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1.
J Hum Hypertens ; 25(3): 164-71, 2011 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20445569

RESUMEN

We investigate associations of fruit and vegetable intake with the risk of future hypertension using home blood pressure in a general population from Ohasama, Japan. We obtained data from 745 residents aged ≥35 years without home hypertension at baseline. Dietary intake was measured using a validated 141-item food frequency questionnaire, and subjects were then divided into quartiles according to the fruit and vegetable intake. Home hypertension was defined as home systolic/diastolic blood pressure of ≥135/85 mm Hg and/or the use of antihypertensive medication. During a 4-year follow-up period, we identified 222 incident cases of home hypertension. After adjustment for all putative confounding factors, the highest quartile of fruit intake was associated with a significantly lower risk of future home hypertension (odds ratio 0.40, 95% confidence interval 0.22-0.74, P=0.004). In conclusion, this study, based on home blood pressure measurement, suggests that higher intake of fruit is associated with a lower risk of future home hypertension.


Asunto(s)
Monitoreo Ambulatorio de la Presión Arterial , Frutas , Hipertensión/epidemiología , Verduras , Antihipertensivos/uso terapéutico , Registros de Dieta , Femenino , Estudios de Seguimiento , Humanos , Hipertensión/dietoterapia , Hipertensión/tratamiento farmacológico , Incidencia , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Riesgo , Factores de Riesgo
2.
Biomaterials ; 22(8): 855-63, 2001 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-11246954

RESUMEN

Collagen (type I from calf-skin) was chemically modified by 4-butyrothiolactone to obtain the mercapto group-bearing collagen (collagenSH), which possessed SH groups in 8-19 M% of a total amino acid residues. The triple helical strands of the collagen was not completely perturbed to exhibit the rotary dispersion [theta]221, which was as much as 70% of an original intensity of the collagen. In the presence of the oxygen dissolved in water, the collagenSH was cross-linked by disulfide bonds to afford the collagenSS. The collagenSS could preserve about 15 and 40% of an original helix structure at 55-70 degrees C and in 2mm sodium dodecyl sulfate, respectively. The film made of the collagenSS exhibited the tensile strength as high as 36 MPa and was insoluble in most organic solvents including water. The collagenSS film was more resistant to degradation by collagenase (type I) than the collagen film. The collagenSS film supported the growth of L929 fibroblast cell in a manner similar to a collagen film.


Asunto(s)
Materiales Biocompatibles/química , Materiales Biocompatibles/aislamiento & purificación , Colágeno/química , Colágeno/aislamiento & purificación , Animales , Fenómenos Biomecánicos , Bovinos , Línea Celular , Dicroismo Circular , Colagenasas , Reactivos de Enlaces Cruzados , Disulfuros/química , Técnicas In Vitro , Ensayo de Materiales , Ratones , Solubilidad
3.
J Biotechnol ; 86(1): 1-8, 2001 Mar 09.
Artículo en Inglés | MEDLINE | ID: mdl-11223139

RESUMEN

Thiol groups were introduced to dermal bovine collagen (DBC) by the reaction with gamma-thiobutyrolactone. Thiolated DBC reacted with 2-pyridyl disulfide group introduced to lysozyme to form DBC-lysozyme conjugate through disulfide bridge. The enzymatic activity of freshly prepared conjugate was almost unchanged during ten consecutive runs over one month. The DBC-lysozyme conjugate showed the maximum activity at pH 6.3, on the contrary, that of native lysozyme was pH 9.0. Thermal stability of lysozyme was enhanced by the conjugation with DBC. The present results showed that the conjugation using thiolated collagen could be one of the useful alternative approaches to modify collagen with bioactive molecules.


Asunto(s)
Colágeno/química , Muramidasa/química , Piel/química , Compuestos de Sulfhidrilo/química , Animales , Bovinos , Disulfuros/química , Estabilidad de Enzimas , Calor , Concentración de Iones de Hidrógeno , Muramidasa/metabolismo
4.
Bioorg Med Chem Lett ; 10(12): 1317-20, 2000 Jun 19.
Artículo en Inglés | MEDLINE | ID: mdl-10890155

RESUMEN

New piperidylpyrimidine derivatives, including quinazolines, were prepared, and their abilities to inhibit TNF-alpha production evaluated. Some compounds showed potent inhibitory activity in mouse macrophages stimulated with LPS. The synthesis and structure activity relationships of these compounds are described.


Asunto(s)
Piperidinas/química , Pirimidinas/química , Factor de Necrosis Tumoral alfa/antagonistas & inhibidores , Animales , Ratones , Estructura Molecular , Piperidinas/farmacología , Pirimidinas/farmacología , Relación Estructura-Actividad , Factor de Necrosis Tumoral alfa/biosíntesis
5.
Biochim Biophys Acta ; 1302(3): 185-92, 1996 Aug 16.
Artículo en Inglés | MEDLINE | ID: mdl-8765138

RESUMEN

A novel glycosphingolipid containing inositol phosphate as an acidic group has been demonstrated in whole tissues of the porcine roundworm, Ascaris suum. The thin layer chromatographic pattern of the total acidic glycolipid revealed the presence of several components, of which a major component (named AGL) with positive reactions toward both orcinol-sulfuric acid (sugar) and molybdate (phosphate) spray reagents was isolated and purified by the use of successive column chromatography on DEAE-Sephadex and silicic acid (latrobeads). From structural studies including compositional sugar analysis, hydrogen fluoride degradation, methylation analysis, periodate oxidation, proton magnetic resonance spectroscopy and fast atom bombardment mass spectrometry, the structure of AGL was deduced to be Gal alpha 1-2Ins(1-->)-P-Cer. Aliphatic constituents were lignoceric acid and its 2-hydroxy homologue as the principal fatty acids, and octadecasphinganine and branched heptadecasphinganine as the major sphingoids.


Asunto(s)
Ascaris suum/química , Glicoesfingolípidos/química , Fosfatos de Inositol/química , Animales , Borohidruros/química , Conformación de Carbohidratos , Secuencia de Carbohidratos , Carbohidratos/análisis , Cromatografía de Gases , Cromatografía en Capa Delgada , Galactosa/química , Cromatografía de Gases y Espectrometría de Masas , Glicoesfingolípidos/análisis , Hidrólisis , Fosfatos de Inositol/análisis , Espectroscopía de Resonancia Magnética , Metilación , Conformación Molecular , Datos de Secuencia Molecular , Oxidación-Reducción , Ácido Peryódico/química , Espectrometría de Masa Bombardeada por Átomos Veloces
6.
Nucleic Acids Symp Ser ; (27): 83-4, 1992.
Artículo en Inglés | MEDLINE | ID: mdl-1289835

RESUMEN

9-[c-4-(1,2-Dihydroxyethyl)cyclopent-2-en-r-1-yl]-9H-adenine , an isomer of BCA, has been synthesized from Diels-Alder adducts prepared by the reaction of 2-iminomalonates with cyclopentadiene under high pressure. The synthetic method involves a novel C-N bond cleavage reaction by NaBH4-K2CO3 (RRA reaction conditions) and has wide applicability for the synthesis of various carbocyclic nucleosides.


Asunto(s)
Adenina/análogos & derivados , Ciclopentanos/síntesis química , Malonatos/química , Adenina/síntesis química , Presión
7.
Nucleic Acids Symp Ser ; (25): 5-6, 1991.
Artículo en Inglés | MEDLINE | ID: mdl-1842092

RESUMEN

The 1'- and 5'-hydroxymethyl derivatives of carbovir and related purine derivatives were synthesized from 5-hydroxymethylcyclopentadiene. The anti-HIV activity evaluation of these compounds has revealed that 9-(c-4,t-5-dihydroxymethylcyclopent-2-en-r-1-yl)-9H-adenine is a prospective chemotherapeutic agent against AIDS.


Asunto(s)
Adenina/análogos & derivados , Adenosina/análogos & derivados , Antivirales/síntesis química , Didesoxinucleósidos/química , VIH/efectos de los fármacos , Adenina/química , Adenina/farmacología , Adenosina/química , Adenosina/farmacología , Antivirales/química , Antivirales/farmacología , Didesoxinucleósidos/farmacología , Estructura Molecular , Estudios Prospectivos
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