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  • 香山 滉一郎, 森下 政夫, 張 国鋒
    粉体および粉末冶金
    2006年 53 巻 5 号 419-429
    発行日: 2006年
    公開日: 2006/12/19
    ジャーナル オープンアクセス
    The phase diagrams of the Ni-Mo-
    B
    and Ni-W-
    B
    ternary systems in the region of less than 50mol%
    B
    were constructed by thermodynamic calculation, based on the data obtained by thermodynamic measurement of the related materials. We found three ternary eutectic points and three or two ternary peritecto-eutectic points as follows:
    E1
    :L (1365K, 71.5mol%Ni-6.
    0
    mol%Mo-
    22
    .5mol%
    B
    )=(Ni)+
    Ni3B
    +
    NiMo2B2

    E2
    :L (1355K, 62.5mol%Ni-2.5mol%Mo-30.5mol%
    B
    )=
    Ni3B
    +
    Ni2B
    +
    NiMo2B2

    E3
    :L (1445K, 42.
    0
    mol%Ni-30.6mol%Mo-10.
    3
    mol%
    B
    )=(Ni)+NiMo+
    NiMo2B2

    P1:L (1812K, 34.
    9
    mol%Ni-42.
    3
    mol%Mo-
    22
    .
    8
    mol%
    B
    )+MoB=
    Mo2B
    +
    NiMo2B2

    P2:L (1633K, 42.
    3
    mol%Ni-40.4mol%Mo-17.
    3
    mol%
    B
    )+Mo=
    Mo2B
    +
    NiMo2B2

    P3
    :L (1812K, 53.5mol%Ni-33.7mol%Mo-12.
    8
    mol%
    B
    )+Mo=NiMo+
    NiMo2B2

    E1
    :L (1622K, 51.
    0
    mol%Ni-31.6mol%W-17.4mol%
    B
    )=(Ni)+W+
    NiW2B2

    E2
    :L (1260K, 71.
    0
    mol%Ni-7.
    0
    mol%W-
    22
    .
    0
    mol%
    B
    )=(Ni)+
    Ni3B
    +
    NiW2B2

    E3
    :L (1291K, 65.4mol%Ni-4.
    8
    mol%W-29.
    8
    mol%
    B
    )=
    Ni2B
    +
    Ni3B
    +
    NiW2B2

    P1:L (2115K, 23.
    8
    mol%Ni-43.1mol%W-33.1mol%
    B
    )+WB=
    W2B
    +
    NiW2B2

    P2:L (1657K, 48.
    9
    mol%Ni-33.1mol%W-18.
    0
    mol%
    B
    )+
    W2B
    =W+
    NiW2B2

    The calculated phase diagrams are expected to be useful for the development of new Ni-based heat-, corrosion- or wear-resistance alloys.
  • Özkan ASLANTAŞ, Ebru Şebnem YILMAZ
    Journal of Veterinary Medical Science
    2017年 79 巻 6 号 1024-1030
    発行日: 2017年
    公開日: 2017/06/16
    [早期公開] 公開日: 2017/04/27
    ジャーナル フリー

    This study aimed to determine the prevalence of fecal carriage of extended spectrum β-lactamase (ESBL) and/or plasmidic AmpC β-lactamase (pAmpC) producing Escherichia coli among dogs (n=428) in Turkey. Polymerase chain reaction (PCR) and sequencing were used to characterize genes encoding β-lactamase and plasmid mediated quinolone resistance (PMQR). Antimicrobial susceptibility testing and PCRs for virulence genes and phylogenetic groups were also performed. Cefotaxime resistant

    E
    . coli isolates were detected in 95 (
    22
    .2%) of the swab samples. Sequencing analysis results showed occurrence of various β-lactamase genes: blaCTX-M-15 (62), blaTEM-
    1b
    (42), blaCMY-2 (
    22
    ), blaCTX-M-
    3
    (16), blaCTX-M-1 (15), blaOXA-1 (
    9
    ) and blaSHV-12 (
    3
    ) alone or in combination. The most frequently encountered phylogenetic group was group A1 (35.
    8
    %), followed by group D2 (
    22
    .1%),
    B
    1 (15.
    8
    %), D1 (
    9
    .5%),
    A0
    (7.4%),
    B22
    (5.
    3
    %) and
    B23
    (4.2%), respectively. PMQR genes, aac(6’)-Ib-cr, qnrS1 and qnrB10 were detected in 25.
    3
    , 10.5 and 1.1% of the isolates, respectively. While all isolates were susceptible to imipenem and amikacin, resistance rates to non-β-lactam antibiotics ranged from 20.
    0
    % for tobramycin to 56.
    8
    % for tetracycline. The virulence genes were only detected in 34 (36.2%) of the isolates and this isolates carried single or various combination of virulence genes of iucD, papC, papE, f17a-A and eaeA. Four isolates were identified as human virulent pandemic CTX-M-15 producing
    E
    . coli
    clone O25
    b
    :ST131/
    B
    2. To the best of our knowledge, this is the first study to show fecal carriage of ESBL/pAmpC type β-lactamase producing
    E
    . coli
    isolates among dogs in Turkey.

  • Hisao Masaki, Atsushi Tabuchi, Yasuhiro Yunoki, Yoshiko Watanabe, Daisuke Mimura, Hiroshi Furukawa, Takahiko Yamasawa, Takeshi Honda, Hiroki Takiuchi, Kazuo Tanemoto
    Annals of Vascular Diseases
    2014年 7 巻 3 号 227-231
    発行日: 2014年
    公開日: 2014/09/25
    [早期公開] 公開日: 2014/07/30
    ジャーナル フリー
    Objective: This study was conducted to determine whether to perform endovascular intervention or bypass surgery as a treatment option for critical limb ischemia (CLI) with lesions in the popliteal artery or below.Subjects and Methods: A total of 150 patients (164 limbs) with CLI underwent endovascular intervention or bypass surgery for lesions in the popliteal artery or below at our department between May 1995 and June 2011. Therapeutic outcomes were examined by surgical technique. An indication for endovascular intervention was established with the combination of (1) poor general condition, and (2) a stenotic or occlusive lesion ≤5 cm.Results: The bypass group (group
    B
    ) comprised 119 patients (
    99
    males, 20 females) with 131 affected limbs at 46 to 89 years of age (mean: 70 years). The endovascular intervention group (group
    E
    ) comprised 31 patients (25 males, 6 females) with 33 affected limbs at 47 to 89 years of age (mean: 72 years). There was no significant difference in patient demography between the two groups. Regarding preoperative complications, hypertension was observed in 54% and 61% of the subjects in groups
    B
    and
    E
    , respectively, diabetes in 36% and 55%, renal dysfunction in 29% and 58%, ischemic heart disease in 27% and 32%, and cerebrovascular disorder in 18% and 23%; renal dysfunction accounted for a significantly higher percentage in group
    E
    . As for early postoperative complications, subjects in group
    B
    experienced wound infections (6 patients), hemorrhage (2), thrombosis (2), pneumonia (1), and another complication (1), and those in group
    E
    experienced wound infections (1) and another complication (1). The hospital mortality rate was
    0
    .
    8
    % (1 patient) for group
    B
    and
    0
    % for group
    E
    . The
    3
    -year cumulative primary patency rate was 72% for group
    B
    and 54% for group
    E
    ; the rate was significantly higher for group
    B
    . The
    3
    -year secondary patency rate was
    82
    % for group
    B
    and 60% for group
    E
    . The
    3
    -year limb salvage rate was 86% for group
    B
    and
    82
    % for group
    E
    ; there was no significant difference between the two groups. The 5-year survival rate was 57% for group
    B
    and 42% for group
    E
    ; the survival rate was significantly lower for group
    E
    .Conclusion: For the study population of CLI patients with lesions in the popliteal artery or below, the patency rate was higher for the bypass group than for the endovascular intervention group, whereas there was no difference in the limb salvage rate. Based on the findings in prognosis for survival, the indication for endovascular intervention at our department is believed to be appropriate. (*English translation of Jpn J Vasc Surg 2013;
    22
    : 715-718)
  • 第1編血清蛋白との結合について
    橋本 孝夫
    CHEMOTHERAPY
    1973年 21 巻 1 号 38-44
    発行日: 1973/01/25
    公開日: 2011/03/08
    ジャーナル フリー
    The binding of penicillin G and other 29 antibiotics to the bovine plasma proteins, a part of the pharmacokinetics of antibiotics, was investigated by the ultrafiltrating technique at 4°C.
    As the rates of the binding, inactivation, recovery and binding activity, following values were obtained in order : 64.
    9
    to
    82
    . 7%, 11. 96 to 56. 85%, 7. 77 to 25. 75% and
    8
    .
    9
    to 34. 11% in penicillin antibiotics;
    0
    to 61. 4%,
    0
    to 10. 66%,
    0
    . 49 to 12.
    8
    % and 14. 91 to 41. 72% in glycoside antibiotics; 91.
    0
    to
    99
    .
    9
    %, 16.
    0
    to 46. 19%, 44. 98 to 71. 01% and 4. 33 to 21. 06% in tetracycline antibiotics; 55.
    22
    to 94. 1%, 5. 37 to 57. 36%, 1. 32 to 31. 5% and
    9
    . 66 to 40. 65% in macrolide antibiotics; and 72. 6 to 95. 68%, 14. 34 to 51. 85%,
    8
    . 19 to 30. 12%, and 17. 28 to 41. 54% in chloramphenicol antibiotics, respectively.
    Optimum pH of the binding of antibiotics to the plasma proteins was in the range 5.
    0
    to
    8
    .
    0
    , i.
    e
    .
    8
    .
    0
    in penicillin antibiotics, 5.
    0
    in glycoside antibiotics, 7.
    0
    to
    8
    .
    0
    in tetracycline antibiotics, 6.
    0
    to 7.
    0
    in macrolide antibiotics, and 7.
    0
    to
    8
    .
    0
    in chloramphenicol antibiotics, respectively.
  • Suguru TAKATSUTO, Kiyomi KOBAYASHI, Tsuyoshi WATANABE, Hiroki KURIYAMA, Tokuo FURUSE
    Agricultural and Biological Chemistry
    1988年 52 巻 12 号 3217-3218
    発行日: 1988年
    公開日: 2006/04/05
    ジャーナル フリー
  • Sen-fang Sui, Erich Sackmann
    The Journal of Biochemistry
    1992年 111 巻 1 号 129-138
    発行日: 1992年
    公開日: 2008/11/18
    ジャーナル フリー
    In the first part of the present work the interaction of glycophorin with dimyristoylphosphatidylcholine (DMPC) is studied by freeze fracture electron microscopy, densitometry, calorimetry, and 90° static light scattering. An exothermic lipid/protein interaction energy of WP=190 kJ•mol-1 was found by application of the well known Van Laar relation for the displacement of the freezing point and the Gibbs-Duhem relationship. Secondly, the effects of Ca2+ on the lipid/protein interaction were studied. Following Ca2+ addition a remarkable decoupling of the interaction of the glycophorin head group with the bilayer surface was revealed by densitometry and gold-labeling electron microscopy. It is estimated that about 80% of lipid once disturbed by the adsorption of glycophorin head groups is decoupled after addition of Ca2+. Thirdly, the selective interaction of glycophorin with binary lipid mixtures was studied, including the mixtures of DMPC with dimyristoylphosphatidylserine (DMPS) and dilauroylphosphatidylcholine (DLPC), and the mixture of dipalmitoylphosphatidylcholine (DPPC) with DLPC.
  • *森元 陽子, 川原 幸一, 菊池 清志, 松山 孝司, 中島 結実子, 小薗(藤崎) 清香, 町頭 三保, 丸山 征郎, 和泉 雄一
    会議録・要旨集 フリー
  • 斉 洋之, 高津戸 秀, 池川 信夫, 田中 洋子, スミス コニー, デルカ F.ヘクター
    Chemical and Pharmaceutical Bulletin
    1984年 32 巻 10 号 3866-3872
    発行日: 1984/10/25
    公開日: 2008/03/31
    ジャーナル フリー
    Chemical synthesis of (
    22
    E
    , 24R)- and (
    22
    E
    , 24S)-1, 24-dihydroxy-
    Δ22
    -vitamin
    D3
    has been achieved starting with the commercially available dinorcholenic acid acetate. Synthesis involved introduction of the 1-hydroxy group by a reduction of the 1, 2-epoxide generated by epoxidation of the 1, 4, 6-trien-
    3
    -one. The side chain on the steroid was then constructed by means of a Wittig reaction followed by introduction of the Δ7 bond by standard methods and its protection with 1-phenyl-1, 2, 4-triazoline-
    3
    , 5-dione. Subsequent reduction of the hydroxy groups in the steroid side chain followed by reduction of the Diels-Alder addition products yielded the both 24-isomers. The 5, 7-dienes were irradiated and the corresponding vitamin D compounds isolated. Nuclear magnetic resonance was used to identify individual isomers. The (
    22
    E
    , 24S)-1, 24-hydroxyvitamin
    D3
    compound bound equally well to the chick intestinal cytosol receptor as 1, 25-dihydroxyvitamin
    D3
    , while the 24R-isomer was approximately ten times less active. In vivo, both isomers were less active than 1, 25-dihydroxyvitamin
    D3
    ; however, the 24S-isomer was considerably more active than the 24R-isomer approaching the activity of 1, 25-dihydroxyvitamin
    D3
    .
  • Yukichi Yamaguchi, Jian-zhi Runan(Gen), Teruaki Nagahara
    Journal of the Physical Society of Japan
    1975年 38 巻 4 号 911-916
    発行日: 1975/04/15
    公開日: 2007/06/01
    ジャーナル 認証あり
    The gamma-ray spectrum and the conversion-electron spectrum are measured in the decay of the 116mIn activity. Directional correlations are also measured for 818–1293 and 1097–1293 keV cascades. The M1-
    E
    2 mixing ratio δ, and the
    E
    0
    -
    E
    2 mixing ratio μk are obtained for 818.7 keV
    22
    +→21+ transition to be δ=1.52
    0.22
    +
    0.26
    , and μk≤6.1×10−4 respectively. The
    E
    2 branching ratio
    B
    (
    E
    2;
    22
    +→
    0g
    +):
    B
    (
    E
    2;
    22
    +→21+):
    B
    (
    E
    2;
    22
    +→01+) is determined to be
    0
    .0158:1.
    0
    :5.86.
  • 小林 優, 神田 扶由子, S. M. D. Kumar, Ch. V. Lakshmana Rao, D. Srinivasa Rao, D. Venkata Rao, C. Bheemasankara Rao
    天然有機化合物討論会講演要旨集
    1990年 32 巻 20
    発行日: 1990/09/25
    公開日: 2017/08/18
    会議録・要旨集 フリー
    Melithasterols A-D (1-4), isolated from a gorgoinan coral Melithaea ocracea of Okinawa, were shown to be cholestane-, 24-methyl-
    22
    -dehydrocholestane-,
    22
    -dehydrocholestane-, and 24-methylenecholestane-derivatives. respectively, having a common
    3
    β, 7α -dihydroxy-5α, 6α-epoxy-Δ^
    8
    steroid nucleus. This was confirmed by direct comparison with the authentic sample prepared by lead tetra-acetate oxydation of cholest-6-ene-
    3
    β, 5α,
    8
    α-triol
    3
    -monoacetate. Twelve new polyhydroxysterols were isolated from an Alcyonium sp. (7,
    8
    ,
    9
    ), and Sclerophytum sp. (14,16,19
    b
    ,20,21,
    22
    a,23,26,28) soft corals collected off the coasts of the Andaman and Nicobar Islands in the Indian Ocean. All the Sclerophytum sp. soft corals contained 17a or its 25-deacetyl derivative. Compounds 7 to
    9
    were identified as 24-methylenecholest-5-ene-
    3
    β, 16β-diol-
    3
    -
    0
    -α-L fucoside (7) and its 7β-(
    8
    ) and 7α-hydroxy (
    9
    ) derivatives. Compound 14 was shown to be 24S-24-methylcholest-5-ene-
    3
    β,25ξ,26-triol and was correlated to the known compound 15 by 5α, 6β-glycolation. Compound 16 was shown to be 5β, 6α-isomer of 17
    b
    , correlating to 17
    b
    by PCC oxidation followed by dehydration. Compound 19
    b
    was identified with 25-deacetyl derivative of the known compound lobosterol (19a) by hydrolysis of authentic lobosterol. Compounds 20 and 21 were shown to be 7-dehydro-(20) and
    22
    E
    -dehydro-(21) derivative of 17a and 17
    b
    , respectively, by comparisons of their spectral data with reference compounds. Compounds
    22
    a and 23 were 24S-methylcholestane-
    3
    β, 5α 25-triol-6-one 25-monoacetate (
    22
    a) and its 25-deacetoxyl derivative (23). Partial PCC oxidation of 17a afforded
    22
    a. Compounds 26 (andamansterol) and 28 (nicobarsterol) were shown to be gorgost-5-ene-
    3
    β,
    9
    α. 11α, 21-tetrol and novel secosteroid, 11,21-cyclo-
    B
    -homo-11-oxa-
    9
    , 11-secoergostane-
    3
    β, 6α, 12ξ-triol-
    9
    -one, respectively, by spectral analyses (H-HCOSY, HMQC, HMBC).
  • 大石 勉, 木村 規
    高分子論文集
    1976年 33 巻 3 号 141-146
    発行日: 1976/03/25
    公開日: 2010/02/26
    ジャーナル フリー
    N-(2-フルオレニル) -マレイミド (I), N-1-(4-アセトキシナフチル) -マレイミド (II), N-2-(
    9
    -アセトキシフルオレニル) -マレイミド (III) の単独重合, 共重合をアゾビスイソブチロニトリル (IV) を開始剤としてテトラヒドロフラン中, 60℃で行った. 単独重合の初速度 (Rp) は, Rp=k [I] 2.11 [IV]
    0.64
    , Rp=k [II] 2.26 [IV]
    0.72
    , Rp=k [III] 1.76 [IV]
    0.52
    となった. kは速度定数である. 全重合の活性化エネルギー (
    E
    ), 頻度係数 (A) は
    E
    =26.4kcal/mol (I), 23.
    3
    kcal/mol (II),
    22
    .
    8
    kcal/mol (III), A=
    3
    .4×1015 (I), 2.7×1011 (II), 1.5×1011 (III) となった. またN置換マレイミドとメタクリル酸メチル (V) との共重合におけるモノマー反応性比, Q,
    e
    値を次のように決定した.
    I (M1) -V (M2) 系で, r1=
    0
    .24, r2=
    0
    .93, Q1=
    0
    .43,
    e1
    =1.
    82
    , II (M1) -V (M2) 系で, r1=
    0
    .17,
    r22.29
    , Q1=
    0
    .51,
    e1
    =1.37, III (M1) -V (M2) 系で, r1=
    0
    .068, r2=1.34, Q1=
    0
    .87,
    e1
    =1.90となった.
  • Masao Morishita, Koichiro Koyama, Kouichi Maeda, Guofeng Zhang
    Materials Transactions, JIM
    1999年 40 巻 7 号 600-605
    発行日: 1999年
    公開日: 2007/06/01
    ジャーナル フリー
    The phase diagram of the Ni–W–
    B
    ternary system in the region of less than 50 mol%
    B
    was constructed by thermodynamic calculation based on the regular solution approximation. We found three ternary eutectic points and two ternary peritecto-eutectic points as follows:
    E1
    : L(1622 K, 51.
    0
    mol%Ni-31.6 mol%W-17.4 mol%
    B
    )=(Ni)+W+
    NiW2B2

    E2
    : L(1260 K, 71.
    0
    mol%Ni-7.
    0
    mol%W-
    22
    .
    0
    mol%
    B
    )=(Ni)+
    Ni3B
    +
    NiW2B2

    E3
    : L(1291 K, 65.4 mol%Ni-4.
    8
    mol%W-29.
    8
    mol%
    B
    )=
    Ni2B
    +
    Ni3B
    +
    NiW2B2

    P1: L(2115 K, 23.
    8
    mol%Ni-43.1 mol%W-33.1 mol%
    B
    )+WB=
    W2B
    +
    NiW2B2

    P2: L(1657 K, 48.
    9
    mol%Ni-33.1 mol%W-18.
    0
    mol%
    B
    )+
    W2B
    =W+
    NiW2B2

    The calculated phase diagram is expected to be useful for the development of new Ni-based heat-, corrosion- and wear-resistance alloys strengthened by
    NiW2B2
    .
  • *嶋田 照子, 菅野 直之, 好士 亮介, 小幡 純, 仙田 直樹, 田中 一, 落合 邦康, 伊藤 公一
    特定非営利活動法人 日本歯周病学会学術大会 プログラムおよび講演抄録集
    2007年 2007s 巻 B-8-1020
    発行日: 2007年
    公開日: 2007/05/07
    会議録・要旨集 フリー
  • Yasuyuki Gono, Manabu Fujioka, Tamotsu Toriyama
    Journal of the Physical Society of Japan
    1970年 29 巻 2 号 255-258
    発行日: 1970/08/05
    公開日: 2007/06/01
    ジャーナル 認証あり
    The gamma-ray spectrum and the conversion-electron spectrum are measured in the decay of the Tb152 activity. The L-subshell electron lines of the 586.7 keV
    22
    +→21+ transition are separated by the ion-free beta-ray spectrometer. The M1-
    E
    2 mixing ratio, δ2, and the dimensionless ratio X of
    E
    0
    -
    E
    2 mixing of the 586.7 keV transition are obtained to be δ2
    0
    .16 and
    0
    .034≤X
    0
    .038, respectively. The
    E
    2 branching ratio
    B
    (
    E
    2;
    22
    +→
    0g
    +):
    B
    (
    E
    2;
    22
    +→21+):
    B
    (
    E
    2;
    22
    +→01+) is determined to be
    0
    .023 : 1.
    0
    : 5.6.
  • Mohd Suhail, Mohd Faizul Suhail, Hina Khan
    Journal of Clinical Biochemistry and Nutrition
    2008年 43 巻 3 号 210-220
    発行日: 2008年
    公開日: 2008/10/31
    ジャーナル フリー
    We compared three groups of pregnant women: placebo with normotensive women, group A which included preeclamptics, and group
    B
    which comprised preeclamptics who were supplemented their diets with vitamins C and
    E
    . MDA increased from 6.
    22
     ± 2.
    8
    (placebo) to
    8
    .48 ± 1.2 (A) and
    8
    .02 ± 1.
    8
     nmol/gHb (
    B
    ). NO concentrations were enhanced from 19.
    3
     ± 4.2 (P) to 23.
    8
     ± 6.4 (A) and 24.1 ± 5.4 μmol/L (
    B
    ). GSH contents were decreased from 10.42 ± 2.81 (P) to
    8
    .02 ± 2.92 (A) and
    9
    .39 ± 1.02 μmol/g Hb (
    B
    ), whereas GSSG concentrations increased from
    0
    .98 ± 
    0
    .28 (P) to 1.24 ± 
    0
    .29 (A) and 1.08 ± 
    0
    .12 μmol/g Hb (
    B
    ). SOD activity decreased 23% in A and 14% in
    B
    ; GRx decreased 27% in A and 5.5% in
    B
    ; GPx decreased 12% in A and
    9
    .6% in
    B
    . Catalase activity, however, increased 27% in A and 29% in
    B
    as compared to control. Thus, we conclude that the use of vitamins C and
    E
    should be considered for the control of certain important biochemical indices during the development of preeclampsia; however, further studies are needed to develop methods for the prevention of preeclampsia in women at high risk.
  • Keishi Hata, Fuyuki Sugawara, Naganori Ohisa, Saori Takahashi, Kazuyuki Hori
    Biological and Pharmaceutical Bulletin
    2002年 25 巻 8 号 1040-1044
    発行日: 2002年
    公開日: 2002/08/01
    ジャーナル フリー
    We screened the differentiation-inducing activities of 39 mushroom extracts from Akita prefecture, Japan, on the mouse osteoblastic cell line, MC
    3
    T
    3
    -
    E
    1. Sixteen phosphate buffered saline (PBS),
    8
    boiled PBS, 14 ethanol and 12 methanol extracts induced alkaline phosphatase (ALP) activities, an indicator of MC
    3
    T
    3
    -
    E
    1 cell differentiation. The enzyme activities were markedly induced by extracts of Tricholoma auratum, and we isolated the active compound from methanol extracts of this mushroom. Physical data for the isolated active compound were identical to those for (
    22E
    ,24R)-ergosta-7,
    22
    -diene-
    ,5α,6β-triol (1). 1 induced ALP activities of MC
    3
    T
    3
    -
    E
    1 cells and promoted cell proliferation. To investigate the relationships between the chemical structure and differentiation-inducing activity of the compound, ALP-inducing activities of MC
    3
    T
    3
    -
    E
    1 cells by 1, ergosterol (2), ergocalciferol (
    3
    ), cholesta-
    ,5α,6β-triol (4), 7-dehydrocholesterol (5) and cholecalciferol (6) were tested. The enzyme activities of MC
    3
    T
    3
    -
    E
    1 cells were increased
    3
    .
    0
    -fold by 10 μM 1 and 2.4-fold by 10 μM 4. However, 2,
    3
    , 5 and 6 did not induce MC
    3
    T
    3
    -
    E
    1 cell ALP activity at
    0
    .1—10 μM. These results suggested that the OH groups at C-5 and/or C-6 of 1 and 4 played an important role in their differentiation-inducing activities on MC
    3
    T
    3
    -
    E
    1 cells. Furthermore, 1 suppressed induction of MC
    3
    T
    3
    -
    E
    1 cell apoptosis by serum starvation.
  • 百目鬼 郁男, 中原 達夫, 山内 亮
    家畜繁殖研究會誌
    1974年 20 巻 2 号 76-80
    発行日: 1974/08/30
    公開日: 2008/05/15
    ジャーナル フリー
    性周期における牛の末梢血中遊離estrogen測定にITTRICH螢光法を応用して次の成績を得た。
    Ittrich colorの最大波長をspectrofluorometer Hitachi MPF-2AおよびType203で測定した結果,励起光538nm,螢光552.5nmであった。この螢光特性は
    E1
    ,
    E2
    および
    E3
    にそれぞれ共通であった。実際の測定では最大波長が接近しているので感度は若干低下するが510~520nmで励起し•螢光側552•5±
    22
    •5nmを読み,ALLENの補正を行なった。この条件において
    E1
    ,
    E2
    および
    E3
    -methyletherの最少検出量は1ngであった。回収率補正の目的で加えた6,7-
    3H
    -
    E2
    -17βの全過程における回収率は平均60.
    3
    ±11.7%であった。正常性周期を示す黒毛和種2頭の頸静脈血についてestrogenを分画測定した。その結果,両牛共
    E1
    ,
    E2
    の各消長型は性周期の全期間を通じてほぼ同じ傾向を示したが,
    E2
    E1
    にくらべ全般に高値であった。また
    E3
    は検出されなかった。これらの牛のtotalestrogenは発情前期に増加し,排卵前に鋭いピーク(35.
    3
    および
    99.8ng
    /l;
    E15.9
    および
    16.0ng
    /l,
    E229.4
    および
    83.8ng
    /l)を形成し,排卵後は急激に減少して最低値(
    3
    .
    8
    ~
    5.3ng
    /l;
    E11.6
    および
    1.9ng
    /l,
    E22.2
    および
    3.4ng
    /l)を示した。黄体期の最高値(10.1および
    27.0ng
    /l;
    E12.4
    および
    3.4ng
    /l,
    E27.7
    および23.6ng/l)は排卵後6~
    8
    日に認めた。すなわちestrogenの血中濃度は性周期の間に2つのピークを形成することを認めた。
  • 小林 優, 家坂 貴子, 中野 江身子, 平山 耕一郎
    天然有機化合物討論会講演要旨集
    1989年 31 巻 71/P2-1
    発行日: 1989/09/17
    公開日: 2017/08/18
    会議録・要旨集 フリー
    Six new cembranoids sarcophytol P (
    3
    ), R (4), S (5), K (
    8
    ), F (11), and T (13) were isolated from the soft coral Sarcophyton glaucum. Sarcophytol P (
    3
    ) was shown to be the 20-hydroxy derivative of the major component sarcophytol A (1), and afforded the cyclization product 6 in CHCl_
    3
    at room temperature, in a same way as in 1. Sarcophytols R (4) and S (5) were correlated to 1, by conversion of its 7R,
    8
    R and 7S,
    8
    S epoxide derivatives. Sarcophytol K(
    8
    ) was a 13, 14-dihydroxycembranoid having a 1
    E
    ,
    3
    Z-diene moiety. The absolute configuration of
    8
    and its 1Z,
    3
    E
    - and 1Z,
    3
    Z-isomers sarcophytol
    B
    (2) and J (10) were determined by circular dichroism study of their bis-p-dimethylaminobenzoate derivatives. Sarcophytols F (11) and T (13) were 1
    E
    - and 1
    E
    ,
    3
    Z-isomers of 1. Compound 11 showed characteristic broadening of the ^1H-NMR chemical shifts, due to the restricted conformational interconversion. Using the three cembranoids sarcophytols F (11, 1
    E
    ,
    3
    E
    ), N (15, 1Z,
    3
    Z) and T (13,1
    E
    ,
    3
    Z), spontaneous autoxidation-cyclization, in CHCl_
    3
    ,was examined, in order to compare the stereochemical course of the reaction with that of 1 (1Z,
    3
    E
    ), which affords trans-fused bicyclo[
    9
    .
    3
    .
    0
    ]tetradecene systems. The 1
    E
    ,
    3
    Z-isomer 13 gave the same cyclization product 18, as in the reaction of 1, even though it is isomeric at C-1,
    3
    . The 1Z,
    3
    Z isomer 15 gave 19, in consequence of the reversed geometry at C-
    3
    of 15. The 1
    E
    ,
    3
    E
    -isomer (11) gave the bicyclic product
    22
    , having an antipodal fusion as compared with 19. This was confirmed by PCC oxidation of 19 and
    22
    , giving enantiomeric ketones 23 and 24 respectively. The 1(14)-epoxide 26 was shown to be the immediate precursor of
    22
    , and acounted for the inversion of the geometry at C-1 of the cyclization product. Compound 26 is isomeric with the epoxide 17 derived from 1. The epoxide 17 is the postulated precursor in the conversion of 13 to 18. It is noteworthy that the mode of antipodal fusion of the cyclopentane rings, in 18 and
    22
    , was controlled by the chirality of the epoxy rings. The C-14 hydroxyl group participates in the transannular cyclization, but was found not to be the requisite functional group for the reaction. Similar treatment of cembrene C (30), the parent hydrocarbon of 1, also reacted in CHCl_
    3
    giving the bicyclic product 32.
  • R. I.・Ittrich-Fluorometry
    田中 啓幹
    日本泌尿器科學會雑誌
    1969年 60 巻 12 号 1125-1142
    発行日: 1969年
    公開日: 2010/07/23
    ジャーナル フリー
    Urinary estrogens have been assayed chiefly with the Kober hydroquinone colorimetry or sulfuric acid fluorimetry. However, it is difficult to determine accurately small amounts of estrogens such as in urines from males, oophorectomized women or menopausal women. In this study, male urinary estrogens were determined by a modification of the method reported by Kambegawa and some experimental studies were made on male urines. 200ml aliquot of 24-hour urine is hydrolyzed by the
    3
    -step hydrolysis, added with estrone-6, 73H, 17β-estradiol-6, 73H and estriol-6, 73H, and extracted with ether, followed by alkaline washes, methylation by a supersonic wave mixer, thin layer and column chromatography, liquid scintillation spectrometry and the Ittrich fluorometry. Results of experimental studies and estimation of urinary estrogens in males are as follows: 1) After the
    3
    -step hydrolysis, 54.5% of the urinary estrogens were collected as the glucuronide, 30% in the solvolyzed fraction and 15.5% as the hot acid hydrolyzate. 2) The methylation of estrogens was achieved 10-20% better by the use of the supersonic wave mixer than by a magnetic stirrer.
    3
    ) Calculating efficiency of the Packard Tri-carb liquid scintillation spectrometer was tested in varieties of the estrogen concentrations using the dilution and the external standardization methods. There was noted no influence of the estrogen concentrations on the counting efficiency in the determination ranges. 4) In the range of 2×10-
    3
    -
    1.0μg
    , a linear relationship on the standard curve was obtained applying the Allen's correction, when fluorometry was conditioned with the excitation light wave length of 510mμ and the fluorescence wave lengths of 530, 550 and 570mμ for each of the three estrogen-methyl ethers. 5) Urinary estrogens were determined in 15 normal males. In 5 subjects (2-13 years old) the values were:
    E1
    : 1.06±1.09;
    E2
    :
    0
    .64±
    0
    .54;
    E3
    :
    0
    .76±
    0
    .68 and the total
    E
    : 2.46±
    1.99μg
    /24hr. In 5 men (
    22
    -38 years old),
    E1
    : 5.02±1.57;
    E2
    : 2.58±
    0
    .21;
    E3
    : 4.11±1.
    82
    and the total
    E
    : 11.72±2.97μg/24hr. In 5 men (46-72 years old),
    E1
    :
    3
    .81±
    0
    .31;
    E1
    : 1.71±
    0
    .48;
    E3
    :
    3
    .51±
    0
    .94 and the total
    E
    :
    9
    .03±1.33μg/24hr. 6) Urinary estrogens were also determined in patients with a variety of clinical syndromes.
  • 山本 哲夫, 三枝 健二, 有水 昇, 国安 芳夫, 伊東 久夫
    RADIOISOTOPES
    2001年 50 巻 8 号 331-342
    発行日: 2001/08/15
    公開日: 2011/03/14
    ジャーナル フリー
    千葉大学病院のホールボディカウンタを用いて, 405名の健常人と186名の患者を対象に, 全身カリウム (K) 量の測定を行った。全身K量は以下に示すレファレンス値として算出した。すなわち20歳代の健康人の全身K量を標準値とし, 体表面積で除し, かつ年齢と男女差を加味して補正し%表示した。405名の健常人のレファレンス値は100.65±
    9
    .
    22
    %であった。各疾患ごとのレファレンス値は以下のようになった。肝硬変: 94.24±11.
    22
    %, 慢性肝炎: 95.74±11.24%, 甲状腺機能亢進症:
    99
    .37±10.
    8
    %, バーター症候群:
    82
    .
    0
    ±
    9
    .01%, 周期性四肢麻痺: 93.
    99
    ±
    9
    .86%, 筋無力症: 97.34±6.42%, 低カリウム血症: 90.64±11.76%であった。また子宮癌, 乳癌, 貧血, 高血圧症ではそれぞれ, 97.78±11.5%,
    99
    .
    22
    ±
    8
    .88%, 96.64±12.73%, 98.5±
    9
    .63%となった。14例が75%以下の異常低値を示した。その内訳は肝硬変1例, 高血圧症
    3
    例, 糖尿病1例, 低カリウム血症
    3
    例, 周期性四肢麻痺1例, バーター症候群2例, 薬物中毒2例, 乳癌1例であった。バーター症候群の1例, 周期性四肢麻痺の
    3
    例, 高血圧症2例, 肝硬変1例, 筋無力症1例では, 経時的に全身K量が測定され, 病状の経過との間に関連が見られた。
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