Effect of thin filament length on the force-sarcomere length relation of skeletal muscle

1991 ◽  
Vol 260 (5) ◽  
pp. C1060-C1070 ◽  
Author(s):  
H. L. Granzier ◽  
H. A. Akster ◽  
H. E. Ter Keurs
Keyword(s):  
Thin Filament ◽  
Sarcomere Length ◽  
Fiber Type ◽  
Thick Filament ◽  
Fiber Types ◽  
Single Region ◽  
Slow Twitch ◽  
The Difference ◽  
Slow Twitch Fibers ◽  
Fast Twitch

We studied a slow- and a fast-twitch muscle fiber type of the perch that have different thin filament lengths. The force-sarcomere length relations were measured, and it was tested whether their descending limbs were predicted by the cross-bridge theory. To determine the predicted relations, filament lengths were measured by electron microscopy. Measurements were corrected for shrinkage with the use of I-band and H-zone periodicities. Thick filament lengths of the two fiber types were found to be similar (1.63 +/- 0.06 and 1.64 +/- 0.10 microns for slow- and fast-twitch fibers, respectively), whereas the thin filament lengths were clearly different: 1.24 +/- 0.10 microns (n = 86) for the slow-twitch type and 0.94 +/- 0.04 microns (n = 94) for the fast type. The descending limbs of the two fiber types are therefore predicted to be shifted along the sarcomere length axis by approximately 0.6 microns. Sarcomere length was measured on-line by laser diffraction in a single region in the center of the fibers. The passive force-sarcomere strain relation increased much more steeply in the slow-twitch fibers. The descending limb of the active force-sarcomere length relation of fast twitch fibers was linear (r = 0.92), but was found at sarcomere lengths approximately 0.1 micron greater than predicted. The descending limb of the slow-twitch fibers was also linear (r = 0.87) but was now found at sarcomere lengths approximately 0.05 microns less than predicted. The difference in position of the descending limbs of the two fiber types amounted to 0.5 microns, approximately 0.1 micron less than predicted. The difference between measured and predicted descending limbs was statistically insignificant.

scholarly journals lncRNA-Six1 Is a Target of miR-1611 that Functions as a ceRNA to Regulate Six1 Protein Expression and Fiber Type Switching in Chicken Myogenesis

Cells ◽  
2018 ◽  
Vol 7 (12) ◽  
pp. 243 ◽  
Author(s):  
Manting Ma ◽  
Bolin Cai ◽  
Liang Jiang ◽  
Bahareldin Ali Abdalla ◽  
Zhenhui Li ◽  
...  
Keyword(s):  
Fiber Type ◽  
Muscle Fibers ◽  
Muscle Fiber Types ◽  
Fiber Types ◽  
Proliferation And Differentiation ◽  
Slow Twitch Muscle ◽  
Fast Twitch Muscle ◽  
Slow Twitch ◽  
Slow Twitch Fibers ◽  
Fast Twitch

Emerging studies indicate important roles for non-coding RNAs (ncRNAs) as essential regulators in myogenesis, but relatively less is known about their function. In our previous study, we found that lncRNA-Six1 can regulate Six1 in cis to participate in myogenesis. Here, we studied a microRNA (miRNA) that is specifically expressed in chickens (miR-1611). Interestingly, miR-1611 was found to contain potential binding sites for both lncRNA-Six1 and Six1, and it can interact with lncRNA-Six1 to regulate Six1 expression. Overexpression of miR-1611 represses the proliferation and differentiation of myoblasts. Moreover, miR-1611 is highly expressed in slow-twitch fibers, and it drives the transformation of fast-twitch muscle fibers to slow-twitch muscle fibers. Together, these data demonstrate that miR-1611 can mediate the regulation of Six1 by lncRNA-Six1, thereby affecting proliferation and differentiation of myoblasts and transformation of muscle fiber types.

Slow to fast alterations in skeletal muscle fibers caused by clenbuterol, a beta 2-receptor agonist

1988 ◽  
Vol 254 (6) ◽  
pp. E726-E732 ◽  
Author(s):  
R. J. Zeman ◽  
R. Ludemann ◽  
T. G. Easton ◽  
J. D. Etlinger
Keyword(s):  
Muscle Fiber ◽  
Receptor Agonist ◽  
Fiber Type ◽  
Fiber Types ◽  
Cross Sectional ◽  
Type Composition ◽  
Slow Twitch ◽  
Beta 2 ◽  
Slow Twitch Fibers ◽  
Fast Twitch

Chronic treatment of rats with clenbuterol, a beta 2-receptor agonist (8–12 wk), caused hypertrophy of histochemically identified fast- but not slow-twitch fibers within the soleus, while the mean areas of both fiber types were increased in the extensor digitorum longus (EDL). In contrast, treatment with the beta 2-receptor antagonist, butoxamine, reduced fast-twitch fiber size in both muscles. In the solei and to a lesser extent in the EDLs, the ratio of the number of fast- to slow-twitch fibers was increased by clenbuterol, while the opposite was observed with butoxamine. The muscle fiber hypertrophy observed in the EDL was accompanied by parallel increases in maximal tetanic tension and muscle cross-sectional area, while in the solei, progressive increases in rates of force development and relaxation toward values typical of fast-twitch muscles were also observed. Our results suggest a role of beta 2-receptors in regulating muscle fiber type composition as well as growth.

scholarly journals Comparative analysis of the transcriptomes of EDL, psoas, and soleus muscles from mice

BMC Genomics ◽  
2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Pabodha Hettige ◽  
Uzma Tahir ◽  
Kiisa C. Nishikawa ◽  
Matthew J. Gage
Keyword(s):  
Skeletal Muscles ◽  
Striated Muscle ◽  
Fiber Type ◽  
Expression Patterns ◽  
Fiber Types ◽  
Muscle Adaptation ◽  
Myosin Heavy Chain Isoform ◽  
Genes Encoding ◽  
Slow Twitch ◽  
Fast Twitch

Abstract Background Individual skeletal muscles have evolved to perform specific tasks based on their molecular composition. In general, muscle fibers are characterized as either fast-twitch or slow-twitch based on their myosin heavy chain isoform profiles. This approach made sense in the early days of muscle studies when SDS-PAGE was the primary tool for mapping fiber type. However, Next Generation Sequencing tools permit analysis of the entire muscle transcriptome in a single sample, which allows for more precise characterization of differences among fiber types, including distinguishing between different isoforms of specific proteins. We demonstrate the power of this approach by comparing the differential gene expression patterns of extensor digitorum longus (EDL), psoas, and soleus from mice using high throughput RNA sequencing. Results EDL and psoas are typically classified as fast-twitch muscles based on their myosin expression pattern, while soleus is considered a slow-twitch muscle. The majority of the transcriptomic variability aligns with the fast-twitch and slow-twitch characterization. However, psoas and EDL exhibit unique expression patterns associated with the genes coding for extracellular matrix, myofibril, transcription, translation, striated muscle adaptation, mitochondrion distribution, and metabolism. Furthermore, significant expression differences between psoas and EDL were observed in genes coding for myosin light chain, troponin, tropomyosin isoforms, and several genes encoding the constituents of the Z-disk. Conclusions The observations highlight the intricate molecular nature of skeletal muscles and demonstrate the importance of utilizing transcriptomic information as a tool for skeletal muscle characterization.

Kinetics of glucose transport in rat muscle: effects of insulin and contractions

1987 ◽  
Vol 253 (1) ◽  
pp. E12-E20 ◽  
Author(s):  
T. Ploug ◽  
H. Galbo ◽  
J. Vinten ◽  
M. Jorgensen ◽  
E. A. Richter
Keyword(s):  
Glucose Transport ◽  
Fiber Type ◽  
Fiber Types ◽  
Simple Diffusion ◽  
Glycogen Repletion ◽  
Gastrocnemius Muscles ◽  
Slow Twitch Fibers ◽  
Fast Twitch ◽  
Kinetics Of ◽  
Red And White Muscles

The effects of insulin and prior muscle contractions, respectively, on 3-O-methylglucose (3-O-MG) transport in skeletal muscle were studied in the perfused rat hindquarter. Initial rates of entry of 3-O-MG in red gastrocnemius, soleus, and white gastrocnemius muscles as a function of perfusate 3-O-MG concentration exhibited Michaelis-Menten kinetics. Uptake by simple diffusion could not be detected. The maximum 3-O-MG transport velocity (Vmax) was increased more by maximum isometric contractions (10- to 40-fold, depending on fiber type) than by insulin (20,000 microU/ml; 3- to 20-fold) in both red and white muscles. The effects of both contractions and insulin were greater in red than in white muscles. In red but not in white muscles, maximum increases in Vmax elicited by contractions and by insulin were additive. Both insulin and contractions decreased the half-saturating substrate concentration for glucose transport (apparent Km) in all three muscles, in fast-twitch fibers from 70 to approximately 7 mM and in slow-twitch fibers from 12 to 7 mM. After contractions, reversal of contraction-induced glucose transport was monoexponential in red fibers, with a half-time of 7 and 15 min in slow- and fast-twitch fibers, respectively. In white muscle, Vmax continued to increase after contractions, reached a plateau after 10 min, and had only decreased 45% after 70 min. In contrast to the prevailing opinion, in all fiber types, reversal of contraction-induced glucose transport took place in the absence of muscle glycogen repletion.

Verapamil and zero Ca2+ alter responses of cat muscle to halothane and caffeine

1986 ◽  
Vol 60 (3) ◽  
pp. 935-941 ◽  
Author(s):  
P. A. Deuster ◽  
E. L. Bockman ◽  
H. Biscardi ◽  
S. M. Muldoon
Keyword(s):  
Electrical Stimulation ◽  
Channel Blocker ◽  
Fiber Type ◽  
Ringer Solution ◽  
Fiber Types ◽  
Slow Twitch ◽  
Fast Twitch ◽  
Ca2 Channels ◽  
Caffeine Contractures

Strips of soleus (slow twitch, oxidative) and gracilis (fast-twitch, glycolytic) muscle were obtained from 27 anesthetized cats and mounted in organ baths filled with oxygenated Krebs-Ringer solution (37 degrees C). The responses to caffeine, halothane (1%), caffeine in the presence of halothane, and electrical stimulation in the presence of halothane were examined in the two fiber types. These responses were compared with those observed in paired strips of muscle that had been treated with verapamil (10 or 28 microM), a slow calcium (Ca2+) channel blocker, with zero Ca2+, or with zero Ca2+ where magnesium (3.7 mM Ca2+) was added to replace the Ca2+. Halothane-induced contractures in the soleus were blocked by verapamil and zero Ca2+. Caffeine-induced contractures and tetanic contractions were attenuated in zero Ca2+ and by verapamil in both fiber types. Halothane overcame verapamil-induced reductions of caffeine contractures and tetanic contractions in both fiber types. In contrast, halothane did not overcome zero Ca2+-induced reductions in caffeine contractures or tetanic contractions in either fiber type. Furthermore, the addition of Mg2+ to the zero Ca2+ did not restore the responses. The findings with verapamil indicate that in cat muscle, both halothane- and caffeine-induced contractures and tetanic contractions are dependent on the influx of extracellular Ca2+. This extracellular Ca2+ may enter through the slow Ca2+ channels. However, because halothane in combination with caffeine or electrical stimulation overcame the effects of verapamil, there may be other sites involved.

Enhanced technique to measure proteins in single segments of human skeletal muscle fibers: fiber-type dependence of AMPK-α1 and -β1

2011 ◽  
Vol 110 (3) ◽  
pp. 820-825 ◽  
Author(s):  
Robyn M. Murphy
Keyword(s):  
Skeletal Muscle ◽  
Human Skeletal Muscle ◽  
Fiber Type ◽  
Significant Advance ◽  
Vastus Lateralis Muscle ◽  
Fiber Types ◽  
Freeze Dried ◽  
Slow Twitch ◽  
Fast Twitch ◽  
Muscle Biopsies

Human physiological studies typically use skeletal muscle biopsies from the heterogeneous vastus lateralis muscle comprised of both fast-twitch and slow-twitch fiber types. It is likely that potential changes of physiological importance are overlooked because fiber-type specific responses may not be apparent in the whole muscle preparation. A technological advance in Western blotting is presented where proteins are analyzed in just one small segment (<2 mm) of individual fibers dissected from freeze-dried muscle samples using standard laboratory equipment. A significant advance is being able to classify every fiber at the level of both contractile (myosin heavy chain and tropomyosin) and sarcoplasmic reticulum [sarco(endo)plasmic reticulum Ca2+-ATPase type 1] properties and then being able to measure specific proteins in the very same segments. This removes the need to fiber type segments before further analyses and, as such, dramatically reduces the time required for sample collection. Compared with slow-twitch fibers, there was less AMP-activated protein kinase (AMPK)-α1 (∼25%) and AMPK-β1 (∼60%) in fast-twitch fibers from human skeletal muscle biopsies.

scholarly journals Comparison of regulated passive membrane conductance in action potential–firing fast- and slow-twitch muscle

2009 ◽  
Vol 134 (4) ◽  
pp. 323-337 ◽  
Author(s):  
Thomas Holm Pedersen ◽  
William Alexander Macdonald ◽  
Frank Vincenzo de Paoli ◽  
Iman Singh Gurung ◽  
Ole Bækgaard Nielsen
Keyword(s):  
Action Potential ◽  
Muscle Fibers ◽  
Membrane Conductance ◽  
Fiber Types ◽  
Channel Inhibition ◽  
Slow Twitch Muscle ◽  
Slow Twitch ◽  
Slow Twitch Fibers ◽  
Fast Twitch ◽  
Passive Membrane

In several pathological and experimental conditions, the passive membrane conductance of muscle fibers (Gm) and their excitability are inversely related. Despite this capacity of Gm to determine muscle excitability, its regulation in active muscle fibers is largely unexplored. In this issue, our previous study (Pedersen et al. 2009. J. Gen. Physiol. doi:10.1085/jgp.200910291) established a technique with which biphasic regulation of Gm in action potential (AP)-firing fast-twitch fibers of rat extensor digitorum longus muscles was identified and characterized with temporal resolution of seconds. This showed that AP firing initially reduced Gm via ClC-1 channel inhibition but after ∼1,800 APs, Gm rose substantially, causing AP excitation failure. This late increase of Gm reflected activation of ClC-1 and KATP channels. The present study has explored regulation of Gm in AP-firing slow-twitch fibers of soleus muscle and compared it to Gm dynamics in fast-twitch fibers. It further explored aspects of the cellular signaling that conveyed regulation of Gm in AP-firing fibers. Thus, in both fiber types, AP firing first triggered protein kinase C (PKC)-dependent ClC-1 channel inhibition that reduced Gm by ∼50%. Experiments with dantrolene showed that AP-triggered SR Ca2+ release activated this PKC-mediated ClC-1 channel inhibition that was associated with reduced rheobase current and improved function of depolarized muscles, indicating that the reduced Gm enhanced muscle fiber excitability. In fast-twitch fibers, the late rise in Gm was accelerated by glucose-free conditions, whereas it was postponed when intermittent resting periods were introduced during AP firing. Remarkably, elevation of Gm was never encountered in AP-firing slow-twitch fibers, even after 15,000 APs. These observations implicate metabolic depression in the elevation of Gm in AP-firing fast-twitch fibers. It is concluded that regulation of Gm is a general phenomenon in AP-firing muscle, and that differences in Gm regulation may contribute to the different phenotypes of fast- and slow-twitch muscle.

scholarly journals Skeletal muscle and fiber type-specific intramyocellular lipid accumulation in obese mice

2021 ◽  
Author(s):  
Nejc Umek ◽  
Simon Horvat ◽  
Erika Cvetko
Keyword(s):  
Muscle Fiber ◽  
Lipid Accumulation ◽  
High Fat Diet ◽  
Fiber Type ◽  
Muscle Fiber Types ◽  
Fiber Types ◽  
Intramyocellular Lipid ◽  
Obese Mice ◽  
Slow Twitch ◽  
Fast Twitch

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.

Influence of fiber type and muscle source on Ca2+ sensitivity of rat fibers

1989 ◽  
Vol 256 (2) ◽  
pp. C420-C427 ◽  
Author(s):  
B. Laszewski-Williams ◽  
R. L. Ruff ◽  
A. M. Gordon
Keyword(s):  
Calcium Concentration ◽  
Fiber Type ◽  
Calcium Sensitivity ◽  
One Dimensional ◽  
Protein Gel ◽  
Fast Twitch Muscle ◽  
Slow Twitch ◽  
Slow Twitch Fibers ◽  
Fast Twitch ◽  
Adductor Longus

This study investigated the influence of muscle source and fiber type on the calcium sensitivity of skinned rat skeletal muscle fibers from predominantly slow muscles [soleus (SOL) and adductor longus (AL)], mixed muscle [posterior gracilis (PG)], and predominantly fast-twitch muscle [extensor digitorum longus (EDL)]. Fibers were characterized histochemically and by one-dimensional protein gel electrophoresis, and calcium-tension relationships were determined. Fiber type and muscle source had significant effects on the negative log of the calcium concentration associated with half-maximal tension (pCa1/2). Slow-twitch fibers had larger values of pCa1/2 than did fast-twitch fibers. Slow-twitch fibers from the predominantly slow muscles, SOL and AL, had similar values of pCa1/2 but slightly smaller values than from the mixed muscle, PG. Fast-glycolytic (FG) fibers from the predominantly fast muscle, EDL, had a higher pCa1/2 than fibers from the mixed fiber type muscle, PG. There were no differences between the pCa1/2 associated with FG and fast-oxidative-glycolytic fibers.

Voluntary Running Exercise Ameliorates Muscle Loss in Mice

2007 ◽  
Author(s):  
Andrea M. Hanson ◽  
Louis S. Stodieck ◽  
Virginia L. Ferguson
Keyword(s):  
Soleus Muscle ◽  
Fiber Type ◽  
Bed Rest ◽  
Muscle Loss ◽  
Running Exercise ◽  
Voluntary Running ◽  
Slow Twitch ◽  
Slow Twitch Fibers ◽  
Fast Twitch

Both spaceflight and bed rest studies are known to cause substantial muscle loss in humans. Of particular interest in atrophy studies is the postural, slow-twitch fiber soleus muscle. It has been demonstrated that during periods of disuse, slow-twitch fibers undergo fiber type switching and morph into fast-twitch fibers [1]. Alternatively, when exercise is prescribed, there is switching of fast-to slow-twitch fibers [2], indicating a profound adaptability of the muscle to exercise.

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