The absorption of tritium-labeled
Escherichia coli
O89 Westphal-type endotoxin from the peritoneal cavity of rats was diminished by bile by 23% and by sodium deoxycholate by 47%, respectively. Practically, there is no endotoxin absorption from the intestinal tract of normal rats. The bile duct of rats was chronically cannulated for experimental purposes. A significant amount of perorally administered endotoxin absorbed from the intestinal canal into the blood in the rats treated thus. Absorption was demonstrated by the lethal effect of endotoxin on rats previously hypersensitized by lead acetate, and by the radioactivities found in the blood samples. The intestinal absorption of endotoxin in rats, rendered bile-deficient, may be prevented by sodium deoxycholate. Supported by their experimental findings, we emphasize the important role of bile acids in the defense mechanism of the macroorganism against bacterial endotoxins.
Acute X-irradiation with 350 R increased the synthesis of interferons induced by poly I : C and endotoxin in individual sera of BALB/c mice. Fractional irradiation with 4.7 or 9.4 I~ daily up to total dose levels of 728, 977 and 1828 R in three different experiments had no influence on serum interferon levels induced by Semliki Forest Virus (SFV), poly I:C or endotoxin. The Newcastle Disease Virus (NDV) induced interferon synthesis decreased in comparison to the non-irradiated control at a total dose of 400 R and attained the control level on further elevation of the total dose. The anti-NDV antibody production fell to one quarter of the control value after exposure to a total dose of 1828 R.
1. The size distribution of aggregates of liver ribosomes and their protein-synthesizing ability in vitro were studied shortly after X-irradiation of guinea pigs. 2. Sucrose-density-gradient analysis of the mitochondrial supernatant after treatment with deoxycholate revealed a gradual increase in the number of polysomes, reaching a maximum between 9 and 15 hr. after irradiation. At that period the amount of ribonucleoprotein particles reached a level 25-30% above the control. This finding was confirmed by analytical-ultracentrifugal analysis and electron microscopy. Experiments were conducted to exclude the possibility that the enrichment of polysomes in the irradiated animals had occurred during the isolation procedure. 3. The protein-synthesizing ability of total ribosomal particles was measured in vitro. This showed an increase in amino acid incorporation parallel to the progressive enrichment of polysomes. At radiation doses of up to 1000r. the protein-synthesizing capacity was dependent on the radiation dose: the higher the dose the higher the amino acid incorporation, reaching 40-60% above the control at the period of maximal polysome enrichment. Amino acid incorporation remained at this level after radiation doses of between 1000 and 3000r. The enhanced protein-synthesizing activity was due solely to the increase in the proportion of polysomes, since irradiation was without effect on the activity of single ribosomes. 4. The results of the experiments are discussed in the light of our knowledge of the effect of radiation on protein synthesis.
1. Liver RNA synthesis was studied within 24h after whole-body X-irradiation of guinea pigs that had been starved for 22-24h. 2. Microsomal RNA was labelled in vivo for 3h with [(14)C]orotic acid and the isolated labelled RNA was fractionated by sucrose-density-gradient centrifugation. Incorporation was 50-100% higher between 3 and 12h after 2000rd X-irradiation and at 22h was not elevated any further. Whole nuclear RNA was labelled with [(14)C]orotic acid for 15min. At 5h after irradiation the incorporation showed a 50-100% increase. Incorporation increased in all types of RNA studied. 3. The RNA phosphorus/DNA phosphorus ratio of whole liver gradually increased after X-irradiation. Maximal increase was found between 24 and 36h, which corresponds to a value about 40% above that of the starved control. The RNA phosphorus content of isolated ribonucleoproteins obtained from various cell fractions of the liver was similarly increased after X-irradiation. 4. Liver microsomes were obtained from X-irradiated and control animals. Microsomes were incubated in vitro with [(14)C]phenylalanine in the presence and absence of polyuridylic acid. After the incubation the microsomes were fractionated by sucrose-density-gradient centrifugation. The polyuridylic acid enhancement was twice as great in the microsomes of the control preparation as in the irradiated one. The experiment demonstrated a higher saturation of microsomes by endogenous messenger after X-irradiation. 5. RNA polymerase activity of the purified nuclear preparation was assayed. The activity of the Mg(2+)-dependent RNA polymerase activity was 50 and 200% respectively above the control values at 6 and 9h after X-irradiation. 6. Animals were treated with actinomycin D shortly before X-irradiation. This treatment abolished the radiation-induced enrichment of polyribosomes and the increase of protein-synthesizing activity. The effect of X-irradiation on the transcription of the genetic code of the liver is discussed.
Adult rats were irradiated (750 R) and were given sheep red blood cells (SRBC), with or without 100 µg E. coli·26 endotoxin, between 1 to 29 days after irradiation. Serum haemolysin titers, plaque forming cell (PFC) counts and relative spleen weights were determined 5 days after SRBC administration. During the 1st week after irradiation endotoxin treatment induced a mild decrease in PFC. From the 10th day on endotoxin resulted in a comparatively earlier regeneration of the antibody forming capacity. By the end of the 1st month the antibody response to SRBC returned to normal levels in the endotoxin + SRBC treated group, while irradiated animals remained impaired. Anti-SRBC PFC and anti-E. coli·26 antibody producing cells showed close parallelism. These results suggest that the antigenic property of endotoxin may play a role in its adjuvant action.
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