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Biomedical subjects

K Rybicka

Publications and source records attributed to K Rybicka.

At least 19 recordsLinked to original sources
PubMed1988

The effect of verapamil cardioplegia on myocardial ultrastructure.

The calcium channel blocker, verapamil, was evaluated as an adjunct to cold cardioplegia in 16 randomized patients with unstable angina pectoris who received saphenous vein bypass grafts. Myocardial biopsies taken before cardioplegia showed various degrees of ischemic change as assessed by ultrastructural parameters (mitochondrial swelling, matrix clearance, and sarcotubular dilatation). After reperfusion, the majority of the patients had progressive changes of ischemia, with marked mitochondrial and sarcotubular swelling, depletion of glycogen, chromatin clumping, and myofibrillar disruption; amorphous mitochondrial densities were occasionally seen. The ultrastructural changes after cardioplegia were dependent primarily on the extent of preexisting ischemic damage and did not correlate with the use of verapamil. Verapamil did not protect the ischemic myocardium during cold cardioplegia as assessed ultrastructurally.

Biopsy↗
PubMed1981

Simultaneous demonstration of glycogen and protein in glycosomes of cardiac tissue.

Cardiac conduction fibers fixed either in glutaraldehyde and OsO4 or treated additionally en bloc with uranyl acetate were studied in order to demonstrate the structure of glycosomes (protein-glycogen complex). Sections were stained histochemically by periodic acid-thiosemicarbazide-silver proteinate (PA--TSC--SP) for glycogen followed by uranyl acetate and lead citrate (U-Pb) for protein. In control sections periodic acid was replaced by hydrogen peroxide (H2O2). Glycogen appeared in all sections stained by PA-TSC-SP. Protein was poorly contrasted in periodic acid treated histochemical sections taken from fixed in glutaraldehyde and OsO4. Simultaneous staining of glycogen and protein was achieved in sections of tissue treated en bloc with uranyl acetate. This treatment revealed two classes of glycosomes: 1) glycosomes deposited freely in the cytoplasm whose structure was disintegrated after treatment with uranyl acetate: 2) glycosomes associated with other cellular structures that remained intact. Staining of glycogen and protein in the same section demonstrated for the first time the structure of intact glycosomes.

Animals↗
PubMed1979

Glycosomes (protein-glycogen complex) in the canine heart. Ultrastructure, histochemistry and changes induced by acidic treatment.

Cardiac conducting fibers were selected from two dogs defined as A and B. The specimens differed in the reaction of their electron dense granules, commonly referred to as glycogen, to the treatment en bloc with uranyl acetate. Material was fixed in glutaraldehyde and OsO4. Blocks were processed either conventionally or immersed in uranyl acetate before dehydration. Sections were examined unsatined, stained with U and/or Pb or with a histochemical technique (PA-TSC-SP) specific for glycogen. Electron dense granules have affinity to Os, U and Pb which suggests ionic reactions specific for protein but improbable for glycogen. Large granules in A turned into pale ghosts and small granules in B disappeared after treatment en bloc with uranyl acetate. PA-TSC-SP in conventional samples showed glycogen particles arranged into aggregates corresponding in size to the electron dense granules. Treatment en bloc slightly affected glycogen aggregates in A and resulted in a formation of large clumps of glycogen particles in B. It was concluded that the electron dense granules represented protein bound to glycogen in the organelles called glycosomes. Acidic action of uranyl acetate removed protein from glycosomes. The degree of this removal depended on the amount of protein present in glycosomes in the moment of fixation.

Acetates↗
PubMed1978

Ultrastructural study on the extrusion of multivesicular bodies from cardiac cells.

Cardiac conducting fibers taken from 12 dogs were studied in the electron microscope. The majority of samples contained a moderate number of multivesicular bodies (MVB's) and an extremely high number occurred in one dog. Single MVB's were found in the perinuclear region and in the cytoplasm separating myofibrils. A high accumulation of MVB's occurred at the cell periphery within cytoplasmic stalks extending into the extracellular space, in the intercalated disc, and also outside of the cell. The latter appeared to be extruded from the cell in the following way: 1) peripheral cytoplasm formed stalk-like extensions which contained MVB's; 2) the stalks detached from the cell; 3) vacuolar and sarcolemmal membranes surrounding the MVB disintegrated; 4) vesicles released from MVB adhered to the cellular surface and the coat of their membrane blended with the coat of the sarcolemma. The above pattern seems to be the same in those parts of sarcolemma which face the interstitial tissue and in the intercalated disc.

Animals↗
PubMed1977

Sarcoplasmic reticulum in the conducting fibers of the dog heart.

The ultrastructure or sarcoplasmic reticulum (SR) was studied in the conducting fibers of the dog heart. A dense network of sarcoplasmic tubules occurred in well preserved cytoplasmic areas. Some of the tubules extended into large sacs filled with finely filamentous material. The sacs often appeared in subsarcolemmal apposition connected to the sarcolemma by electron dense projections. The flattened cisternae of SR occurred beneath the sarcolemma in the myofibrillar region of the cell. Long flattened cisternae only partially apposed to the sarcolemma were quite common in one specimen. Sarcoplasmic reticulum was continuous throughout the interfibrillar spaces surrounding each myofibril. At the level of the Z-line the SR formed a quasi tubular flattened structure surrounding the Z-line and closely adhering to it.

Animals↗