scholarly journals THE ACTION OF X-RAYS ON EUPLOTES TAYLORI AND ASSOCIATED BACTERIA

1933 ◽  
Vol 16 (3) ◽  
pp. 397-406 ◽  
Author(s):  
Morden G. Brown ◽  
J. Murray Luck ◽  
Grace Sheets ◽  
C. V. Taylor

1. The minimum lethal dose of x-rays for Euplotes taylori was determined. Under the conditions of this investigation a 220 second exposure (2110 Roentgen units per second) was required to kill the protozoon. Much less exposure was sufficient to kill the associated bacteria. This difference in resistance permits the sterilization of protozoa with comparative ease. 2. Irradiation of Euplotes for 100 to 220 seconds caused a complete but temporary cessation of ciliary activity in many of the organisms, the percentage so affected increasing with the length of irradiation. 3. Pure cultures of Pseudomonas fluorescens and Bacillus coli, K13, separately irradiated, were found to be killed much more readily than protozoa,—the former in 15 seconds exposure (2530 Roentgen units per second) and the latter in 45 seconds. 4. The death of these organisms by irradiation was not due to the action of toxic products in the medium since separately irradiated media were not found to be toxic. 5. Irradiated bacteria were found unsatisfactory for the nutrition of Euplotes, previously sterilized either by irradiation or washing.

1918 ◽  
Vol 28 (5) ◽  
pp. 571-583
Author(s):  
Julia T. Parker

1. The livers of rabbits inoculated with cultures of Bacillus typhosus or Bacillus prodigiosus under certain conditions contain a toxic substance extractable with salt solution. When the toxic extracts are injected intravenously into normal rabbits the latter animals develop symptoms resembling those of anaphylactic shock and succumb. The lethal doses of the toxic extracts are far smaller than those of normal liver extract. 2. The livers of rabbits injected with typhoid antigen also yield a toxic extract. 3. Boiling as well as filtration through a Berkefeld filter only partially detoxicates the extract. 4. Tolerance to one to two lethal doses of the poisonous extracts can be induced by cautious immunization. 5. Rabbits actively immunized to Bacillus typhosus or Bacillus prodigiosus usually resist one lethal dose of the homologous liver poison; and animals tolerant to the typhoid liver poison resist one minimum lethal dose at least of Bacillus typhosus. 6. Typhoid immune serum is not detoxicating either in vivo or in vitro for the typhoid liver poison. 7. The liver poisons are specific, since rabbits actively immunized to either Bacillus typhosus or Bacillus prodigiosus withstand at least one minimum lethal dose of the homologous but not of the heterologous-liver poisons.


1919 ◽  
Vol 30 (5) ◽  
pp. 417-436 ◽  
Author(s):  
Wade H. Brown ◽  
Louise Pearce

The essential facts to be gathered from these studies of the toxicologic action of N-phenylglycineamide-p-arsonic acid may be summarized very briefly. The substance is one which lends itself well to almost any method of administration and can be given to animals in very large doses. The tolerance of different animal species varies rather widely but with one exception the reaction of laboratory animals to toxic doses of the drug is of favorable character. That is, toxic effects are confined to doses relatively close to the minimum lethal dose and the recovery of animals from sublethal intoxications is remarkably rapid and complete. This feature of the action of the drug makes possible the repeated administration of even very large doses at comparatively short intervals of time without incurring the dangers incident to cumulative action or to superposition of toxic effects. On the contrary, by taking advantage of this peculiarity of action, it is possible to develop such a degree of tolerance on the part of animals that the dose of the drug administered can be progressively increased to a point well above that which is fatal to the normal animal, and this stands out as the feature of the toxicologic action of N-phenylglycineamide-p-arsonic acid which is of greatest significance in the use of the drug for therapeutic purposes.


1919 ◽  
Vol 29 (5) ◽  
pp. 485-512 ◽  
Author(s):  
Samuel A. Levine

1. Cats vary considerably in their susceptibility to strophanthin and in the extent of the difference between the minimum lethal dose and the minimum toxic dose. 2. The amount of strophanthin necessary to produce a toxic effect in a given cat is independent of the speed of administration to a period of 4 hours. An improvement in the clinical administration of the drug is thereby indicated. 3. A theory of the action of strophanthin is formulated which reconciles the results which point to the importance of the total amount taken up by the heart with those inidicate that the concentration of the drug is the determining factor.


1956 ◽  
Vol 33 (3) ◽  
pp. 502-507
Author(s):  
A. H. MOHAMED ◽  
O. ZAKY

1. Two methods for preparation of the toxin in a purified crystalline form are described. 2. The toxin is probably a secondary proteose. 3. It has an excitatory parasympathetic effect on the uterus of the guinea-pig and on the intestine of the rabbit. The effect is abolished by atropine. 4. It causes excessive salivary secretion, again abolished by atropine. 5. It causes partial or complete block of perfused isolated amphibian and mammalian hearts. It also causes extrasystoles. Both effects are abolished by atropine. 6. The minimum lethal dose for rats is 0.035-0.05 mg. toxin/100 g. body weight. Atropine did not save the life of the animal although it prolonged it. 7. The possibility of a histamine-like action of the venom is discussed.


1961 ◽  
Vol 200 (5) ◽  
pp. 1039-1042 ◽  
Author(s):  
Bernard D. Newsom ◽  
Donald J. Kimeldorf

A lethal dose of X irradiation can be made sublethal by the fractionation of a dose into a series of smaller doses separated by adequate time intervals. The results reported here demonstrate how an environmental stress, such as cold, may affect this mitigating action of dose fractionation. Rats were maintained at 6 C while receiving a total dose of 600 r in one or eight exposures with various intervals between exposures. A greater interval was required between radiation exposures at 6 C than at 23 C to reduce the lethal response following irradiation. From the results of the food consumption measurements, it appears that cold exposure emphasizes the consequence of the reduced food intake which follows daily doses of 75 r in the rat. The irradiated rat was able to increase the amount of food consumed during cold exposure; however, the increase was not sufficient for adaptation. The lowered consumption which followed eight daily 75-r exposures was sufficient to cause death in pair-fed rats maintained at 6 C, but not at 23 C.


1935 ◽  
Vol 118 (809) ◽  
pp. 316-320 ◽  

Any means of increasing the sensitiveness of human tumours to X-rays or gamma rays would certainly change the outlook on the treatment of cancer in many sites, more especially for the types of tumours which are sometimes termed radio-resistant. The experiments recorded here were mainly carried out with a fairly rapidly growing sarcoma of the rat (F. 16), originally given us by the Imperial Cancer Research Fund in 1921. We (1933) have already referred to the modification which it has since undergone, particularly to the extraordinary increase in its rate of growth and cellularity of structure. These changes are probably due to the technique used in its transplantation, and to the use of a strain of rats particularly sensitive to tumour implantation. With Jensen’s rat sarcoma, 100% of progressive tumours is generally obtained from grafts and 90% is looked upon as a rather poor result. Another obvious advantage for experiments of the type described here is that spontaneous absorption of an established tumour of either F. 16 or J. R. S. is extremely rare. In the first experiments established tumours were exposed for varying lengths of time to carefully measured doses of X-rays generated at about 170 kV and filtered by 10 mm of aluminium. The minimum amount of radiation necessary to cause the disappearance of all tumours of each type is referred to here as the “lethal” dose. It is expressed by time—for sarcoma F. 16 it is 200 minutes, approximately equivalent to 1000 r. A dose of X-rays amounting to 30-40% of the lethal dose generally has some deterrent effect on the growth of the tumour; 40% of the lethal dose very rarely causes the disappearance of a well-established tumour. The effect becomes more definite and lasts longer as the dose is increased and the majority of tumours disappear after a dose which is 75% of the lethal dose. Great care has always been taken to expose only the tumour, as it has been observed that the dose of X-rays required to cause complete disappearance is considerably less when even a small area of surrounding tissue is irradiated. The actual size of the tumour at the time of irradiation also influences the final result; quite small, young tumours may disappear with a comparatively small dose of X-rays, while very large ones are sometimes little affected by a much larger dose, in spite of strict attention to the principle of dosage which is measured by the ionization at the lowest level of the tumour. Most of the tumours used for these experiments were between 16 mm and 22 mm in diameter at the time of exposure to X-rays.


2016 ◽  
Author(s):  
John H. Duffus ◽  
Monica Nordberg ◽  
Douglas M. Templeton

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