[Clotting and fibrinolytic activities in acute alcoholic golden hamsters with or without ether anaesthesia].

Fluid cadaveric blood is generally known as a characteristic of sudden death. However, it has been reported that soft blood clots have been observed in a number of cases of sudden death after alcohol drinking. Such a tendency was also recognized on autopsy cases in our laboratory.

[Radiation therapy for human renal cell carcinoma transplantable to the nude mice].

Efficacy of radiation therapy was studied using human renal cell carcinoma strain (AM-RC-3) implantable in nude mice. Cobalt 60 gamma-ray was used dosage of 5 Gy, 10 Gy, 15 Gy and 20 Gy in single, localized exposures of subcutaneously implanted tumors of the lower right femoral region. Therapeutic efficacy was determined using the Battelle Columbus Standard and evaluation of histological changes based on National Cancer Research Institute (Shimosato's classifications).

[Effects of radiation on the human renal cell carcinoma transplantable to the nude mice].

Effects of irradiation were studied using human renal cell carcinoma (AM-RC-3) implanted subcutaneously in nude mice. Tumors were irradiated locally with 60Co gamma-ray as a single dose of 5, 10, 15 and 20 Gy, then the tumor volume was measured periodically. Efficacy of irradiation was determined using Battelle Columbus Standard.

[Radiosensitization of Lewis lung tumor by perfluorochemical emulsion comparison between single and fractionated irradiation].

Previously perfluorochemical emulsion (FDAS) was shown to enhance tumor growth delay, when applied together with breathing carbogen (95% O2+5% CO2) before and during irradiation. In the present paper, radiosensitizing effects of FDAS in tumor bearing mice were examined on a single (10 Gy) and fractionated irradiation (4 Gy, 4 times) and on the dose of administration. The results were as follows; 1) All groups of single irradiation with injection of FDAS 10-40 ml/kg could enhance the radiosensitivity of LLC bearing mice.

Characterization of a mode of specific binding of fibrin monomer through its amino-terminal domain by macrophages and macrophage cell-lines.

The studies reported here probe the existence of a receptor-mediated mode of fibrin-binding by macrophages that is associated with the chemical change underlying the fibrinogen-fibrin conversion (the release of fibrinopeptides from the amino-terminal domain) without depending on fibrin-aggregation. The question is pursued by 1) characterization of binding in relation to fibrinopeptide content of both the intact protein and the CNBr-fragment comprising the amino-terminal domain known as the NDSK of the protein, 2) tests of competition for binding sites, and 3) photo-affinity labeling of macrophage surface proteins. The binding of intact monomers of types lacking either fibrinopeptide A alone (alpha-fibrin) or both fibrinopeptides A and B (alpha beta-fibrin) by peritoneal macrophages is characterized as proceeding through both a fibrin-specific low density/high affinity (BMAX congruent 200-800 molecules/cell, KD congruent to 10(-12) M) interaction that is not duplicated with fibrinogen, and a non-specific high density/low affinity (BMAX greater than or equal to 10(5) molecules/cell, KD greater than or equal to 10(-6) M) interaction equivalent to the weak binding of fibrinogen.