Abstract
The avian anterior latissimus dorsi (ALD) is unique amongst vertebrates since it has been considered to be a true slow (or tonic) skeletal muscle. While the structure and function of the extrafusal fibers in the ALD have been intensively investigated, the intrafusal fibers of its muscle spindles and their relationship to the surrounding extrafusal fibers in this muscle have been virtually neglected. Serial frozen sections of this muscle from normal adult domestic chickens were tested for two separate enzymes: myosin ATPase after preincubations at differing pH (Brooke and Kaiser, '69) and NADHโtetrazolium reductase, a mitochondrialโbound oxidative enzyme. Both enzyme reactions were able to detect two distinct categories of extrafusal fibers in this muscle, as well as two classes of intrafusal fibers in its muscle spindles.
Neither of the extrafusal fiberโtypes reacted like typical fast (or twitch) fibers for myosin ATPase; they did not show a characteristic reversal in their relative staining patterns throughout the alkaline (pH 9.4) to acid (pH 4.6 and 4.3) preincubation range. The majority of fibers (type 1) were significantly larger in their crossโsectional size, consistently stained lightly for ATPase, and showed high NADHโTR activity. They represented about 84% of the total fiber population (n = 3540 ยฑ 75). The other set of extrafusal fibers (type 2) constituted the remaining 16% of the total fiber population. They were smaller in diameter, exhibited high myosin ATPase activity, and reacted less intensely for the oxidative enzyme.
The histochemical characteristics of the two kinds of intrafusal fibers were profoundly different from those observed in the extrafusal fibers. Their crosssectional fiber diameters were not significantly different from each other, and they exhibited a reversal in their staining reactions for myosin ATPase following acid preincubation for this enzyme.
The results of this study concur with recently published reports of extrafusal fiber heterogeneity in the slow ALD muscle of the chicken. In addition, this work clearly demonstrates a histochemical dichotomy amongst the intrafusal fibers of muscle spindles in this muscle.