Sodium MRI of the human kidney at 3 Tesla.

The sodium concentration gradient in the kidney (from the cortex to the medulla) serves to regulate fluid homeostasis and is tightly coupled to renal function. It was previously shown that renal function and pathophysiology can be characterized in rat kidneys by measuring the sodium gradient with (23)Na MRI. This study demonstrates for the first time the ability of (23)Na MRI to map the distribution of sodium in the human kidney and to quantify the corticomedullary sodium gradient. The study was performed on a 3T Signa LX scanner (GE) using an in-house-built quadrature surface coil. (23)Na images of volunteers were acquired using a 3D coronal gradient-echo sequence at a spatial resolution of 0.3 x 0.3 x 1.5 cm(3) in a 25-min scan time. The signal intensity (relative to the noise) increased linearly from the cortex to each of the medullae with a mean slope of 1.6 +/- 0.2 in relative arbitrary units per mm (Rel.u./mm, N = 6) and then decreased, as expected, toward the renal pelvis. Water deprivation (12 hr) induced a significant increase of 25% (P < 0.05) in this gradient. Based on these results, we suggest that sodium MRI can serve as a valuable noninvasive method for functional imaging of the human kidney.     

The inhibitory effect of polysaccharide on mumps virus multiplication

Polysaccharides derived from type-specific Friedl?nder bacilli cause inhibition of the multiplication of mumps virus in the allantoic sac of the chick embryo. As little as 5 microg. of polysaccharide is effective as an inhibitor. Inhibition of multiplication is obtained when polysaccharide is injected as long as 4 days after inoculation of virus. Chemical studies have shown that the structural configurations of the polysaccharide responsible for specific serological activity are not identical with those which determine the inhibitory effect relative to mumps virus. The possible mechanisms of the inhibition of viral multiplication by means of polysaccharides are discussed.     

The antibody response in rabbits to killed suspensions of pathogenic T. pallidum

The intravenous injection into rabbits of suspensions of dead T. pallidum derived from rabbit testicular chancres regularly caused the appearance of Wassermann and flocculation antibodies in significantly increased titer. Control suspensions of cultured treponemes (Reiter strain) added to extracts of normal testes were ineffective. This suggests that the Wassermann and flocculation reagin elaborated during syphilitic infection may be an antibody to T. pallidum which happens to cross-react with alcoholic extracts of mammalian tissue. The antisera did not cause the agglutination of suspensions of pathogenic T. pallidum, living or dead, did not give specific complement fixation with those suspensions, and did not usually cause the living treponemata to lose their infectiousness. Animals immunized with such aqueous suspensions for as long as 4 months, or with organisms suspended in a water-in-oil emulsion, were not demonstrably resistant to infection. As few as ten living organisms inoculated intradermally into animals "immunized" with as many as 38 billion dead treponemata regularly produced typical darkfield positive infections; and two of five animals inoculated intratesticularly with ten organisms were also infected. The contradiction involved in the production of antibodies cross-reacting with a non-specific antigen, and the non-appearance of specific antibodies against the organism used as antigen, is discussed in the text.