Anatomic capillarization is elevated in the medial gastrocnemius muscle of mighty mini mice

2009 ◽  
Vol 106 (5) ◽  
pp. 1660-1667 ◽  
Author(s):  
Lisa E. Wong ◽  
Theodore Garland ◽  
Sharon L. Rowan ◽  
Russell T. Hepple

House mice selectively bred for high voluntary wheel running display a mini-muscle (MM) phenotype wherein mass-specific mitochondrial enzyme activities are double that of normal, but muscle mass is reduced by half. In addition, mini-muscles are characterized by small muscle fibers in the superficial region of the plantaris and medial gastrocnemius muscles. To determine the structural alterations facilitating aerobic metabolism in these mini-muscles, cross-sections of the medial gastrocnemius muscle of normal (N; n = 6) and mini-muscle (MM; n = 6) mice were histo- and immunochemically labeled and analyzed for fiber size, capillarization, and fiber type. On the basis of the higher mitochondrial enzyme activities in muscles of MM mice, we hypothesized that they would have greater fiber capillarization in the medial gastrocnemius than N mice. Furthermore, we hypothesized that augmented capillarization in MM would principally be a function of the smaller fibers in the superficial aspect of this muscle. On average, MM had higher capillary-to-fiber ratio and higher capillary density. Binning fibers according to size revealed that it was primarily the normal-sized fibers of the MM that had higher capillarity. The small fibers seen in the superficial region of MM were distinct from N mice in that they had heterogeneous myofibrillar ATPase staining and patchy succinate dehydrogenase staining in the interior of the fibers. These results support the hypothesis that the MM have higher indexes of capillarity, caused primarily by greater capillary number around normally sized fibers. These alterations are consistent with the superior mass-specific aerobic function of these muscles.

1996 ◽  
Vol 81 (2) ◽  
pp. 933-942 ◽  
Author(s):  
C. J. De Ruiter ◽  
P. E. Habets ◽  
A. de Haan ◽  
A. J. Sargeant

The purpose of the present study was to investigate to what extent fast-twitch IIX and IIB fiber recruitment was related to the natural existing muscle compartments (subvolumes of muscle innervated by different primary nerve branches) in rat medial gastrocnemius. Three groups (n = 6) of rats trotted on a motor-driven treadmill (20 degrees incline) at different speeds. A fourth group served as controls, and a fifth group received in situ electrical stimulation of all medial gastrocnemius muscle fibers. Postexercise glycogen levels (periodic acid-Schiff staining intensities) were made. Running caused more and in situ stimulation caused less glycogen breakdown in the proximal IIX and IIB fibers compared with the fibers of the same type in the most distal compartment. Furthermore, the boundaries of the most distal compartment could often be recognized in the periodic acid-Schiff-stained cross sections. It was concluded that during running the proximal IIX and IIB fibers were recruited to a greater extent (and at lower treadmill speeds) compared with the distal IIX and IIB fibers, respectively.


Neuroscience ◽  
1981 ◽  
Vol 6 (4) ◽  
pp. 725-739 ◽  
Author(s):  
R.F. Mayer ◽  
R.E. Burke ◽  
J. Toop ◽  
J.A. Hodgson ◽  
K. Kanda ◽  
...  

2019 ◽  
Vol 68 ◽  
pp. 187-192 ◽  
Author(s):  
Tatsunori Watanabe ◽  
Ippei Nojima ◽  
Hideshi Sugiura ◽  
Basma Yacoubi ◽  
Evangelos A. Christou

1994 ◽  
Vol 76 (6) ◽  
pp. 2663-2671 ◽  
Author(s):  
L. J. Einsiedel ◽  
A. R. Luff

The aim of the study was to determine whether increased motoneuron activity induced by treadmill walking would alter the extent of motoneuron sprouting in the partially denervated rat medial gastrocnemius muscle. An extensive partial denervation was effected by unilateral section of the L5 ventral root, and it is very likely that all units remaining in the medial gastrocnemius were used in treadmill walking. Rats were trained for 1.5 h/day and after 14 days were walking at least 1 km/day. Motor unit characteristics were determined 24 days after the partial denervation and were compared with units from partially denervated control (PDC) animals and with units from normal (control) animals. In PDC rats, force developed by slow, fast fatigue-resistant, and fast intermediate-fatigable motor units increased substantially compared with control animals; that of fast-fatigable units did not increase. In partially denervated exercised animals, force developed by slow and fast-fatigue-resistant units showed no further increase, but fast-intermediate- and fast-fatigable units showed significant increases compared with those in PDC animals. The changes in force were closely paralleled by changes in innervation ratios. We concluded that neuronal activity is an important factor in determining the rate of motoneuron sprouting.


1980 ◽  
Vol 238 (1) ◽  
pp. C62-C71 ◽  
Author(s):  
R. G. Holly ◽  
J. G. Barnett ◽  
C. R. Ashmore ◽  
R. G. Taylor ◽  
P. A. Mole

A new model of stretch-induced growth is evaluated in four chicken wing muscles stretched to different extents by a spring-loaded tubular assembly. Muscles grew in length and cross section in proportion to the extent to which they were stretched. Longitudinal growth was essentially completed within 1 wk, while muscles grew in cross section through at least 5 wk of stretch. The muscles were neither denervated nor immobilized, and muscle activity as measured by EMG was not increased. Oxidative enzyme activities increased substantially with stretch in the patagialis (PAT), a twitch muscle, but were relatively unchanged in the slow-tonic anterior latissimus dorsi (ALD). Stretch altered mitochondrial enzyme proportions in the PAT, but had little effect in the ALD. Capillary density was unchanged with stretch in the PAT, but decreased in the ALD. Capillary density was unchanged with stretch in the PAT, but decreased in the ALD. Capillary-to-fiber ratio, however, increased in both muscles. We conclude that muscles grow and adapt enzymatically due to stretch, but that these responses are dissimilar in twitch and tonic muscles.


Sign in / Sign up

Export Citation Format

Share Document