbers of actin and myosin... 

The analytic validity of an abstract parallel elastic component rests on an assumption. On the basis of its presumed separate physical basis, it is ordinarily taken that the resistance to stretch present at rest is still there during activation. In short, it is in parallel with the filaments which generate active force. This assumption is especially attractive since the actin-myosin system has no demonstrable resistance to stretch in skeletal muscle. However, one should keep in mind, for example, that in smooth muscle cells there is an intracellular filament system which runs in parallel with the actin-myosin system, the intermediate filament system composed of an entirely different set of proteins, (vimentin, desmin, etc.), whose mechanical properties are essentially unknown. Moreover, as already mentioned, different smooth muscles have different extracellular volumes and different kinds of filaments between the cells. 

The compliance in series with the active force. Force exerted by the activated elements must be transmitted or borne by whatever structural elements are in series with them. In skeletal muscle there is clearly a tendon in series but not so with smooth muscle. In smooth muscle, the total length of contractile apparatus is broken up into individual cells with intercalating extracellular connective structures. In addition, the portions of the crossbridges in series with the pulling site must also be stretched before force can rise to isometric levels. Taken together, the... 

In the sarcoplasm of smooth muscle cells there is a membrane bound compartment usually referred to as the SR by analogy with skeletal muscle. However, it is not at all clear that the interior of these membrane-bound regions are continuous as they are in skeletal muscle. The primary properties of this system seem to be quite similar to those of the endoplasmic reticulum of many other cell types. In general, calcium is concentrated into the membrane-bound reticulum and then released to initiate the characteristic action of the cell. 

It has been shown that inositol triphosphate (IP3) is involved in the excitation-contraction coupling in smooth muscle (Vergara et al., 1985), but presently no clear evidence has been reported for a similar involvement in skeletal muscle. If IP3 functions as a messenger for Ca release, it would bridge the gap between muscle metabolic changes and Ca release, as ATP is a prerequisite for IP3 regeneration. 

Schneider, M.F. Chandler, W.K. (1973). Voltage dependent charge movement in skeletal muscle A possible step in excitation-contraction coupling. Nature 242,244-246. 

Sjogaard, G., Adams, R.P., Saltin, B. (1985). Water and ion shifts in skeletal muscle of humans with intense dynamic knee extension. Am. J. Physiol. 248, R190-R196. 

Spriet, L.L., Soderlund, K., Bergstrom, M., Hultman, E. (1987a). Anaerobic energy release in skeletal muscle during electrical stimulation in men. J. Appl. Physiol. 62, 611-615. 

Westerblad, H., Lee, J.A., Lamb, A.G., Bolsover, S.R., Allen, D.G. (1990). Spatial gradients of intracellular calcium in skeletal muscle during fatigue. Pfluegers Arch. 415, 734-740. 

The gene for myophosphoiylase has been assigned to chromosome 1 lql3. The enzyme is a dimer of two identical 97 IcDa subunits and is the sole isoform present in skeletal muscle. Heart and brain also contain this isoform in addition to a distinct brain isoenzyme and a hybrid muscle/brain isoform. Smooth muscle also contains a phosphorylase isoform distinct from the muscle isoenzyme. If regenerating muscle fibers are present they also contain phosphorylase activity due to the presence, in fetal and developing muscle, of an isoform said to be identical with brain phosphorylase. 

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