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J H Rust

Publications and source records attributed to J H Rust.

At least 37 records · Page 2Linked to original sources
PubMed1967

A transport medium for specimens containing Pasteurella pestis.

A medium, originally designed by Stuart and co-workers and later modified by Cary & Blair, for the maintenance and transport, without multiplication, of pathogenic bacteria contained in bacteriological specimens was tested in the laboratory and in the field in Viet-Nam to determine its effectiveness in preserving specimens known to contain Pasteurella pestis.The results indicate that this medium should be useful in diagnostic plague studies in areas where transport facilities are inadequate. Properly collected clinical specimens, sent to a central laboratory by any means and under any climatic conditions likely to be encountered in the hot tropics, should yield viable Pasteurella pestis for at least 30 days.

Culture Media↗
PubMedDate not supplied

Time sequence of cancer occurrence. Implications in low level radiation risk assessment.

A total of 8,229 C57 Black mice of both sexes were randomly assigned to various groups. In some groups, mice aged 33 +/- 3 days were submitted to either sham, neutron or cobalt external radiation at 32, 45, 63, 88 and 123 mGy or at 18, 25, 36 and 51 cGy dose levels, respectively. In other groups, mice either at birth or weaning, were injected with tritiated thymidine or tritiated water, or were given tritiated water as drinking water for the entire lifespan. The main purpose of the experiment was to investigate the low dose-response relationship of cancer induction, especially leukemogenesis and to evaluate the excess risk, using actuarial age-specific rates. Following neutron or cobalt exposure, the phenotypic occurrence of lymphocytic lymphomas was earlier in appearance and higher in yield during the first decades of lifespan in irradiated groups versus matching controls, whereas such occurrence was markedly lower in yield at a later age. Under parallel experimental conditions, induction of reticulum cell lymphomas, however, was uniformly enhanced throughout the entire lifespan. Induction rates of all tumors (reticular and solid) pooled were significantly increased, and more so following cobalt than neutron irradiation. In mice injected with tritiated thymidine, the overall tumor incidence was increased monotonically throughout the lifespan. In mice exposed to tritiated water, the incidence of lymphocytic lymphomas was markedly increased throughout the lifespan, whereas no such effect was observed for reticulum cell tumors. In the light of tumor data analysis, it appears that selection of a particular type of tumor as a dependent variable for dose-response assessment cannot disregard the primary modulation of the whole tumor spectrum, In C57 Black murine leukemogenesis, the shape and structure of the dose-response regression curve over the entire lifespan dose not fit the linear-quadratic model. It is, however, theorized that our data are consistent with the two-mutation clonal expansion model, assuming creation of initiated cells which are added to the pool of spontaneously occurring initiated cells and implying that the excess risk is initially high at early age and then decreases with increasing age following exposure. It is concluded that murine radiocarcinogenesis investigation may contribute to improving the assessment as well as understanding the underlying mechanisms of low level radiation hazards.

Animals↗
PubMedDate not supplied

Effects in animals of chronic administration of spironolactone--a review.

Spironolactone, an aldosterone antagonist, has been found effective in the treatment of certain forms of hypertension, ascites, and edematous conditions. Since patients may receive daily doses of spironolactone for many years, it is important to determine the chronic effects on tissues. This study reviews the tissue changes in rats, dogs, and monkeys receiving spironolactone daily for up to two years. Dose levels were frequently in excess of 100 times the recommended human dose. The pituitary, adrenals, and kidneys of all animals showed no significant changes. Histologic changes were noted in rat livers, thyroid, and male internal genitalia. There were alterations in monkey testes and male mammary glands. This study found no evidence to suggest that spironolactone is tumorigenic or carcinogenic. Species differences in metabolism may account for the diversity of tissue observations.

Animals↗