In any given muscle different fibre types can be found interspersed among one another.

Successive cross-sections of the same muscle stained for different properties.  (A) for slow myosin-ATPase; (B) for succinic dehydrogenase (oxidative phosphorylation) activity; and (C) for glycolytic capacity. 

Fast fibres (Type II) express a relatively potent myosin-ATPase variant.  These fibres are specialised to contract rapidly and powerfully.  They need to obtain a rich and ready supply of ATP.  ATP from glycolysis is produced in the cytosol right in the vicinity of the myofibrils.  Fast fibres are therefore designed to preferentially use glycolysis. 

Since glycogen provides 3 ATP per glucose molecule, and can be stored right in the cytoplasm, they also 'prefer' this source over glucose from the blood (which will provide only 2 ATP per molecule).  They do not rely on ATP produced by oxidative phosphorylation (OP). 

 

Type I - slow oxidative (red)

Type IIA*- fast  oxidative (red)

Type IIB – fast glycolytic (white)

Myosin isozyme (ATPase)

Slow

Fast

Fast

SR calcium-ATPase

Moderate

High

High

Fibre diameter

Moderate

Small

Large

Oxidative capacity (mito-

chondria, myoglobin etc.)

High

Very high

Low

Glycolytic capacity

Moderate

High

High

*Rare in humans & other primates     

Oxidative Phosphorylation produces ATP efficiently and in abundance for each molecule of glucose or FFA burnt, but the ATP is made in the mitochondria and the process is dependent upon inward diffusion of oxygen.  All this is too slow for fast fibres, which abandon OP.  They are therefore supplied by relatively few capillaries, have few mitochondria and store relatively little myoglobin (but lots of glycogen and glycolytic enzymes).  They are therefore pale in colour (white meat).  The fibres are quite large in diameter, since diffusion is not a problem - but they do need to generate powerful contractions.  The SR is usually abundant (to supply large quantities or Ca2+) and has a potent Ca2+-ATPase to rapidly resequester the released Ca2+.    Sprinters have proportionately large numbers of fast fibres in their muscles.

Slow fibres express a relatively weak myosin-ATPase variant.  Since they are not in so much of a hurry, they rely on the more efficient oxidative processes to produce ATP.  The fibres are relatively thin, rich in mitochondria and myoglobin, richly supplied with capillaries, poor in glycogen, and have relatively sparse SR, with a relatively weak Ca2+-ATPase.  These fibres are dark in colour (red meat).  Long distance runners have abundant slow fibres in their muscles. 

Fast fibres sacrifice durability for power.  They produce pyruvate + NADH + H+ as end products which react to produce lactate and NAD+ in order to preserve the redox balance of the cells.  The lactate does not leave the fibre easily. The intracellular pH therefore falls, impairing functioning of the Ca2+-ATPase in the SR and of the actomyosin ATPase.  The fast fibres thus fatigue readily. 

Fast & slow fibres do not readily interconvert, but training can increase capillary density, buffering capacity and ability to extract oxygen from the blood.  An intermediate type of fibre (IIA) may convert more to fast type with strength training and  more to slow type with endurance training.

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