Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.6.4.1 (myosin ATPase)
 1,140 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Endurance exercise training has been found to enhance the functional capacity of the myocardium in several animal models. The sub-cellular phenomena accompanying the augmented function are yet to be explained. The present study sought to determine if the myosin ATPase activity of cardiac muscle increased as a result of endurance conditioning. Five beagles trained by running on a motor driven treadmill (T) and five control (NT) animals were studied. Follwoing 10 weeks of training the T group had a significantly (P less than .05) lower heart rate than the NT while performing the same submaximal exercise and the gastrocnemius cytochrome oxidase activity was significantly greater (P less than .005) in the T than in the NT. These two measurements established that the exercised animals were physically trained. Myosin was isolated from the left ventricular myocardium and activated in a medium containing K-EDTA. No significant (P less than .05) difference in maximum myosin ATPase activity was observed between the NT and T groups in cardiac muscle. It was concluded that cardiac muscle myosin ATPase activity was not affected by 10 weeks of endurance conditioning induced by treadmill running in dogs.
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PMID:Effect of endurance training on myocardial myosin adenosine triphosphatase activity of the dog. 16 Apr 87

1. Using histochemical staining methods for myosin ATPase oxidative and glycolytic enzymes, three major types of muscle fibre could be identified in the skeletal muscle of hamsters and mice. 2. Muscle fibre counts showed that the proportions of the different fibres were not entirely stable with age. In the hamster biceps brachii which is predominantly composed of ATPase-high fibres there was a decrease in the number of ATPase-low fibres. In the soleus muscle which is predominantly composed of ATPase-low fibres there was a decrease in ATPase-high fibres with age. 3. Although there was a change in the proportions of fibre types there was no change in the total number of fibres within the muscles with age. It is suggested that some reinnervation may take place during growth and that this is why the less dedominant fibre type decreases. 4. The response of the different fibre types to partial starvation was studied. The ATPase-high fibres showed the greatest decrease in size. Of these, the ATPase-high glycolytic type responded more than the ATPase-high oxidative type. The effects of the under-nutrition on the different fibre types were found to be completely reversible. Starvation did not affect the total number of fibres or the numbers of any fibre type. 5. The response of the different types to high intensity exercise (weight lifting) was studied. This type of exercise resulted in hypertrophy of all three major fibre types. However, the extent of the response varied according to the fibre type and the exact nature of the exercise. In most cases the ATPase-high fibres underwent hypertrophy more readily than the ATPase-low fibres. Where distinction was made between the two types of ATPase-high fibres, the ATPase-high glycolytic were found to hypertrophy more than the ATPase-high oxidative fibres. The effects of post exercise recovery (return to relative inactivity) were also studied and the changes in size of the fibres were found to be completely reversible.
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PMID:Changes in rodent muscle fibre types during post-natal growth, undernutrition and exercise. 16 Sep 29

Whereas dissociation of rabbit skeletal muscle myosin light chains occurs at an increased temperature (25 degrees) and in the absence of divalent cations, reassociation of the myosin oligomer requires a low temperature (4 degrees C) and the presence of divalent cations, thus resulting in the original light to heavy chain stoichiometry. With a 5-10 per cent release of alkali light chains, LC1 and LC3, and a 50 per cent dissociation of the Ca2+ binding light chain, LC2, there is no significant decrease in myosin ATPase activity irrespective of the cation activator, however, there is an approximate 15-20 per cent decrease in actomyosin ATPase activity. With reassociation of the myosin oligomer, actomyosin ATPase activity is partially restored as well as the original number of Ca2+ binding sites.
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PMID:Dissociation and reassociation of rabbit skeletal muscle myosin. 16 9

This review summarizes the results obtained by biochemical and physiological studies on the functional implications of the two-headed structure of the myosin molecule. Our nonidentical two-head hypothesis of myosin is supported by biochemical studies on myosin ATPase. The reaction mechanism of the Mg2+-ATPase reaction catalyzed by one head of the myosin molecule is shown to be different from that catalyzed by the other head, and the reaction intermediate, MPADP, is produced in head B but not in head A. Evidence for differences in the chemical structures of the two heads of myosin is also presented. The myosin preparation is shown to be a mixture of homodimers with respect to its g-chain composition, but every homodimer has the non-identical two heads, B and A. Furthermore, the molecular mechanism for acceleration of the Mg2+-ATPase reaction by F-actin and that for its control by Ca2+ ions and Mg2+-ATP are discussed, based on the nonidentical two-head hypothesis of the myosin molecule. It was shown that the formation and decomposition of the key intermediate, A(B)MPADP are required for tension development and shortening. One cycle of ATP hydrolysis by crossbridges synchronously initiated by a rapid stretch or a sudden release of a slow stretch, indicating that the probability of dissociation of a crossbridge by its interaction with ATP depends on its angular position. It is also demonstrated that rotation of the base of nucleoside triphosphate about the glycosyl bond is essential for formation of MPXDP from M2XTP, as well as for muscle contraction. Based on these biochemical and physiological studies on the movement of the myosin head in muscle contraction, a molecular mechanism for muscle contraction is proposed.
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PMID:Functional implications of the two-headed structure of myosin. 16 89

Myosin isolated under phosphorylation conditions, showed an additional band of phosphorylated light chain. In the case of cardiac myosin, LC2 is the phosphorylated light chain whereas in skeletal myosin, it is the 18,000 dalton component known as DTNB light chain. There are no differences in K+-EDTA and Ca2+ activated myosin ATPase of cardiac and skeletal of control and phosphorylated myosins. Our experiments showed that the rat heart and skeletal muscle myosins isolated under phosphorylating conditions exhibited high phosphate content which is associated with higher actin activated Mg2+ ATPase activity of myosin as compared to control. Control myosin phosphorylated using myosin light chain kinase and Ca2+ also showed high actin activated myosin ATPase activity. Beef heart myosin isolated in the presence of phosphate buffer, also exhibited a higher level of phosphate followed by an increase in actin activation as compared to myosin isolated in the absence of phosphate buffer. All these experimental data suggest that there is a direct relationship between actin activation and the amount of phosphate incorporated as a result of phosphorylation.
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PMID:Phosphorylation and its effects on ATPase activity of cardiac and skeletal myosins. 16 48

The kinetic parameters of the inhibition of monovalent cation activated myosin ATPase by ADP were investigated. The inhibitor constant (KI) was 1.65 X 10(-4) M and the maximal velocity (V) was 1.28 mumol Pi/mg myosin/min in the presence of 0.3M Kcl at 20 degrees C. The dependence of 1/VO on inhibitor concentration and the pH dependence of KI and Km (i.e. pKi approximately equal to pKm) show that the inhibition has a pure competitive character. The results are supported by energetic parameters, too. The enthalpy of the formation of (EI) complex was calculated. Similar results were obtained also in the presence of Rb+ activated myosin ATPase and subfragment-I K+ ATPase.
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PMID:Kinetic study of the inhibition of myosin ATPase activity by ADP. 16 61

The histochemical and ultrastructural effects of extracorporeal circulation and aortic cross-clamping during coronary heart surgery have been examined in drill biopsy samples of the left ventricle in 22 patients. The biopsies were obtained before and after bypass with a DeSoutter drill. Histochemical studies indicated definite differences between control and experimental biopsies, with increased succinic dehydrogenase, cytochrome oxidase, and LDH activity, while phosphorylase A and myosin ATPase activities declined. Furthermore, free phospholipid levels increased, as determined by the acid hematein reaction. Ultrastructural examination demonstrated loss of glycogen, intracellular swelling, and mitochondrial damage, which included loss of matrix density, loss of cristae, and eventual disruption in the postbypass biopsy. These results, which closely resemble the effects of ischemia and reperfusion observed in animal experiments, suggest that the initial insult is a change in membrane permeability regulation.
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PMID:Histochemical and structural changes in human myocardial cells after cardiopulmonary bypass. 16 88

Electron-microscopic, morphometric, histochemical and biochemical studies were carried out on muscle biopsies from a patient with the characteristic clinical and pathological findings of nemaline myopathy. The mean fiber diameter was decreased, and the vastus lateralis muscle biopsy consisted exclusively of slow twitch (Type I) fibers. Quantitative biochemical investigations revealed significantly low calcium uptake and ATPase activity of the fragmented sarcoplasmic reticulum and decreased myosin ATPase activity. The electrophoretogram of myosin showed an abnormality in the light chain pattern which could not be explained by a disproportion of normal fiber types.
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PMID:Characteristics of myosin in nemaline myopathy. 17 35

A 35--70% ammonium sulfate fraction of smooth muscle actomyosin was prepared from guinea pig vas deferens. This fraction also contains a smooth muscle myosin kinase and a phosphatase that phosphorylates and dephosphorylates, respectively, the 20,000-dalton light chain of smooth muscle myosin. Phosphorylated and dephosphorylated smooth muscle myosin. Phosphorylated and dephosphorylated smooth muscle myosin were purified from this ammonium sulfate fraction by gel filtration, which also separated the kinase and the phosphatase from the myosin. Purified phosphorylated and dephosphorylated myosin have identical stained patterns after sodium dodecyl sulfate/polyacrylamide gel electrophoresis. They also have similar ATPase activities measured in 0.5 M KCl in the presence of K+-EDTA and Ca2+. However, the actin-activated myosin ATPase activity is markedly increased after phosphorylation. Moreover, the actin-activated ATPase activity of phosphorylated myosin is inhibited by the removal of Ca2+ in the absence of any added regulatory proteins. Dephosphorylation of myosin results in a decrease in the actin-activated ATPase activity. Skeletal muscle tropomyosin markedly increased the actin-activated ATPase activity of phosphorylated but not dephosphorylated myosin in the presence, but not in the absence, of Ca2+.
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PMID:Effect of phosphorylation of smooth muscle myosin on actin activation and Ca2+ regulation. 18 2

Myocardial contractility can be regulated by two types of control mechanism. A "tonic control mechanism", which allows the heart to respond to sustained changes in circulatory dynamics, appears to operate through changes in the structure of various constituents of the myocardium, best understood of these being changes in the myosin molecule that cause alterations in both myosin ATPase activity and contractility. Beat-to-beat changes in myocardial contractility are affected by a "phasic control mechanism" that involves changes in at least five calcium fluxes in the myocardium. The effects of catecholamines, many of which appear to be mediated by cyclic AMP, can be understood in terms of the modification of several of the calcium fluxes involved in the phasic control of myocardial contractility.
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PMID:"Tonic" and "phasic" mechanisms in the regulation of myocardial contractility. 18 48


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