Daisuke Ono 교수

In mammals, circadian rhythms, such as sleep/wake cycles, are regulated by the central circadian clock located in the suprachiasmatic nucleus (SCN) of the hypothalamus. The SCN consists of thousands of individual neurons, which exhibit circadian rhythms. They synchronize with each other and produce robust and stable oscillations. Although several neurotransmitters are expressed in the SCN, almost all SCN neurons are γ-amino butyric acid (GABA)-ergic. Several studies have attempted to understand

In mammals, the temporal order of physiology and behavior is primarily regulated by the circadian pacemaker located in the hypothalamic suprachiasmatic nucleus (SCN). Rhythms are generated in cells by an auto-regulatory transcription/translation feedback loop, composed of several clock genes and their protein products. Taking advantage of bioluminescence reporters, we have succeeded in continuously monitoring the expression of clock gene reporters Per1-luc, PER2::LUC and Bmal1-ELuc in the SCN of

Abstract In mammals, the circadian rhythms are regulated by the central clock located in the hypothalamic suprachiasmatic nucleus (SCN), which is composed of heterogeneous neurons with various neurotransmitters. Among them an inhibitory neurotransmitter, γ-Amino-Butyric-Acid (GABA), is expressed in almost all SCN neurons, however, its role in the circadian physiology is still unclear. Here, we show that the SCN of fetal mice lacking vesicular GABA transporter (VGAT −/− ) or GABA synthesizing enz

The mammalian central circadian clock is located in the suprachiasmatic nucleus (SCN) of the hypothalamus. The SCN contains multiple circadian oscillators which synchronize with each other via several neurotransmitters. Importantly, an inhibitory neurotransmitter, γ-amino butyric acid (GABA), is expressed in almost all SCN neurons. In this review, we discuss how GABA influences circadian rhythms in the SCN. Excitatory and inhibitory effects of GABA may depend on intracellular Cl^- conc

New soap‐type surfactants bearing a 1,3‐dioxolane ring were prepared in good yields by the acid‐catalyzed condensation of 1‐ O ‐alkylglycerols (alkyl: decyl, dodecyl, tetradecyl, heptadecyl, octadecyl, or cis ‐9‐octadecenyl) with oxocarboxylic acid esters, followed by alkaline hydrolysis without any expensive reagent and special equipment. These surfactants were soluble in alkaline water at room temperature. Their critical micelle concentrations were much smaller than that of sodium dodecanoate.

It has been 50 years since the suprachiasmatic nucleus (SCN) was first identified as the central circadian clock and 25 years since the last overview of developments in the field was published in the <i>Journal of Biological Rhythms</i>. Here, we explore new mechanisms and concepts that have emerged in the subsequent 25 years. Since 1997, methodological developments, such as luminescent and fluorescent reporter techniques, have revealed intricate relationships between cellular and network-level

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTPreparation of new acetal type cleavable surfactants from epichlorohydrinDaisuke Ono, Araki Masuyama, and Mitsuo OkaharaCite this: J. Org. Chem. 1990, 55, 14, 4461–4464Publication Date (Print):July 1, 1990Publication History Published online1 May 2002Published inissue 1 July 1990https://pubs.acs.org/doi/10.1021/jo00301a048https://doi.org/10.1021/jo00301a048research-articleACS PublicationsRequest reuse permissionsArticle Views307Altmetric-Citations39LEA

Bis(sodium sulfate) surfactants each bearing two alkyl groups were easily prepared by the acid-catalyzed transesterification of diethyl tartrate with fatty alcohols (octyl, decyl, or dodecyl) and subsequent sulfation with sulfamic acid without any expensive reagents and special equipment. These surfactants had better water-solubility, smaller critical micelle concentration (cmc) and lower surface tension at cmc compared to sodium dodecylsulfate and sodium tetradecylsulfate. These surfactants bea

Abstract The biodegradability of new carboxylate types of “acid‐sensitive” cleavable surfactants bearing a 1,3‐dioxolane ring was measured by the biochemical oxygen demand (BOD) method in the presence of activated sludge. The result for sodium dodecanoate, measured under the same conditions, was used as a standard for evaluating the biodegradability of these cleavable surfactants. For cleavable surfactants derived from epoxides and oxocarboxylates, the biodegradation was considerably influenced

The mammalian central circadian clock, located in the suprachiasmatic nucleus (SCN), coordinates the timing of physiology and behavior to local time cues. In the SCN, second messengers, such as cAMP and Ca²⁺, are suggested to be involved in the input and/or output of the molecular circadian clock. However, the functional roles of second messengers and their dynamics in the SCN remain largely unclear. In the present study, we visualized the spatiotemporal patterns of circadian rhythms

Clock genes Cryptochrome (Cry1) and Cry2 are essential for expression of circadian rhythms in mice under constant darkness (DD). However, circadian rhythms in clock gene Per1 expression or clock protein PER2 are detected in the cultured suprachiasmatic nucleus (SCN) of neonatal Cry1 and Cry2 double deficient (Cry1 (-/-)/Cry2 (-/-)) mice. A lack of circadian rhythms in adult Cry1 (-/-)/Cry2 (-/-) mice is most likely due to developmentally disorganized cellular coupling of oscillating neurons in t

The temporal order of physiology and behaviour in mammals is regulated by the coordination of the master circadian clock in the suprachiasmatic nucleus (SCN) and peripheral clocks in various tissues outside the SCN. Because the circadian oscillator(s) in the olfactory bulb (OB) is regarded as SCN independent, we examined the relationship between the SCN master clock and the circadian clock in the OB. We also examined the role of vasoactive intestinal peptide receptor 2 in the circadian organizat

Clock genes Cry1 and Cry2, inhibitory components of core molecular feedback loop, are regarded as critical molecules for the circadian rhythm generation in mammals. A double knockout of Cry1 and Cry2 abolishes the circadian behavioral rhythm in adult mice under constant darkness. However, robust circadian rhythms in PER2::LUC expression are detected in the cultured suprachiasmatic nucleus (SCN) of Cry1/Cry2 deficient neonatal mice and restored in adult SCN by co-culture with wild-type neonatal S