Journal of Histochemistry and Cytochemistry Priciples for Free Access to Science
  Search:   
    >> Advanced Search

Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Staron, R. S.
Right arrow Articles by Toma, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Staron, R. S.
Right arrow Articles by Toma, K.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Journal of Histochemistry and Cytochemistry, Vol. 48, 623-630, May 2000, Copyright © 2000, The Histochemical Society, Inc.


ARTICLE

Fiber Type Composition of the Vastus Lateralis Muscle of Young Men and Women

Robert S. Starona, Fredrick C. Hagermana, Robert S. Hikidaa, Thomas F. Murraya, David P. Hostlerc, Mathew T. Crillc, Kerry E. Raggb, and Kumika Tomac
a Department of Biomedical Sciences, College of Osteopathic Medicine, Ohio University, Athens, Ohio
b Student Health Service, Ohio University, Athens, Ohio
c Department of Biological Sciences, Ohio University, Athens, Ohio

Correspondence to: Robert S. Staron, Dept. of Biomedical Sciences, College of Osteopathic Medicine, Ohio University, Irvine Hall, Rm 430, Athens, OH 45701. E-mail: staron@ohiou.edu


*   Summary
*Top
*Summary
*Introduction
*Materials and Methods
*Results
*Discussion
*Literature Cited

This study presents data collected over the past 10 years on the muscle fiber type composition of the vastus lateralis muscle of young men and women. Biopsies were taken from the vastus lateralis muscle of 55 women (21.2 ± 2.2 yr) and 95 men (21.5 ± 2.4 yr) who had volunteered to participate in various research projects. Six fiber types (I, IC, IIC, IIA, IIAB, and IIB) were classified using mATPase histochemistry, and cross-sectional area was measured for the major fiber types (I, IIA, and IIB). Myosin heavy chain (MHC) content was determined electrophoretically on all of the samples from the men and on 26 samples from the women. With the exception of fiber Type IC, no significant differences were found between men and women for muscle fiber type distribution. The vastus lateralis muscle of both the men and women contained approximately 41% I, 1% IC, 1% IIC, 31% IIA, 6% IIAB, and 20% IIB. However, the cross-sectional area of all three major fiber types was larger for the men compared to the women. In addition, the Type IIA fibers were the largest for the men, whereas the Type I fibers tended to be the largest for the women. Therefore, gender differences were found with regard to the area occupied by each specific fiber type: IIA>I>IIB for the men and I>IIA>IIB for the women. These data establish normative values for the mATPase-based fiber type distribution and sizes in untrained young men and women. (J Histochem Cytochem 48:623–629, 2000)

Key Words: fiber types, human skeletal muscle, muscle biopsies, myosin heavy chains, mATPase histochemistry


*   Introduction
*Top
*Summary
*Introduction
*Materials and Methods
*Results
*Discussion
*Literature Cited

It is often desirable to obtain muscle samples for direct analyses in order to study the effects of diet, exercise, disuse, or disease on human skeletal muscle. Although invasive, the percutaneous muscle biopsy technique (Bergstrom 1975 Down) is safe, rapid, and repeatable. It is excellent for allowing the extraction of a small piece of muscle (~80–160 mg) with minimal discomfort and scarring. The vastus lateralis muscle, a portion of the quadriceps femoris muscle group, has been the muscle of choice for biopsies because of its mixed fiber type composition, trainability, and accessibility. Therefore, a large body of data concerning this muscle exists in the literature, potentially facilitating comparisons among studies ( Saltin and Gollnick 1983 Down).

However, direct comparisons of morphometric data may be hindered for a number of reasons, including the use of small biopsy samples and/or a small number of subjects (usually less than 12), disregard for possible gender and age differences, different methodologies for fiber type delineation, and different fitness levels (e.g., Edstrom and Nystrom 1969 Down; Edstrom and Ekblom 1972 Down; Johnson et al. 1973 Down; Gollnick et al. 1974 Down; Edgerton et al. 1975 Down; Tesch and Karlsson 1978 Down; Lexell et al. 1984 Down; Simoneau et al. 1985 Down). Because young men and women are often used as subjects and because the vastus lateralis muscle is most often investigated, it is important to establish mean values for morphometric data from this muscle in this age group. Recently, six fiber types have been delineated in human skeletal muscle and these have been correlated with a specific myosin heavy chain (MHC) profile (Staron 1991 Down).

The purpose of this investigation was to present normative data on muscle fiber types and sizes within the superficial region of vastus lateralis muscle of healthy, untrained young men and women, and to establish specific gender differences using this entire range of histochemically defined fiber types. Biopsy data were gathered from individuals who had participated in various research projects at Ohio University over the past 10 years.


*   Materials and Methods
*Top
*Summary
*Introduction
*Materials and Methods
*Results
*Discussion
*Literature Cited

Subjects
A total of 150 healthy college-aged men and women volunteered to participate in various research projects at Ohio University over the past 10 years (e.g., Staron et al. 1990 Down, Staron et al. 1991 Down, Staron et al. 1994 Down; Allemeier et al. 1994 Down; and recent unpublished data). In all cases, the Ohio University Institutional Review Board gave approval before the beginning of each project. All subjects were informed of the procedures, risks, and benefits, and provided written consent before participation. Subjects consisted of 95 young men and 55 young women ( Table 1). Although physically active, all subjects were considered untrained and had not participated in any regular exercise program for at least 6 months before the start of each research project. Anthropometric measurements were taken immediately before the extraction of the muscle biopsies (Table 1). Body composition was estimated using skinfold measurements from three sites for the men (chest, umbilicus, and anterior thigh) (Jackson and Pollock 1978 Down) and women (anterior thigh, posterior brachium, and suprailium) (Jackson et al. 1980 Down).


 
View this table:
[in this window]
[in a new window]
 
Table 1. Anthropometric measurements a

Muscle Biopsies
Muscle biopsies (80–160 mg) were extracted from the superficial portion of the vastus lateralis muscle by the percutaneous needle biopsy technique (Bergstrom 1962 Down). The muscle samples were removed from the needle, oriented in tragacanth gum, immediately frozen in isopentane cooled by liquid nitrogen to -159C, and stored at -74C. Because of possible anatomic variations ( Willan et al. 1990 Down), as well as potential variations in fiber type distribution and size from superficial to deep and proximal to distal (Blomstrand and Ekblom 1982 Down; Elder et al. 1982 Down; Lexell et al. 1983 Down, Lexell et al. 1985 Down; Mahon et al. 1984 Down; Lexell and Taylor 1989 Down), attempts were made to extract samples from each individual at approximately the same location. Biopsies were therefore taken ~16 cm proximal to the superior border of the patella from the superficial portion of the vastus lateralis muscle (25–30 mm deep to the fascia lata). Depth was gauged by interval markings engraved in the biopsy needles. To ensure the procurement of adequate sample sizes, large biopsy specimens were obtained using a double-chop method (Staron et al. 1990 Down) combined with suction ( Evans et al. 1982 Down).

Fiber Type and Cross-sectional Area Determinations
The frozen biopsy specimens were thawed to -24C and serially sectioned (12 µm thick) for histochemical analysis. Myofibrillar adenosine triphosphatase (mATPase) histochemistry was performed using preincubation pH values of 4.3, 4.6, and 10.4 ( Brooke and Kaiser 1970 Down) to determine the muscle fiber type composition. Six fiber types (I, IC, IIC, IIA, IIAB, and IIB) were distinguished on the basis of their staining intensities (Fig 1). Fiber Types IIAB and IIB have more recently been referred to as IIAX and IIX, respectively ( Smerdu et al. 1994 Down; Ennion et al. 1995 Down). A composite photomontage of each mATPase preparation after preincubation at pH 4.6 was made using Polaroid micrographs (x 56 magnification). These were used in combination with the other mATPase preparations to determine fiber type percentages and total fiber number in each biopsy. Because of the scarcity of hybrid fibers (IC, IIC, and IIAB), only the major fiber types were used for area determinations. Cross-sectional area was determined on at least 50 fibers per major fiber type (I, IIA, and IIB) per biopsy, using either direct tracings (x 200) and a digitizing tablet or an image analysis computer program (NIH Image software program). The six histochemically delineated fiber types were subsequently collapsed into the three major types (I, IIA, and IIB) using the following formulae: I + IC = I, IIC + IIA + 1/ 2IIAB = IIA, 1/2IIAB + IIB = IIB. These three types were then combined with the respective area measurements to yield fiber type percent area that has been shown to correlate with relative MHC isoform percentages (Fry et al. 1994 Down).



View larger version (56K):
[in this window]
[in a new window]
 
Figure 1. Serial cross-sections of a pretraining muscle sample taken from a subject demonstrating the fiber type delineation by mATPase histochemistry after preincubation at pH 10.4 (a), 4.3 (b), and 4.6 (c). I, Type I; IC, Type IC; IIC, Type IIC; A, Type IIA; AB, Type IIAB; B, Type IIB. Bar = 100 µm.

Myosin Heavy Chain Analysis
MHC analysis was performed on all the biopsy samples from the men and on 26 of the 55 samples from the women using sodium dodecyl sulfate (SDS)-polyacrylamide electrophoretic techniques. The protocol for analyzing the specimens was based on the procedures of Perrie and Bumford 1986 Down, with modifications used for single fiber analysis (Staron 1991 Down; Staron and Hikida 1992 Down). Briefly, four to six serial cross-sections (20 µm thick) from each biopsy were placed in 0.5 ml of a lysing buffer containing 10% (w/v) glycerol, 5% (v/v) 2-mercaptoethanol, and 2.3% (w/v) SDS in 62.5 mM Tris (hydroxymethyl) aminomethane HCl buffer (pH 6.8) and were heated for 10 min at 60C. Small amounts of the extracts (3–5 µl) were loaded on 4–8% gradient SDS-polyacrylamide gels with 4% stacking gels (Bar and Pette 1988 Down), run overnight (19–21 hr) at 120 V, and stained with Coomassie Blue. MHC isoforms were identified according to their apparent molecular masses compared with those of marker proteins and migration patterns from single fiber analyses. Relative MHC isoform content was subsequently determined using a laser densitometer.

Statistical Analysis
The statistical package SPSS was utilized for all statistical analyses. Descriptive statistics were used to derive mean ± SD for all variables. Anthropometric data were compared between groups using independent t-tests. Muscle fiber characteristics (fiber type distribution, cross-sectional area, percentage fiber type area, and MHC content) were analyzed using repeated-measures one-way and two-way analysis of variance (ANOVA). Significant differences were then determined using Tukey's HSD post hoc test. Correlation analyses were performed to compare percentage fiber type area with MHC content. Differences were considered significant at p<= 0.05.


*   Results
*Top
*Summary
*Introduction
*Materials and Methods
*Results
*Discussion
*Literature Cited

Anthropometric Data
The men were taller, heavier, and had a lower percentage of body fat compared to the women (Table 1).

Fiber Type Distribution
Large sample sizes were obtained for the determination of fiber type composition. Only four of the 150 biopsy specimens contained less than 400 fibers. The distribution of the six fiber types was almost identical for the young men and women (Table 2). The lone exception was a significantly lower percentage of Type IC fibers for the men. The superficial region of the vastus lateralis muscle for both men and women contained a fiber type distribution of approximately 41% I, 1% IC, 1% IIC, 31% IIA, 6% IIAB, and 20% IIB (Table 2). However, there was a wide range for the percentage of Type I fibers for both the men (17.6–65.6%) and the women (16.5–97.4%). Most of the vastus lateralis muscle samples (132 of the 150) had between 25–60% Type I fibers. A total of 6% of the vastus lateralis samples (four women and five men) contained >60% Type I fibers and 6% (three women and six men) contained <25% Type I fibers. Similar to the data of Simoneau and Bouchard 1989 Down, individuals with a percentage of Type I fibers <35% were found almost twice as often for the men (38%) compared to the women (20%).


 
View this table:
[in this window]
[in a new window]
 
Table 2. Muscle fiber type percentages ab

Cross-sectional Area Measurements
As previously shown for the vastus lateralis muscle ( Simoneau and Bouchard 1989 Down), the cross-sectional areas of all three major fiber types (I, IIA, and IIB) were significantly larger for the men compared to the women (Table 3). On average, the Type I, IIA, and IIB fibers were 18.6%, 59.2% and 65.5% larger for the men than the respective fiber types for the women. For the men, the Type IIA fibers were the largest (with no significant difference between Types I and IIB), and for the women Type I and IIA fibers were larger than Type IIB fibers ( Table 3).


 
View this table:
[in this window]
[in a new window]
 
Table 3. Cross-sectional area (µm2) a

Percentage Fiber Type Area
Percentage fiber type areas were determined following the collapse of the original six fiber types into the three major groups (see Materials and Methods). Although no differences were found between the men and women for fiber type proportions (with the exception of the IC population), the area made up of each of the major fiber types was very different between the men and the women. The percentage area of Type I was significantly smaller and the percentage area of Type IIA significantly larger for the men compared to the women (Table 4). The hierarchy of the percentage fiber type area from largest to smallest was IIA>I>IIB for the men and I>IIA>IIB for the women (Table 4).


 
View this table:
[in this window]
[in a new window]
 
Table 4. Percentage fiber type area a

Myosin Heavy Chain Content
The relative content of the three MHC isoforms (MHCI, MHCIIa, and MHCIIb) paralleled the fiber type area data. Thus, the relative percentage of MHCI was significantly smaller and the relative percentage of MHCIIa significantly larger for the men compared to the women (Table 5). Likewise, in order from largest to smallest, the relative MHC content for the men was MHCIIa>MHCI>MHCIIb and for the women was MHCI=MHCIIa>MHCIIb ( Table 5). As expected, correlations between fiber type area and relative MHC percentages were all significant, including correlations for the men and women separately as well as together (Table 6).


 
View this table:
[in this window]
[in a new window]
 
Table 5. Relative myosin heavy chain isoform percentages a


 
View this table:
[in this window]
[in a new window]
 
Table 6. Correlation analyses a


*   Discussion
*Top
*Summary
*Introduction
*Materials and Methods
*Results
*Discussion
*Literature Cited

Not surprisingly, anthropometric data from the present study revealed gender differences. The young men were significantly taller, heavier, and had a lower percentage of body fat compared to the young women. Similar findings have been previously reported by many others (e.g., Komi and Karlsson 1978 Down; Simoneau et al. 1985 Down; Glenmark et al. 1992 Down; Miller et al. 1993 Down).

Gender differences have also been previously reported for fiber size within the vastus lateralis muscle. Shortly after birth, muscle fibers are small (12–18 µm diameter), with the Type I fibers slightly larger than the Type II and no difference between male and female ( Oertel 1988 Down). However, after puberty, fiber cross-sectional area in males tends to be larger than in females ( Brooke and Engel 1969 Down; Edstrom and Nystrom 1969 Down; Saltin et al. 1977 Down; Simoneau et al. 1985 Down; Essen-Gustavsson and Borges 1986 Down; Simoneau and Bouchard 1989 Down; Miller et al. 1993 Down). Recently, all three major fiber types (I, IIA, and IIB) have been shown to be larger in the vastus lateralis muscle of men. Simoneau and Bouchard 1989 Down found that the cross-sectional areas of fiber Types I, IIA, and IIB from the vastus lateralis muscle of young men were 14%, 38%, and 56% larger compared to young women. Similarly, fiber Types I, IIA, and IIB in the present study were approximately 19%, 59% and 66% larger for the men compared to the women. In addition, Type II fibers tend to be larger than Type I in the muscles of men, whereas the reverse is true for women ( Brooke and Engel 1969 Down; Saltin et al. 1977 Down; Simoneau et al. 1985 Down; Simoneau and Bouchard 1989 Down). For both men and women, the Type IIA cross-sectional area appears to be larger than the Type IIB, contributing to the hierarchy of fiber sizes (from largest to smallest) found in the present study: IIA>IIB=I for the men and I=IIA>IIB for the women.

Although many studies have found gender differences related to fiber size, conflicting reports have been published regarding the overall proportion of fast and slow fibers in the vastus lateralis muscle of men vs women (see Table 7). Investigations have reported a higher percentage of Type I fibers in women compared to men ( Simoneau et al. 1985 Down; Simoneau and Bouchard 1989 Down; Miller et al. 1993 Down), a higher percentage of Type I fibers in men (Komi and Karlsson 1978 Down; Essen-Gustavsson and Borges 1986 Down), and no difference between men and women (Saltin et al. 1977 Down; Nygaard 1982 Down). These different findings may be related to differences in sample size, age, methodology, hormone profiles, and/or physical activity level.


 
View this table:
[in this window]
[in a new window]
 
Table 7. Summary of published data on muscle fiber type percentages in the vastus lateralis muscle of untrained young men and women a b

Many studies on human muscle have used small sample sizes and/or have histochemically delineated only two fiber types, I and II (e.g., Brooke and Engel 1969 Down; Edstrom and Ekblom 1972 Down; Gollnick et al. 1972 Down; Johnson et al. 1973 Down; Komi and Karlsson 1978 Down; Oertel 1988 Down; Willan et al. 1990 Down; Miller et al. 1993 Down). Other studies have combined data from both men and women ( Gollnick et al. 1974 Down; Edgerton et al. 1975 Down). Because of the large amount of inter- and intraindividual variations in the percentages of fast and slow fibers in the vastus lateralis muscle, it is important not only to use large biopsy samples but also to use large numbers of subjects. Indeed, even investigations with relatively large numbers of subjects have reported mean values for the percentage of slow fibers ranging from 37 to 55% in women and 36 to 58% men (Table 7).

Although Simoneau and Bouchard 1989 Down presented cumulative data gathered over a number of years on fiber type composition and area measurements in the vastus lateralis muscle of 270 sedentary young men and women (range 16–33 years old), 148 post-training biopsies were also included in the analysis. In addition, only three muscle fiber types (I, IIA, and IIB) were histochemically delineated using a single-step histochemical technique (Mabuchi and Sreter 1980 Down). Such methods do not allow adequate identification of hybrid fibers (IC, IIC, and IIAB), and will therefore result in fiber misclassification ( Staron 1997 Down). It should be made clear, however, that the primary purpose of Simoneau and Bouchard 1989 Down was to investigate the extent of variation in these morphometric parameters in human skeletal muscle, rather than to establish normative fiber type data. To our knowledge, this is the only study presenting normative data on the entire range of histochemically defined fiber types collected from a large number of untrained young men and women. Data from the current investigation suggest that there may not be a true gender difference between men and women with regard to the fiber type distribution in the vastus lateralis muscle.

Perhaps the most interesting gender difference relates to the percentage area occupied by the major fiber types. Although it appears that men and women have similar overall distributions of fast and slow fiber types in the vastus lateralis muscle, significant gender differences exist with regard to the total area occupied by each fiber type within the muscle. In the present investigation, the slow fibers were found to occupy a greater area in the women, whereas the fast IIA fibers occupied a greater area in the men. Of importance is the fact that these data were verified by the MHC profile. Similar findings with regard to percentage fiber type area have been previously reported for the vastus lateralis ( Essen-Gustavsson and Borges 1986 Down). On an applied level, these differences in percent fiber type area may result in differences in performance (Gollnick and Matoba 1984 Down).

In conclusion, important aspects of the current investigation are the compilation of data from a large number of healthy untrained individuals, relatively large biopsy specimens, the delineation of the entire range of mATPase-based fiber types, and verification of the histochemical data by comparing percent fiber type area and relative MHC content. These data support previous findings demonstrating that the mean fiber cross-sectional area in the vastus lateralis muscle is smaller in women compared to men and that the Type II fibers of males tend to be larger than the Type I, whereas the reverse is true for the female. The current data suggest that the overall proportion of fast and slow fibers in the vastus lateralis muscle of young men and women is similar. There are, however, gender differences in percent fiber type areas that relate to differences in the hierarchy of cross-sectional areas of the major fiber types. Although the percentages of fast and slow fiber types are similar between young men and women, the slow fibers occupy a greater area in the women compared to the men and the fast fibers occupy a greater area in the men.


*   Acknowledgments

We thank the Ohio University College of Osteopathic Medicine photographic and graphic departments for help with the figures and tables. Special thanks to all those young men and women who participated in various research projects in our laboratory over the past 10 years.

Received for publication November 23, 1999; accepted January 19, 2000.


*   Literature Cited
*Top
*Summary
*Introduction
*Materials and Methods
*Results
*Discussion
*Literature Cited

Allemeier CA , Fry AC , Johnson P , Hikida RS , Hagerman FC , Staron RS (1994 ) Effects of sprint cycle training on human skeletal muscle. J Appl Physiol 77:2385-2390 [Abstract/Free Full Text]

Bär A , Pette D (1988 ) Three fast myosin heavy chains in adult rat skeletal muscle. FEBS Lett 235:153-155 [Medline]

Bergström J (1962 ) Muscle electrolytes in man. Scand J Clin Lab Invest 14(suppl 68):1-110

Bergström J (1975 ) Percutaneous needle biopsy of skeletal muscle in physiological and clinical research. Scand J Clin Invest 35:609-616 [Medline]

Blomstrand E , Ekblom B (1982 ) The needle biopsy technique for fibre type determination in human skeletal muscle—a methodological study. Acta Physiol Scand 116:437-442 [Medline]

Brooke MH , Engel WK (1969 ) The histographic analysis of human muscle biopsies with regard to fiber types. Neurology 19:221-233 [Free Full Text]

Brooke MH , Kaiser KK (1970 ) Three "myosin ATPase" systems: the nature of their pH lability and sulfhydryl dependence. J Histochem Cytochem 18:670-672 [Medline]

Campbell CJ , Bonen A , Kirby RL , Belcastro AN (1979 ) Muscle fiber composition and performance capacities of women. Med Sci Sports 11:260-265 [Medline]

Doriguzzi C , Mongini T , Pamucci L , Gagnor E , Schiffer D (1984 ) Quantitative analysis of quadriceps muscle biopsy. Results in 30 healthy females. J Neurol Sci 66:319-326 [Medline]

Edgerton V , Smith JL , Simpson DR (1975 ) Muscle fibre type populations of human leg muscles. Histochem J 7:259-266 [Medline]

Edström L , Ekblom B (1972 ) Differences in sizes of red and white muscle fibres in vastus lateralis of musculus quadriceps femoris of normal individuals and athletes. Relation to physical performance. Scand J Clin Lab Invest 30:175-181 [Medline]

Edström L , Nyström B (1969 ) Histochemical types and sizes of fibres in normal human muscles . Acta Neurol Scand 45:257-269 [Medline]

Elder GCB , Bradbury K , Roberts R (1982 ) Variability of fiber type distributions within human muscles. J Appl Physiol 53:1473-1480 [Abstract/Free Full Text]

Ennion S , Sant'ana Pereira J , Sargeant AJ , Young A , Goldspink G (1995 ) Characterization of human skeletal muscle fibres according to the myosin heavy chains they express. J Muscle Res Cell Motil 16:35-43 [Medline]

Essén–Gustavsson B , Borges O (1986 ) Histochemical and metabolic characteristics of human skeletal muscle in relation to age. Acta Physiol Scand 126:107-111 [Medline]

Evans WJ , Pinney SD , Young VR (1982 ) Suction applied to a muscle biopsy maximizes sample size. Med Sci Sports Exerc 14:101-102 [Medline]

Fry AC , Allemeier CA , Staron RS (1994 ) Correlation between percentage of fiber type area and myosin heavy chain content in human skeletal muscle. Eur J Appl Physiol 68:246-251

Glenmark B , Hedberg G , Jansson E (1992 ) Changes in muscle fibre type from adolescence to adulthood in women and men. Acta Physiol Scand 146:251-259 [Medline]

Gollnick PD , Armstrong RB , Saubert CW, IV , Piehl K , Saltin B (1972 ) Enzyme activity and fiber composition in skeletal muscle of untrained and trained men. J Appl Physiol 33:312-319 [Free Full Text]

Gollnick PD , Matoba H (1984 ) The muscle fiber composition of skeletal muscle as a predictor of athletic success. An overview. Am J Sports Med 12:212-217 [Free Full Text]

Gollnick PD , Sjödin B , Karlsson J , Jansson E , Saltin B (1974 ) Human soleus muscle: a comparison of fiber composition and enzyme activities with other leg muscles. Pfluegers Arch 348:247-255 [Medline]

Jackson AS , Pollock ML (1978 ) Generalized equations for predicting body density of men. Br J Nutr 40:497-504 [Medline]

Jackson AS , Pollock ML , Ward A (1980 ) Generalized equations for predicting body density of women. Med Sci Sports 12:175-182

Johnson MA , Polgar J , Weightman D , Appelton D (1973 ) Data on the distribution of fibre types in thirty-six human muscles. An autopsy study. J Neurol Sci 18:111-129 [Medline]

Komi PV , Karlsson J (1978 ) Skeletal muscle fibre types, enzyme activities and physical performance in young males and females. Acta Physiol Scand 103:210-218 [Medline]

Lexell J , Downham D , Sjöström M (1984 ) Distribution of different fibre types in human skeletal muscles. A statistical and computational study of the fibre type arrangement in m. vastus lateralis of young, healthy males. J Neurol Sci 65:353-365 [Medline]

Lexell J , Henriksson–Larsén K , Sjöström M (1983 ) Distribution of different fibre types in human skeletal muscles. 2. A study of cross-sections of whole m. vastus lateralis. Acta Physiol Scand 117:115-122 [Medline]

Lexell J , Taylor CC (1989 ) Variability in muscle fibre areas in whole human quadriceps muscle. How much and why? Acta Physiol Scand 136:561-568 [Medline]

Lexell J , Taylor C , Sjöström M (1985 ) Analysis of sampling errors in biopsy techniques using data from whole muscle cross sections. J Appl Physiol 59:1228-1235 [Abstract/Free Full Text]

Mabuchi K , Sréter FA (1980 ) Actomyosin ATPase. Fiber typing by histochemical ATPase reaction . Muscle Nerve 3:233-239 [Medline]

Mahon M , Toman A , Willan PLT , Bagnall KM (1984 ) Variability of histochemical and morphometric data from needle biopsy specimens of human quadriceps femoris muscle. J Neurol Sci 63:85-100 [Medline]

Miller AEJ , MacDougall JD , Tarnopolsky MA , Dale DG (1993 ) Gender differences in strength and muscle fiber characteristics . Eur J Appl Physiol 66:254-262

Nygaard E (1982 ) Skeletal muscle fibre characteristics in young women. Acta Physiol Scand 112:299-304

Oertel G (1988 ) Morphometric analysis of normal skeletal muscles in infancy, childhood and adolescence. An autopsy study. J Neurol Sci 88:303-313 [Medline]

Perrie WT , Bumford SJ (1986 ) Electrophoretic separation of myosin isoenzymes. Implications for the histochemical demonstration of fibre types in biopsy specimens of human skeletal muscle. J Neurol Sci 73:89-96 [Medline]

Saltin B , Gollnick PD (1983 ) Skeletal muscle adaptability: significance for metabolism and performance. In Peachey LD , Adrian RH , Geiger SR , eds. Handbook of Physiology—Skeletal Muscle. New York , Williams & Wilkins, 555-631

Saltin B , Henriksson J , Nygaard E , Andersen P (1977 ) Fiber types and metabolic potentials of skeletal muscles in sedentary man and endurance runners. Ann NY Acad Sci 301:3-29 [Medline]

Simoneau J-A , Bouchard C (1989 ) Human variation in skeletal muscle fibre-type proportion and enzyme activities. Am J Physiol 257:E567-572 [Abstract/Free Full Text]

Simoneau J-A , Lortie G , Boulay MR , Thibault M-C , Thériault G , Bouchard C (1985 ) Skeletal muscle histochemical and biochemical characteristics in sedentary male and female subjects. Can J Physiol Pharmacol 63:30-35 [Medline]

Smerdu V , Karsch–Mizrachi I , Campione M , Leinwand L , Schiaffino S (1994 ) Type IIx myosin heavy chain transcripts are expressed in type IIb fibers of human skeletal muscle. Am J Physiol 267:C1723-1728 [Abstract/Free Full Text]

Staron RS (1991 ) Correlation between myofibrillar ATPase activity and myosin heavy chain composition in single human muscle fibers. Histochemistry 96:21-24 [Medline]

Staron RS (1997 ) Human skeletal muscle fiber types: delineation, development, and distribution. Can J Appl Physiol 22:307-327 [Medline]

Staron RS , Hikida RS (1992 ) Histochemical, biochemical, and ultrastructural analyses of single human muscle fibers with special reference to the C fiber population . J Histochem Cytochem 40:563-568 [Abstract]

Staron RS , Karapondo DL , Kraemer WJ , Fry AC , Gordon SE , Falkel JE , Hagerman FC , Hikida RS (1994 ) Skeletal muscle adaptations during early phase of heavy-resistance training in men and women. J Appl Physiol 76:1247-1255 [Abstract/Free Full Text]

Staron RS , Leonardi MJ , Karapondo D , Malicky ES , Falkel JE , Hagerman FC , Hikida RS (1991 ) Strength and skeletal muscle adaptations in heavy resistance-trained women after detraining and retraining. J Appl Physiol 70:631-640 [Abstract/Free Full Text]

Staron RS , Malicky ES , Leonardi MJ , Falkel JE , Hagerman FC , Dudley GA (1990 ) Muscle hypertrophy and fast fiber type conversions in heavy resistance-trained women. Eur J Appl Physiol 60:71-79

Tesch P , Karlsson J (1978 ) Isometric strength performance and muscle fibre type distribution in man. Acta Physiol Scand 103:47-51 [Medline]

Willan PLT , Mahon M , Golland JA (1990 ) Morphological variations of the human vastus lateralis muscle. J Anat 168:235-239[Medline]


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Eur J EndocrinolHome page
C. Brufani, A. Tozzi, D. Fintini, P. Ciampalini, A. Grossi, R. Fiori, D. Kiepe, M. Manco, R. Schiaffini, O. Porzio, et al.
Sexual dimorphism of body composition and insulin sensitivity across pubertal development in obese Caucasian subjects
Eur. J. Endocrinol., May 1, 2009; 160(5): 769 - 775.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
T. Suga, K. Okita, N. Morita, T. Yokota, K. Hirabayashi, M. Horiuchi, S. Takada, T. Takahashi, M. Omokawa, S. Kinugawa, et al.
Intramuscular metabolism during low-intensity resistance exercise with blood flow restriction
J Appl Physiol, April 1, 2009; 106(4): 1119 - 1124.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
F. X. Pizza, B. C. Clark, R. E. De Meersman, S. M. Phillips, N. Stupka, S. Sipila, V. Kovanen, H. Suominen, G. L. Warren, D. A. Lowe, et al.
Comments on Point:Counterpoint: Estrogen and sex do/do not influence post-exercise indexes of muscle damage, inflammation, and repair
J Appl Physiol, March 1, 2009; 106(3): 1016 - 1020.
[Full Text] [PDF]


Home page
Exp PhysiolHome page
R. C. I. Wust, C. I. Morse, A. de Haan, D. A. Jones, and H. Degens
Sex differences in contractile properties and fatigue resistance of human skeletal muscle
Exp Physiol, July 1, 2008; 93(7): 843 - 850.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
L. A. Burnes, S. J. Kolker, J. F. Danielson, R. Y. Walder, and K. A. Sluka
Enhanced muscle fatigue occurs in male but not female ASIC3-/- mice
Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2008; 294(4): R1347 - R1355.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
R. A. Kley, Y. Hellenbroich, P. F. M. van der Ven, D. O. Furst, A. Huebner, V. Bruchertseifer, S. A. Peters, C. M. Heyer, J. Kirschner, R. Schroder, et al.
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients
Brain, December 1, 2007; 130(12): 3250 - 3264.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
B. Phakdeekitcharoen, S. Phudhichareonrat, C. Pookarnjanamorakot, C. Kijkunasathian, N. Tubtong, W. Kittikanokrat, and P. Radinahamed
Thyroid Hormone Increases mRNA and Protein Expression of Na+-K+-ATPase {alpha}2 and {beta}1 Subunits in Human Skeletal Muscles
J. Clin. Endocrinol. Metab., January 1, 2007; 92(1): 353 - 358.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
S. Fujita, B. B. Rasmussen, J. A. Bell, J. G. Cadenas, and E. Volpi
Basal muscle intracellular amino acid kinetics in women and men
Am J Physiol Endocrinol Metab, January 1, 2007; 292(1): E77 - E83.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
F. M. Gabhann and A. S. Popel
Interactions of VEGF isoforms with VEGFR-1, VEGFR-2, and neuropilin in vivo: a computational model of human skeletal muscle
Am J Physiol Heart Circ Physiol, January 1, 2007; 292(1): H459 - H474.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
M. T. Korhonen, A. Cristea, M. Alen, K. Hakkinen, S. Sipila, A. Mero, J. T. Viitasalo, L. Larsson, and H. Suominen
Aging, muscle fiber type, and contractile function in sprint-trained athletes
J Appl Physiol, September 1, 2006; 101(3): 906 - 917.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Sports. Med.Home page
J S Volek, C E Forsythe, and W J Kraemer
Nutritional aspects of women strength athletes
Br. J. Sports Med., September 1, 2006; 40(9): 742 - 748.
[Abstract] [Full Text] [PDF]


Home page
Journals of Gerontology Series A: Biological Sciences and Medical SciencesHome page
A. M. Abbatecola, L. Ferrucci, G. Ceda, C. R. Russo, F. Lauretani, S. Bandinelli, M. Barbieri, G. Valenti, and G. Paolisso
Insulin Resistance and Muscle Strength in Older Persons
J. Gerontol. A Biol. Sci. Med. Sci., October 1, 2005; 60(10): 1278 - 1282.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
N. Yasuda, E. I. Glover, S. M. Phillips, R. J. Isfort, and M. A. Tarnopolsky
Sex-based differences in skeletal muscle function and morphology with short-term limb immobilization
J Appl Physiol, September 1, 2005; 99(3): 1085 - 1092.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
A. E. Oskouei and W. Herzog
Observations on force enhancement in submaximal voluntary contractions of human adductor pollicis muscle
J Appl Physiol, June 1, 2005; 98(6): 2087 - 2095.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
Y. C. Luiking, M. M. Hallemeesch, W. H. Lamers, and N. E. P. Deutz
NOS3 is involved in the increased protein and arginine metabolic response in muscle during early endotoxemia in mice
Am J Physiol Endocrinol Metab, June 1, 2005; 288(6): E1258 - E1264.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
B. C. Clark, T. M. Manini, D. J. The, N. A. Doldo, and L. L. Ploutz-Snyder
Gender differences in skeletal muscle fatigability are related to contraction type and EMG spectral compression
J Appl Physiol, June 1, 2003; 94(6): 2263 - 2272.
[Abstract] [Full Text] [PDF]


Home page
ptjournalHome page
C S. Bickel, J. M Slade, G. L Warren, and G. A Dudley
Fatigability and Variable-Frequency Train Stimulation of Human Skeletal Muscles
Physical Therapy, April 1, 2003; 83(4): 366 - 373.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
J.A.M. Korfage and T.M.G.J Van Eijden
Myosin Heavy Chain Composition in Human Masticatory Muscles by Immunohistochemistry and Gel Electrophoresis
J. Histochem. Cytochem., January 1, 2003; 51(1): 113 - 119.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
E. Hagstrom-Toft, V. Qvisth, I. Nennesmo, M. Ryden, H. Bolinder, S. Enoksson, J. Bolinder, and P. Arner
Marked Heterogeneity of Human Skeletal Muscle Lipolysis at Rest
Diabetes, December 1, 2002; 51(12): 3376 - 3383.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
L. J Beaton, M. A Tarnopolsky, and S. M Phillips
Contraction-induced muscle damage in humans following calcium channel blocker administration
J. Physiol., November 1, 2002; 544(3): 849 - 859.
[Abstract] [Full Text] [PDF]


Home page
Journals of Gerontology Series A: Biological Sciences and Medical SciencesHome page
J. O. Marx, W. J. Kraemer, B. C. Nindl, and L. Larsson
Effects of Aging on Human Skeletal Muscle Myosin Heavy-Chain mRNA Content and Protein Isoform Expression
J. Gerontol. A Biol. Sci. Med. Sci., June 1, 2002; 57(6): B232 - 238.
[Abstract] [Full Text]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Staron, R. S.
Right arrow Articles by Toma, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Staron, R. S.
Right arrow Articles by Toma, K.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?


Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact