Architecture of the pectoralis muscle of the Japanese quail (Coturnix japonica): histochemical and ultrastructural characterization, and distribution of muscle fiber types

1987 ◽  
Vol 65 (1) ◽  
pp. 63-71 ◽  
Author(s):  
B. W. C. Rosser ◽  
J. C. George ◽  
S. K. Frombach

The muscle fibers in the pectoralis muscle of the Japanese quail (Coturnix japonica) are classified as fast-twitch glycolytic (FG), fast-twitch oxidative-glycolytic (FOG), and slow-tonic on the basis of their histochemical and ultrastructural characteristics. There is an increasing proportion of FOG/FG fibers along a superficial to deep gradient throughout the entire belly of the muscle. Slow-tonic fibers are present in low numbers, and are restricted to a tiny area located in the deepest fasciculi of the cranial third of the muscle. This distribution of muscle fiber types is typical of those vertebrate muscles adapted to a locomotory function. The slow-tonic fibers are alkali-stable and acid-stable when preincubated for myofibrillar adenosine triphosphatase (mATPase) activity. Slow fibers in the chicken pectoralis and mouse soleus muscle, both types previously described as alkali-labile, acid-stable for mATPase activity, cannot be distinguished from each other or Japanese quail slow-tonic fibers on the basis of several ultrastructural characteristics: Z-line width, metabolic differences, or fusion of myofibrils. While mammalian slow fibers have one large motor end plate, all avian slow fibers have small multiple motor end plates. Mammalian slow fibers are slow-twitch, and avian slow fibers are probably slow-tonic. More complex secondary synaptic clefts distinguish mammalian from all avian fiber types.

1983 ◽  
Vol 245 (2) ◽  
pp. H265-H275 ◽  
Author(s):  
B. G. Mackie ◽  
R. L. Terjung

Blood flow to fast-twitch red (FTR), fast-twitch white (FTW), and slow-twitch red (STR) muscle fiber sections of the gastrocnemius-plantaris-soleus muscle group was determined using 15 +/- 3-microns microspheres during in situ stimulation in pentobarbital-anesthetized rats. Steady-state blood flows were assessed during the 10th min of contraction using twitch (0.1, 0.5, 1, 3, and 5 Hz) and tetanic (7.5, 15, 30, 60, and 120/min) stimulation conditions. In addition, an earlier blood flow determination was begun at 3 min (twitch series) or at 30 s (tetanic series) of stimulation. Blood flow was highest in the FTR (220-240 ml X min-1 X 100 g-1), intermediate in the STR (140), and lowest in the FTW (70-80) section during tetanic contraction conditions estimated to coincide with the peak aerobic function of each fiber type. These blood flows are fairly proportional to the differences in oxidative capacity among fiber types. Further, their absolute values are similar to those predicted from the relationship between blood flow and oxidative capacity found by others for dog and cat muscles. During low-frequency contraction conditions, initial blood flow to the FTR and STR sections were excessively high and not dependent on contraction frequency. However, blood flows subsequently decreased to values in keeping with the relative energy demands. In contrast, FTW muscle did not exhibit this time-dependent relative hyperemia. Thus, besides the obvious quantitative differences between skeletal muscle fiber types, there are qualitative differences in blood flow response during contractions. Our findings establish that, based on fiber type composition, a heterogeneity in blood flow distribution can occur within a whole muscle during contraction.


1984 ◽  
Vol 51 (3) ◽  
pp. 529-537 ◽  
Author(s):  
D. W. Sickles ◽  
T. G. Oblak

We have examined the oxidative metabolism of rat alpha-motoneurons innervating muscles composed predominantly of one muscle-fiber type. Intramuscular injections of horseradish peroxidase (HRP) into the tensor fasciae latae (TFL) (approximately 94% fast-twitch glycolytic fibers, FG), tibialis anterior (TA) (approximately 66% fast-twitch oxidative-glycolytic, FOG; 32% FG), and soleus (SOL) (approximately 84% slow-twitch oxidative, SO) muscles permitted identification of motoneurons innervating these muscles. gamma-Motoneurons (less than 25-micron average soma diameter) were eliminated from the sampling. The alpha-motoneurons innervating the TFL were considered as FG, those innervating the tibialis anterior as FOG, and those of the soleus as SO. Alternate 5-micron serial cryostat sections were processed for HRP and nicotinamide adenine dinucleotide-diapharase (NADH-D) (oxidative enzyme) activities. Controls were included to assure reliability of reaction product quantitation. Motoneuron pools of each muscle were characterized by their shape and location within the ventral horn. Cells identified on HRP sections as innervating each of the muscles were located on sections processed for NADH-D activity. The optical density of motoneurons in sections processed for NADH-D activity was measured with a Zeiss Zonax MPM 03 microdensitometer. The mean relative NADH-D activities (optical density) of alpha-motoneurons innervating the TFL (FG), TA (FOG), and SOL(SO) muscles were 0.261, 0.305, and 0.447, respectively. Although some overlap in distribution of enzyme activities was observed, statistical analysis indicated significant differences between the NADH-D activities of each type of alpha-motoneuron. This is the first report of any metabolic difference in alpha-motoneurons belonging to different motor-unit types.(ABSTRACT TRUNCATED AT 250 WORDS)


Author(s):  
Nejc Umek ◽  
Simon Horvat ◽  
Erika Cvetko

In obesity, accumulation of lipid droplets in skeletal muscle fibers and a shift towards fast muscle fiber types can both contribute to insulin resistance. However, it is not yet clear how intramyocellular lipid accumulation and fiber type changes are associated. Therefore, we investigated to what extent the lipids accumulated in a fiber type-specific manner in the functionally similar fast-, intermediate- and slow‑twitch gastrocnemius, plantaris, and soleus muscles, respectively, in high-fat diet-induced obese 54-week-old female C57BL/6JOlaHsd mice (n=9) compared to control standard-diet-treated lean mice (n=9). A high-fat diet was administered for 26 weeks. Fiber-type specific intramyocellular lipid content analysis and muscle fiber typing were performed using histochemical analysis of lipids with Sudan Black and immunohistochemical analysis of myosin heavy chains on serial sections of skeletal muscles. Compared to the lean mice, the lipid accumulation was most prominent in types 2a and 2x/d fibers (p<0.05) of fast-twitch gastrocnemius and intermediate plantaris muscles in the obese mice, while in slow-twitch soleus muscle, there was no significant lipid accumulation in the obese animals. Furthermore, the slow-twitch soleus muscle of the obese mice with no significant change in muscle fiber diameters exhibited the most pronounced shift towards fast-type myosin heavy chain isoform expression (p<0.05). In contrast, the fast-twitch and intermediate-twitch gastrocnemius and plantaris muscles, respectively, in which the muscle fiber diameters increased (p<0.05), were more resistant toward myosin heavy chain expression changes. In conclusion, we demonstrated both muscle- and fiber-type specificity in intramyocellular lipid accumulation in obese mice, suggesting that in obesity, similar muscle fiber types in different muscles accumulate lipids differentially.


1986 ◽  
Vol 251 (3) ◽  
pp. C395-C402 ◽  
Author(s):  
S. P. Kirkwood ◽  
E. A. Munn ◽  
G. A. Brooks

High-voltage electron microscopy at 1,500 kV was used to examine mitochondrial morphology in three skeletal muscles of the rat. The soleus, deep portion of the vastus lateralis, and superficial portion of the vastus lateralis muscles were examined to represent slow-twitch oxidative, fast-twitch oxidative, glycolytic, and fast-twitch glycolytic skeletal muscle fiber types, respectively. Muscle samples were removed from six female Wistar rats. The tissues were fixed using standard electron microscopic techniques and were sectioned transversely with respect to muscle fiber orientation to approximately 0.5-micron thickness. The sections were stained on grids with uranyl acetate and Reynolds' lead citrate. Results revealed a mitochondrial reticulum in all three skeletal muscle fiber types. Stereological analyses of the electron micrographs were performed to measure volume densities and surface-to-volume ratios of mitochondria in the muscle samples. Cross-sectional volume densities of mitochondria in the soleus (15.5 +/- 1%) and deep portion of the vastus lateralis (16.1 +/- 2%) were significantly greater (P less than 0.05) than in the superficial portion of the vastus lateralis (8.7 +/- 1%). Surface-to-volume ratios of mitochondria were not significantly different between fiber types. It was concluded that the mitochondria in mammalian limb skeletal muscle are a reticulum, or network.


1993 ◽  
Vol 41 (7) ◽  
pp. 1013-1021 ◽  
Author(s):  
S Boudriau ◽  
M Vincent ◽  
C H Côté ◽  
P A Rogers

We used immunochemical quantification and indirect immunofluorescence to investigate the cell content, distribution, and organization of microtubules in adult rat slow-twitch soleus and fast-twitch vastus lateralis muscles. An immunoblotting assay demonstrated that the soleus muscle (primarily Type I fibers) was found to have a 1.7-fold higher relative content of alpha-tubulin compared with the superficial portion of the vastus lateralis muscle (primarily Type IIb fibers). Both physiological muscle types revealed a complex arrangement of microtubules which displayed oblique, longitudinal, and transverse orientations within the sarcoplasmic space. The predominance of any one particular orientation varied significantly from one muscle tissue section to another. Nuclei were completely surrounded by a dense net-like structure of microtubules. Both muscle fiber types were found to possess a higher density of microtubules in the subsarcolemmal region. These microtubules followed the contour of the sarcolemma in slightly contracted fibers and showed a fine punctate appearance indicative of a restricted distribution. The immunofluorescence results indicate that microtubules are associated with the sarcolemma and therefore may form a part of the membrane cytoskeletal domain of the muscle fiber. We conclude that the microtubule network of the adult mammalian skeletal muscle fiber constitutes a bone fide component of the exosarcomeric cytoskeletal lattice domain along with the intermediate filaments, and as such could therefore participate in the mechanical integration of the various organelles of the myofibers during the contraction-relaxation cycle.


2001 ◽  
Vol 49 (8) ◽  
pp. 1033-1044 ◽  
Author(s):  
Guillermo H. Graziotti ◽  
Clara M. Ríos ◽  
José-Luis L. Rivero

Skeletal muscle fiber types classified on the basis of their content of different myosin heavy chain (MHC) isoforms were analyzed in samples from hindlimb muscles of adult sedentary llamas ( Lama glama) by correlating immunohistochemistry with specific anti-MHC monoclonal antibodies, myofibrillar ATPase (mATPase) histochemistry, and quantitative histochemistry of fiber metabolic and size properties. The immunohistochemical technique allowed the separation of four pure (i.e., expressing a unique MHC isoform) muscle fiber types: one slow-twitch (Type I) and three fast-twitch (Type II) phenotypes. The same four major fiber types could be objectively discriminated with two serial sections stained for mATPase after acid (pH 4.5) and alkaline (pH 10.5) preincubations. The three fast-twitch fiber types were tentatively designated as IIA, IIX, and IIB on the basis of the homologies of their immunoreactivities, acid denaturation of their mATPase activity, size, and metabolic properties expressed at the cellular level with the corresponding isoforms of rat and horse muscles. Acid stability of their mATPase activity increased in the rank order IIA>IIX>IIB. The same was true for size and glycolytic capacity, whereas oxidative capacity decreased in the same rank order IIA>IIX>IIB. In addition to these four pure fibers (I, IIA, IIX, and IIB), four other fiber types with hybrid phenotypes containing two (I + IIA, IIAX, and IIXB) or three (IIAXB) MHCs were immunohistochemically delineated. These frequent phenotypes (40% of the semitendinosus muscle fiber composition) had overlapped mATPase staining intensities with their corresponding pure fiber types, so they could not be delineated by mATPase histochemistry. Expression of the three fast adult MHC isoforms was spatially regulated around islets of Type I fibers, with concentric circles of fibers expressing MHC-IIA, then MHC-IIX, and peripherally MHC-IIB. This study demonstrates that three adult fast Type II MHC isoproteins are expressed in skeletal muscle fibers of the llama. The general assumption that the very fast MHC-IIB isoform is expressed only in small mammals can be rejected. (J Histochem Cytochem 49:1033–1044, 2001)


1980 ◽  
Vol 49 (5) ◽  
pp. 851-855 ◽  
Author(s):  
B. G. Mackie ◽  
G. A. Dudley ◽  
H. Kaciuba-Uscilko ◽  
R. L. Terjung

The influence of muscle stimulation (3 Hz) on the uptake of exogenously administered chylomicron 14C-labeled triglycerides (14C-TG) in the three different muscle fiber types was evaluated in fed and fasted pentobarbital-anesthetized rats. The fractional uptake of 14C-TG in the nonstimulated muscles was lowest in the fast-twitch white, intermediate in the fast-twitch red, and highest in the slow-twitch red muscle fiber section. Fasting doubled the uptake in both high-oxidative red fibers. These 14C-TG uptakes were directly proportional (r = 0.993) to their respective activities of lipoprotein lipase in these fiber types of fed and fasted animals reported by others. Muscle stimulation caused a significant increase in the fractional 14C-TG uptake in all of the fiber types. Although the TG uptake could account for only a small fraction of the total energy needs of the working muscle, it could contribute to the turnover of endogenous TG, especially in the slow-twitch red fibers. Further, the estimated TG uptake rate is sufficient to replace endogenous TG loss with an overnight rest following exercise. These results suggest that plasma TG could play an important role in lipid metabolism, especially in the high-oxidative slow and fast muscle fiber types.


1996 ◽  
Vol 270 (4) ◽  
pp. C1067-C1074 ◽  
Author(s):  
P. C. Tullson ◽  
P. G. Arabadjis ◽  
K. W. Rundell ◽  
R. L. Terjung

Inosine 5'-monophosphate (IMP) reamination in skeletal muscle fiber sections of the rat hindlimb was studied. High IMP concentrations were established during ischemic contractions in each fiber section: 3.1, 2.8, or 0.6 mumol/g in the fast-twitch white (FTW), fast-twitch red (FTR), and slow-twitch red (STR) muscle sections, respectively. Thereafter blood flow was restored and stimulation was discontinued to allow reamination of IMP. After 0, 2, 5, 10, 15, or 20 min of recovery, muscle sections were freeze-clamped and analyzed for metabolite contents. IMP was nearly fully reaminated after 10 and 20 min of recovery in STR and FTR muscles, respectively. Reamination in TW fibers was delayed and slower, with only 50% of the IMP reaminated after 20 min of recovery. Significant recovery (approximately 75%) of phosphocreatine occurs in each fiber section before the onset of reamination. Reamination was also evaluated after high-speed treadmill running with or without inhibition of reamination by hadacidin. Running resulted in large accumulations of IMP in FTW and FTR fibers (3.5 and 1.4 mumul/g, respectively); IMP in FTR fibers was higher with hadacidin treatment. Reamination after running was much greater in FTR than in FTW fibers and was associated with recovery of phosphocreatine. After running, the purine degradation products inosine and hypoxanthine were increased in FTW and FTR fibers in normal and hadacidin-treated animals. Plasma inosine, hypoxanthine, and urate increased after exercise; concentrations continued to increase if reamination was inhibited by hadacidin. These results demonstrate that when muscle IMP is increased, subsequent degradation and loss of purines occur. Rapid reamination should minimize the quantity of purine lost from muscle and limit the metabolic cost of replenishing purines by the de novo synthesis or salvage pathways.


1979 ◽  
Vol 82 (2) ◽  
pp. 391-400 ◽  
Author(s):  
G F Gauthier

In a fast-twitch muscle, three types of fibers (red, intermediate, and white) can be distinguished on the basis of mitochondrial content. Red fibers, identified by abundant mitochondria, can be further differentiated on the basis of a positive or negative response to antibodies specific for white ("fast") myosin. Because there is also a difference in Z-line width among fibers of the same muscle, the possibility existed that the two red fibers, which differ in type of myosin, might also differ in dimensions of the Z line. We therefore examined, with the electron microscope, fibers which had been exposed to antibody against white myosin. In those fibers which react with the antibody, an electron-opaque band is evident in the H-band region, thereby distinguishing reactive from unreactive fibers. The red fiber can now be subdivided on the basis of a positive or negative response to anti-white myosin visualized directly with the electron microscope. Both categories of red fibers ("fast" and "slow") have wide Z lines, and thus are distinguished from white and intermediate fibers, which react with the antibody but which have narrow Z lines. On the basis of combined immunocytochemical and ultrastructural characteristics, four types of fibers can be recognized in a single muscle. Moreover, it is demonstrated here that a wide Z line does not necessarily imply a slow speed of contraction.


2015 ◽  
Vol 309 (7) ◽  
pp. F638-F647 ◽  
Author(s):  
Luz M. Acevedo ◽  
Alan Peralta-Ramírez ◽  
Ignacio López ◽  
Verónica E. Chamizo ◽  
Carmen Pineda ◽  
...  

This study describes fiber-type adaptations in hindlimb muscles, the interaction of sex, and the role of hypoxia on this response in 12-wk ⅚ nephrectomized rats (Nx). Contractile, metabolic, and morphological features of muscle fiber types were assessed in the slow-twitch soleus and the fast-twitch tibialis cranialis muscles of Nx rats, and compared with sham-operated controls. Rats of both sexes were considered in both groups. A slow-to-fast fiber-type transformation occurred in the tibialis cranialis of Nx rats, particularly in males. This adaptation was accomplished by impaired oxidative capacity and capillarity, increased glycolytic capacity, and no changes in size and nuclear density of muscle fiber types. An oxidative-to-glycolytic metabolic transformation was also found in the soleus muscle of Nx rats. However, a modest fast-to-slow fiber-type transformation, fiber hypertrophy, and nuclear proliferation were observed in soleus muscle fibers of male, but not of female, Nx rats. Serum testosterone levels decreased by 50% in male but not in female Nx rats. Hypoxia-inducible factor-1α protein level decreased by 42% in the tibialis cranialis muscle of male Nx rats. These data demonstrate that 12 wk of Nx induces a muscle-specific adaptive response in which myofibers do not change (or enlarge minimally) in size and nuclear density, but acquire markedly different contractile and metabolic characteristics, which are accompanied by capillary rarefaction. Muscle function and sex play relevant roles in these adaptations.


Sign in / Sign up

Export Citation Format

Share Document