Myotube Protein Content Associates with Intracellular L-Glutamine Levels.

BACKGROUND/AIMS: Skeletal mass loss is reported in several catabolic conditions and it has been associated with a reduced intracellular L-glutamine content. We investigated the association of intracellular L-glutamine concentration with the protein content in skeletal muscle cells. METHODS: We cultivated C2C12 myotubes in the absence or presence of 2 (reference condition), 8 or 16 mM L-glutamine for 48 hours, and the variations in the contents of amino acids and proteins measured. We used an inhibitor of L-glutamine synthesis (L-methionine sulfoximine - MSO) to promote a further reduction in intracellular L-glutamine levels. Amino acids contents in cells and media were measured using LC-MS/MS. We measured changes in phosphorylated Akt, RP-S6, and 4E-BP1contents in the absence or presence of insulin by western blotting. RESULTS: Reduced intracellular L-glutamine concentration was associated with decreased protein content and increased protein breakdown. Low intracellular glutamine levels were also associated with decreased p-Akt contents in the presence of insulin. A further decrease in intracellular L-glutamine caused by glutamine synthetase inhibitor reduced protein content and levels of amino acids generated from glutamine metabolism and increased bAib still further. Cells exposed to high medium glutamine levels did not have any change in protein content but exhibited increased contents of the amino acids derived from L-glutamine metabolism. CONCLUSION: Intracellular L-glutamine levels per se play a role in the control of protein content in skeletal muscle myotubes.

Histochemical and morphometric analyses of the musculature of the forelimb of the subterranean rodent Ctenomys talarum (Octodontoidea).

Histochemical and morphometric analyses were performed to characterize the fibre-type composition of two forelimb muscles of the South American subterranean rodent Ctenomys talarum. The studied muscles were the triceps lateralis, an extensor of the elbow, and the teres major, a flexor of the shoulder. It was found that these muscles had an elevated proportion of fast oxidative-glycolytic (FOG) fibres, and lower proportions of slow oxidative (SO) and fast glycolytic (FG) fibres. This composition probably qualifies the teres major and triceps muscles to perform the sustained effort required in tunnelling excavation. The results were discussed considering published data on fibre-type composition of mammals having different modes of life and digging behaviour. We here suggest that C. talarum has the potential of generating forces linked to rapid, powerful movements during sustained periods by means of an elevated proportion of FOG fibres, together with osteological changes that result in a great mechanical advantage of the forelimb muscles.

Incidence of humeral head of biceps brachii muscle: anatomical insight / Incidencia de la cabeza humeral del músculo bíceps braquial - visión anatómica

Biceps brachii is stated as one of the muscles that shows most frequent anatomical variations. Its most commonly reported anomaly is the presence of an accessory fascicle arising from the humerus which is termed as the humeral head of biceps brachii. Evidence shows a clear racial trend in the incidence of the humeral head of biceps brachii. Therefore, detailed knowledge of this variation in different populations is important for surgical interventions of the arm, nerve compression syndromes and in unexplained pain syndromes in the arm or shoulder region. The goal of this study was to elucidate the incidence and morphological features of this muscle in an adult Sri Lankan population. Upper extremities of the total of one hundred thirty five cadavers were dissected and studied for the presence of accessory heads of the biceps brachii muscle. The proximal and distal attachments of the humeral heads as well as their cranio-caudal, antero-posterior and medio-lateral dimensions were recorded. The incidence of humeral head of biceps brachii was found to be 3.7 percent. In all cases, it was found unilaterally and only in male subjects. The humeral head originated from the antero-medial aspect of the humeral shaft and descended and merged with the other two heads to form a common tendon. The results of the present study further highlight the racial variations in the incidence of humeral head of biceps brachii among Sri Lankans. Knowledge of the occurrence of humeral head of biceps brachii may facilitate preoperative diagnosis as well as the surgical procedures of the upper limb thus avoiding iatrogenic injuries.

El músculo bíceps braquial se conoce como uno de los músculos que muestra las variaciones anatómicas más frecuentes. Su anomalía más común es la presencia de un fascículo accesorio proveniente del húmero, que se denomina cabeza humeral del músculo bíceps braquial. La evidencia muestra una clara tendencia racial en la incidencia de la cabeza humeral del músculo bíceps braquial. El conocimiento acabado de esta variación, en las diferentes poblaciones, es importante para las intervenciones quirúrgicas del brazo, en los síndromes de compresión nerviosa y en los síndromes de dolor inexplicable en la región del brazo o del hombro. El objetivo de este estudio fue determinar la incidencia y las características morfológicas de este músculo en una población adulta de Sri Lanka. Fueron estudiados los miembros superiores en 135 cadáveres, disecados para evaluar la presencia de las cabezas del músculo bíceps braquial accesorio. Fueron registrados el origen e inserción de la cabeza humeral del músculo bíceps braquial, así como su dimensión cráneo-caudal, anteroposterior y mediolateral. La incidencia de la cabeza humeral del músculo bíceps braquial se encontró en el 3,7 por ciento de los miembros estudiados. En todos los casos, su presencia era unilateral y sólo presente en hombres. La cabeza humeral se originó en la región antero-medial de la diáfisis del húmero, descendió y se fusionó con las otras dos cabezas para formar un tendón común. Los resultados de este estudio resaltan aún más las variaciones raciales en la incidencia de la cabeza humeral del músculo bíceps braquial, entre los habitantes de Sri Lanka. El conocimiento de la presencia de la cabeza humeral del músculo bíceps braquial puede facilitar el diagnóstico preoperatorio, así como los procedimientos quirúrgicos del miembro superior, evitando las lesiones iatrogénicas.

Up-regulation of the vitamin C transporter SVCT2 upon differentiation and depolarization of myotubes.

In addition to its role as a strong antioxidant, vitamin C regulates the differentiation of several cell lineages. In vertebrate skeletal muscle, the vitamin C transporter SVCT2 is preferentially expressed in slow muscle fibers. To gain insights into the possible involvement of intracellular vitamin C on early myogenesis, we investigated the regulation of SVCT2 expression in cultures of chick fetal myoblasts. SVCT2 expression increases in cultures of both, slow and fast muscle-derived myoblasts, as they fuse to form mainly fast myotubes. Interestingly, we found that SVCT2 could be positively modulated by potassium-induced depolarization of myotubes. These findings suggest that SVCT2-mediated uptake of vitamin C could play diverse roles on skeletal muscle development and physiology.

Effects of exercise training on atrophy gene expression in skeletal muscle of mice with chronic allergic lung inflammation

We evaluated the effects of chronic allergic airway inflammation and of treadmill training (12 weeks) of low and moderate intensity on muscle fiber cross-sectional area and mRNA levels of atrogin-1 and MuRF1 in the mouse tibialis anterior muscle. Six 4-month-old male BALB/c mice (28.5 ± 0.8 g) per group were examined: 1) control, non-sensitized and non-trained (C); 2) ovalbumin sensitized (OA, 20 µg per mouse); 3) non-sensitized and trained at 50 percent maximum speed _ low intensity (PT50 percent); 4) non-sensitized and trained at 75 percent maximum speed _ moderate intensity (PT75 percent); 5) OA-sensitized and trained at 50 percent (OA+PT50 percent), 6) OA-sensitized and trained at 75 percent (OA+PT75 percent). There was no difference in muscle fiber cross-sectional area among groups and no difference in atrogin-1 and MuRF1 expression between C and OA groups. All exercised groups showed significantly decreased expression of atrogin-1 compared to C (1.01 ± 0.2-fold): PT50 percent = 0.71 ± 0.12-fold; OA+PT50 percent = 0.74 ± 0.03-fold; PT75 percent = 0.71 ± 0.09-fold; OA+PT75 percent = 0.74 ± 0.09-fold. Similarly significant results were obtained regarding MuRF1 gene expression compared to C (1.01 ± 0.23-fold): PT50 percent = 0.53 ± 0.20-fold; OA+PT50 percent = 0.55 ± 0.11-fold; PT75 percent = 0.35 ± 0.15-fold; OA+PT75 percent = 0.37 ± 0.08-fold. A short period of OA did not induce skeletal muscle atrophy in the mouse tibialis anterior muscle and aerobic training at low and moderate intensity negatively regulates the atrophy pathway in skeletal muscle of healthy mice or mice with allergic lung inflammation.

Effects of exercise training on atrophy gene expression in skeletal muscle of mice with chronic allergic lung inflammation.

We evaluated the effects of chronic allergic airway inflammation and of treadmill training (12 weeks) of low and moderate intensity on muscle fiber cross-sectional area and mRNA levels of atrogin-1 and MuRF1 in the mouse tibialis anterior muscle. Six 4-month-old male BALB/c mice (28.5 +/- 0.8 g) per group were examined: 1) control, non-sensitized and non-trained (C); 2) ovalbumin sensitized (OA, 20 microg per mouse); 3) non-sensitized and trained at 50% maximum speed _ low intensity (PT50%); 4) non-sensitized and trained at 75% maximum speed _ moderate intensity (PT75%); 5) OA-sensitized and trained at 50% (OA+PT50%), 6) OA-sensitized and trained at 75% (OA+PT75%). There was no difference in muscle fiber cross-sectional area among groups and no difference in atrogin-1 and MuRF1 expression between C and OA groups. All exercised groups showed significantly decreased expression of atrogin-1 compared to C (1.01 +/- 0.2-fold): PT50% = 0.71 +/- 0.12-fold; OA+PT50% = 0.74 +/- 0.03-fold; PT75% = 0.71 +/- 0.09-fold; OA+PT75% = 0.74 +/- 0.09-fold. Similarly significant results were obtained regarding MuRF1 gene expression compared to C (1.01 +/- 0.23-fold): PT50% = 0.53 +/- 0.20-fold; OA+PT50% = 0.55 +/- 0.11-fold; PT75% = 0.35 +/- 0.15-fold; OA+PT75% = 0.37 +/- 0.08-fold. A short period of OA did not induce skeletal muscle atrophy in the mouse tibialis anterior muscle and aerobic training at low and moderate intensity negatively regulates the atrophy pathway in skeletal muscle of healthy mice or mice with allergic lung inflammation.

Muscle fibre types and connective tissue morphometry in frontal muscle of Norfolk rabbits (Oryctolagus cuniculus) / Morfometría de los tipos de fibra muscular y del tejido conectivo en músculo frontal de conejos Norfolk (Oryctolagus cuniculus)

The frontal muscle is formed by a complex of contractile elements which compose the set of facial muscles responsible for the expression of emotions. In view of its functional characteristics the frontal muscle consists of a mixture of high (type I) and low oxidative (type II) muscle fibres. The objective of the present study was to determine the area, diameter, and relative volume occupied by each fibre type in frontal muscles of Norfolk rabbits using nicotinamide adenine dinucleotide tetrazolium reductase (NADH-TR) histochemistry combined with morphometry. In addition, the connective tissue area (endomysium) and the number of blood vessels per fibre were evaluated. Female rabbits ranging in age from 6 to 8 months and weighing 2.8 to 3.1 kg were used. Four quadrants of samples from 12 animals were analysed. Type IIB fibres occupied the largest area compared to the other fibre types. The fibre diameter and relative volume were similar among the different fibre types identified by NADH-TR staining. No significant difference in the number of vessels per fibre was observed between the different fibre types. The endomysial area occupied the smallest area among the parameters analyzed. These findings demonstrated the intense activity of this muscle in the facial architecture of the animal. However, the low oxidative type II fibres predomination indicates more prone to muscle fatigue. The present findings may contribute to the study of myopathies involving this muscle.

El músculo frontal está formado por un complejo de elementos contráctiles que componen el conjunto de músculos faciales responsables de la expresión de emociones. A la vista de las características funcionales, el músculo frontal está constituido de una mezcla de fibras musculares de alto (tipo I) y bajo nivel de oxidación (tipo II). El objetivo del presente estudio fue determinar área, diámetro y volumen relativo ocupado por cada tipo de fibra en los músculos frontales de conejos Norfolk utilizando histoquímica para nicotinamide adenina dinucleotide tetrazolium reductasa (NADH-TR), combinado con su morfología. Además, fueron evaluados la zona de tejido conectivo (endomisio) y el número de vasos sanguíneos por fibras. Fueron utilizados conejos hembras, de edades comprendidas entre los 6 a 8 meses y con un peso de 2,8 a 3,1 kg. Se analizaron cuatro cuadrantes de las muestras de 12 animales. Las fibras tipo IIB ocuparon la mayor superficie, en comparación con los otros tipos de fibras. Los diámetros y volúmenes relativos de las fibras fueron similares entre los diferentes tipos identificados por NADH-TR. No se observaron diferencias significativas en el número de vasos por fibra, entre los diferentes tipos de fibras. El área ocupada por el endomisio fue la superficie más pequeña entre los parámetros analizados. Estos resultados demostraron la intensa actividad de este músculo en la arquitectura facial del animal. Sin embargo, el predominio de las fibras tipo II, de baja oxidación, indica más propensión a la fatiga muscular. El presente hallazgo pueden contribuir al estudio de las miopatías con la participación de este músculo.

Fiber type composition in semitendinous muscle of Wistar rats and effects of intermittent training on its hypertrophy / Composición de los tipos de fibras del músculo semitendinoso de ratas Wistar y los efectos del entrenamiento intermitente en su hipertrofia

Skeletal muscles respond to several stimuli changing their phenotype. Muscular fibers adaptation capability is related to the presence of several myosin heavy chains (MHC). These express four types of pure fibers: I, IIA, IID and IIB containing MHCI, IIa, IId and IIb, respectively. Among pure fibers, there are hybrid fibers, which can express two or more types of myosins. In this study, types of fibers constituting male Wistar rats semitendinous and their myosin heavy chains, as well as influence of intermittent training on hypertrophy of these fibers have been checked through MATPase histochemical technique and electrophoretic proteins separation. All types of pure and hybrid muscular fiber have been found, however the fibers of the types IIA, IID and IIB were predominant, featuring muscle as a fast-contracting one. Training has promoted muscular fibers transition with a significant increase of fibers of IC, IIAD and IIDB type. A cross-section increase of fibers of IIDB and IIB type has also been noticed. In summary, semitendinous muscle is essentially constituted by fast-contracting fibers and training could promote transition and hypertrophy of these fast fibers.

Los músculos esqueléticos responden a diversos estímulos cambiando su fenotipo. La capacidad de adaptación de las fibras musculares está relacionada con la presencia de diversas miosinas de cadena pesada (MHC). Estas miosinas expresan cuatro tipos de fibras puras: I, IIA, IID, IIB, que contienen MHCI IIa IId IIb, respectivamente. Entre las fibras puras hay fibras híbridas, las cuales pueden expresar dos o más tipos de miosinas. En este trabajo, se observaron los tipos de fibras y las cadenas pesadas de miosinas del músculo semitendinoso en ratas Wistar macho, así como también, la influencia del entrenamiento intermitente en la hipertrofia de aquellas fibras, a través de la técnica histoquímica de mATPasa y separación eletroforética de proteínas. Todos los tipos de fibras musculares puras e híbridas fueron encontradas, siendo las fibras de tipo IIA IID y IIB predominantes, por ser un músculo de contracción rápida. El entrenamiento promovió la transición de las fibras musculares con un aumento significativo de las fibras del tipo IC, IIAD y IIDB. En una sección transversal, un incremento de fibras del tipo IIDB y IIB también fue reportada. En resumen, el músculo semitendinoso está compuesto esencialmente por fibras de contracción rápida y el entrenamiento puede promover la transición e hipertrofia de las fibras musculares rápidas.

Association between the muscle-specific proteins desmin and caveolin-3 in muscle cells.

The muscle-specific intermediate filament protein desmin is expressed in mononucleated myoblasts and in differentiated myotubes. Desmin has been shown to associate with the sarcolemma in specific structures, such as neuromuscular junctions and the dystrophin-associated protein complex. Since these are specialized membrane regions, the study of a possible association between desmin and liquid-ordered membrane microdomains is of particular interest. We have carried out an analysis of the association between desmin and the muscle-specific protein caveolin-3, a major component of caveolar microdomains. Our results demonstrate that (1) desmin precisely co-localizes with caveolin-3 in myoblasts and multinucleated myotubes, (2) caveolin-3 is up-regulated during in vitro chick muscle development, (3) desmin is detectable in caveolae-enriched membrane fractions prepared from skeletal muscle, and (4) caveolin-3 co-immunoprecipitates with desmin. We have thus shown, for the first time, an association between the intermediate filament protein desmin and caveolin-3 in myogenic cells.

Difference in adhesion molecule expression (ICAM-1 and VCAM-1) in juvenile and adult dermatomyositis, polymyositis and inclusion body myositis.

To assess the differential expression of adhesion molecules ICAM-1 and VCAM-1 in vessels and muscle fibers in acquired inflammatory myopathy, a series comprising thirty-seven muscle biopsy specimens from patients with JDM, fifteen with DM, fifteen with PM and seven with IBM was studied. Histochemical and immunohistochemical tests (StreptABCcomplex/HRP) for ICAM-1 and VCAM-1 (Dakopatts) were performed in serial frozen sections. ICAM-1 expression in vessels was significantly (p<0.0001) more present in JDM than PM, DM or IBM. However, in muscle fibers, ICAM-1 expression was absent in both JDM and IBM, but present in 33.4% and 40% in PM and DM respectively (p<0.0001). VCAM-1 expression in vessels was significantly more present in PM and DM than JDM and IBM (p<0.0001) while VCAM-1 expression in muscle fibers was almost absent in the four groups (p=0.2632). These findings emphasize the importance of adhesion molecules in the pathophysiology of the inflammatory myopathies, mainly the marked ICAM-1 expression in vessels in JDM, corroborating the microvascular involvement in this disease. In contrast, VCAM-1 seems not to play a major role in JDM, as previously described in PM, DM and IBM. Adhesion molecule expression in JDM presents a differential characteristic when compared to PM, DM and IBM.

Aerobic training, but not creatine supplementation, alters the gluteus medius muscle.

The aim of the present study was to investigate the effect of oral supplementation of creatine on the muscular responses to aerobic training. Twelve purebred Arabian horses were submitted to aerobic training for 90 d, with and without creatine supplementation, and evaluated with respect to BW and BCS and to the area and frequency of the different types of muscle fibers in the gluteus medius. Supplementation consisted of the daily administration of 75 g of creatine monohydrate mixed into the ration for the 90 d of training. Physical conditioning was conducted on a high-performance treadmill, and training intensity was stipulated by calculating the velocity at which blood lactate reaches 4 mmol/L, determined monthly for each animal. The individual intensity of physical force at 80% of aerobic threshold was established. Morphometry of gluteus medius muscle fibers was performed on frozen sections processed for histochemical analysis of myosin adenosine triphosphatase and immunohistochemistry of slow-contracting myosin. The results demonstrated that the animals maintained a moderate BCS without alteration of BW during the course of training, providing evidence of equilibrium between food intake and caloric expenditure during the study period. The present study demonstrated that aerobic training for 90 d caused hypertrophy of fiber types I (P = 0.04), IIA (P = 0.04), and IIX (P = 0.01), as well as an increase in the relative area occupied by type I fibers (P = 0.02) at the expense of type IIX fibers (P = 0.03), resulting in modifications of the contractile and metabolic characteristics of the gluteus medius muscle. It was not possible to show any beneficial effect from creatine on the skeletal muscle characteristics examined.

Muscular myosin isoforms of Taenia solium (Cestoda).

Type II myosin, the primary component of the thick filament of muscle fibers, is organized as a dimeric high molecular weight protein, and is composed of a pair of heavy chains (MHC) and two pairs of light chains. Myosin II transforms ATP energy into mechanical force. All type II myosins are conserved proteins but they have two variable regions that are located in different places of the molecule. Myosin molecules are encoded by a multigene family and many isoforms are generated. The expression of myosins depends on the developmental stage and on the type and degree of contractile activity and tissue, therefore several myosin isoforms are found in the same organism. Here we describe the use of different techniques that allowed demonstrating the presence of isoforms of the heavy chain type II myosin of Taenia solium cysticerci (larvae) and tapeworms (adults), a cestode parasite of importance in public health in many developing countries. Myosin was purified and used in comparative proteolytic fragmentation, ATPase activity, detection of antigenic differences and electrophoretic separation. The results obtained showed biochemical and immunochemical differences among cysticerci and tapeworms, and demonstrate the presence of myosin isoforms in T. solium that are probably associated to physiological requirements of each developmental stage.

Distribution and morphometry of skeletal muscle fibers in patients with chronic obstructive pulmonary disease and chronic hypoxemia.

This study was designed to assess the size and distribution of muscle fiber types in patients with severe chronic obstructive pulmonary disease and stable chronic hypoxemia. Brachial biceps biopsies were performed in 8 patients and 12 controls. Histochemistry was used to count and determine the cross-sectional area of the various fiber-types (1, 2a, and 2b). A significant reduction (P < 0.05) in the proportion of type 2a fibers and an increase in the proportion and cross-sectional area of type 2b fibers were seen in hypoxemic patients. These findings suggest an adaptation of the muscle fibers to a low partial pressure of oxygen in arterial blood.

Ventricular expression of atrial natriuretic peptide in chronic chagasic cardiomyopathy is not induced by myocarditis.

BACKGROUND: The ventricles of the normal heart are virtually devoid of atrial natriuretic peptide (ANP). Although ANP occurs in ventricles submitted to elevated wall stress, it is not clear whether ANP expression is affected by myocarditis. We investigated the immunohistochemical expression of ANP in chronic chagasic cardiomyopathy, an inflammatory cardiomyopathy caused by infection with the protozoan Trypanosoma cruzi. METHODS: Necropsy samples from the left and right ventricles of 16 patients exhibiting chronic chagasic cardiomyopathy were evaluated for myocarditis, fibrosis, T. cruzi parasites and ANP immunoreactivity. The diameters of 50 myocytes per sample were measured. RESULTS: ANP was present in myocytes of the subendocardial region in 13/16 (81.3%) left and 10/16 (62.5%) right ventricular samples (P=0.25). Myocytes present in the inflammatory foci, near the infiltrating inflammatory cells but distant from the subendocardial region, did not express ANP. Trypanosoma cruzi parasites exhibited intense immunoreactivity for ANP. The mean myocyte diameter and the incidence of myocarditis, fibrosis, and T. cruzi parasites was similar between the left and right ventricular samples. No statistical differences were found between the ANP-positive and ANP-negative cases. CONCLUSIONS: In chronic chagasic cardiomyopathy, both ventricles exhibit hypertrophy, fibrosis and ANP in the subendocardial region. The inflammatory infiltrate does not induce ANP expression in the myocytes. Regional stress but not myocarditis itself, is probably responsible for ventricular ANP expression in myocarditis.

The pore region of the skeletal muscle ryanodine receptor is a primary locus for excitation-contraction uncoupling in central core disease.

Human central core disease (CCD) is caused by mutations/deletions in the gene that encodes the skeletal muscle ryanodine receptor (RyR1). Previous studies have shown that CCD mutations in the NH2-terminal region of RyR1 lead to the formation of leaky SR Ca2+ release channels when expressed in myotubes derived from RyR1-knockout (dyspedic) mice, whereas a COOH-terminal mutant (I4897T) results in channels that are not leaky to Ca2+ but lack depolarization-induced Ca2+ release (termed excitation-contraction [EC] uncoupling). We show here that store depletion resulting from NH2-terminal (Y523S) and COOH-terminal (Y4795C) leaky CCD mutant release channels is eliminated after incorporation of the I4897T mutation into the channel (Y523S/I4897T and Y4795C/I4897T). In spite of normal SR Ca2+ content, myotubes expressing the double mutants lacked voltage-gated Ca2+ release and thus exhibited an EC uncoupling phenotype similar to that of I4897T-expressing myotubes. We also show that dyspedic myotubes expressing each of seven recently identified CCD mutations located in exon 102 of the RyR1 gene (G4890R, R4892W, I4897T, G4898E, G4898R, A4905V, R4913G) behave as EC-uncoupled release channels. Interestingly, voltage-gated Ca2+ release was nearly abolished (reduced approximately 90%) while caffeine-induced Ca2+ release was only marginally reduced in R4892W-expressing myotubes, indicating that this mutation preferentially disrupts voltage-sensor activation of release. These data demonstrate that CCD mutations in exon 102 disrupt release channel permeation to Ca2+ during EC coupling and that this region represents a primary molecular locus for EC uncoupling in CCD.

Stretch-induced alkalinization of feline papillary muscle: an autocrine-paracrine system.

Myocardial stretch is a well-known stimulus that leads to hypertrophy. Little is known, however, about the intracellular pathways involved in the transmission of myocardial stretch to the cytoplasm and nucleus. Studies in neonatal cardiomyocytes demonstrated stretch-induced release of angiotensin II (Ang II). Because intracellular alkalinization is a signal to cell growth and Ang II stimulates the Na+/H+ exchanger (NHE), we studied the relationship between myocardial stretch and intracellular pH (pHi). Experiments were performed in cat papillary muscles fixed by the ventricular end to a force transducer. Muscles were paced at 0.2 Hz and superfused with HEPES-buffered solution. pHi was measured by epifluorescence with the acetoxymethyl ester form of the pH-sensitive dye 2',7'-bis(2-carboxyethyl)-5,6-carboxyfluorescein (BCECF-AM). Each muscle was progressively stretched to reach maximal developed force (Lmax) and maintained in a length that was approximately 92% Lmax (Li). During the "stretch protocol," muscles were quickly stretched to Lmax for 10 minutes and then released to Li; pHi significantly increased during stretch and came back to the previous value when the muscle was released to Li. The increase in pHi was eliminated by (1) specific inhibition of the NHE (EIPA, 5 micromol/L), (2) AT1-receptor blockade (losartan, 10 micromol/L), (3) inhibition of protein kinase C (PKC) (chelerythrine, 5 micromol/L), (4) blockade of endothelin (ET) receptors with a nonselective (PD 142,893, 50 nmol/L) or a selective ETA antagonist (BQ-123, 300 nmol/L). The increase in pHi by exogenous Ang II (500 nmol/L) was also reduced by both ET-receptor antagonists. Our results indicate that after myocardial stretch, pHi increases because of stimulation of NHE activity. This involves an autocrine-paracrine mechanism in which protein kinase C, Ang II, and ET play crucial roles.

Gender does not influence neuromuscular properties in dimorphic skeletal muscles of the toad.

The aim of this work was to study gender differences on the physiology of the dimorphic brachial musculature involved in the clasp reflex of the toad (Bufo marinus L.). The neuromuscular transmission, the sensitivity to acetylcholine (ACh) and the cholinesterase activity were compared on the forelimb sternoradialis muscles (SR) from male and female toads. The interosseous muscles of the first finger were used to compare the properties of the nicotinic receptor/ionic channel complex (AChR). All the muscles studied were dimorphic, i.e. significantly smaller in the female than in the male frog in otherwise similar size animals. The SR of either sex contracted to bath application of ACh with similar EC50. In physiological solution the frequency of the miniature end-plate potentials (mepps) was very low (0.1 s-1) and no gender difference was detected. The mepp amplitudes were 0.62 +/- 0.03 and 0.58 +/- 0.03 mV in SR from male and female toads, respectively. To increase exocytosis the muscles were incubated in hypertonic solution (158 mM NaCl). Under this condition mepp frequency was increased by five and seven times and mepp amplitude increased by 1.3 and 1.6 times in SR from male and female toads, respectively. The cholinesterase activity measured by the colorimetric method, did not differ in SR from male and female toads. In muscle fibers dissociated from the dimorphic interosseous muscles of male and female toads, the ionic channel conductance was 43 +/- 5.3 and 44 +/- 4.5 pS, respectively. The mean channel open time was voltage-dependent and not significantly different in preparations from both genders. These observations indicate that neither the ACh-nicotinic receptor interaction, nor the AChR complex kinetics and the nicotinic excitation-contraction coupling or the cholinesterase activity differ in dimorphic muscles from Bufo genders. No gender difference was detected in neuromuscular transmission of the studied muscle. Only a slight increase in mepp frequency and amplitude could be detected when the muscles were incubated in hypertonic solution.

Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophies.

While present in the surface membrane of embryonic muscle fibers, in adult normal muscle fibers, utrophin is restricted to the motor endplate and cells of blood vessel walls. However, the observation that utrophin is maintained in the extrajunctional plasma membrane in Duchenne (DMD) and in mdx muscle fibers has led to the suggestion that excess utrophin might compensate for dystrophin deficiency in the Xp21 muscular dystrophies. In order to detect an inverse correlation of utrophin presence and clinical severity, we have assessed utrophin distribution and quantity in DMD and Becker (BMD) patients of different ages and stages of clinical severity. All patients showed a positive discontinuous immunolabeling of utrophin on the sarcolemma, staining equally small and large muscle fibers, indicating that immature characteristics are maintained in such fibers. On Western blot, utrophin bands with concentrations 2- to 10-fold greater than in normal controls were detected in all DMD/BMD patients. However, no negative correlation was found between the amount of utrophin and the severity of clinical course, implying that the detectable utrophin levels in these patients did not compensate for dystrophin deficiency. In a DMD patient with growth hormone (GH) deficiency and a BMD-like clinical course, utrophin levels were comparable to the other typical DMD cases, which reinforces the hypothesis that the observed increase in utrophin is apparently not responsible for a milder clinical course in some patients with Xp21 muscular dystrophies.

Immunohistochemical alterations of dystrophin in congenital muscular dystrophy

Foi estudada a distribuiçäo da distrofina na membrana plasmática das fibras musculares em 22 crianças com distrofia muscular congênita, através de técnicas de imuno-histoquímica. A distrofina foi identificada nas biópsias musculares processadas a fresco, por técnicas de imunofluorescência utilizando anticorpos policlonais. Todos os casos tinham interrupçöes da imunofluorescência na membrana plasmática. Em 17 elas eram grandes, em 12 eram pequenas e em 7 eram de ambos os tipos. Fibras com interrupçöes pequenas e constantes, como um rosário, foram vistas em 15 casos. Essas anormalidades estavam presentes em todas as fibras em 5 casos, eeram freqüentes em 8, ocasionais em 5 e raras em 4. Cinco casos mostraram fibras sem distrofina. Esses dados sugerem que a expressäo da distrofina é anormal nesse grupo de crianças. Essas anormalidades podem também ser encontradas em casos precoces de distrofia muscular de Becker e distrofia autossômica recessiva da infância. Portanto, isoladamente a imuno-histoquímica näo permite a diferenciaçäo

From collagen type I solution to fibers with a helical pattern: a self-assembly phenomenon.

To determine whether collagen solubilized from tendons can regenerate the most relevant characteristics of the tendon supraorganization was the aim of the present study. Extracted and purified collagen in acetic acid solutions subjected to precipitation and extensive dialysis was found to produce gels with rheological properties that allowed them to form threads and rubber-like rods. Molecular order and the ordered aggregational state of the fibers were detected by optical anisotropy at the polarization microscope. Self-assembly and self-organization resulted in a supraorganized structure in which the fibers are ordered parallel to the long axis of the thread or the rod, and in an intertwined helical organization. The highly birefringent fibers and their geometrically ordered self-organization resembled the original tendons. Some questions related to morphogenesis, recognition and adhesion events, biomechanical properties of collagen-containing structures and development of biomaterial for medical use may be answered by this model. In terms of perspectives it would be important to consider collagen fibers as models for producing organic-inorganic interface depositions to achieve optical properties.