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Biomedical subjects

B A Kakulas

Publications and source records attributed to B A Kakulas.

At least 109 records · Page 6Linked to original sources

On the specificity of the histochemical technique for sarcoplasmic reticular adenosine triphosphatase: a light and electron microscopic study.

The specificity of the histochemical localization of the calcium activated adenosine triphosphatase (ATPase) activity of the sarcoplasmic reticulum (SR) at pH 7.4 was studied using a calcium-citro-phosphate technique. The latter involves the splitting of ATP by ATPase producing phosphate ions which then react with calcium and citrate to form an insoluble reaction product. This reaction product was detected by both light and electron microscopy. Light microscopic examination showed a darkly stained continuous reticular pattern of reaction product which surrounded individual myofibrils. This reticular pattern of reaction product was distinctly dissimilar to that found when the histochemical reactions for mitochondrial or myofibrillar ATPase were performed. Ultrastructural investigations demonstrated the presence of discrete foci of electron dense reaction product in close association with the membranes of the SR in striated muscle fibres. Only occasional flecks were seen in the vicinity of mitochondria or myofilaments. The possibility is considered that the reticular pattern of staining achieved by the calcium-citro-phosphate technique may reflect the distribution of the "extra ATPase" of the SR, an enzyme implicated in the process of calcium uptake and muscle relaxation.

Adenosine Triphosphatases↗

Gliomas: a review of an 11-year series.

A series of gliomas is reviewed in an endeavour to establish the efficacy or otherwise of the various forms of treatment available. In general, it would seem that prognosis depends upon the activity of tumour cells and the anatomical relationships of the lesion. From the experience of this series it appears that wide resection, if this is possible, offers a longer survival time than any other form of treatment.

Adolescent↗

Experimental muscle diseases.

The mode of pathological reaction of the skeletal muscle fibres to injury is now well understood as a result of the large number of experimental studies and the wide variety of techniques applied to the problem, as recounted above. The most notable aspect of the reaction of the injured muscle fibre is the remarkable stereotyped character of the resulting changes as demonstrated by many diverse agents producing surprisingly similar results. The initial lesion is essentially local coagulative necrosis of the muscle fibre. If the animal survies, such necrosis is inevitably followed by a series of biological reactions inherent in muscle and which lead to the removal of dbris and the proliferation of myoblasts...

Animals↗

Muscular dystrophy in young girls.

Muscular dystrophy occurred in four girls. In only one of these was the syndrome both proximal and with pseudo-hypertrophy, thus clinically resembling the x-linked Duchenne type of the disease. The evidence for a primary dystrophic process existing in the four individuals is based on the laboratory findings of very high serum creatine kinase levels, myopathic E.M.G. appearances and muscle biopsies. However, each case is clinically different (one is proximal with contractures, another limb girdle with facial involvement and the fourth is distal) and worthy of documentation. The recent demonstration of a neurogenic basis for several myopathies previously considered to be dystrophic in nature has not caused us to revise our view that true muscular dystrophy does occur in girls but that the "Duchenne-like" type is rare.

Adolescent↗