Okayama University Medical School

1. When hemolysed blood is administered orally to rabbits, in cases of healthy and those with blocked reticulo-endothelial systems, a transient increase in the verdohemoglobin (M. Engel) is seen in circulating blood, while in that of rabbits with impaired parenchymal liver cells, no such increase occurs. 2. On irrigation of hemolysed blood through rabbit livers, in healthy rabbits production of indirect bilirubin may be demonstrated while in that with blockage of the reticulo-endothelial system or with impaired liver parenchymal cells, this may not be seen. Moreover, in this case of blockade of the reticulo-endothelial system. production of verdohemoglobin may be demonstrated. while none whatsoever may be demonstrated in cases of impaired liver parenchmal. On the other hand on irrigation of verdohemoglobin and biliverdin solutions, in healthy and in impaired liver parenchymal cell cases, production of bilirubin may be observed while absolutely none was detected in cases of blocked reticulo-endothelial systems, 3. Concluding from the results stated above and those of clinical experiments stated elsewhere, the following process is assumed: when blood is imposed on the organism it is primarily phagocytosed by the reticulo-endothelial system, next dissolved to verdohemoglobin {M. Engel) in the parenchymal cells of the liver, and then dissolved into globin, iron, and biliverdin in the reticulo-endothelial system, of which biliverdin is further reduced to bilirubin. A portion of this remains in the circulating blood as indirect bilirubin, while the majority of it is esterized in the parenchymal cells of the liver, and proceeds to the bile ducts as direct bilirubin.

1. In the bile of rabbits, the metabolisms of biliverdin and bilirubin are in a solucible state, and which have a ratio of 2: 1 in normal animals. 2. In the production of biliverdin, the liver, especially the parenchyma of the liver has a very important role, while that of the reticulo-endothelial system is rather minor. However, in the case of glucose administration, the reduction of bilirubin from biliverdin is performed in the reticulo-endothelial system, thus conferring an important part of this system. 3. The production of bilirubin is performed primarily extrahepatically, and the participation of the extrahepatical reticuloendothelial system is of a conservative nature, thus denying us any willingness to agree to the theory of bilirubin production in the reticulo-endothelial system. 4. On administration of hemolysed blood, bile pigments in bile demonstrate a remarkable increase, while as compared when injected into the auricle veins in cases of administration through the portal vein a decline in the functions of the liver reticulo-endothelial system is seen, causing a decrease in biliverdin amount. In the former modus of administration, an occasional stimulation of the liver reticulo- endothelial system is seen, causing reduction of biliverdin to bilirubin. 5. Concluding from these facts, biliverdin in rabbit bile occupies the role of an intermediate product in the production and metabolism of bilirubin.

1. The proteolytic action of papayotin is activated by X-ray irradiation with 60 r and 1000 r, and inhibited with 200 r and 400 r. 2. The influences of X-rays upon papayotin are direct and remain unchanged for definite periods of time. 3. The proteolytic action of papayotin show wavy phenomena which correspond to the time and dose of the X-ray irradiation. 4. The proteolytic action of papayotin is considered to be inhibited by the decomposition products (polypeptides) of substrate only in the presence of some other factors.

Caryophyllaeidae Claus, 1879 1. Glaridacris limnodrili Yamaguti, 1934 Bothriocephalidae Blanchard, 1849 2. Bothriocephalus fluviatilis n. sp. 3. B. lateolabracis n. sp. 4. B. branchiostegi n. sp. 5. B. acheilognathi Yamaguti, 1934 6. B. brotulae n. sp. 7. B. apogonis n. sp. 8. Oncodiscus sauridae Yamaguti, 1934 9. Glossobothrium nipponicum n. g., n. sp. Amphicotylidae Ariola, 1899 10. Amphicotyle quinquarii n. sp. 11. Eubothrioides lamellatus n. g., n. sp. Phyllobothriidae Braun, 1900 12. Phyllobothrium triacis n. sp. 13. P. filiforme n. sp. 14. P. serratum n. sp. 15. P. laciniatum (Linton, 1889) 16. P. loculatum n. sp. 17. P. squali n. sp. 18. P. lactuca van Beneden, 1850 19. Anthobothrium rajae n. sp. 20. A. pteroplateae n. sp. 21. A. bifidum n. sp. 22. A. parvum Stossich, 1895 23. Orygmatobothrium musteli (van Beneden, 1850) 24. O. versatile Die3ing, 1854 25. Monorygma megacotyla n. sp. 26. Pithophorus vulpeculae n. sp. 27. Echeneibothrium bifidum n. sp. 28. E. tobijei Yamaguti, 1934 29. Marsupiobothrium alopias n. g ., n. sp. 30. Dinobothrium spinulosum n. sp. 31. Gastrolecithus planus (Linton, 1922) n. g. Onchobothriidae Braun, 1900 32. Acanthobothrium triads n. sp. 33. A. micracantha n. sp. 34. A. latum n. sp. 35. A. gracile n. sp. 36. A. dasybati Yamaguti, 1934 37. A. ijimai Yoshida, 1917 38. A. grandiceps n. sp. 39. Calliobothrium verticillatum (Rud., 1819) van Bened., 1850 40. Platybothrium auriculatum n. sp. 41. P. musteli n. sp. Aberrant Tetraphyllidea 42. Pelichnibothrium speciosum Montic., 1889 43. Discobothrium japonicum Yamaguti, 1934 Tentaculariidae Poche, 1926 44. Nyelinia manazo n. sp. 45. N. sphyrnae n. sp. Floricipitidae Dollfus, 1929 46. Floriceps uncinatus (Linton, 1924) Tetrarhynchidean larvae 47. Pintneriella musculicola Yamaguti. 1934 48. Microbothriorhynchus coelorhynchi n. g., n. sp. 49. Oncomegas wageneri (Linton, 1890) 50. Pterobothrium chaeturichthydis n. sp. 51. P. hira n. sp. 52. Callotetrarhynchus speciosus (Linton, 1897) 53. Symbothriorhynchus uranoscopi n. g., n. sp. 54. Nybelinia anguillae n. sp. 55. N. nipponica n. sp. 56. Otobothrium dipsacum Linton, 1897

The following results were obtained through the experiments on the cytochrome c oxidase activities and the analysis of the glycolysis and high energy phosphorus compounds in the normal bacteria and those fast to penicillin, sulfathiazol, 2.4-dimethylthiazdl, and macramin. 1. In the normal bacteria, the cytochrome c oxidase activities, glycolysis and high energy phosphorylated cycles increase accordto the order of S.57 s-type<S.57 r-type<staphylococcus aureus F. D. A. strain <staphylococcus aureus Terazima strain. 2. In the bacteria fast to penicillin originated these normal bacterial strain, the cytochrome c oxidase activities, glycolysis and high energy phosphorylated cycles increase, especially glycolysis. 3. In the bacteria fast to sulfathiazol, there are shown the same results as in the case of penicillin. 4. In the bacteria fast to 2.4-dimethylthiazol, the cytochrome c oxidase activities decrease, glycolysis increases markedly and high energy phosphorylated cycle decreases. 5. In the bacteria fast to macramin, these activities and cycles show no specific changes.

1) I designed a new micro-method for complement fixation test by means of a capillary pipette. 2) By this method, the complement-fixing antibodies in an individual mouse could be tested without taking its life. 3} The complement fixation titers in mice immunized with Japanese B encephalitis had a considerable individuality. 4) An adjuvant containing anhydrous lanoline and paraffin-oil, when mixed with Japanese B encephalitis vaccine, was effective to potent complement-fixing antibody productions in mice to this antigen.

1. In normal adults and in patients of non-hepatic diseases a transient hyperbilirubinemia occurs after peroral administration of hemolysed blood. 2. In cases of severe anchylostomiasis the serum bilirubin displays a remarkable decrease, and on imposition of hemolysed blood, no hyperbilirubinemia occurs but a relative one may be seen. 3. In patients with highly impaired functions of the parenchymal cells of the liver, neither absolute nor relative hyperbilirubinemia occurs on similar imposition of hemolysed blood. 4. Imposed blood or hemoglobin seems primarily to be phagocytosed by the reticulo-endothelial system. 5. A similar transient hyperbilirubinemia is also seen in rabbits after peroral imposition of hemohsed blood. 6. When the functions of the reticulo-endothelial system are accelerated by administration of "Koha", even incases of nonimposition of blood a hyperbilirubinemia occurs, but when hemolysed blood is imposed an additional transient increase in the hyperbilirubinemia may be detected. 7. In cases of blockage of the reticulo- endothelial system, this degree in the occurrence of hyperbilirubinemia is somewhat lower. 8. In cases of impaired liver cells by carbon tetrachloride, this decline is especially remarkable, and only a tendency of occurence can be dected. Since it is very difficult to explain this fact only by the co-existing impairment in the reticulo-endothelial system, the decline in the functions of the parenchymal cells of the liver must be placed under consideration. 9. By absorption tests of the intestines and by serological procedures, it is apparent that the perorally administerred hemoglobin may be readily absorbed from the jejunum, under any of these conditions. 10. Consequently, as for the cause of the hyperbilirubinemia occurring after peroral administration of hemolysed blood, most naturaly the reticulo-endothelial system participates, but it is impossible to neglect the part payed by the parenchymal cells of the liver.