BACKGROUND: The unbiased estimation of the capillary length density in skeletal muscle tissue Lv(cap/mus) has been performed in this study applying a new stereological methodology based on the use of vertical slices and the intersections of cycloid test curves with capillaries in a three-dimensional space defined by systematically chosen fields of vision and the thickness of the sections. METHODS: The following simple requirements must be fulfilled: selection of a fixed vertical axis in skeletal muscle, adequate systematic muscle sampling, obtention of vertical slices of constant and known thickness but indifferent in magnitude, superposition of a cycloid test system with the minor axis of cycloid curves positioned perpendicularly to the vertical axis, and counting the intersections between cycloid curves and capillaries. In our study, the vertical axis was defined as that which is parallel to the natural, major axis of the muscle where fibres and capillaries are arranged parallel to this axis. The muscle sampling was performed using the fractionator method, and 25 microns thick sections were chosen. RESULTS: The application of the equation for estimation of Lv(cap/mus) permits determination of an average of 1,480 mm of capillaries per mm3 of muscle tissue, knowing the number of intersections, section thickness, and the points hitting the muscle with a known ratio between cycloid test curve length to a test point. CONCLUSIONS: The estimation of Lv(cap/mus) is efficient, unbiasedly obtained, and no assumptions on the degree of capillary anisotropy are required.
BACKGROUND: The unbiased estimation of the capillary length density in skeletal muscle tissue Lv(cap/mus) has been performed in this study applying a new stereological methodology based on the use of vertical slices and the intersections of cycloid test curves with capillaries in a three-dimensional space defined by systematically chosen fields of vision and the thickness of the sections. METHODS: The following simple requirements must be fulfilled: selection of a fixed vertical axis in skeletal muscle, adequate systematic muscle sampling, obtention of vertical slices of constant and known thickness but indifferent in magnitude, superposition of a cycloid test system with the minor axis of cycloid curves positioned perpendicularly to the vertical axis, and counting the intersections between cycloid curves and capillaries. In our study, the vertical axis was defined as that which is parallel to the natural, major axis of the muscle where fibres and capillaries are arranged parallel to this axis. The muscle sampling was performed using the fractionator method, and 25 microns thick sections were chosen. RESULTS: The application of the equation for estimation of Lv(cap/mus) permits determination of an average of 1,480 mm of capillaries per mm3 of muscle tissue, knowing the number of intersections, section thickness, and the points hitting the muscle with a known ratio between cycloid test curve length to a test point. CONCLUSIONS: The estimation of Lv(cap/mus) is efficient, unbiasedly obtained, and no assumptions on the degree of capillary anisotropy are required.