The Use of 5 Per Cent Dextrose in 0.2 Per Cent Saline as a Priming Solution

Transfusion ◽  
1966 ◽  
Vol 6 (S1) ◽  
pp. 397-399
Author(s):  
Bruce C. Paton ◽  
Yoshimasa Miyauchi
Keyword(s):  
1949 ◽  
Vol 89 (6) ◽  
pp. 631-641 ◽  
Author(s):  
Sydney M. Friedman ◽  
Constance L. Friedman

Desoxycorticosterone acetate in pellet form was administered for 51 days to albino rats of the Sherman strain which also received 1 per cent saline as drinking water. Treatment was stopped in representative groups at 25, 37, and 51 days so that the regression of blood pressure and renal changes could be observed. It was noted that both the elevation in blood pressure during treatment and its reversal when treatment was stopped were closely correlated with corresponding changes in renal mass. In the time for which the process was studied it did not become irreversible. Removal of both kidneys from DCA-treated animals aggravated the hypertension, suggesting that the kidneys are actively concerned with the excretion and possible inactivation of the steroid.


1966 ◽  
Vol 45 (3) ◽  
pp. 366???371 ◽  
Author(s):  
WARREN W. FIEBER ◽  
JOHN R. JONES
Keyword(s):  

1948 ◽  
Vol 87 (4) ◽  
pp. 329-338 ◽  
Author(s):  
Sydney M. Friedman ◽  
John R. Polley ◽  
Constance L. Friedman

Small doses of DCA administered at intervals in pellet form are capable of raising the blood pressure, altering renal function, and changing the electrolyte pattern in the intact rat. The concomitant feeding of 1 per cent saline intensifies the process. The elevation in blood pressure occurs prior to demonstrable changes in renal excretory function. The alteration in renal function consists first of a reduction in CPAH with the maintenance of a normal filtration rate. Filtration fraction is elevated while there is no reduction in renal plasma flow per unit of tubular excretory tissue. Later, filtration is interfered with and renal ischemia occurs. The electrolyte change is characterized by a sustained fall in plasma K and Cl, a rise in plasma Na, an increase in the Na/Cl ratio, and finally an elevation of Na plus K. Plasma Ca is unaffected. These observations suggest the possible etiological significance of the adrenal cortex in some types of hypertension.


Blood ◽  
1963 ◽  
Vol 22 (6) ◽  
pp. 703-717 ◽  
Author(s):  
ISAAC DJERASSI ◽  
ALBERT ROY

Abstract Rat platelets were frozen in liquid nitrogen (-195 C.) without losing their morphologic integrity and their ability to circulate in thrombocytopenic recipient animals. The simultaneous presence of two preservative agents—a sugar and dimethylsulfoxide—was instrumental in this respect. The use of single agents was only slightly or not at all effective. The combination of 5 per cent Dextrose and 5 per cent DMS in plasma permitted in individual experiments a circulating yield of frozen platelets as high as 70 to 87 per cent of the numbers observed when fresh platelets were given. The bleeding time was reduced to normal whenever the platelet levels were increased to more than 300,000/mm3.


1942 ◽  
Vol 88 (372) ◽  
pp. 407-414 ◽  
Author(s):  
R. Ström-Olsen ◽  
E. de C. Kite

In 1936 Tomesco (1) and his co-workers described changes in the crystallization of sodium chloride produced by the addition of small amounts of cerebrospinal fluid to 0.8 per cent. saline. A drop of *8 per cent. NaCl solution dried on a microscope slide at 75° C. produces a thin circumference of crystals surrounding an empty space. If normal C.S.F. is added in proportions of 1 C.S.F. to 20, 40 or 60 parts saline the central empty space is replaced by a thin translucent film of crystals, which in the higher dilutions begins to show lacunae. In a dilution of 1 in 120 this translucent film is reduced to a narrow strip along the inner margin of the circumference. Microscopically the translucent area is found to consist of concentric circles, feather- or spear-shaped crystals, parallel lines, needles, etc., well organized in the low dilutions, but not organized in a dilution of 1 in 120. This is regarded as the normal crystal picture.


1918 ◽  
Vol 27 (3) ◽  
pp. 425-442 ◽  
Author(s):  
Hideyo Noguchi

1. The virulence of vaccine virus for the testicular tissues increases until its maximum is finally reached. The selective increase is not associated with any loss, reduction, or modification in its virulence for the skin. A highly potent testicular vaccine is also highly active for the skin. 2. The testicular strain of vaccine virus has no more tendency to localize in various organs than the ordinary skin strain. Both may localize in adjacent lymph nodes when introduced intravenously, subcutaneously, or intratesticularly in sufficiently large quantities, but other organs are not involved. 3. Intravenous inoculation of an excessive amount of a powerful vaccine virus (1 to 2 cc. of undiluted stock emulsion), irrespective of whether it is from the testis or the skin, will result in a generalized eruption over the entire body surface of rabbits. The eruption may be confluent on mucous membranes of the mouth, nostrils, genitalia, etc. Intratesticular or subcutaneous inoculations of the same virus fail to produce this effect. 4. Subcutaneous or intravenous introduction of much smaller quantities of the virus does not cause an appreciable local or general reaction in the rabbit. But the animals which have once received these injections become refractory to a subsequent vaccination as applied to the skin. It seems probable that an active immunity has been conferred. 5. Experiments on the viability and resistance of the testicular strain of vaccine virus indicate that the virus is best preserved when emulsified with Ringer's solution or 0.9 per cent saline solution. Distilled water, while apparently one of the best diluents, fails to keep the virus active as long as Ringer's or saline solutions. As would be expected, the lower the temperature is, the longer the virus retains its viability. At 18° or 37°C., the deterioration of the virus proceeds rapidly. However, a small part of the virus survives after many weeks' standing at 37°C. 6. Of the two most commonly employed chemical agents for the ripening (eliminating bacteria) process of the green vaccine pulp, glycerol and phenol, the latter is the less injurious. Phenol in concentration above 2 per cent destroys the virus within 24 hours at any temperature, but it has almost no injurious effect when used in 0.5 to 1 per cent. On the other hand, glycerol is a powerful vaccinicide. When used in full strength it destroys the virus within 24 hours, even at 4°C. In a concentration of 40 per cent, that ordinarily recommended for the ripening, the virus retains some of its virulence for about half a year at 4°C., while at higher temperatures the same concentration kills the virus within 1 to 2 months. The virus preserved in distilled water or Ringer's solution under similar temperature conditions remains more active during this period. From this it may be concluded that glycerol is not an indifferent agent, as is assumed by many, but a powerful vaccinicide when used in high concentrations. The injurious effect is markedly accelerated at 18° or 37°C. 7. The vaccine virus retains its virulence better in a sealed tube containing either hydrogen, nitrogen, or air than in an open receptacle. The virus deteriorates when placed in a sealed tube with oxygen or carbon dioxide. 8. Desiccation decreases to a considerable degree the virulence of the vaccine virus. In the dried state the virus retains its viability about as long as does the emulsion, but it is not protected from the deterioration caused by age under various conditions. 9. Iodine is a powerful disinfectant for the vaccine virus, but its sodium and potassium salts have no effect. Various bile salts destroy the vaccine virus when employed in sufficient concentration.


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