Biomedical subjects

R J Talmadge

Publications and source records attributed to R J Talmadge.

At least 19 recordsLinked to original sources

PubMed1997

Modulation of MHC isoforms in functionally overloaded and exercised rat plantaris fibers.

The effects of 1 and 10 wk of functional overload (FO) of the rat plantaris with (FOTr) and without daily endurance treadmill training on its myosin heavy chain (MHC) composition were studied. After 1 and 10 wk of FO, plantaris mass was 22 and 56% greater in FO and 37 and 94% greater, respectively, in FOTr rats compared with age-matched controls. At 1 wk, pure type I and pure type IIa MHC fibers were hypertrophied in FO (39 and 44%) and FOTr (70 and 87%) rats. By 10 wk all fiber types comprising >5% of the fibers sampled showed a hypertrophic response in both FO groups. One week of FO increased the percentage of hybrid (containing both type I and type IIa MHC) fibers and of fibers containing embryonic MHC. By 10 wk, the percentage of pure type I MHC fibers was approximately 40% in both FO groups compared with 15% in controls, and the percentage of fibers containing embryonic MHC was similar to that in controls. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analyses showed an increase in type I MHC and a decrease in type IIb MHC in both FO groups at 10 wk, whereas little change was observed at 1 wk. These data are consistent with hypertrophy and transformation from faster to slower MHC isoforms in chronically overloaded muscles. The additional overload imposed by daily endurance treadmill training employed in this study (1.6 km/day; 10% incline) results in a larger hypertrophic response but appears to have a minimal effect on the MHC adaptations.

Animals↗

PubMed1996

Myosin heavy chain composition of adult feline (Felis catus) limb and diaphragm muscles.

The myosin heavy chain (MHC) compositions of adult feline limb and diaphragm muscles were determined. Sodium dodecyl sulfate-polyacrylamide gels (SDS-PAGE) were able to separate three different MHC isoforms. This was in contrast to rat muscles, in which four MHC isoforms were separated by SDS-PAGE. The fastest migrating cat MHC migrated similar to rat type I MHC and labeled in Western blots with a monoclonal antibody (mAb) specific for slow MHC and was categorized as type I. The other two MHC isoforms labeled in Western blots with a mAb specific for fast MHC and were categorized as type II. The slowest migrating fast isoform migrated similar to rat type IIa MHC and labeled with mAb N2.261, specific for types I and IIa; therefore, this MHC was categorized as type IIa. The intermediate migrating cat MHC did not migrate similar to either rat type IIx or type IIb and was not reactive with mAbs N2.261, 35 (specific for rat I, IIa, and IIb MHCs), or F3 (specific for rat IIb MHC). In tissue sections, type IIB fibers (based on myofibrillar ATPase histochemistry) were also unstained with mAbs N2.261 and 35. Therefore, the intermediate migrating cat MHC was categorized as type IIx. Consequently, feline limb and diaphragm muscles were composed of fibers containing type I, IIa, or IIx MHCs. The observations that type I and IIa isoforms, but not IIx, had similar electrophoretic mobilities in the cat and rat and that type IIb was absent from cat limb muscles suggest that there is greater diversity in MHC isoforms IIb and IIx compared to I and IIa in cats compared to rats.

Animals↗

PubMed1996

Myosin heavy chain isoforms in adult equine skeletal muscle: an immunohistochemical and electrophoretic study.

BACKGROUND: The aim of this study was to characterize the myosin heavy chain (MyHC) isoforms present in equine skeletal muscle. METHODS: Muscle biopsies were removed from the superficial region of the gluteus medius muscle of five mature horses and analyzed by immunohistochemistry (using a battery of monoclonal antibodies specific for rat MyHC isoforms) and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. RESULTS: Immunohistochemistry allowed subdivision of three different muscle fiber populations containing a single MyHC, one slow and two fast, and two hybrid populations, one containing slow and fast MyHCs and another with both fast-MyHC isoforms. Electrophoresis of MyHC confirmed the existence of three resolvable bands, with an electrophoretic mobility parallel to type I, IIa, and IIx rat MyHCs. The identities of two of these MyHCs were easily comparable with slow type I and fast type IIa MyHCs from rat skeletal muscle. However, a precise identification of the second fast MyHC was not made. CONCLUSIONS: These results show the presence of three different MyHC isoforms in mature equine skeletal muscle, whose differential distribution defines three fiber types containing a single MyHC and two hybrid fiber populations containing either both slow and fast type IIa MyHCs or both fast MyHC isoforms.

Animals↗

PubMed1996

Correlation between myofibrillar ATPase activity and myosin heavy chain composition in equine skeletal muscle and the influence of training.

BACKGROUND: The histochemical myofibrillar ATPase (mATPase) method is used routinely for identification of equine skeletal muscle fiber types, but important problems have been observed with the subdivision of fast fiber population when using this method. To verify the use of this qualitative method, a number of equine muscle biopsies were analyzed with a combination of histochemical, immunohistochemical, electrophoretic, and morphometric techniques. The influence of training on these interrelations was also evaluated. METHODS: Five young (2-3 years old) thoroughbred horses were intensively trained for 8 months on a high-speed treadmill. Biopsies were taken from the gluteus medius muscle at the beginning, after 4 months, and at the end of the training program. Serial sections of the samples were stained by mATPase histochemistry and immunohistochemistry by using a number of monoclonal antibodies specific to selected myosin heavy chain (MyHC) isoforms. The histochemical and immunohistochemical categorization of a large number of fibers (N = 2,078) was compared fiber by fiber. The MyHC content of homogenates of the same biopsies were quantified by densitometry of a sensitive gel electrophoretic technique and compared with histochemical and immunohistochemical fiber types. RESULTS: A large proportion of fibers examined (approximately 20%) were misclassified by traditional mATPase histochemistry. Many fibers histochemically identified as type IIB displayed both type IIa and type IIb MyHC isoforms, and nearly all type IIAB fibers in mATPase contained only the type IIa MyHC isoform by immunohistochemistry. Correlation analyses suggested a weak relation between the histochemically assessed relative cross-sectional area occupied by the three major fiber types (I, IIA, and IIB) and the electrophoretically assessed MyHC content, whereas a stronger relation was found between immunohistochemically defined fiber types and electrophoretic data. The four fiber type populations delineated according to MyHC content (I, IIA, IIAB, and IIB) had sizes and oxidative capacities significantly different from each other. No adaptation of any parameter measured to training was found. Training had no significant effect on the number of fibers misclassified by mATPase histochemistry. CONCLUSIONS: These data demonstrate a significant limitation in mATPase histochemistry for assessing fibers containing fast MyHC isoforms. The use of monoclonal antibodies against specific MyHC isoforms seems to be a more sensitive and less subjective method.

Animals↗

PubMed1996

Myosin heavy chain profile of cat soleus following chronic reduced activity or inactivity.

To determine the role that normal neuromuscular activity plays in maintaining the myosin heavy chain (MHC) profile of adult cat soleus muscles, the spinal cords of 4 cats were transected (ST) and 8 cats were spinal isolated (SI) for 6 months. Nine nonoperated cats served as controls. Electrophoresis demonstrated that the soleus from control cats contained 98% type I, and 2% IIa MHCs. Both ST and SI resulted in decreased type I and increased IIa MHC, as well as de novo expression of IIb MHC. Immunohistochemistry with MHC-specific antibodies demonstrated that the soleus from control cats contained 99% type I, 1% IIa, and < 1% hybrid fibers (containing both type I and II MHCs). Following ST there were 67% type I, 17% IIa, 3% IIb, and 13% hybrid fibers. After SI, 48% of the fibers were type I, 11% were IIa, 1% were IIb, 25% were hybrid, and 15% contained embryonic MHC. Thus, normal levels of neuromuscular activity appear to be necessary for maintenance of the normal adult MHC profile in some fibers. Complete inactivation results in developmental MHC isoform expression in some fibers. Therefore, the dependence of a fiber on activity as a source of MHC modulation differs substantially among fibers even in a relatively homogeneous muscle.

Animals↗

PubMed1996

Synergistic ablation does not affect atrophy or altered myosin heavy chain expression in the non-weight bearing soleus muscle.

The purpose of this study was to investigate whether the soleus muscle undergoes atrophy and alterations in myosin heavy chain (MHC) composition during non-weight bearing in the absence of synergists. Thirty-two female rats were randomly assigned to four groups: control (C), synergistic ablation (ABL) of the gastrocnemius and plantaris muscles to overload the soleus muscle, hindlimb suspension (HLS), or a combination of synergistic ablation and hindlimb suspension (HLS-ABL). After 28 days of hindlimb suspension, soleus atrophy was more pronounced in HLS (58%) than in HLS-ABL (43%) rats. Compared to C rats, non-weight bearing decreased mixed and myofibrillar protein contents and Type I MHC 49%, 45%, and 7%, respectively, in HLS animals. In addition, de novo expression of fast Type IIx and Type IIb MHC (5% and 2%, respectively) was observed in HLS animals. Similarly, when compared to C rats, mixed and myofibrillar protein contents and Type I MHC decreased 43%, 46%, and 4%, respectively, in HLS-ABL animals. Also, de novo expression of Type IIx (4%) and IIb (1%) MHC was observed. Collectively, these data indicate that the loss of muscle protein and Type I MHC, and the de novo expression of Type IIx and Type IIb MHC in the rat soleus occur independently of the presence of synergists during non-weight bearing. Furthermore, these results confirm the contention that soleus mass and MHC expression are highly sensitive to alterations in mechanical load.

Animals↗

PubMed1996

MHC and sarcoplasmic reticulum protein isoforms in functionally overloaded cat plantaris muscle fibers.

To determine whether the adaptations in myosin heavy chain (MHC) isoform expression after functional overload (FO) are accompanied by commensurate adaptations in protein isoforms responsible for relaxation [sarco(endo)plasmic reticulum (SR) Ca(2+)-adenosinetriphosphatase (SERCA) and phospholamban (PHL)] in single muscle fibers, the isoforms of MHC and SERCA and the presence or absence of PHL were determined for cat plantaris fibers 3 mo after FO. In control plantaris the relative MHC isoform composition was 23% type I, 21% type IIa, and 56% type IIb. FO resulted in a shift toward slower isoforms (33% type I, 44% type IIa, and 23% type IIb). In the deep region of the plantaris the proportions of type I MHC and hybrid MHC fibers (containing type I and II MHCs) were 40 and 200% greater in FO cats, respectively. FO resulted in a 47% increase in the proportion of fibers containing only the slow SERCA isoform (SERCA2) and a 41% increase in the proportion of fibers containing PHL. The proportions of fibers containing type I MHC, SERCA2, and PHL in control and FO plantaris were linearly correlated. These data show that adaptations in MHC isoform expression are accompanied by commensurate adaptations in sarcoplasmic reticulum protein isoforms in single muscle fibers after FO.

Animals↗

PubMed1996

IGF-I, growth hormone, and/or exercise effects on non-weight-bearing soleus of hypophysectomized rats.

The effects of insulin-like growth factor (IGF-I) or growth hormone (GH) with and without exercise on predominantly slow muscles of hypophysectomized hindlimb-suspended (HS) rats were determined. HS resulted in a 21, 23, and 30% decrease in soleus, adductor longus, and vastus intermedius masses, respectively, compared with ambulatory rats. Compared with values in HS rats, IGF-I increased the vastus intermedius mass and GH or exercise alone increased both the soleus and vastus intermedius masses. There was a strong interactive effect between GH, but not IGF-I, and exercise in all three muscles of HS rats. The soleus fiber type distribution of HS rats was not affected by any treatment. HS resulted in a 24, 18 (P > 0.05), 32, and 20% (P > 0.05) decrease in the size of soleus fibers containing type I, IIa, I + IIa, and IIa + IIx myosin heavy chains, respectively, compared with ambulatory hypophysectomized rats. Hormone or exercise alone had no effect on fiber size in HS rats. However, all fiber sizes (except for type IIa + IIx in IGF-I with exercise rats) were larger in HS rats treated with GH or IGF-I and exercise than those in HS rats. These data indicate an interactive effect of both GH and IGF-I with exercise in maintaining fiber size of chronically non-weight-bearing predominantly slow muscles. Furthermore, the results suggest that the myosin heavy-chain phenotype in rats deficient in all pituitary factors is unresponsive to short-term administration of either GH or IGF-I or to exercise or HS.

Animals↗

PubMed1996

Distribution of myosin heavy chain isoforms in non-weight-bearing rat soleus muscle fibers.

The effects of 14 days of spaceflight (SF) or hindlimb suspension (HS) (Cosmos 2044) on myosin heavy chain (MHC) isoform content of the rat soleus muscle and single muscle fibers were determined. On the basis of electrophoretic analyses, there was a de novo synthesis of type IIx MHC but no change in either type I or IIa MHC isoform proportions after either SF or HS compared with controls. The percentage of fibers containing only type I MHC decreased by 26 and 23%, and the percentage of fibers with multiple MHCs increased from 6% in controls to 32% in HS and 34% in SF rats. Type IIx MHC was always found in combination with another MHC or combination of MHCs; i.e., no fibers contained type IIx MHC exclusively. These data suggest that the expression of the normal complement of MHC isoforms in the adult rat soleus muscle is dependent, in part, on normal weight bearing and that the absence of weight bearing induces a shift toward type IIx MHC protein expression in the preexisting type I and IIa fibers of the soleus.

Animals↗

PubMed1996

Size and myosin heavy chain profiles of rat hindlimb extensor muscle fibers after 2 weeks at 2G.

METHOD: The effects of 14 d of continuous centrifugation at approximately 2G on the hindlimb extensor musculature of male rats were studied. RESULTS: The mean body mass of centrifuged rats was 17% smaller than age-matched controls. In centrifuged rats, the mean absolute masses of the soleus and medial gastrocnemius (MG) were similar to control, while the mean relative masses (expressed as milligram muscle mass/gram of body mass) were larger than control. Based on a battery of monoclonal antibodies for specific myosin heavy chains (MHC), the soleus of centrifuged rats had a lower percentage (68 vs. 74%) of fibers expressing type I MHC only and a higher percentage (15 vs. 10%) that co-expressed type I and IIa MHC's. The MHC composition of fibers from the deep portion of the MG was unaffected by centrifugation. The MHC compositions based on SDS-PAGE gel electrophoresis for each muscle were similar in the two groups. Mean fiber size of each fiber type in the soleus was unaffected by centrifugation. In the MG, the fibers, expressing only type IIb MHC were smaller in the centrifuge compared to control rats. CONCLUSION: Although 2 weeks of chronic centrifugation at 2G resulted in a cessation of body growth, there was essentially no effect on the muscle masses or fiber size in either a slow or fast extensor muscle. These data suggest that periods of centrifugation may be beneficial in maintaining extensor muscle mass in an animal that is not growing at a normal rate e.g., during chronic unloading.

Adaptation, Physiological↗

PubMed1995

Prominence of myosin heavy chain hybrid fibers in soleus muscle of spinal cord-transected rats.

The effect of a midthoracic spinal cord transection (ST) on myosin heavy chain (MHC) isoform expression in the rat soleus muscle was studied. Electrophoretic analyses demonstrated that 15 days after ST there were significant proportional increases in type IIx, decreases in type IIa, and no change in type I MHC composition. Thirty days after ST, some type IIb MHC was expressed, there were further proportional increases in type IIx, an increase in type IIa (compared with 15-day ST), and a decrease in type I MHC. At both time periods after ST, many fibers expressed multiple MHCs, as demonstrated by immunohistochemistry where a battery of monoclonal antibodies specific to MHC isoforms was used. Fibers were observed containing types I and II together or multiple type II MHC isoforms. These data suggest that the expression of the normal complement of MHC isoforms in the adult rat soleus muscle is dependent, in part, on normal neuromuscular activation.

Animals↗

PubMed1995

Plasticity of myonuclear number in hypertrophied and atrophied mammalian skeletal muscle fibers.

Although a mammalian skeletal muscle fiber may contain thousands of myonuclei, the importance of this number or the potential to modulate it in adult muscle has not been clearly demonstrated. Using immunohistochemistry and confocal microscopy, we examined the plasticity of myonuclear number and fiber size in isolated fast and slow fiber segments from adult cat hindlimb muscles in response to chronic alterations in neuromuscular activity and loading. Compared with slow fibers in the soleus of control cats, myonuclear number in presumably transformed fast fibers was 32% lower and fiber size was decreased 73% after elimination of neuromuscular activation for 6 mo by spinal isolation. Slow fibers in the soleus of spinal-isolated cats had smaller cross-sectional areas, whereas myonuclear number was not significantly different than that in the control cats. Myonuclear number in fast plantaris fibers was more than threefold higher and fiber size was 2.8-fold higher after 3 mo of functional overload compared with the plantaris of control cats. Compared with control slow plantaris fibers, myonuclear number and fiber size also increased in overloaded slow plantaris fibers. These results demonstrate that changes in myonuclear number are associated with changes in myosin type and suggest that modulations in the amount of available DNA may be a factor in regulating cytoplasmic volume of muscle fibers in response to chronic changes in neuromuscular activity.

Animals↗

PubMed1995

Myofibrillar ATPase activity of feline muscle fibers expressing slow and fast myosin heavy chains.

The interrelationships among myofibrillar ATPase activity (Quant-mATPase), qualitative myofibrillar ATPase staining after acid (Acid-mATPase) and alkaline (Alk-mATPase) preincubations, and myosin heavy chain (MHC) composition were determined in frozen sections of soleus (Sol) and medial gastrocnemius (MG) muscle fibers from adult control cats and cats 6 months after complete spinal cord transection (Sp). Fibers were categorized as either fast, slow, or fast and slow (Fast-Slow) based on monoclonal antibody labeling. Slow fibers had low Quant-mATPase activity and stained lightly with Alk-mATPase and darkly with Acid-mATPase. Fast fibers had high Quant-mATPase activity (approximately twice that of slow fibers) and stained darkly with Alk-mATPase and lightly with Acid-mATPase. Fast-Slow fibers had intermediate Quant-mATPase activity and stained intermediately for Acid-mATPase and darkly for Alk-mATPase. There was a positive linear relationship between Alk-mATPase and Quant-mATPase for all fibers of Sol and MG from control and Sp cats. There was a negative linear relationship between Acid-mATPase and Quant-mATPase for all fibers of Sol and MG. However, within the fast fiber population of the MG there was a positive relationship between these two measures of mATPase. In summary, quantitative and qualitative measures of mATPase are highly correlated with the types of MHC expressed by single fibers from control and Sp cat muscles.

Animals↗

PubMed1994

Limited capacity for glyconeogenesis from alanine by diaphragm muscle.

The mammalian diaphragm (Dia) is a unique skeletal muscle because of its chronic contractile activity. Chronically active muscles have higher capacities for glycogen synthesis from lactate and glucose. In this study, the contribution of alanine to glycogen synthesis in the predominantly fast-twitch mouse Dia was determined. Chronically active fast- and slow-twitch muscles from dy2J/dy2J pseudomyotonic mice were also analyzed. Alanine aminotransferase (AlaAT) activity was significantly (P < 0.05) greater in Dia and chronically active gastrocnemius muscle (Gast) than control Gast. 14C-label incorporation into glycogen following in vivo injection of 14C-alanine, was significantly higher in Dia and chronically active Gast than control Gast. A direct incorporation of 14C from 14C-alanine into glycogen is also observed in vitro. The incorporation rate shows a linear concentration dependent relationship and a pH optimum of 6.3. Insulin had no effect on glycogen synthesis from alanine by Dia in vitro. The extensor digitorum longus muscle (EDL) and chronically active EDL and soleus muscle (Sol) had higher rates of glycogen synthesis from alanine than control Sol and Dia. The oxidation of alanine to CO2 was the primary route for alanine metabolism by the Dia. These results demonstrate that the Dia can synthesize glycogen from alanine, but only at low rates.

Alanine↗

PubMed1993

Muscle fiber types and function.

In this review, we address current concepts and recent experimental results that relate to heterogeneity in the physiologic, biochemical, and morphologic properties of mammalian skeletal muscle fibers. Recent data reinforce some of these current concepts while questioning others. The biochemical bases of the concepts of fiber types continue to evolve, particularly in reference to the combinations of the myosin light and heavy chains that are expressed in most mammalian skeletal muscle fibers. Further, it is becoming increasingly clear that specific myosin isoforms relate to contractile function. What remains unclear, however, are the bases for a continuum in functional properties, eg, the maximum velocity of shortening, rather than distinct increments in these properties as might be predicted based on myosin isoforms alone. Clearly, there are factors other than myosin that play a role in defining the characteristics of a fiber, and some of these other factors are discussed. A second general issue addressed in this review is the source of the control of the heterogeneity among fibers of a skeletal muscle. Data are presented that demonstrate that this heterogeneity is not simply a function of the patterns of activation of motoneurons. It appears that the motoneuron can maintain practically all type-related features of fibers in the absence of neuromuscular activity. Although the motoneuron can influence muscle protein expression, it is equally clear that there are myogenic and hormonal factors that have significant regulatory roles. In effect, muscle fiber types reflect a complex interaction of multiple sources of control of protein expression, and the net effect of the control ultimately defines its functional properties.

Animals↗

PubMed1993

Glucose uptake and glycogen synthesis in normal and chronically active muscles.

The hindlimb muscles of the C57Bl6J dy2J/dy2J (dy2J) mouse suffer from a chronic neural stimulation (pseudomyotonia), resulting in increased contractile activity. In response to the increased contractile activity, these muscles store increased amounts of glycogen. In this study, glucose uptake and glycogenesis (glycogen synthesis from glucose) were analyzed in chronically active and normal muscles. In vivo experiments demonstrate increased 3-O-methylglucose (3-MG) uptake rates and glycogenesis by chronically active dy2J gastrocnemius muscles (Gast) vs. normal control Gast. The chronically active diaphragm muscle (Dia) showed the highest rates of 3-MG uptake, as well as glycogenesis in vivo when compared with other skeletal muscles. No differences were observed between dy2J and control Dia. The levels of blood glucose were similar between dy2J and control animals. In vitro experiments demonstrated an increased sensitivity and responsiveness to insulin for glucose uptake in the dy2J soleus muscle (Sol). Glycogenesis by dy2J Sol was elevated only at the highest insulin concentration tested (10,000 microU/ml). In contrast, the dy2J extensor digitorum longus muscle had an increased sensitivity and responsiveness to insulin for both glucose uptake and glycogenesis. This study demonstrates that chronically active muscles have elevated capacities for glucose uptake and glycogenesis and may help to explain the elevated glycogen levels in the dy2J hindlimb muscles.

3-O-Methylglucose↗

PubMed1993

Electrophoretic separation of rat skeletal muscle myosin heavy-chain isoforms.

A new technique for the sodium dodecyl sulfate-polyacrylamide gel electrophoretic separation of rat skeletal muscle myosin heavy-chain (MHC) isoforms is presented. This technique allows for the separation of the four identified MHC isoforms known to be present in adult rat skeletal muscle. These types of MHC are commonly called I, IIa, IIx or IId, and IIb. The procedure can be performed using minigel electrophoresis systems and does not involve preparation of gradient-separating gels or the use of special cooling devices. The procedure accommodates both silver and Coomasie Blue staining. Thus the procedure is simple to perform and highly repeatable, providing high-resolution separation of MHC protein isoforms. The percent composition of the four adult MHCs in rat soleus, medial gastrocnemius, diaphragm, and levator ani muscles by use of this procedure and Coomasie Blue staining is similar to that previously reported. This new technique provides a novel and easy-to-perform method for the separation of rat skeletal muscle MHC isoforms.

Animals↗

PubMed1991

Glyconeogenic and glycogenic enzymes in chronically active and normal skeletal muscle.

The chronically active (pseudomyotonic) gastrocnemius muscle in the C57B16J dy2J/dy2J mouse contains both elevated lactate and glycogen as well as fibers that have high amounts of glycogen and enhanced glyconeogenic activity. In the present study we analyze the activities of some key glyconeogenic enzymes to assess the causes of elevated muscle glycogen and to determine the pathway for glycogen synthesis from lactate. Glycogen synthase, malate dehydrogenase, phosphoenolpyruvate carboxykinase, and malic enzyme were all elevated in homogenates of the chronically active muscle. Activities of glycogen phosphorylase and fructose 1,6-bisphosphatase were decreased in whole muscle homogenates. Histochemistry demonstrated that the high-glycogen fibers were typically fast-twitch glycolytic fibers that had high glycogen synthase, glycogen phosphorylase, and malic enzyme activities. Malate dehydrogenase activity followed succinate dehydrogenase activity and did not correlate to high-glycogen fibers. Thus the high-glycogen fibers have an elevated enzymatic capacity for glycogen synthesis from lactate, and the pathway may involve use of the pyruvate kinase bypass enzymes.

Animals↗