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J Exerc Rehabil > Volume 10(6);2014 > Article
Choi: Differential susceptibility on myosin heavy chain isoform following eccentric-induced muscle damage

Abstract

Based on myosin heavy chain (MHC) isoform, human skeletal muscle fibers can be categorized into three fiber types, type I, IIa, IIx fibers, and each fiber type has different characteristics. Typical characteristics are difference in force production, shortening velocity, and fatigue resistance. When the muscle is contract and stretched by a force that is greater than the force generated by the muscle, contraction-induced muscle damage frequently occurs. Several experimental models involving both human and animal have considered the susceptibility of different muscle fiber type and part of muscles to eccentric induced muscle damage. General consensus is a greater susceptibility of fast-twitch fiber or type II fiber to damage following eccentric contractions. However, the results from these previous efforts were not enough to conclude the susceptibility between each individual fiber types after eccentric contraction. Therefore, the purpose of this review is to explore detail limitation and interpretation of previous studies, and review the recent study that eliminated the prior limitations, such as strain magnitude, lengthening velocity, fiber type heterogeneity, and muscle architecture issue.

INTRODUCTION

Muscle is a heterogeneous tissue, containing cells with different contractile properties, metabolic profiles, and fatigue resistance. Much of this diversity is correlated with the myosin heavy chain (MHC) isoform expressed by the cell. Small mammals express nine MHC isoforms of which four, type I or β, type IIa, type IIx, and type IIb, are expressed in adult limb muscles (Ennion et al., 1995; Smerdu et al., 1994). The type IIb isoform is not found in the limb muscles of large mammals, including humans. Human muscle fibers can be categorized into three fiber types: type I, IIa, and IIx (Ennion et al., 1995; Smerdu et al., 1994). These isoform can also be co-expressed, resulting in hybrid fiber types: type I/IIa, and type IIa/IIx or even type I/IIa/IIx (Caiozzo et al., 2003; Pette and Staron, 2001). Typical characteristics of fiber types are force production, and shortening velocity. Type IIa or IIx fiber produce higher force and contract faster than type I fibers, whereas type I fibers appear to be more fatigue resistant than other fiber types. Type IIx fiber contract and relax slightly faster than type IIa fibers, but both are faster than type I fiber.
As well known, an eccentric contraction is much more likely to injury a muscle compared to an isometric contraction or a contraction in which the force producing muscle shortens (Allen, 2001; Faulkner et al., 1993; Lieber and Friden, 2002; Proske and Allen, 2005; Warren et al., 2001). It is also generally accepted that fast muscle fibers are more susceptible to eccentric contraction than slow muscle fibers (Friden et al., 1983; Jones et al., 1986; Lieber and Friden, 1988; Warren et al., 1994). This idea is based on histological and functional experiments performed on human and animal models. However, a critical appraisal of this body of work shows that the evidence supporting the idea that fast muscle fibers are more susceptible to eccentric injury is far from complete or conclusive. Therefore, in this review the detail limitation of previous work on distinct susceptibility on MHC isoform will be discussed first, and then recent work on differential susceptibility of MHC heterogeneity will be reviewed.

PREVIOUS STUDIES IN DISTINCT SUSCEPTIBILITY ON MHC ISOFORM

Studies on humans have reported a greater susceptibility of fast-twitch fibers to damage (Asp et al., 1998; Friden et al., 1983; Jones et al., 1986). However, these studies have used indirect methods to quantify the muscle injury such as histological markers of damage (Friden et al., 1983) or the plasma creatine kinase (CK) concentration (Jones et al., 1986). Plasma CK concentration is frequently used as an index of the muscle damage after eccentric contraction. However, no significant correlation was observed between CK concentration and muscle strength (Friden and Lieber, 2001). Another study investigated muscle glycogen content after eccentric exercise, and it revealed type II fibers were predominantly recruited (Asp et al., 1998). Thus the authors concluded a selective effect of eccentric contractions on type II fiber but it could not be readily accepted that the glycogen content represents the susceptibility of muscle structure and functional to damage.
Functional approaches performed on isolated mouse muscle (soleus and extensor digitorum longus (EDL)) are limited by fiber type heterogeneity and muscle architectural differences. For instance, mouse soleus muscles are not constituted with only slow fiber types, and mouse EDL muscle express an extra MHC isoform, type IIb, which is not founded in human limb muscle (Ennion et al., 1995; Smerdu et al., 1994). Furthermore, its slow type I MHC isoform has a faster velocity than the human slow type I MHC (Widrick et al., 1997). Thus, these species differences could confound generalization of animal data to humans. Also, the differences of muscle architecture between mouse soleus and EDL muscle resulted in the differentiation of applied strain amount to each muscle, due to differences in the fiber length to muscle length ratios of these muscles (Warren et al., 1994).
Studies using single muscle fibers, obtained from animals report that muscles comprised of predominantly fast fibers are preferentially damaged (Brockett et al., 2002; Friden and Lieber, 1992; Lieber and Friden, 1988; Lynch et al., 2008; Macpherson et al., 1996; Rader et al., 2007; Vijayan et al., 2001). Only three of these studies have directly examined muscle fiber function: two studies examined fibers from the predominately slow soleus and the predominately fast EDL of the rat (Lynch et al., 2008; Macpherson et al., 1996), and another study examined fibers from normal and congenitally clefted goat palates (Rader et al., 2007). Most of these studies have been performed using muscles from rodents. As discussed above, small mammals and humans do not express all of the same MHC isoforms. Sarcomere heterogeneity after eccentric contractions was also measured with fiber type identification by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) (Patel et al., 2004). However, they used the pooled fiber bundles from the frog tibialis anterior muscle, which is comprised of two equal part of fastest amphibian muscle fiber type (Lutz et al., 1998). Brockett (Brockett et al., 2002) also studied the vulnerability of different motor units that consisted of mixed fiber types using the cat muscle without identifying the fiber types. None of these studies examined MHC isoform content and function in the same fibers, making it difficult to draw conclusions about damage to individual fiber types.
Although most studies show greater susceptibility of fast-twitch fibers, a few studies report that slow-twitch, or type I fibers, were selectively damaged during eccentric contractions. Armstrong (Armstrong et al., 1983) showed that the deeply embedded slow-twitch fibers were predominantly damaged after downhill running compare to level running. However, downhill running may preferentially recruit the slow fiber type, and this may obscure which type is actually more susceptible. Another study indicated the increased fragment rate in slow-twitch skeletal MHC through magnetic resonance imaging (Mair et al., 1992), and plasma creatine kinase (CK) concentration, which is not a highly correlated index of muscle damage.

POTENTIAL MECHANISM OF PREFERENTIAL DAMAGE TO FAST TWITCH MUSCLE AFTER ECCENTRIC CONTRACTION

Even though there is no conclusive mechanism yet, several potential mechanisms were proposed to explain the greater vulnerability of fast-twitch fibers. One proposed mechanism was that fast-twitch fibers fatigued faster than slow-twitch fiber, and the fast-twitch fibers stay in rigor binding stage during cross-bridge cycle due to impaired ATP regeneration, which results in mechanical damage as these rigor fibers are stretched (Friden and Lieber, 1992). However, this hypothesis does not hold up because studies report that fatigued muscle is less susceptible to damage or fatigue has no effect (Choi and Widrick, 2009; Friden and Lieber, 1992; Mair et al., 1996; Morgan et al., 2004) and other studies support the fatigued muscle is more resistible to eccentric-induced muscle injury (Nosaka and Clarkson, 1997). It has been suggested that the ultrastructural differences between type I and type II fibers explain the greater vulnerability of fast-twitch fibers to eccentric-induced muscle damage. Fast-twitch fibers have narrower Z-lines compared to slow-twitch fibers (Friden et al., 1983), which reflect fewer attachments for thick and thin filaments (Yamaguchi et al., 1985). Type II fibers contain smaller isoforms of the sarcomeric proteins myomesion and nebulin, which play a role in sarcomere assembly (Agarkova et al., 2004; Prado et al., 2005). Therefore, relatively greater stress is applied to the cytoskeleton of fast fiber, resulting in a higher susceptibility to damage. This phenomenon also confirmed from the reloaded human soleus fiber after 17 days of bed rest and spaceflight (Widrick et al., 1999). He found that the fibers, have weak connections between sarcomeres were relatively weaker than fibers, have normal connection between sarcomeres, due to greater workload. Also, fast fibers express a lower molecular weight, and less elastic, titin isoform than slow fibers (Prado et al., 2005) The less compliant titin in fast fibers may transmit greater stress during eccentric contractions (Horowits, 1992).
Accordingly, it is widely accepted that fast-twitch, or type II fibers tend to be more vulnerable to eccentric-induced muscle injury (Byrne et al., 2004; Proske and Morgan, 2001). However, none of above studies has investigated the relationship between fiber MHC isoform content and its susceptibility to eccentric contraction using single fiber preparation, isolated from human muscle, with the identification of fiber type.

RECENT STUDIES IN DISTINCT SUSCEPTIBILITY ON MHC ISOFORM

Accordingly, it is clear that more data examining the relationship between fiber type expression and susceptibility after eccentric contraction are required. Chemically skinned single muscle fiber preparations can avoid limitations of previous studies by allowing the investigator control over strain magnitude and velocity under standard experimental conditions of temperature, ionic strength and activating Ca2+ concentration. The issue of fiber type heterogeneity can also be overcome by identification of MHC isoforms in the same of single muscle fiber segments used for the physiological assays.
There is a study that utilizes the single fiber approach to examine the differential susceptibility on MHC isoform (Choi and Widrick, 2010). Ca2+-activated skinned muscle fiber segments, prepared from healthy untrained young subjects (25±2 yr, n=10) were subjected to standardized an eccentric contraction, in terms of strain magnitude (25% of fiber length) and lengthening velocity (50% of maximum shortening velocity). Maximal force was measured before and after a single eccentric or fixed-end contraction, and fiber MHC isoform contents were confirmed by gel electrophoresis. A model was developed using multiple linear regression to describe how each of major fiber type populations present in human limb muscle responds to a single eccentric contraction, The best model reveals a fiber type independent factor (pre-treatment force) and a fiber type dependent factor (MHC expressions) to the damage process. Regardless of fiber type, fiber generating greater pre-eccentric specific force showed greater post-eccentric force deficits. When this pre-treatment force was controlled, fiber expressing type I or IIa MHC had identical force change to the eccentric contraction, whereas fiber co-expressing the type IIa and IIx MHC isoforms showed 3-folder greater force deficit. These results could be interpreted as evidence that the fastest MHC isoforms, in this case type IIx, were associated with greater damage. However, an equally valid interpretation would be that the co-expression of multiple MHC isoforms within the same fiber is the critical factor.
Note
However, a limitation of the skinned fiber approach is that fibers are studied in an artificial milieu (although one thought to represent the intracellular milieu). In addition, the skinning process may remove or allow efflux of structural (e.g. dystrophin) or enzymatic (e.g. calpain) proteins that may be involved in the damage process. Finally, fibers are maximally activated where in vivo, different fiber types may be differentially recruited by the nervous system, altering their apparent susceptibility to injury. Therefore, additional studies need to address the response of living cells to in vivo eccentric exercise.

CONCLUSIONS

While most studies conclude that type II fibers are more susceptible to eccentric-induced muscle injury, these finding are based on indirect measures of damage, conducted on muscles instead of fibers, and if conducted on fibers, have not confirmed MHC isoform context by gel electrophoresis which provide a more accurate determination of the fiber types including hybrid fiber (Glaser et al., 2010; Pandorf et al., 2010). Since most muscles are heterogeneous in the fiber type composition, whole muscle or motor unit studies cannot effectively evaluate changes of function occurring in type I and type II fibers following eccentric contractions. However, recent single muscle fiber study found a single eccentric treatment (25% strain with 50% lengthening velocity) resulted in 9 kN/m2 (8.1%) and 12 kN/m2 (9.8%) of force drop compare to pre-treatment force for fibers expressing a single MHC isoform (I and IIa, respectively). However, hybrid fibers containing IIa and IIx MHC isoform showed 3-folders greater force deficit (38 kN/m2, 28.4%) than either type I or type IIa fibers. These results indicate that human fast hybrid fibers (IIa/IIx) are further sensitive to a standardized in vitro eccentric contraction.

Notes

CONFLICT OF INTEREST

No potential conflict of interest relevant to this article was reported.

ACKNOWLEDGMENTS

This research was supported by Kyungsung University Research Grants in 2014.

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