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1.
J Nutr Sci Vitaminol (Tokyo) ; 59(3): 178-86, 2013.
Article in English | MEDLINE | ID: mdl-23883688

ABSTRACT

Recent studies have shown that the urinary excretion levels of water-soluble vitamins can be used as biomarkers for the nutritional status of these vitamins. To determine changes in the urinary excretion levels of water-soluble vitamins during pregnant and lactating stages, we surveyed and compared levels of nine water-soluble vitamins in control (non-pregnant and non-lactating women), pregnant and lactating women. Control women (n=37), women in the 2nd (16-27 wk, n=24) and 3rd trimester of pregnancy (over 28 wk, n=32), and early- (0-5 mo, n=54) and late-stage lactating (6-11 mo, n=49) women took part in the survey. The mean age of subjects was ~30 y, and mean height was ~160 cm. A single 24-h urine sample was collected 1 d after the completion of a validated, self-administered comprehensive diet history questionnaire to measure water-soluble vitamins or metabolites. The average intake of each water-soluble vitamin was ≍ the estimated average requirement value and adequate intake for the Japanese Dietary Reference Intakes in all life stages, except for vitamin B6 and folate intakes during pregnancy. No change was observed in the urinary excretion levels of vitamin B2, vitamin B6, vitamin B12, biotin or vitamin C among stages. Urine nicotinamide and folate levels were higher in pregnant women than in control women. Urine excretion level of vitamin B1 decreased during lactation and that of pantothenic acid decreased during pregnancy and lactation. These results provide valuable information for setting the Dietary Reference Intakes of water-soluble vitamins for pregnant and lactating women.


Subject(s)
Ascorbic Acid/urine , Diet , Lactation/urine , Nutritional Status , Pregnancy/urine , Vitamin B Complex/urine , Adult , Ascorbic Acid/administration & dosage , Biomarkers/urine , Data Collection , Energy Intake , Female , Humans , Japan , Recommended Dietary Allowances , Surveys and Questionnaires , Vitamin B Complex/administration & dosage
2.
J Artif Organs ; 12(1): 40-6, 2009.
Article in English | MEDLINE | ID: mdl-19330504

ABSTRACT

This study aimed to map the elasticity of a natural artery at the micron level by using a tactile mapping system (TMS) that was recently developed for characterization of the stiffness of tissue slices. The sample used was a circumferential section (thickness, approximately 1 mm) of a small-caliber porcine artery (diameter, approximately 3 mm). Elasticity was measured with a probe of diameter 1 microm and a spatial resolution of 2 microm at a rate of 0.3 s per point, without significant sample invasion. Topographical measurements were also performed simultaneously. Wavy regions of high elasticity, layered in the circumferential direction, were measured at the tunica media, which was identified as an elastin-rich region. The Young's modulus of the elastin-rich region in the media was 50.8 +/- 13.8 kPa, and that of the elastin-rich region of the lamina elastica interna was 69.0 +/- 12.8 kPa. Both these values were higher than the Young's modulus of the other regions in the media, including smooth muscle cells and collagen fibrils (17.0 +/- 9.0 kPa). TMS is simple and inexpensive to perform and allows observation of the distribution of the surface elastic modulus at the extracellular matrix level in vascular tissue. TMS is expected to be a powerful tool in evaluation of the maturation and degree of reconstruction in the development of tissue-engineered or artificial tissues and organs.


Subject(s)
Arteries/diagnostic imaging , Elasticity Imaging Techniques , Animals , Biomechanical Phenomena , Elastic Modulus , In Vitro Techniques , Swine
3.
Chem Commun (Camb) ; (21): 2133-5, 2007 Jun 07.
Article in English | MEDLINE | ID: mdl-17520113

ABSTRACT

A novel FRET based strategy for DNA sequence analysis utilising base-discriminating fluorescence (BDF) nucleoside, (Py)U/(2-Ant)U, as donor in the dual-labelled oligonucleotide probe is reported; a selective/specific emission from acceptor, was observed upon excitation at the donor, only when the opposite base of the "smart" fluorescently labeled BDF nucleoside, (Py)U/(2-Ant)U, is adenine on the complementary target sequence.


Subject(s)
Adenosine/analysis , Adenosine/genetics , Fluorescence Resonance Energy Transfer , Fluorescent Dyes/chemistry , Oligonucleotide Probes/chemistry , Polymorphism, Single Nucleotide , Amino Acid Sequence , Genotype , Molecular Sequence Data , Molecular Structure
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