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Biomedical subjects

H Schmalbruch

Publications and source records attributed to H Schmalbruch.

At least 91 records · Page 5Linked to original sources

A freeze-fracture study of the plasma membrane of muscle fibres of a patient with chronic creatine kinase elevation suspected for malignant hyperthermia.

The muscle biopsy from a 12-year-old boy with chronic creatine kinase elevation was studied by electron microscopy. At the age of 7 years the patient had a possible abortive attack of malignant hyperthermia. The biopsy specimen contained many fibres with segmental contracture and necrosis; thin sections showed defects of the plasma membrane with loss of glycogen granules into the interstitium. Freeze-fracturing of the plasma membrane showed clustering of intramembranous particles and some membrane areas were devoid of particles and of pinocytotic caveolae. The E-face showed irregular elevations and the P-face corresponding defects. These deviations of the fracture-plane were due to manifest membrane openings, to abnormalities of the structure of the lipid bilayer, to clustering of membrane particles or to the fact that intracellular membranes often were abnormally close to the plasma membrane. The findings suggest that a disintegration of the lipid-protein system of the membrane precedes the formation of manifest defects. The manifest defects resembled those in Duchenne muscular dystrophy. It is unknown whether the changes seen by freeze-fracturing were specific for a myogenic disorder and whether they were due to a basic membrane abnormality or to defects in other systems of the muscle cell.

Anesthesia↗

Satellite cells of rat muscles as studied by freeze-fracturing.

Satellite cells in rat muscles were studied by freeze-fracturing. They were found not to be fusiform but to have several narrow projections embedded in grooves of the muscle fibre membrane. Short projections of the muscle fibre covering the outer face of the satellite cells were observed as well. In the P-face of the cell membrane of satellite cells, membrane particles and caveolae were less frequently seen than in the P-face of the muscle membrane. Thus the surface of the satellite cells looked more smooth than that of the muscle fibres. Junctions between muscle fibre and satellite cell were not found. The presence of cytoplasmic extensions of satellite cells may suggest that these cells are motile.

Animals↗

Regeneration of soleus muscles of rat autografted in toto as studied by electron microscopy.

Rat soleus muscles were autografted from right to left legs, and regeneration following necrosis of all original myofibres was studied after 7 to 250 days. The best regenerates were from grafts replacing all calf muscles and sutured to the tendon stumps. After 30 days the size of such regenerates was equal to those from minced gastrocnemius muscles: the cross sectional area of muscle tissue was 30% (1.7 mm2) and the number of fibres was 180% (4500) of normal soleus muscles; the fibre diameters were 10 to 40mum. To increase the number of myoblasts before grafting some muscles were injured by Ringer solution of 70 degrees C and transplanted after 2 days. Nevertheless, this did not influence regeneration. After 7 days clusters of myotubes occurred in the periphery of the muscle. These myotubes originated from myoblasts growing like endothelial cells on the inner face of the persisting basal lamina tubes of necrotic fibres. After 30 days the muscles were vascularized. Fibres formed in a common basal lamina detached and so looked "split". Satellite cells of new fibres came from undifferentiated cells associated with myotubes, i.e. from myoblasts. After 30 days and more regenerates contained three sorts of fibres. 1. Thin (5 to 20 mum) fibres resembling fetal muscle fibres. They were most prominent after 30 days, and probably not yet innervated. 2. Thin (10 mum) degenerating fibres as in long-time denervated muscles. 3. Thick (more than 30 mum) mature looking fibres which were innervated and revealed end-plates. Half of the grafts studied after 30 and 60 days contained unmyelinated and myelinated axons which had grown along strands of surviving Schwann cells. After 250 days, only two muscles were studied which both lacked innervation. Almost all regenerates contained muscle spindles, which, however, were not innervated. Within the persisting spindle capsules new muscle fibres had been formed from satellite cells of the former intrafusal fibres.

Animals↗

The number of nuclei in adult rat muscles with special reference to satellite cells.

The number and the size of different populations of nuclei were studied in skeletal muscles and in the diaphragm of male Wistar rats of 200-250 g weight. Nuclei on cross-sections were counted and classified by electron microscopy, their incidence was corrected for their different lengths, and the number of nuclei per mm3 of muscle was determined by light microscopy. The total number of nuclei per mm3 was 5-10(4) in the superficial part of the anterior tibial muscle, it was 10-10(4) in the soleus, and it was 15-10(4) in the diaphragm. Half of the nuclei were localized inside muscle fibres. The incidence of satellite cell nuclei on cross sections was 4% of muscle nuclei in the anterior tibial muscle, and 8% in soleus and diaphragm. The number of satellite cells per mm3 muscle were 900, 4,900, and 5,300 in these muscles. More than half of the satellite cells were closely associated with a capillary. In the anterior tibial muscle, and in 1-micron sections no satellite cells could be identified by light microscopy. In the soleus muscle and in the diaphragm, satellite cells were more rich in cytoplasm and many were visible in the light microscope.

Animals↗

The number of satellite cells in normal human muscle.

The satellite cell population in skeletal muscles of ten normal subjects aged 7 to 73 years was quantitated by electron microscopy. In all 1,414 nuclei were assessed. Satellite cell nuclei comprised 4% (standard deviation 2%) of all nuclei within the fibre basal lamina. The lowest incidence (0.6%) was found in a 73-year-old man. The study confirms, that satellite cells are regularly present in human skeletal muscle.

Adolescent↗

The morphology of regeneration of skeletal muscles in the rat.

Muscle regeneration was studied by light and electron microscopy in soleus muscles of rat. After segmental crushing the number of fibres increased in some muscles within 30 days, indicating that numerical hyperplasia can take place. Locally applied Ringer solution of 60-70 degrees C caused necrosis of myofibres but left satellite cells and blood supply largely intact. Following phagocytosis, four mechanisms of regeneration were seen. (1) Lost fibres were replaced by clusters of myotubes formed by satellite cells within persisting basal lamina tubes. These clusters displaced the surrounding endomysium and looked like longitudinally 'split' fibres. (2) Viable fibre fragments fused with satellite cells. (3) Satellite cells of surviving fibres proliferated and fused to myotubes localized beneath the basal lamina. (4) Thin new fibres occurred in the interstitium. Their origin remained unknown. After 6 months the mean size of the new myofibres was normal, but the scatter of diameters was increased, central nuclei, fibre 'spliting' and branching, and fibrosis were prominent. Staining for acetylcholinesterase revealed that many fibres were short and not innervated. The similarity with dystrophic muscles in man suggested, that the most prominent histological changes in myopathic muscles may be due to attempts of regeneration.

Acetylcholinesterase↗

Segmental fibre breakdown and defects of the plasmalemma in diseased human muscles.

Thick round fibres common in cross sections of muscle biopsies from patients with muscular dystrophy are due to contracted and swollen segments of otherwise normal muscle fibres. This contracture leads to segmental fibre breakdown, which is identical with Zenker's waxy degeneration. In biopsies from 90 patients suspected of neuromuscular disease, segmental contracture was seen in all or nearly all patients with infantile muscular dystrophy, necrotic myopathy or acute alcoholic myopathy. It was present in half of the patients with polymyositis or myotonic dystrophy. In resticted forms of muscular dystrophy it was rare as it was in neurogenic atrophy. In 9 clinically normal patients it was absent. In electron micrographs of the initial stage sarcomeres were moderately shortened, the sarcoplasmic reticulum was distended and the mitochondria were normal. In the plasmalemma holes were found, through which glycogen granules were lost into the interstitial tissue. In later stages myofibrils were overcontracted and homogenized; in large areas the plasmalemma was absent. Based on these findings a hypothesis for the development of waxy degeneration is proposed: locally defects of the plasmamembrane cause segmental contracture, glycogen granules and water soluble enzymes are lost through holes in the plasma membrane, and finally the affected fibre segment becomes necrotic.

Adolescent↗

Histochemical fiber typing and staining intensity in cat and rat muscles.

In the gastrocnemius muscle of cat and rat, staining for oxidative enzymes differentiated three fiber types (A,B,C) and staining for adenosine triphosphate at pH 9.4 differentiated two fiber types (I, II) with a reliability of 90% and 98%, respectively. In cat 96% and in rat 90% of the fibers were typed identically after staining for nicotinamide adenine dinucleotidelinked lactic dehydrogenase (LDH) and succinic dehydrogenase (SDH). When differentiated by staining for LDH, A and B fibers were of type I. IN RAT, 80-90% OF ALL FIBERS WERE OF TYPE 22, COMPPRISING A, B and C fibers. Type I fibers stained for LDH intensely as did C fibers of type II, but stained intermediately for SDH. The degree of staining was measured by photometry. When fibers were stained for LDH, histograms of density showed three peaks corresponding to A, B and C fibers in cat, but only two peaks corresponding to A and C fibers in rat, In cat and rat, the densities of A, B and C fibers belonged to different populations. In soleus muscle of cat and rat stained for LDH, menadione-linked alpha-glycerophosphate dehydrogenase and adenosine triphosphatase at pH 9.4, the degree of staining differed from thatin any type of fiber in gastrocnemius muscle

Adenosine Triphosphatases↗