The effect of long‐term high‐frequency stimulation on capillary density and fibre types in rabbit fast muscles.

Rabbit fast muscles (tibialis anterior, t.a.; extensor digitorum longus, e.d.l.; and peroneal muscles) were stimulated for up to 28 days by electrodes implanted in the vicinity of the lateral popliteal (peroneal) nerve for 8 h/day, using either intermittent high‐frequency (three trains at 40 Hz/min, each 5 s duration), or continuous stimulation at 10 Hz. This did not result in muscle hypertrophy even after 28 days. Capillary density (number of capillaries/mm2) was increased in e.d.l. from 251 +/‐ 3 to 366 +/‐ 6 after 14 days of stimulation and from 251 +/‐ 3 to 514 +/‐ 13 after 28 days of stimulation at 40 Hz. In t.a., capillary density increased from 373 +/‐ 5 to 583 +/‐ 10 after 14 days of stimulation at 40 Hz. The capillary/fibre ratio increased in e.d.l. from 1.25 +/‐ 0.02 to 1.86 +/‐ 0.04 at 14 days and to 2.07 +/‐ 0.06 at 28 days. In t.a., capillary/fibre ratio increased from 1.40 +/‐ 0.03 to 1.83 +/‐ 0.05 at 14 days. All these changes were significant (P less than 0.0005). Analysis of capillary density, capillary/fibre ratio, fibre areas and proportion of different fibre types in muscles stimulated for shorter periods showed no changes in capillary density, capillary/fibre ratio or fibre areas in e.d.l. or t.a. stimulated for 4 days; there was a decrease in the proportion of fast glycolytic fibres from 42 to 32% (P less than 0.0025) and increase in fast oxidative from 37.6 to 41.2% in e.d.l. Muscles stimulated for 7 days showed increases in capillary density and capillary/fibre ratio in fast predominantly glycolytic fibres in e.d.l., and a decrease in capillary density in fast and slow oxidative fibres in t.a. This was partly due to the increase in fibre areas in these groups (capillary/fibre ratio in t.a. was not significantly changed). No changes were observed in fibre areas in e.d.l. Stimulation at 10 Hz produced increase in capillary/fibre ratio in the vicinity of glycolytic fibres after only 4 days. High‐frequency intermittent stimulation leads to a massive capillary growth which starts first in the muscle with a higher proportion of glycolytic fibres (e.d.l.), has a later onset than continuous low‐frequency stimulation, and may be due to a combination of high blood flow and metabolic factors.

[1]  E. Valdivia Total capillary bed in striated muscles of guinea pigs native to the Peruvian mountains. , 1958, The American journal of physiology.

[2]  J. Henriksson,et al.  Capillary supply of the quadriceps femoris muscle of man: adaptive response to exercise , 1977, The Journal of physiology.

[3]  O. Hudlická,et al.  Capillary growth in chronically stimulated adult skeletal muscle as studied by intravital microscopy and histological methods in rabbits and rats. , 1978, Microvascular research.

[4]  J. Folkman,et al.  Role of cell shape in growth control , 1978, Nature.

[5]  R. Bannister,et al.  LOCALIZED AREAS OF HIGH ALKALINE PHOSPHATASE ACTIVITY IN THE TERMINAL ARTERIAL TREE , 1962, The Journal of cell biology.

[6]  B. Folkow,et al.  A comparison between “red” and “white” muscle with respect to blood supply, capillary surface area and oxygen uptake during rest and exercise , 1968 .

[7]  T. Lømo,et al.  DIFFERENT STIMULATION PATTERNS AFFECT CONTRACTILE PROPERTIES OF DENERVATED RAT SOLEUS MUSCLES , 1980 .

[8]  F. Jolesz,et al.  Fast to slow transformation of fast muscles in response to long-term phasic stimulation , 1982, Experimental Neurology.

[9]  O. Hudlická Resting and postcontraction blood flow in slow and fast muscles of the chick during development. , 1969, Microvascular research.

[10]  N. Banchero,et al.  Capillary Density of Skeletal Muscle in Andean Dogs 1 , 1976, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[11]  G. Vrbóva,et al.  Growth of capillaries during long-term activity in skeletal muscle. , 1973, Bibliotheca anatomica.

[12]  E. M. Renkin,et al.  Microvascular supply in relation to fiber metabolic type in mixed skeletal muscles on rabbits. , 1978, Microvascular research.

[13]  S Salmons,et al.  The influence of activity on some contractile characteristics of mammalian fast and slow muscles , 1969, The Journal of physiology.

[14]  G. Imre STUDIES ON THE MECHANISM OF RETINAL NEOVASCULARIZATION , 1964, The British journal of ophthalmology.

[15]  P. Björntorp,et al.  Metabolic Activity in Human Skeletal Muscle Effect of Peripheral Arterial Insufficiency , 1972, European journal of clinical investigation.

[16]  D. Pette,et al.  Response of succinate dehydrogenase activity in fibres of rabbit tibialis anterior muscle to chronic nerve stimulation. , 1983, The Journal of physiology.

[17]  M. Houston,et al.  Cross-adaptive responses to different forms of leg training: skeletal muscle biochemistry and histochemistry. , 1982, Canadian journal of physiology and pharmacology.

[18]  E. M. Renkin,et al.  Early changes in fiber profile and capillary density in long-term stimulated muscles. , 1982, The American journal of physiology.

[19]  G. Vrbóva,et al.  Functional specializations of the vascular bed of soleus , 1970, The Journal of physiology.

[20]  M. Brooke,et al.  SOME COMMENTS ON THE HISTOCHEMICAL CHARACTERIZATION OF MUSCLE ADENOSINE TRIPHOSPHATASE , 1969, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[21]  Eliot R. Clark,et al.  Microscopic observations on the growth of blood capillaries in the living mammal , 1939 .