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1.
Nihon Rinsho ; 73(6): 924-8, 2015 Jun.
Article in Japanese | MEDLINE | ID: mdl-26065121

ABSTRACT

The rate of those who have sleep problems increases due to aging. In Japan, a super-aging society, insomnia is a common disease. It is reported that the ratio of insomniacs over sixty year-old is 29.5 %. The sleep disturbance in the elderly is caused by multi factors, such as physiological, physical, psychosociological, psychiatric, and pharmacological factors. According to the latest diagnostic criteria of sleep disorders, ICSD-3, the concept of primary or secondary insomnia was abolished. Instead of that, insomnia is categorized by the duration of disease, and general doctors can diagnose sleep disorders more easily than the past. However, it is not necessary to consider the pathophysiological mechanism, there is a concern that the clinical level of insomnia treatment might decline in quality.


Subject(s)
Aging/physiology , Diagnostic and Statistical Manual of Mental Disorders , Mental Disorders/psychology , Sleep Initiation and Maintenance Disorders/etiology , Sleep/physiology , Humans , Mental Disorders/complications , Mental Disorders/diagnosis , Sleep Initiation and Maintenance Disorders/classification , Sleep Initiation and Maintenance Disorders/diagnosis , Stress, Physiological/physiology
2.
J Phys Chem A ; 116(33): 8523-9, 2012 Aug 23.
Article in English | MEDLINE | ID: mdl-22799591

ABSTRACT

Rate coefficients for three daytime atmospheric reactions of (Z)-3-hexenal (3HA)-photolysis (J(1)), reaction with OH radicals (k(2)), and reaction with ozone (k(3))-were measured at 760 Torr and 298 K using a 6 m(3) photochemical reaction chamber. The UV absorption cross sections (σ(3HA)(λ)) were obtained in the wavelength range 240-350 nm. The photodissociation rate of 3HA relative to that of NO(2) was measured by a solar simulator at 760 Torr and was determined to be J(1)/J(NO2) = (4.7 ± 0.4) × 10(-3). Using the obtained σ(3HA)(λ) and J(1)/J(NO2), the effective photodissociation quantum yield was calculated to be Φ(3HA) = 0.25 ± 0.06. The rate coefficient for the reaction with OH radicals was measured by the relative rate method with three reference compounds and was determined to be k(2) = (6.9 ± 0.9) × 10(-11) cm(3) molecule(-1) s(-1). The rate coefficient for the reaction with ozone was measured by an absolute method and was determined to be k(3) = (3.5 ± 0.2) × 10(-17) cm(3) molecule(-1) s(-1). Using the obtained rate coefficients, the daytime atmospheric lifetime of 3HA was estimated.


Subject(s)
Aldehydes/chemistry , Atmosphere/chemistry , Hydroxyl Radical/chemistry , Kinetics , Ozone/chemistry , Photolysis , Spectrophotometry, Ultraviolet
3.
Genome Res ; 20(1): 28-35, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19923254

ABSTRACT

Acetaminophen-induced liver toxicity is the most frequent precipitating cause of acute liver failure and liver transplant, but contemporary medical practice has mainly focused on patient management after a liver injury has been induced. An integrative genetic, transcriptional, and two-dimensional NMR-based metabolomic analysis performed using multiple inbred mouse strains, along with knowledge-based filtering of these data, identified betaine-homocysteine methyltransferase 2 (Bhmt2) as a diet-dependent genetic factor that affected susceptibility to acetaminophen-induced liver toxicity in mice. Through an effect on methionine and glutathione biosynthesis, Bhmt2 could utilize its substrate (S-methylmethionine [SMM]) to confer protection against acetaminophen-induced injury in vivo. Since SMM is only synthesized in plants, Bhmt2 exerts its beneficial effect in a diet-dependent manner. Identification of Bhmt2 and the affected biosynthetic pathway demonstrates how a novel method of integrative genomic analysis in mice can provide a unique and clinically applicable approach to a major public health problem.


Subject(s)
Acetaminophen/adverse effects , Analgesics, Non-Narcotic/adverse effects , Betaine-Homocysteine S-Methyltransferase/genetics , Chemical and Drug Induced Liver Injury/genetics , Liver Failure, Acute/genetics , Vitamin U/metabolism , Acetaminophen/metabolism , Acetaminophen/pharmacokinetics , Animals , Betaine-Homocysteine S-Methyltransferase/metabolism , Chemical and Drug Induced Liver Injury/etiology , Chemical and Drug Induced Liver Injury/pathology , Chemical and Drug Induced Liver Injury/prevention & control , Diet , Gene Expression Profiling , Liver/metabolism , Liver/pathology , Liver Failure, Acute/chemically induced , Liver Failure, Acute/pathology , Liver Failure, Acute/prevention & control , Magnetic Resonance Spectroscopy , Mice , Mice, Inbred Strains , Molecular Sequence Data , Oligonucleotide Array Sequence Analysis , Sequence Analysis, DNA
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