JaLCDOI | 10.18926/AMO/32533 |
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FullText URL | fulltext.pdf |
Author | Szirmai, Endre| Sachs, Volkmar| |
Abstract | Die Autoren berichten uber die guten Behandlungsmoglichkeiten in der Praxis bei verschiedenen peripheren venosen Durchblutungsstorungen bei Erkrankungen der Bewegungsapparate, bei leichteren Fallen von arteriellen DurchblutungsstOrungen und bei einigen Fallen von Hirnblutungen mit Vasotonin und Vasotonin-forte und auch in vitro-Blutgerinnungsuntersuchungen. Bei den erwahnten Fallen kann man die therapeutische Wirkung noch mit Vasotonin-forte-Salbe gut unterstutzen. Die Autoren konnen nachweisen, daB Extr. Arnicae insbesonder in dem Vasotonin-forte die hamodynamische und die blutgerinnungshemmende Wirkung von extr. Aesculi Hippercastani gut verstairkt. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 137 |
End Page | 147 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
NAID | 120002311362 |
JaLCDOI | 10.18926/AMO/32534 |
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FullText URL | fulltext.pdf |
Author | Gray, C. H.| |
Abstract | In this review of the chemistry, biochemistry and chemical pathology of the bile pigments I am well aware that I shall ask many more questions than I am able to answer. It seems appropriate that the subject should be considered under the five headings: -Chemistry; Formation from Haem Proteins; Transport in the Blood; Conjugation and Transport to the Bile; and Changes in the Gut. I shall conclude with a brief account of the early labelled bilirubin. Because investigation of the pathological significance of the chemical changes undergone in the body is possible only if the chemical structures of the bile pigments are accurately known, my department in London has been very much concerned during the last 15 years with the chemistry of the bile pigments. The work I shall describe has been carried out in collaboration with Dr. NICHOLSON, Dr. KULCZYCKA, Dr. COLE, Dr. PETRYKA and more recently by Mr. STOLL and Miss LEMMON. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 149 |
End Page | 163 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 4242308 |
NAID | 120002311535 |
JaLCDOI | 10.18926/AMO/32535 |
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FullText URL | fulltext.pdf |
Author | Kaneda, Shoken| |
Abstract | In the mixed tissue culture of mouse lymphocytes with addition of PHA the rate of the appearance of large and intermediate cells increases markedly, but which side of the two cell groups have reacted stronger remains obscure. In order to solve this problem, mixed cultures were conducted in such a way that only one cell group of the two would react. Namely, one cell group was exposed to C0 6).irradiation (Table 2) prior to the culture and cultured with another viable cell group (FJ test group, Table 2) to see the percentage of the appearance of large and intermediate cells. Simultaneously, the skin homograft from respective donor mouse was transplanted to each other and the survival days of each skin graft were compared. As a result it has been shown that the percentage of blastformation and the survival time of the skin transplant in each group prove to be in an inverse relation. The results of these mixed cultures indicate that the extent of blast. formation reflects significantly the difference in B-2 histocompatibility antigens. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 89 |
End Page | 94 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 4242309 |
NAID | 120002312263 |
JaLCDOI | 10.18926/AMO/32536 |
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FullText URL | fulltext.pdf |
Author | Nakashima, Youichi| |
Abstract | The regional lymph node cells of the mice sensitized with Ehrlich ascites tumor cells is known to possess a substance that shows antitumor activity on target cells (JTC-II cells). For the purpose to clarify the localization of this substance the regional lymph node cells from such sensitized mice were treated with trypsin solution of different concentrations (1.0 %, 0.2 %, and 0.01 %), and the tissue culture was carried out with JTC.II cells. As a result it was found that these lymph node cells lost antitumor activity. Next, by the differential contrifugation of these sensitized lymphocytes we obtained F1 fraction (700 g, sediment), F2 (8,500 g sediment), F3 (100,000 g sediment) and F4 (100,000 g supernatant). In the presence of each of these fractions tissue culture was conducted with JTC-II cells as target cells, and it was found that the substance with antitumor activity is contained abundantly in F2 fraction (8,500 g sediment) and F4 fraction (100,000 g supernatant). After giving due consideration to the results of these two experiments and also to the available data in the literature, we assume that the substance with antitumor activity is contained in the cell membrane component. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 95 |
End Page | 104 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 4242310 |
NAID | 120002312235 |
JaLCDOI | 10.18926/AMO/32537 |
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FullText URL | fulltext.pdf |
Author | Wakabayashi, Akira| |
Abstract | <P>The mitochondrial, the microsomal, and the supernatant fractions were prepared from the cell homogenate of tumors induced by viruses, such as adenovirus type 12, SV 40, and Rous sarcoma virus, etc. and the antigenicities of these fractions were investigated. In the virus-induced tumors, there existed no antigenicity common to the mitochondrial and the microsomal fractions as in the tumors induced by chemical carcinogens, and the highest antigenicity was recognized in the mitochondrial fraction. Therefore, the properties of the tumor cell mitochondria were precisely investigated with virus-induced tumor mitochondria. 1. The mitochondria of tumors induced by viruses have clearly the specific antigenicity. 2. This specific antigenicity of virus.induced tumor mitochondria IS common to all the virus-induced tumors used in the present study. 3. This tumor mitochondria.specific antigenicity is found commonly in all the tumor mitochondria in the present experiments. 4. The specific cancer antigenicity of tumor cell mitochondria does not exist in normal organ mitochondria, but the regenerating organ mitochondria exhibit a slight antigenicity common to cancer cell mitochondria. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 105 |
End Page | 124 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 4310523 |
NAID | 120002311874 |
JaLCDOI | 10.18926/AMO/32538 |
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FullText URL | fulltext.pdf |
Author | Seki, Shuji| |
Abstract | 1. A cytochrome oxidase-rich submitochondrial membrane (green membrane) was obtained from beef heart mitochondria after extraction of flavoproteins, cytochrome b, Cll C, etc. by treating with deoxycholate and potassium chloride. 2. The green membrane was formed by self assembly from the membrane fragments (flat sheets), which derived from the cristae membrane of mitochondria and had essentially the same particulate structure as the green membrane. 3. The green membrane exhibited regular arrays of small particles on the surface, measuring approximately 50 to 60 A in diameter with center to center distance of about 70 A. These particles sometime were arranged in a woven structure on the surface. 4. Both the configuration of the particles and the regularity of the arrangement were influenced by detergents and temperature. 5. Green membranes as well as beef heart mitochondria and electron transfer particles commonly retained membrane-structure after sonication and exhibited higher specific activity of cytochrome oxidase than that of purified cytochrome oxidase, if the activity is calculated on the basis of heme a concentration (sec1 / 10 m,lJ.moles of heme a/3 ml). The results suggest that the active sites of cytochrome oxidase are arranged on the surface of these membranes. 6. From these results and other experimental findings, an intimate correlation between cytochrome oxidase and the particles observed on the green membranes is suggested. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 69 |
End Page | 88 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 4310524 |
NAID | 120002312173 |
JaLCDOI | 10.18926/AMO/32539 |
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FullText URL | fulltext.pdf |
Author | Hasegawa, Makoto| |
Abstract | The following conclusions were drawn from the above data concerning the RES function to sequestrate 51Cr-labelled heat-damaged iso-erythrocytes in mice. (l) When the hematological disorders of mice were induced, the RES of the liver and spleen reacted in the same manner. (2) The RES function of the bone marrow and liver were observed to react reversely except in the case of splenectomized mice. (3) Human gamma globulin hypersensitization and chloramphenicol administrations suppressed RES function of the bone marrow and augmented that of the liver and spleen. (4) The RES function of the bone marrow was activated after splenectomy. (5) The massive human gumma globulin administration was followed by the increased RES function of the bone marrow and by the suppressed one of the liver and spleen. |
Amo Type | Article |
Publication Title | Acta Medicinae Okayama |
Published Date | 1969-04 |
Volume | volume23 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 125 |
End Page | 136 |
NCID | AA00041342 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 4186811 |
NAID | 120002311603 |