The relationship between capillarisation and fibre types during compensatory hypertrophy of the plantaris muscle in the rat.

H Degens, Z Turek, LJC Hoofd, MA Van't Hof… - Journal of …, 1992 - ncbi.nlm.nih.gov
H Degens, Z Turek, LJC Hoofd, MA Van't Hof, RA Binkhorst
Journal of anatomy, 1992ncbi.nlm.nih.gov
Compensatory hypertrophy of the plantaris muscle was obtained by denervation of its
synergists. This hypertrophy is characterised by a 32% increase in muscle mass. The
muscle consists of type I and IIa (oxidative), and IIb (glycolytic) fibres. Fibres of all types were
enlarged in hypertrophied muscles and the proportion of type I fibres was increased. We
investigated the capillarisation after hypertrophy as related to fibre type. In order to obtain
this information a new technique was used, capable of estimating not only the traditional …
Abstract
Compensatory hypertrophy of the plantaris muscle was obtained by denervation of its synergists. This hypertrophy is characterised by a 32% increase in muscle mass. The muscle consists of type I and IIa (oxidative), and IIb (glycolytic) fibres. Fibres of all types were enlarged in hypertrophied muscles and the proportion of type I fibres was increased. We investigated the capillarisation after hypertrophy as related to fibre type. In order to obtain this information a new technique was used, capable of estimating not only the traditional overall capillary density (CD) but also an index of heterogeneity in capillary spacing (LogSD), the'local capillary to fibre ratio'(LCFR), obtained separately for each muscle fibre type, and finally a capillary density for each respective fibre type, the'capillary fibre density'(CFD). It was found in both control and hypertrophied muscles that CD was higher in the deep (few IIb fibres) than in the superficial part of the muscle (considerable number of IIb fibres). The LogSD was lower, indicating less heterogeneity, in the deep than in the superficial part of the muscle. The LCFR and CFD of each fibre type was greater in the deep than in the superficial region of both control and hypertrophied muscles. Furthermore the CFD and LCFR were larger in type I and IIa fibres than in IIb fibres in each region of control and hypertrophied muscles. In hypertrophied muscles the CD was not significantly different from that of control muscles. However, LCFR of all fibre types was increased significantly in hypertrophied muscles as compared with controls, demonstrating capillary proliferation. The decreased CFD of type I and IIa fibres in the deep region of hypertrophied muscles as compared with controls suggests that here the capillary proliferation lags behind the increase in muscle mass. Endurance training had no significant effects for any region in any of the indices that were used.
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