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Query: UNIPROT:P20020 (
adenosine triphosphatase
)
3,299
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The purpose of this study was to examine the distribution of
myosin
isozymes in rodent (Rattus norvegicus) hindlimb skeletal muscles and regions of muscle known to have contrasting fiber-type composition. Muscle samples were analyzed for Ca2+-regulated myofibril
adenosine triphosphatase
(
ATPase
) activity, Ca2+-activated myosin ATPase activity,
myosin
isozyme profile, and myosin light chain profile. Four isozymes of
myosin
were identified based on native protein and light chain electrophoresis patterns: one associated primarily with slow-twitch muscle (SM) and three associated primarily with fast-twitch muscle (FM). Multiple linear regression analysis of Ca2+-regulated myofibril
ATPase
activity (pCA 4) vs. measured isozyme profile was used to estimate the myofibril
ATPase
activities of the individual isozymes (FM1 = 0.86, FM2 = 0.52, FM3 = 0.31, and SM = 0.15 mumol Pi formed . mg myofibril protein-1 . min-1 at 25 degrees C, n = 180, P less than 0.001). Differences in the native isozyme profiles and myofibril
ATPase
activities between muscles and muscle regions of similar fiber type composition indicate that a given fiber type may not necessarily express a single isozyme profile. These data are consistent with the hypothesis that, among rodent hindlimb skeletal muscles and inherently their motor units, a range of
myosin
isozyme profiles exists that may provide a broad range of mechanical expression.
...
PMID:Myosin isozyme distribution in rodent hindlimb skeletal muscle. 294 6
By means of histological methods for revealing
adenosine triphosphatase
of
myosin
(pH 4.6) and succinate dehydrogenase activity, using postmortem material, development of various muscle fibers of the femoral m. quadriceps and m. soleus has been studied in human ontogenesis. The first stage of rearrangements lasts from the 5th-6th month of the uterine development up to 2 years of age and is characterized by formation (from non-differentiated) of oxidative, glycolytic and oxidative-glycolytic fibers. During the period from 2 up to 7-8 years of age the ratio in the types changes slightly, but transversal section size of the muscle fiber increases intensively. Then from 11 up to 17 years of age, together with maximal increment of the fibers transversal section, there is an essential change in the type relation. By the 17th years of age, in the femoral m. quadriceps the part of the fibers with glycolytic type of energy supply increases, while in the m. soleus the oxidative fibers become more numerous. By the 70th years of age in the femoral m. quadriceps relative amount of intermediate fibers increases.
...
PMID:[Development of various types of muscle fibers in the quadriceps femoris and the soleus during human ontogenesis]. 294 54
A non-failing hypertrophy of the left ventricle was produced in the pig heart by supravalvular banding of aorta for 4, 8 and 12 weeks and the
myosin
and myofibrillar
adenosine triphosphatase
activities were measured. A significant increase in
myosin
Ca2+-ATPase activity was seen at 4 weeks of hypertrophy, but at 8 and 12 weeks this activity was significantly decreased compared to sham control. Similar changes were also seen in actin-activated myosin ATPase activities at 4, 8 and 12 weeks of hypertrophy. There were no changes in the K+- and NH4+-EDTA-stimulated ATPAse activities of
myosin
. Basal ATPase activities of myofibrils were decreased at 4 and 8 weeks of hypertrophy and there was no change in this activity at 12 weeks of hypertrophy. Ca2+ stimulated ATPase activity of myofibrils was significantly increased at 4 weeks, normal at 8 weeks and significantly reduced at 12 weeks of hypertrophy. The changes in ATPase activities were not due to any alterations of proteins by high concentrations of salts during the purification of
myosin
. The non-hypertrophied right ventricle from the banded animals did not show any change in the basal or Ca2+ stimulated myofibrillar ATPase activities. It is suggested that hypertrophy of the myocardium is accompanied by specific changes in the enzyme activities of the contractile proteins and the biphasic responses may correlate with the functional state of the myocardium subjected to a chronic increase in pressure.
...
PMID:A biphasic change in contractile proteins during the development of cardiac hypertrophy in pigs. 295 33
1. Normal and chronically stimulated peroneus longus muscles of the cat's hind limb were studied with respect to fibre size and staining properties for myofibrillar (
myosin
)
adenosine triphosphatase
(
ATPase
) and succinate dehydrogenase (SDH) activity. The intensity of staining for SDH activity was measured by microphotometry from the central portions of the muscle fibres ('core-SDH staining'). For comparison, histochemical properties were also studied in non-stimulated soleus muscles. 2. On account of the pH sensitivity of their myofibrillar
ATPase
, about 18% of the fibres in normal peroneus longus muscles were classified as type I, and about half of the remainder as II A and II B respectively. 3. In the normal peroneus longus muscles, the mean diameter of single muscle fibres generally varied between about 25 and 75 micron, whereby the average size of type I less than type II. 4. In the normal peroneus longus muscles the staining intensity for core SDH varied over a wide range. The average heaviness of staining was clearly ranked in the order type I greater than type II A greater than type II B. 5. Chronic stimulation was given to the deafferented common peroneal nerve by aid of a portable and remotely controlled mini-stimulator. The stimulation was delivered in 'tonic' patterns (greater than or equal to 50% of total time taken up by activity) of 'fast' (20 or 40 Hz) or 'slow' (5 or 10 Hz) rates. 6. Prior to the period of long-term stimulation, the cats had been subjected to a dorsal rhizotomy and hemispinalization on the ipsilateral (left) side. In the absence of chronic stimulation, these operations had no evident effects on the sizes or staining properties of peroneus longus fibres. 7. After 8 weeks of treatment with tonic patterns of stimulation, the fibres of peroneus longus muscles clearly became more similar to each other with respect to their diameter as well as their staining for
ATPase
and SDH activity. With respect to
ATPase
staining, however, the chronically stimulated peroneus longus fibres had become more similar to non-stimulated soleus fibres than to non-stimulated type I fibres of peroneus longus. With respect to the staining for core SDH, the chronically stimulated fibres all became similar to normal II A fibres of peroneus longus. The 'fast' and 'slow' patterns of chronic stimulation had the same effects on the staining properties. 8. Chronically stimulated peroneus longus muscles showed a decrease in fibre diameter which corresponded, roughly, to the concomitant decrease in muscle weight.(ABSTRACT TRUNCATED AT 400 WORDS)
...
PMID:Fibre sizes and histochemical staining characteristics in normal and chronically stimulated fast muscle of cat. 295 93
M. semitendinosus and m. trapezius (portion) were removed from eight miniature pigs ranging from 21 to 160 days of age and eight age-control as well as eight weight-control commercial Large White pigs. Complete transverse frozen sections were obtained for each muscle sample and stained for various enzyme activities including
myosin
adenosine triphosphatase
activity which enabled the identification of 'metabolic bundles'. This in turn enabled conclusions to be made about the prenatal development of the muscle in terms of primary and secondary myofibres. The Large White pigs contained 173% more muscle fibres in m. semitendinosus than did the miniature pigs. Primary myofibre number was found to be about four times more important than secondary to primary myofibre ratios in determining myofibre number in the two breeds of pigs. Both primary myofibre number and secondary to primary myofibre ratios were, however, significantly greater in Large White than in miniature pigs. When the age- and weight-control Large Whites were compared with the miniature pigs it was found that at any given live weight the miniature pigs had thicker myofibres whereas at the same age there was no significant difference. The total area of m. semitendinosus occupied by slow myofibres was about three times greater in the Large White pigs; the functional aspects of this are discussed. It was concluded that genetically smaller animals develop fewer muscle fibres in their muscles by a different mechanism to that exhibited by animals which are smaller due to nutritional deprivation in utero.
...
PMID:The numbers and types of muscle fibres in large and small breeds of pigs. 296 20
Muscle fiber subtypes, determined with the actomyosin Ca+2,Mg+2-
adenosine triphosphatase
(
ATPase
) reaction in chicken anterior latissimus dorsi and posterior latissimus dorsi muscles, were demonstrated only after acid or alkaline preincubation followed by a 60-min enzyme incubation. In contrast, subtypes were demonstrated in the sartorius muscle either with or without preincubation. A single-step procedure was therefore possible with this muscle. The results were generally similar to those obtained previously with the mycosin Ca+2-
ATPase
procedure. Both methods revealed corresponding muscle fiber subtypes, with the exceptions noted below. The actomyosin Ca+2,Mg+2-
ATPase
procedure, following preincubation at pH 9.4 and 10.3, resulted in a similar reaction intensity in all fiber types. With the
myosin
Ca+2-
ATPase
procedure, the IRA (slow) type in anterior latissimus dorsi and sartorius muscles and the I (slow), IIR (fast oxidative-glycolytic), and IIW (fast glycolytic) types in posterior latissimus dorsi muscle had a higher reaction intensity following preincubation at pH 9.4 than at pH 10.3. Fiber Types IIR and IIW in sartorius muscle were easily distinguished with the actomyosin Ca+2,Mg+2-
ATPase
procedure.
...
PMID:Determination of fiber types of chicken skeletal muscles based on reaction for actomyosin, calcium+2, magnesium+2-dependent adenosine triphosphatase. 297 Jun 33
Isomyosin analyses by biochemical, immunochemical, and histochemical investigations have been carried out in five sheep following unilateral recurrent laryngeal nerve paralysis and direct functional electrostimulation of the denervated cricoarytenoid posterior muscle. Myosin light chains were identified by two-dimensional gel electrophoresis. Myosin heavy chains were analyzed by one-dimensional SDS-polyacrylamide gel electrophoresis. Slow myosin heavy chain was identified by orthogonal peptide mapping and immunochemistry. The stimulation effect at cellular level was determined using
adenosine triphosphatase
(
ATPase
) histochemistry. A dramatic increase of the type 1 fiber area (slow, fatigue-resistant fibers) could be seen after many weeks of an increasing regime of low-frequency direct electrical stimulation. Biochemically, the amount of slow
myosin
was always higher than in normal muscles. Some muscles were transformed almost completely to the slow type. At the time they were studied and with the methods employed, the expression of embryonic isomyosin was not observed. In conclusion, after numerous weeks of maintained functional activity, elicited by direct electrostimulation, the denervated muscle regionally showed areas of hypertrophy or at least lack of atrophy of slow myofibers without major signs of muscle damage.
...
PMID:Isomyosin changes after functional electrostimulation of denervated sheep muscle. 297 27
Motor units were studied in the soleus muscle of normal adult cats and adult cats that had undergone complete spinal cord transection approximately 4 mo earlier. Intracellular recording and stimulation techniques were used to study selected electrical properties of the motoneuron and isometric contractile properties of the muscle unit. Motor unit fibers were depleted of their glycogen through repetitive stimulation of the motoneuron and identified by a quantitative histochemical determination of glycogen. A sample of muscle fibers from the glycogen-depleted unit and from fibers not depleted of glycogen were analyzed for cross-sectional area, succinate dehydrogenase (SDH), alpha-glycerolphosphate dehydrogenase (GPD), and alkaline myofibrillar
adenosine triphosphatase
. It was observed that the fiber-to-fiber variability in cross-sectional area and SDH and GPD activity within units of normal and transected cats was significantly larger than that measured in repeated samples from a single fiber. Additionally, for each of these properties, the range found among fibers within a unit was similar to that found among nondepleted fibers of the same
myosin
type. The influence of spinal cord transection on some muscle fibers seemed to result in a metabolic shift from the generalized category of slow-oxidative toward fast-oxidative glycolytic. This shift in metabolic properties appeared to be coupled with a similar shift in the physiological properties of the muscle unit and motoneuron from slow to fast.
...
PMID:Coordination of electromechanical and metabolic properties of cat soleus motor units. 297 41
The amount of inorganic phosphate liberated by the
adenosine triphosphatase
activity of
myosin
in a thin section of cardiac tissue can be measured quantitatively by precipitation with calcium in an alkaline medium under a defined set of conditions. Specificity of the procedure for
myosin
adenosine triphosphatase
has been confirmed by the response to inhibitors and to different degrees of contractile filament overlap. Precise quantitation of
adenosine triphosphatase
activity has been demonstrated by (1) constant rate over time, (2) linearity with amount of enzyme, (3) correct values for the Km of adenosine triphosphate, and (4) a similar value for Vmax to those determined by more traditional procedures. Stimulation of the beta-adrenergic system by the release of catecholamines following injection of the animal with 6-hydroxydopamine causes a rise and then a fall of both calcium- and actin-activated
adenosine triphosphatase
in parallel with the changes in blood levels of the transmitter. Tyramine injection of rats produces a dose related increase in
myosin
adenosine triphosphatase
. Perfusion of isolated hearts with isoproterenol increases
myosin
adenosine triphosphatase
in dose-related manner. Addition of cyclic adenosine monophosphate and phosphodiesterase inhibitor to the solution bathing frozen, dried sections of heart increases both calcium- and actin-activated
adenosine triphosphatase
activity by almost 150%. The data show that the beta-adrenergic system, through cyclic adenosine monophosphatate, regulates the enzymatic activity of
myosin
, independent of the concentration of calcium. The possible role of this regulatory mechanism in the physiological modulation of cardiac contractility is discussed.
...
PMID:Adrenergic regulation of myosin adenosine triphosphatase activity. 300 59
Calcium initiates smooth muscle contraction by binding to calmodulin and activating the enzyme myosin light chain kinase. The activated form of myosin light chain kinase phosphorylates
myosin
on the 20,000-dalton light chain and contractile activity ensues. Calcium may also enhance smooth muscle contractile activity by binding directly to
myosin
, the main component of the thick filament. Recent studies raise the possibility that the calcium-calmodulin complex may also modulate smooth muscle contractile activity by removing the inhibition imposed by caldesmon, a protein that is bound to the thin (i.e., actin-containing) filaments of smooth muscle. In vitro studies have demonstrated that the calcium-activated, phospholipid-dependent kinase, protein kinase C, can phosphorylate smooth muscle
myosin
at a different site than does myosin light chain kinase and down-regulate its actin-activated magnesium
adenosine triphosphatase
activity. This raises the possibility that protein kinase C phosphorylation of
myosin
may play a role in modulating vascular contractile activity in vivo.
...
PMID:Effects of calcium on vascular smooth muscle contraction. 302 18
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