日本獣医師会雑誌
Online ISSN : 2186-0211
Print ISSN : 0446-6454
ISSN-L : 0446-6454
18 巻, 10 号
選択された号の論文の5件中1~5を表示しています
  • 有沢 道弥, 高橋 健, 内野 富弥, 渡辺 仙, 中井 隆夫, 野田 宗兵, 中村 良一
    1965 年18 巻10 号 p. 620-625
    発行日: 1965/10/20
    公開日: 2011/06/17
    ジャーナル フリー
    total of 49 cases of various diseases were treated by intramuscular injection with kanamycin sulfate solution.
    1) Eight adult cows affected with bronchopneumonia, bronchitis, or liver abscess were injected with 3 to 5g daily for 1 to 4 days. Seven of them recovered in 2 to 8 days.
    2) Five calves affected with bronchitis, bronchopneumonia, or calf scour were injected with 1 to 3g daily for 1 to 3 days. All of them recovered in 2 to 6 days.
    3) A horse affected with bronchitis was given once and recovered in 2 days.
    4) Three adult swine affected with puerperal fever or erysipelas were injected with 2 to 3g once or for 2 days and recovered in 2 to 4 days.
    5) Two piglets suffering from bronchopneumonia were injected with 0.5g once. One of them recovered in 2 days, and the other died at 2 days.
    6) Twenty-eight dogs affected with distemper, bronchitis, bronchopneumonia, black tongue, nephritis, endometritis, and suppurative trauma and 2 cats with external otitis were injected with 0.25×0.5g daily for 1 to 6 days. Of the 30 cases, 22 recovered in 3 to 15 days.
    7) The rate of recovery due to kanamycin therapy was 73.3% in the small animals, 92.8% in the large animals, and 80.0% in the swine.
    8) When injected jointly with penicillin, kanamycin seemed to show a powerful antibacterial effect.
  • 野田 周作, 堀江 牧夫, 野村 正行, 大西 堂文
    1965 年18 巻10 号 p. 626-628
    発行日: 1965/10/20
    公開日: 2011/06/17
    ジャーナル フリー
  • 村上 大蔵
    1965 年18 巻10 号 p. 631-632
    発行日: 1965/10/20
    公開日: 2011/06/17
    ジャーナル フリー
  • 松岡 恵爾, 来住 輝彦, 長瀬 烝治
    1965 年18 巻10 号 p. 633-635
    発行日: 1965/10/20
    公開日: 2011/06/17
    ジャーナル フリー
    Two mammals, Meles anakuma and Felis catus, kept in separate cages at the Tennoji zoo in Osaka succumbed, two months apart, showing a cut watery diarrhea.
    At antopsy, Salmonella enteritidis was isolated from the intestinal contents of both animals.
  • 免疫発現の時期と接種鶏体内のウイルス分布について
    西村 豊, 川島 秀雄, 山本 富史, 小山 敬之
    1965 年18 巻10 号 p. 636-640
    発行日: 1965/10/20
    公開日: 2011/06/17
    ジャーナル フリー
    In the first part of this series (17) living Newcastle disease virus (NDV) vaccine made by the Philips-Duphar Company in the Netherlands was tested for immunity and proved to be very effective to prevent the infection of NDV. This time, living NDV vaccine made by Dr. Salsbury's Laboratory in the U. S. A. was examined for safety and potency, and the following results were obtained.
    1) Some 3-to 8-day-old chickens were vaccinated per os and intranasally with 2 doses, and then challenged with the virulent strain SATO 21 days, 1 month, and 2 months after vaccination. The survival rate was 80 to 100%. A similar experiment was performed with laying hens, and a 100% survival rate was obtained. The titers of HI and SN of these vaccinated birds were <1-320 and 10-1000, respectively; that is, they were higher than those of non-vaccinated birds, which were <5 and <1, respectively.
    2) The development of immunity seemed to occur 7 days after vaccination.
    3) The presence of vaccine-virus was proved in the alimentary canal and trachea of chickens sacrificed on the first to 7th day after vaccination, the feces of a chicken killed 3 days after vaccination, and the heart blood, a mixed tissue emulsion (spleen, pancreas, lung, and kidney) of a chicken slaughtered 14 days after vaccination. It was also demonstrated in the liver and a mixed tissue emulsion (spleen, pancreas, kidney, and lung) of non-vaccinated chickens which had been raised in the same cage with the vaccinated birds, 14 and 21days after vaccination.
    4) In the course of immunization, only three birds died from bacterial contamination (1.4%). The other birds showed no clinical abnormality nor drop in laying rate. Thirty-day-old chickens vaccinated per os with 10 to 50 doses survived for 14 days, without showing any clinical abnormality.
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