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  <title>DSpace コレクション: 1995-06</title>
  <link rel="alternate" href="http://hdl.handle.net/10564/1494" />
  <subtitle>1995-06</subtitle>
  <id>http://hdl.handle.net/10564/1494</id>
  <updated>2026-04-10T15:42:05Z</updated>
  <dc:date>2026-04-10T15:42:05Z</dc:date>
  <entry>
    <title>AUDITORY P300 EVENT-RELATED POTENTIALS AND MINI MENTAL STATE EXAMINATION PERFORMANCE IN DEMENTIA ; EFFECTS OF IDEBENONE AND VINPOCETINE</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/825" />
    <author>
      <name>Kishimoto, Toshifumi</name>
    </author>
    <author>
      <name>Hiraoka, Yukie</name>
    </author>
    <author>
      <name>Oribe, Hiroaki</name>
    </author>
    <author>
      <name>Inoue, Makoto</name>
    </author>
    <author>
      <name>Ueda, Atsushi</name>
    </author>
    <author>
      <name>Matsuyama, Mitsuharu</name>
    </author>
    <author>
      <name>Inoue, Yuichiro</name>
    </author>
    <author>
      <name>Itoh, Takashi</name>
    </author>
    <author>
      <name>Yoshitomi, Katsunari</name>
    </author>
    <author>
      <name>Miyagi, Tetsuro</name>
    </author>
    <author>
      <name>Masuda, Nobuaki</name>
    </author>
    <author>
      <name>Tatsuda, Hiroshi</name>
    </author>
    <author>
      <name>Nakanishi, Yasuo</name>
    </author>
    <author>
      <name>Negoro, Hideki</name>
    </author>
    <author>
      <name>Ikawa, Genro</name>
    </author>
    <id>http://hdl.handle.net/10564/825</id>
    <updated>2017-06-11T23:20:26Z</updated>
    <published>1995-06-29T15:00:00Z</published>
    <summary type="text">タイトル: AUDITORY P300 EVENT-RELATED POTENTIALS AND MINI MENTAL STATE EXAMINATION PERFORMANCE IN DEMENTIA ; EFFECTS OF IDEBENONE AND VINPOCETINE
著者: Kishimoto, Toshifumi; Hiraoka, Yukie; Oribe, Hiroaki; Inoue, Makoto; Ueda, Atsushi; Matsuyama, Mitsuharu; Inoue, Yuichiro; Itoh, Takashi; Yoshitomi, Katsunari; Miyagi, Tetsuro; Masuda, Nobuaki; Tatsuda, Hiroshi; Nakanishi, Yasuo; Negoro, Hideki; Ikawa, Genro
抄録: One group of twenty-one demented patients were administered Idebenone &#xD;
90 mg/day for eight weeks, the other group of thirty-two demented patients were adminis- &#xD;
tered Idebenone 90 mg/day plus Vinpocetine 15 mg/day for eight weeks. Mini Mental State &#xD;
Examination (MMSE) was carried out and auditory event-related potentials (ERPs) were &#xD;
recorded pre-treatment, after four weeks treatment and after eight weeks treatmet. &#xD;
MMSE performance was significantly improved with treatment in both groups. Central &#xD;
P300 latency was shortened in the group which was treated with Idebenone and Vinpocetine, &#xD;
but not in the group which was treated with Idebenone alone. Based on the obtained results, &#xD;
we were convinced that administration of Idebenone and Vinpocetine was very useful in the &#xD;
treatment of vascular dementia.</summary>
    <dc:date>1995-06-29T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA) AND MIDLATENCY AUDITORY EVOKED RESPONSES</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/824" />
    <author>
      <name>Kishimoto, Toshifumi</name>
    </author>
    <author>
      <name>Higashiura, Naoto</name>
    </author>
    <author>
      <name>Hiraoka, Yukie</name>
    </author>
    <author>
      <name>Sakiyama, Shinobu</name>
    </author>
    <author>
      <name>Kirita, Ikuhiro</name>
    </author>
    <author>
      <name>Noriyama, Yoshinobu</name>
    </author>
    <author>
      <name>Itoh, Naoto</name>
    </author>
    <author>
      <name>Ueda, Atsushi</name>
    </author>
    <author>
      <name>Oribe, Hiroaki</name>
    </author>
    <author>
      <name>Ikawa, Genro</name>
    </author>
    <id>http://hdl.handle.net/10564/824</id>
    <updated>2017-06-11T23:20:26Z</updated>
    <published>1995-06-29T15:00:00Z</published>
    <summary type="text">タイトル: DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA) AND MIDLATENCY AUDITORY EVOKED RESPONSES
著者: Kishimoto, Toshifumi; Higashiura, Naoto; Hiraoka, Yukie; Sakiyama, Shinobu; Kirita, Ikuhiro; Noriyama, Yoshinobu; Itoh, Naoto; Ueda, Atsushi; Oribe, Hiroaki; Ikawa, Genro
抄録: The human 'P1' middle latency evoked potential is postulated to be generat- &#xD;
ed in the thalamus by a cholinergic component of the ascending reticular activating system. &#xD;
To test the midbrain function of dentatorubral-pallidoluysian atrophy (DRPLA), recording &#xD;
of middle latency response to click stimuli were carried out in a DRPLA family which was &#xD;
detected with the aid of molecular diagnosis. Comparisons between the DRPLA members &#xD;
and the normal members indicated normal Pa responses but P1 component is abnormal in &#xD;
DRPLA. This P1 abnormality suggests that the midbrain cholinergic cells in DRPLA may &#xD;
be dysfunctional.</summary>
    <dc:date>1995-06-29T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>担癌マウスにおける腫瘍の発育, 生存, 血中リンパ球サブセットに及ぼす脾摘の影響</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/823" />
    <author>
      <name>渡邉, 巌</name>
    </author>
    <id>http://hdl.handle.net/10564/823</id>
    <updated>2017-06-11T23:20:26Z</updated>
    <published>1995-06-29T15:00:00Z</published>
    <summary type="text">タイトル: 担癌マウスにおける腫瘍の発育, 生存, 血中リンパ球サブセットに及ぼす脾摘の影響
著者: 渡邉, 巌
抄録: The spleen is the largest peripheral lymphoid tissue and plays an important &#xD;
role as one of the immune associated organs, but the effect of splenectomy in cancer therapy &#xD;
remains obscure. The tumor growth, host survival, and the change of T-lymphocyte subsets &#xD;
(Lyt2⁺, L3 T4⁺) in blood and spleen were studied using tumor bearing mice (Colon 26 &#xD;
bearing BALB/c mice) to investigate the effect of splenectomy, and the following results &#xD;
were obtained. &#xD;
1. In cotrol group (CONT), the subcutaneous mass appeared macroscopically in the 8th &#xD;
day after tumor inoculation (Colon 26,2×10⁴), and started to death on the 30th day. Lyt2⁺ &#xD;
and L3 T4⁺ ratio of spleen elevated to the highest level on the 6th day and returned to the &#xD;
same level with tumor growth, on the other hand, Lyt2⁺ ratio of blood kept constant &#xD;
regardless of tumor growth, and L3 T4⁺ ratio dropped to the lowest level on the 9th day, &#xD;
and returned to the same level with tumor growth. &#xD;
2. When splenectomy was done on the 5th day after tumor inoculation (SPN 5 ; early &#xD;
phase), Lyt2⁺ ratio of blood was significantly decreased (p&lt;0.05) as compared with other &#xD;
groups, and subsequent enhancement of tumor growth and the shortening of survival period &#xD;
were observed (p&lt;0.05). &#xD;
3. On the 10th day after tumor inoculation (SPN 10 ; middle phase), Lyt2⁺ ratio of blood &#xD;
was significantly elevated (p&lt;0.05) as compared with other groups, and subsequent inhibition of tumor growth and elongation of survival period were observed. &#xD;
4. On the 20th day after tumor inoculation (SPN 20 ; late phase), blood T-cell subsets did &#xD;
not show great change, and subsequent enhancement of tumor growth and the shortening of &#xD;
survival period were observed. &#xD;
These results suggest that splenectomy of tumor bearing mice induces the change of &#xD;
blood T-cell subsets, and affects the tumor growth and host survival ; early splencectomy &#xD;
works tumor-enhancement, and middle splenectomy works tumor-inhibition ; also surgical &#xD;
damage as well as late splenectomy works tumor-inhibition.</summary>
    <dc:date>1995-06-29T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>好酸球における活性化抗原CD69の発現</title>
    <link rel="alternate" href="http://hdl.handle.net/10564/822" />
    <author>
      <name>森井, 武志</name>
    </author>
    <id>http://hdl.handle.net/10564/822</id>
    <updated>2017-05-29T06:07:23Z</updated>
    <published>1995-06-29T15:00:00Z</published>
    <summary type="text">タイトル: 好酸球における活性化抗原CD69の発現
著者: 森井, 武志
抄録: The activation antigen, CD69, has been shown to be expressed on activated &#xD;
lymphocytes. CD69 has also been shown to be associated with the signal transduction &#xD;
process. In this study, the author performed flowcytometric analysis of CD69 expression on &#xD;
eosinophils obtained from the bronchoalveolar lavage fluid (BALF), pleural effusion, or &#xD;
peripheral blood (PB) of various patients. Whatever the diseases were, lung eosinophils &#xD;
obtained from BALF or pleural effusion expressed significant levels of CD69, whereas most &#xD;
PB eosinophils did not express CD69. Further, CD69 expression was induced on PB &#xD;
eosinophils by the activation of interleukin-3 (IL-3), IL-5, granulocyte macrophage colony &#xD;
stimulating factor (GM-CSF), interferon-a (IFN-α) and phorbol myristate acetate (PMA), &#xD;
but platelet activating factor (PAF) did not induce CD69 expression. CD69 expression &#xD;
induced by IL-3 or GM-CSF was in a dose and time dependent manner. The expression &#xD;
could be induced significantly at low concentration of 10 pg/ml and was detected after &#xD;
stimulation for two hours. These findings suggest that CD69 expressions are restricted to &#xD;
local eosinophils, and that local eosinophils may stand at a different activating state from &#xD;
PB eosinophils.</summary>
    <dc:date>1995-06-29T15:00:00Z</dc:date>
  </entry>
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