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Biomedical subjects

B M Wagner

Publications and source records attributed to B M Wagner.

At least 127 records · Page 7Linked to original sources

Primary myocardial disease in the cat. A model for human cardiomyopathy.

Thirty-four cats with primary myocardial disease were studied. The cats were divided into two groups, depending on the clinical, hemodynamic, angiocardiographic, and pathologic findings. Group A consisted of those cats with hypertrophic cardiomyopathy and Group B consisted of those cats with congestive cardiomyopathy. Similarity in the characteristics of cardiomyopathy in the human cat was found. Both Group A and Group B consisted predominantly of mature adult male cats. The most common presenting signs were dyspnea and/or thromboembolism, systolic murmurs with gallop rhythms on auscultation, cardiomegaly with (Group A) or without (Group B) pulmonary edema, abnormal electrocardiograms, elevated left ventricular end diastolic pressures, and angiocardiographic evidence of mitral regurgitation with left ventricular concentric hypertrophy (Group A) or left ventricular dilatation (Group B). Some cats in Group A also had evidence of left ventricular outflow obstruction. The principal pathologic findings in these cats were left atrial dilatation, symmetric hypertrophy or asymmetric septal hypertrophy of the left ventricle (Group A), and dilatation of the four cardiac chambers (Group B). Aortic thromboembolism was commonly observed in both groups. These clinical and pathologic findings indicate that cardiomyopathy in the cat is similar to the two most common forms of cardiomyopathy in the human (hypertrophic cardiomyopathy, with and without obstruction, and congestive cardiomyopathy).

Age Factors↗

Studies on the mechanism of lithium action: preliminary report.

Preliminary observations in a small animal sample reveal that chronic lithium treatment in rats produced significant changes in the microvillous processes on the cell surface of the choroid plexus. These alterations may be associated with increased intracellular choroidal volume. The type of changes noted by SEM suggest an alteration in movement of water into the extracellular areas of the brain. This basic alteration produced by lithium in the secretory/absorptive capacity of the chorid plexus is probably reversible.

Animals↗

In memoriam.

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History, 20th Century↗

Studies in rheumatic fever. VI. Ultrastructure of chronic rheumatic heart disease.

The fine structure alterations in the atrium and atrial appendage, mitral valve and papillary muscle are described in 11 matched patients with chronic rheumatic heart disease. The muscle changes consisted of loss of myofilaments and accumulation of lipid and osmiophilic dense bodies. The connective tissue stroma of the atrium and the mitral valve showed extensive deposition of collagen and elastic fibers. There were numerous foci of collagen degeneration, characterized by fraying of the collagen fibers and accumulation of homogeneous granular material at these sites. Although the muscle changes were more striking, the connective tissue alterations appear important in the evolution of the chronic disease. The extent of collagen degeneration appeared to parallel the degree of collagen formation. The muscle fiber degeneration and connective tissue alterations did not correlate with the clinical findings. At the resolution of the electron microscope, the continuing process in the rheumatic heart appears to be primarily collagen formation and degradation rather than primary degeneration of the muscle fibers. It is the balance of these processes which determine the clinical state of the patient. Acute muscle damage along with evidence of inflammation do not seem to be associated with progressive, chronic rheumatic heart disease.

Adult↗