We compared three groups of pregnant women: placebo with normotensive women, group A which included preeclamptics, and group which comprised preeclamptics who were supplemented their diets with vitamins C and . MDA increased from 6. ± 2. (placebo) to .48 ± 1.2 (A) and .02 ± 1. nmol/gHb (). NO concentrations were enhanced from 19.3 ± 4.2 (P) to 23. ± 6.4 (A) and 24.1 ± .4 μmol/L (). GSH contents were decreased from 10.42 ± 2. (P) to .02 ± 2.92 (A) and .39 ± 1.02 μmol/g Hb (), whereas GSSG concentrations increased from 0.98 ± 0.28 (P) to 1.24 ± 0.29 (A) and 1.08 ± 0.12 μmol/g Hb (). SOD activity decreased 23% in A and 14% in ; GRx decreased 27% in A and .% in ; GPx decreased 12% in A and .6% in . Catalase activity, however, increased 27% in A and 29% in as compared to control. Thus, we conclude that the use of vitamins C and 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.

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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

. coli isolates were detected in 95 (.2%) of the swab samples. Sequencing analysis results showed occurrence of various β-lactamase genes: bla_CTX-M-15 (62), blaTEM-

1b

(42), bla_CMY-2 (

22

), bla_CTX-M-3 (16), bla_CTX-M-1 (15), bla_OXA-1 (

9

) and bla_SHV-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.

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The phase diagrams of the Ni-Mo- and Ni-W- ternary systems in the region of less than 50mol% 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:
:L (1365K, 71.mol%Ni-6.0mol%Mo-.mol%)=(Ni)++
:L (1355K, 62.mol%Ni-2.mol%Mo-30.mol%)=++
:L (1445K, 42.0mol%Ni-30.6mol%Mo-10.3mol%)=(Ni)+NiMo+
P₁:L (1812K, 34.mol%Ni-42.3mol%Mo-.mol%)+MoB=+
P₂:L (1633K, 42.3mol%Ni-40.4mol%Mo-17.3mol%)+Mo=+
P₃:L (1812K, 53.mol%Ni-33.7mol%Mo-12.mol%)+Mo=NiMo+
:L (1622K, 51.0mol%Ni-31.6mol%W-17.4mol%)=(Ni)+W+
:L (1260K, 71.0mol%Ni-7.0mol%W-.0mol%)=(Ni)++
:L (1291K, 65.4mol%Ni-4.mol%W-29.mol%)=++
P₁:L (2115K, 23.mol%Ni-43.1mol%W-33.1mol%)+WB=+
P₂:L (1657K, 48.mol%Ni-33.1mol%W-18.0mol%)+=W+
The calculated phase diagrams are expected to be useful for the development of new Ni-based heat-, corrosion- or wear-resistance alloys.

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At low levels, enterohemorrhagic Escherichia coli should be selectively isolated by suppressing competing microflora in meat samples. In conventional methods, MacConkey II Agar with C-T Sorbitol (cefixime-tellurite, CT-SMAC) which utilizes the ability of

E

. coli O157 to ferment sorbitol, and media containing -specific chromogenic substrates, are used for detecting

E

. coli O157.
In this study, we compared two types of CHROMagar^TM O157 for the isolation of enterohemorrhagic

E

. coli O157 (improved CHROMagar^TM O157 and conventional CHROMagar^TM O157) with CT-SMAC by using the Miles-Misra method and evaluating the recovers from ground beef and human fecal samples. The results obtained are described below:
1. In the inoculation test with three media by the Miles-Misra method, improved CHROMagar^TM O157 inhibited the growth of all organisms except

E

. coli O157 better than the two other media and allowed easy differentiation from

E

. hermannii, which could not be distinguished on CT-SMAC.
2. In the

E

. coli O157 detection test for ground beef artificially inoculated with

E

. coliO157 at 1 cfu/g, the detection rate of improved CHROMagar ^TM O157 was 95%, CTSMAC 75% and conventional CHROMagar^TM O157 40%, respectively.
4. In the

E

. coli O157 detection test for

E

. coli O157 positive human fecal samples, the detection rate of improved CHROMagar^TM O157 was 54.%, CT-SMAC 50% and conventional CHROMagar^TM O157 .7%, respectively.

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魚市場およびと畜場のドブネズミにおけるStaphylococcus auresの保有率はそれぞれ74.6% (44/59), 34.6% (/26) であった. 魚市場のネズミ由来S. aureus104株の生物型はC型株 (77.%), 型16株 (15.4%), A型6株 (.%), 型別不能1株 (1%) で, と畜場由来株はG型株 (88.%), 型1株 (11.1%) であった. 魚市場のネズミ由来株のコアグラーゼ型は, VIII型 (26.%), 1型 (.1%), VII型 (13.%), IV型 (.7%), II型 (.%), III型 (2.%), V型 (2.%), VI型 (2.%), 同定不能 (14.4%) で, と畜場由来株は, VIII型 (44.4%), V型 (.2%), VI [型 (.2%), 同定不能 (11.1%) であった.魚市場のネズミ匹由来の12株からはエンテロトキシンA (11株) および (1株) が産生された.

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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 W_P=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.

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Pironetin 1 (PA-48153C) is a novel unsaturated δ-lactone derivative isolated from the fermentation broths of Streptomyces species which shows immunosuppressive and plant growth regulating activities. Several total syntheses of 1 have been reported to date, but we show here a novel approach to 1 via a convergent route using our chiral building block, (1S,S,6R)--hydroxybicyclo[4.1.0]heptan-2-one . We dissected pironetin at C6-C7 and employed the coupling of the epoxide 16 with the dithiane 25, which would be derived from , as a key step. The THP ether of was methylated and the following reduction gave an inseparable mixture of four diastereomers . After etherification, removal of THP group afforded separable isomers a and in a ratio of 13 to 1. The desired major isomer a was oxidized to ketone 6. Oxidation of 6 via silyl enol ether with osmium tetroxide gave ketol 21 in quantitative yield. Reduction of cyclopropylketone moiety of 21 under Birch condition afforded a mixture of a and . The ketol moiety of a and was oxidatively cleaved with lead tetraacetate in benzene-methanol to give the single aldo-ester 23. Acetalization of 23 followed by reduction of ester group gave aldehyde 24. Introduction of C2-unit via Takai's protocol as -olefin formation followed by thioacetalization afforded the dithiane 25, as C7-C14 unit of pironetin. Meanwhile, the epoxide 16 as C1-C6 unit was prepared from known epoxy alcohol 3 in 6 steps. Coupling reaction of two units, the dithiane 25 and the the epoxide 16, successfully gave the product with the whole skeleton 26 in high yield. Mercuric ion assisted hydrolysis of the thioacetal 26 gave ketol 27. Selective reduction of β-hydroxyketone 27 by Mori's method afforded and-diol 28a predominantly (: ). Finally, desilylation and oxidation with manganese dioxide afforded pironetin 1.

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Background : Usefulness of endoscopic microwave coagulation therapy (-MCT) was examined in 27 patients with hepatocellular carcinoma (HCC).
Material and Methods : HCC was found in patients with type liver cirrhosis (LC), 16 patients with type C LC, and 3 patients with non non C LC. Median tumor size was 23 mm (solitary lesion , multiple ). Laparoscopic MCT was performed for S_2-6 lesion and thoracoscopic MCT for lesion under general anesthesia. Linear type ultrasonography was used in every case for monitoring lesion ant therapeutic effect.
Results : Complete tumor necrosis was obtained in 24 cases (%) and local recurrence was found in cases after the observation period of maximum 34 months. Pleural abscess, hemorrhage and hepatic infarction were found in 3 cases without serious outcome.
Conclusions : We conclude that -MCT is quite promising therapy for surface type HCC in term of minimally invasive and curative procedure a time. It is important that sufficient marginal coagulation should be obtained.

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Brassinolide analogues, (R, 23R, 24R)-2α, 3α, , 23-tetrahydroxy--homo-7-oxa--ergostan-6-one (24-epibrassinolide) (10) and (S, 23S, 24R)-2α, 3α, , 23-tetrahydroxy--homo-7-oxa--ergostan-6-one (), were synthesized from brassicasterol (3a) in five steps and with ca. 20% overall yield. The key steps are the direct formation of (, 24R)-3α, -cyclo--ergost--en-6-one (4) from brassicasterol mesylate (3), the acid-catalyzed rearrangement of 4 to (, 24R)--ergosta-2, -dien-6-one (6), and the Baeyer-Villiger oxidation of the tetrahydroxy -ergostan-6-ones 7 and .

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Potassic-ferropargasite, ideally KCa₂(Fe₄²⁺Al)(OH)₂, is a new member of the amphibole group occurring in a schistose calcareous hornfels from Kabutoichiba, Kameyama, Mie Prefecture, central Japan. The amphibole occurs as black subhedral to anhedral crystals, up to about 700 μm long, associated with calcite, biotite, K-feldspar, plagioclase, scapolite, chlorite and titanite. Potassic-ferropargasite is optically biaxial negative with α = 1.680(2), β = 1.690 (calc.), γ = 1.698(2) and 2V = 80-90°. The mineral is monoclinic, space group C2/m, with refined unit-cell parameters a = .937(), = 18.108(), c = .335(4) Å, β = 105.30(3)°, V = 926.0() ų, Z = 2. The three strongest lines in the X-ray powder-diffraction pattern [d in Å (I) hkl] are 2.72 (100) 151, .48 () 110 and 2.61 (59) 061. Electron-microprobe gave SiO₂ 38.08, TiO₂ 1.92, Al₂O₃ 15.12, Cr₂O₃ 0.44, FeO 19.96, MnO 0., MgO 6., CaO 11.73, Na₂O 1.57, K₂O 2.74, F 0.13, Cl not detected, O = F + Cl -0.05, total 98.08 wt%, corresponding to (K_0.54Na_0.42)_Σ0.96(Ca_1.95Na_0.05)_Σ2.00(Fe²⁺

2.59Mg_1.44Al_0.67Ti_0.22Cr_0.05Mn_0.03

)

Σ5.00

(

Si_5.91Al_2.09

)

Σ8.00O₂₂

(OH_1.94F_0.06)_Σ2.00 on the basis of O = 23, assuming OH + F + Cl = 2. The crystal structure of the clinoamphibole type was refined to an R of 6.

5

%.

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Six full-length cDNAs encoding pig cytochrome P450 (CYP) enzymes, CYP1A1, CYP2A19, CYP2, CYP2C33v4, CYP2C49, and CYP21, were isolated and sequenced. The cDNA sequences of pig CYP1A1, CYP2A19, CYP2, CYP2C49, and CYP21 showed high similarity to human CYP1A1 (85.4%), CYP2A13 (88.6%), (.1%), CYP2C18 (85.3%), and (82.%), respectively, and pig CYP2C33v4 cDNA showed high similarity to rat CYP2C23 (79.2%). Reverse transcription-polymerase chain reaction (RT-PCR) assays revealed hepatic gene expression of all these pig CYP enzymes: the order of expression was CYP2C33v4 and > CYP2C49 > CYP1A1 and CYP2A19 > . In the kidney, the CYP2C33v4 gene was expressed at the same level as in the liver, but the CYP1A1, CYP2A19, and genes were expressed at lower levels than in the liver. Little renal gene expression of CYP2C49 and CYP21 was observed. We revealed for the first time the full-length cDNA sequences encoding pig CYP1A1 and five CYP enzymes belonging to the CYP2 gene family, thus making it possible to examine the gene expression levels of these CYP enzymes in pig tissues by RT-PCR.

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Melithasterols A-D (1-4), isolated from a gorgoinan coral Melithaea ocracea of Okinawa, were shown to be cholestane-, 24-methyl--dehydrocholestane-, -dehydrocholestane-, and 24-methylenecholestane-derivatives. respectively, having a common 3β, 7α -dihydroxy-α, 6α-epoxy-Δ^ steroid nucleus. This was confirmed by direct comparison with the authentic sample prepared by lead tetra-acetate oxydation of cholest-6-ene- 3β, α, α-triol 3-monoacetate. Twelve new polyhydroxysterols were isolated from an Alcyonium sp. (7,,), and Sclerophytum sp. (14,16,19,20,21,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 were identified as 24-methylenecholest--ene- 3β, 16β-diol-3-0-α-L fucoside (7) and its 7β-() and 7α-hydroxy () derivatives. Compound 14 was shown to be 24S-24-methylcholest--ene-3β,25ξ,26-triol and was correlated to the known compound 15 by α, 6β-glycolation. Compound 16 was shown to be β, 6α-isomer of 17, correlating to 17 by PCC oxidation followed by dehydration. Compound 19 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 -dehydro-(21) derivative of 17a and 17, respectively, by comparisons of their spectral data with reference compounds. Compounds a and 23 were 24S-methylcholestane-3β, α 25-triol-6-one 25-monoacetate (a) and its 25-deacetoxyl derivative (23). Partial PCC oxidation of 17a afforded a. Compounds 26 (andamansterol) and 28 (nicobarsterol) were shown to be gorgost--ene-3β, α. 11α, 21-tetrol and novel secosteroid, 11,21-cyclo--homo-11-oxa-, 11-secoergostane-3β, 6α, 12ξ-triol--one, respectively, by spectral analyses (H-HCOSY, HMQC, HMBC).

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