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1.
J Appl Phys ; 130(7): 070907, 2021 Aug 21.
Article in English | MEDLINE | ID: mdl-34483360

ABSTRACT

Progress in computing architectures is approaching a paradigm shift: traditional computing based on digital complementary metal-oxide semiconductor technology is nearing physical limits in terms of miniaturization, speed, and, especially, power consumption. Consequently, alternative approaches are under investigation. One of the most promising is based on a "brain-like" or neuromorphic computation scheme. Another approach is quantum computing using photons. Both of these approaches can be realized using silicon photonics, and at the heart of both technologies is an efficient, ultra-low power broad band optical modulator. As silicon modulators suffer from relatively high power consumption, materials other than silicon itself have to be considered for the modulator. In this Perspective, we present our view on such materials. We focus on oxides showing a strong linear electro-optic effect that can also be integrated with Si, thus capitalizing on new materials to enable the devices and circuit architectures that exploit shifting computational machine learning paradigms, while leveraging current manufacturing infrastructure. This is expected to result in a new generation of computers that consume less power and possess a larger bandwidth.

2.
Clin Microbiol Infect ; 27(1): 69-75, 2021 Jan.
Article in English | MEDLINE | ID: mdl-32272171

ABSTRACT

OBJECTIVES: Recently, rapid phenotypic antimicrobial susceptibility testing (AST) based on microscopic imaging analysis has been developed. The aim of this study was to determine whether implementation of antimicrobial stewardship programmes (ASP) based on rapid phenotypic AST can increase the proportion of patients with haematological malignancies who receive optimal targeted antibiotics during early periods of bacteraemia. METHODS: This randomized controlled trial enrolled patients with haematological malignancies and at least one positive blood culture. Patients were randomly assigned 1:1 to conventional (n = 60) or rapid phenotypic (n = 56) AST. The primary outcome was the proportion of patients receiving optimal targeted antibiotics 72 hr after blood collection for culture. RESULTS: The percentage receiving optimal targeted antibiotics at 72 hr was significantly higher in the rapid phenotypic AST group (45/56, 80.4%) than in conventional AST group (34/60, 56.7%) (relative risk (RR) 1.42, 95% confidence interval (CI) 1.09-1.83). The percentage receiving unnecessary broad-spectrum antibiotics at 72 hr was significantly lower (7/26, 12.5% vs 18/60, 30.0%; RR 0.42, 95% CI 0.19-0.92) and the mean time to optimal targeted antibiotic treatment was significantly shorter (38.1, standard deviation (SD) 38.2 vs 72.8, SD 93.0 hr; p < 0.001) in the rapid phenotypic AST group. The mean time from blood collection to the AST result was significantly shorter in the rapid phenotypic AST group (48.3, SD 17.6 vs 83.1, SD 22.2 hr). DISCUSSION: ASP based on rapid phenotypic AST can rapidly optimize antibiotic treatment for bacteraemia in patients with haematological malignancy. Rapid phenotypic AST can improve antimicrobial stewardship in immunocompromised patients.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Antimicrobial Stewardship/methods , Bacteremia/drug therapy , Hematologic Neoplasms/drug therapy , Microbial Sensitivity Tests/methods , Adult , Anti-Bacterial Agents/pharmacology , Bacteremia/complications , Female , Hematologic Neoplasms/complications , Humans , Male , Middle Aged , Time-to-Treatment , Treatment Outcome
3.
J Chem Inf Model ; 60(12): 5832-5852, 2020 12 28.
Article in English | MEDLINE | ID: mdl-33326239

ABSTRACT

We present a supercomputer-driven pipeline for in silico drug discovery using enhanced sampling molecular dynamics (MD) and ensemble docking. Ensemble docking makes use of MD results by docking compound databases into representative protein binding-site conformations, thus taking into account the dynamic properties of the binding sites. We also describe preliminary results obtained for 24 systems involving eight proteins of the proteome of SARS-CoV-2. The MD involves temperature replica exchange enhanced sampling, making use of massively parallel supercomputing to quickly sample the configurational space of protein drug targets. Using the Summit supercomputer at the Oak Ridge National Laboratory, more than 1 ms of enhanced sampling MD can be generated per day. We have ensemble docked repurposing databases to 10 configurations of each of the 24 SARS-CoV-2 systems using AutoDock Vina. Comparison to experiment demonstrates remarkably high hit rates for the top scoring tranches of compounds identified by our ensemble approach. We also demonstrate that, using Autodock-GPU on Summit, it is possible to perform exhaustive docking of one billion compounds in under 24 h. Finally, we discuss preliminary results and planned improvements to the pipeline, including the use of quantum mechanical (QM), machine learning, and artificial intelligence (AI) methods to cluster MD trajectories and rescore docking poses.


Subject(s)
Antiviral Agents/chemistry , COVID-19 Drug Treatment , SARS-CoV-2/drug effects , Viral Nonstructural Proteins/chemistry , Artificial Intelligence , Binding Sites , Computer Simulation , Databases, Chemical , Drug Design , Drug Evaluation, Preclinical , Humans , Molecular Docking Simulation , Protein Conformation , Spike Glycoprotein, Coronavirus/chemistry , Structure-Activity Relationship
4.
Biochemistry (Mosc) ; 85(12): 1554-1559, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33705293

ABSTRACT

The circadian clock is the biological mastermind governing orderly execution of bodily processes throughout the day. In recent years, an emerging topic of broad interest is clock-modulatory agents, including small molecules both of synthetic and natural origins, and their potential applications in disease models. Nobiletin is a naturally occurring flavonoid with the greatest abundance found in citrus peels. Extensive research has shown that Nobiletin is endowed with a wide range of biological activities, yet its mechanism of action remains unclear. We recently found through unbiased chemical screening that Nobiletin impinges on the clock machinery to activate temporal control of downstream processes within the cell and throughout the body. Using animal models of diseases and aging, we and others illustrate potent beneficial effects of Nobiletin on cellular energetics in both periphery and brain to promote healthy aging. Given its excellent safety profile, Nobiletin may represent a promising candidate molecule for development of nutraceutical and chronotherapeutic agents against chronic and age-related neurodegenerative diseases.


Subject(s)
Circadian Clocks/drug effects , Energy Metabolism/drug effects , Flavones/pharmacology , Animals , Humans , Mitochondria/metabolism
5.
J Biosci ; 42(1): 131-138, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28229972

ABSTRACT

The aim of this study was to investigate whether neonatal maternal separation (MS) - chronic stress experience in early life - affects the anorectic efficacy of leptin in the offspring at adolescence. Sprague-Dawley pups were separated from the dam daily for 3 h during postnatal day 1-14 or left undisturbed as non-handled controls (NH). NH and MS male pups received an intraperitoneal leptin (100 µg/kg) or saline on postnatal day (PND) 28, and then food intake and body weight gain were recorded. The hypothalamic levels of leptin-signalling-related genes, phosphorylated signal transducer and activator of transcription-3 (pSTAT3) and protein-tyrosine phosphatase 1B (PTP1B) were examined at 40 min after a single injection of leptin on PND 39 by immunohistochemistry and Western blot analysis. Leptin-induced suppressions in food intake and weight gain was observed in NH pups, but not in MS. Leptin increased pSTAT3 in the hypothalamic arcuate nucleus of NH pups, but not of MS. Interestingly, basal levels of the hypothalamic PTP1B and pSTAT3 were increased in MS pups compared with NH controls. The results suggest that neonatal MS experience may blunt the anorectic efficacy of leptin later in life, possibly in relation with increased expressions of PTP1B and/or pSTAT3 in the hypothalamus.


Subject(s)
Leptin/metabolism , Protein Tyrosine Phosphatase, Non-Receptor Type 1/biosynthesis , STAT3 Transcription Factor/biosynthesis , Stress, Psychological/genetics , Animals , Animals, Newborn , Arcuate Nucleus of Hypothalamus/metabolism , Body Weight , Eating , Hypothalamus/metabolism , Leptin/administration & dosage , Male , Protein Tyrosine Phosphatase, Non-Receptor Type 1/genetics , Rats , Rats, Sprague-Dawley , STAT3 Transcription Factor/genetics , Signal Transduction/genetics , Stress, Psychological/metabolism
6.
Br J Pharmacol ; 165(3): 683-92, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21718307

ABSTRACT

BACKGROUND AND PURPOSE: Transient receptor potential ion channel vanilloid 3 (TRPV3) is expressed in skin keratinocytes and plays an important role in thermal and chemical nociceptions in the periphery. The presence of TRPV3 inhibitors would improve our understanding of TRPV3 function and help to develop receptor-specific analgesics. However, little is known about physiological substances that specifically inhibit TRPV3 activity. Here, we investigated whether 17(R)-resolvin D1 (17R-RvD1), a naturally occurring pro-resolving lipid specifically affects TRPV3 activity. EXPERIMENTAL APPROACH: We examined the effect of 17R-RvD1 on sensory TRP channels using Ca(2+) imaging and whole cell electrophysiology experiments in a HEK cell heterologous expression system, cultured sensory neurons and keratinocytes. We also examined changes in sensory TRP agonist-specific acute licking/flicking or flinching behaviours and mechanical and thermal pain behaviours using Hargreaves, Randall-Selitto and von Frey assay systems in the absence and presence of inflammation. KEY RESULTS: We showed that 17R-RvD1 specifically suppresses TRPV3-mediated activity at nanomolar and micromolar concentrations. The voltage-dependence of TRPV3 activation by camphor was shifted rightwards by 17R-RvD1, which indicates its inhibitory mechanism is as a result of a shift in voltage-dependence. Consistently, TRPV3-specific acute pain behaviours were attenuated by locally injected 17R-RvD1. Moreover, the administration of 17R-RvD1 significantly reversed the thermal hypersensitivity that occurs during an inflammatory response. Knockdown of epidermal TRPV3 blunted these antinociceptive effects of 17R-RvD1. CONCLUSIONS AND IMPLICATIONS: 17R-RvD1 is a novel natural inhibitory substance specific for TRPV3. The results of our behavioural studies suggest that 17R-RvD1 has acute analgesic potential via TRPV3-specific mechanisms.


Subject(s)
Analgesics/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Docosahexaenoic Acids/therapeutic use , Pain/drug therapy , TRPV Cation Channels/antagonists & inhibitors , Analgesics/pharmacology , Animals , Anti-Inflammatory Agents/pharmacology , Capsaicin , Carrageenan , Cell Line , Docosahexaenoic Acids/pharmacology , Freund's Adjuvant , Ganglia, Spinal/cytology , HEK293 Cells , Hot Temperature , Humans , Inflammation/chemically induced , Inflammation/drug therapy , Inflammation/physiopathology , Keratinocytes/drug effects , Keratinocytes/physiology , Male , Mice , Mice, Inbred ICR , Mice, Knockout , Pain/chemically induced , Pain/physiopathology , Rats , Rats, Sprague-Dawley , Sensory Receptor Cells/drug effects , Sensory Receptor Cells/physiology , TRPV Cation Channels/deficiency , TRPV Cation Channels/genetics , TRPV Cation Channels/physiology
7.
Caries Res ; 45(4): 327-35, 2011.
Article in English | MEDLINE | ID: mdl-21720161

ABSTRACT

There are over 750 species of bacteria that inhabit the human oral cavity, but only a small fraction of those are attributed to causing plaque-related diseases such as caries. Streptococcus mutans is accepted as the main cariogenic agent and there is substantial knowledge regarding the specific virulence factors that render the organism a pathogen. There has been rising interest in alternative, target-specific treatment options as opposed to nonspecific mechanical plaque removal or application of broad-spectrum antibacterials that are currently in use. The impact of diet on oral health is undeniable, and this is directly observable in populations that consume high quantities of polyphenol-rich foods or beverages. Such populations have low caries incidence and better overall oral health. Camellia sinensis, the plant from which various forms of tea are derived, and Vaccinium macrocarpon (American cranberry fruit) have received notable attention both for their prevalence in the human diet as well as for their unique composition of polyphenols. The biologically active constituents of these plants have demonstrated potent enzyme-inhibitory properties without being bactericidal, a key quality that is important in developing therapies that will not cause microorganisms to develop resistance. The aim of this review is to consider studies that have investigated the feasibility of tea, cranberry, and other select plant derivatives as a potential basis for alternative therapeutic agents against Streptococcus mutans and to evaluate their current and future clinical relevance.


Subject(s)
Cariostatic Agents/pharmacology , Plant Extracts/pharmacology , Polyphenols/pharmacology , Streptococcus mutans/drug effects , Tea , Vaccinium macrocarpon , Apigenin/pharmacology , Cariostatic Agents/chemistry , Farnesol/pharmacology , Glucosyltransferases/antagonists & inhibitors , Humans , Plant Extracts/chemistry , Polyphenols/chemistry , Propolis/chemistry , Streptococcus mutans/enzymology , Structure-Activity Relationship , Tea/chemistry , Vaccinium macrocarpon/chemistry
8.
Opt Express ; 19(14): 13245-56, 2011 Jul 04.
Article in English | MEDLINE | ID: mdl-21747479

ABSTRACT

We demonstrate a fully-reconfigurable fourth-order optical lattice filter built by cascading identical unit cells consisting of a Mach-Zehnder interferometer (MZI) and a ring resonator. The filter is fabricated using a commercial silicon complementary metal oxide semiconductor (CMOS) process and reconfigured by current injection into p-i-n diodes with a reconfiguration time of less than 10 ns. The experimental results show full control over the single unit cell pole and zero, switching the unit cell transfer function between a notch filter and a bandpass filter, narrowing the notch width down to 400 MHz, and tuning the center wavelength over the full free spectral range (FSR) of 10 GHz. Theoretical and experimental results show tuning dynamics and associated optical losses in the reconfigurable filters. The full-control of each of the four cascaded single unit cells resulted in demonstrations of a number of fourth-order transfer functions. The multimedia experimental data show live tuning and reconfiguration of optical lattice filters.


Subject(s)
Filtration/instrumentation , Interferometry/instrumentation , Refractometry/instrumentation , Silicon/chemistry , Transistors, Electronic , Computer-Aided Design , Equipment Design , Equipment Failure Analysis
9.
J Dent Res ; 89(12): 1455-60, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20935279

ABSTRACT

Er,Cr:YSGG lasers are used clinically in dentistry. The advantages of laser therapy include minimal thermal damage and the alleviation of pain. This study examined whether the Er,Cr:YSGG laser has in vivo and in vitro antinociceptive effects in itself. In capsaicin-evoked acute licking/shaking tests and Hargreaves tests, laser irradiation with an aerated water spray suppressed nociceptive behavior in mice. Laser irradiation attenuated TRPV1 activation by capsaicin in Ca(2+) imaging experiments with TRPV1-overexpressing cells and cultured trigeminal neurons. Therefore, the laser-induced behavioral changes are probably due to the loss of TRPV1 activity. TRPV4 activity was also attenuated, but limited mechanical antinociception by the laser was observed. The laser failed to alter the other receptor functions, which indicates that the antinociceptive effect of the laser is dependent on TRPV1. These results suggest that the Er,Cr:YSGG laser has analgesic effects via TRPV1 inhibition. Such mechanistic approaches may help define the laser-sensitive pain modality and increase its beneficial uses.


Subject(s)
Lasers, Solid-State/therapeutic use , Nociceptors/radiation effects , Pain/prevention & control , TRPV Cation Channels/radiation effects , Animals , Behavior, Animal/drug effects , Behavior, Animal/radiation effects , Calcium Channel Blockers/pharmacology , Calcium Signaling/drug effects , Calcium Signaling/radiation effects , Capsaicin/pharmacology , Dinoprostone/pharmacology , HEK293 Cells , HeLa Cells , Hot Temperature , Humans , Male , Mice , Mice, Inbred ICR , Mice, Knockout , Neurons/drug effects , Neurons/radiation effects , Nociceptors/drug effects , Pain Threshold/radiation effects , Reaction Time/radiation effects , Ruthenium Red/pharmacology , Sensory System Agents/pharmacology , Sensory Thresholds/radiation effects , TRPV Cation Channels/drug effects , Thermosensing/radiation effects , Touch/radiation effects , Trigeminal Nerve/drug effects , Trigeminal Nerve/radiation effects
10.
Br J Dermatol ; 163(3): 557-63, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20412090

ABSTRACT

BACKGROUND: Dermatological procedures can result in disfiguring bruises that resolve slowly. OBJECTIVES: To assess the comparative utility of topical formulations in hastening the resolution of skin bruising. METHODS: Healthy volunteers, age range 21-65 years, were enrolled for this double (patient and rater) blinded randomized controlled trial. For each subject, four standard bruises of 7 mm diameter each were created on the bilateral upper inner arms, 5 cm apart, two per arm, using a 595-nm pulsed-dye laser (Vbeam; Candela Corp., Wayland, MA, U.S.A.). Randomization was used to assign one topical agent (5% vitamin K, 1% vitamin K and 0·3% retinol, 20% arnica, or white petrolatum) to exactly one bruise per subject, which was then treated under occlusion twice a day for 2 weeks. A dermatologist not involved with subject assignment rated bruises [visual analogue scale, 0 (least)-10 (most)] in standardized photographs immediately after bruise creation and at week 2. RESULTS: There was significant difference in the change in the rater bruising score associated with the four treatments (anova, P=0·016). Pairwise comparisons indicated that the mean improvement associated with 20% arnica was greater than with white petrolatum (P=0·003), and the improvement with arnica was greater than with the mixture of 1% vitamin K and 0·3% retinol (P=0·01). Improvement with arnica was not greater than with 5% vitamin K cream, however. CONCLUSIONS: Topical 20% arnica ointment may be able to reduce bruising more effectively than placebo and more effectively than low-concentration vitamin K formulations, such as 1% vitamin K with 0·3% retinol.


Subject(s)
Arnica , Contusions/drug therapy , Emollients/therapeutic use , Phytotherapy/methods , Plant Preparations/therapeutic use , Administration, Topical , Adult , Aged , Contusions/etiology , Contusions/pathology , Double-Blind Method , Female , Humans , Lasers/adverse effects , Male , Middle Aged , Observer Variation , Petrolatum/therapeutic use , Photography , Vitamin K/therapeutic use , Young Adult
11.
J Food Sci ; 74(2): C134-40, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19323727

ABSTRACT

Omija (Schizandra chinensis) is used as an ingredient in traditional medicine in East Asia. It is consumed as tea and wine and display pinkish-red color and beneficial physiological activity. However, the origin of Omija's unique color and bioactivity has not been studied extensively and its application is very limited. Thus, it was required to determine the chemical structure of major phenolic compounds of Omija fruit and evaluate their antioxidant activity. The colorants extracted from a domestic Omija cultivar were concentrated by a Sep-pak(R) Plus C(18) cartridge. A major high-performance liquid chromatography (HPLC) peak of anthocyan represented 94.1% of total absorbable compounds at 520 nm, which was further identified by LC-ESI-MS. The mass-to-charge ratio (m/z) of the major anthocyan was determined to be 727. Highly pure anthocyan fraction with a semipreparative HPLC was acid-hydrolyzed, and the sugar moieties linked to anthocyan (cyanidin) were characterized by thin layer chromatography (TLC) and high-performance anion exchange chromatography (HPAEC) analyses. The linkage patterns of sugars and core cyanidin structure were determined by (1)H- and (13)C-NMR analyses. Antioxidant activity of the extract and the purified anthocyanin was evaluated by 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) methods. As a result, the structure of the purified colorant was identified as Cya-3-O-xylrut. At the same molar level of the samples tested, the purified Cya-3-O-xylrut (31.2% and 39.2%) had substantially greater antioxidant activity than l-ascorbic acid (17.1% and 10.1%) from DPPH and ABTS methods, respectively. In this study, Omija colorant mostly consisted of Cya-3-O-xylrut explained 86% (DPPH) and 98% (ABTS) of total antioxidant activity derived from water extract from Omija.


Subject(s)
Antioxidants/analysis , Fruit/chemistry , Schisandra/chemistry , Anthocyanins/analysis , Chromatography, High Pressure Liquid , Magnetic Resonance Spectroscopy , Mass Spectrometry , Phenols/analysis
12.
J Food Sci ; 73(8): C577-84, 2008 Oct.
Article in English | MEDLINE | ID: mdl-19019099

ABSTRACT

Pork loin and belly cuts were pumped to 110% of their original weight with solutions containing 5% of various ingredients (sodium ascorbate, garlic, and onion powder), and evaluated the physicochemical properties, and antioxidant and antimicrobial activities during refrigerated storage at 8 degrees C. The addition of garlic and onion powder tended to increase redness (a) and yellowness (b) in both the belly lean and loin with the exception of a few cases. Free fatty acid values in both pork belly and loin cuts were reduced with the addition of these ingredients, as compared to the control. Significant differences in peroxide values were observed in sodium ascorbate and garlic-injected belly, and in sodium ascorbate and onion-injected loin, as compared to the control. Thiobarbituric acid reactive substance values in the pork belly with garlic or onion powder were significantly lower than in the belly without these ingredients or with sodium ascorbate (P < 0.05). Total plate counts were lower in both the belly and loin containing garlic and onion powder, as compared to the control. In both the belly and loin cuts, the content of oxidative products (volatile compounds) was reduced with the addition of garlic and onion powder, particularly the aldehydes (hexanal). Overall, garlic and onion in enhanced meats showed an antioxidant activity as effective as that of sodium ascorbate and also an antimicrobial effect to inhibit the growth of total bacteria and Enterobacteriaceae.


Subject(s)
Anti-Infective Agents/pharmacology , Antioxidants/pharmacology , Food Preservation/methods , Garlic/chemistry , Meat , Onions/chemistry , Ascorbic Acid/pharmacology , Chemical Phenomena , Cold Temperature , Enterobacteriaceae/drug effects , Enterobacteriaceae/growth & development , Fatty Acids/analysis , Hydrogen-Ion Concentration , Lipid Peroxidation/drug effects , Meat/analysis , Meat/microbiology , Volatilization
13.
J Food Sci ; 73(5): C367-72, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18576981

ABSTRACT

After deesterification of commercial pectins with a pectin methyl esterase (PME), their gelling properties were characterized using instrumental texture analysis. The final degree of esterification (DE) of the high- and low-methoxy pectins reached approximately 6% after the PME treatment, while deesterification of low-methoxy amidated pectin stopped at 18% DE. Furthermore, DE of high-methoxy pectin was tailored to be 40%, which is equivalent to the DE of commercial low-methoxy pectin. As a result, significant changes in molecular weight (Mw) distribution were observed in the PME-treated pectins. The texture profile analysis showed that PME modification drastically increased hardness, gumminess, and chewiness, while decreasing cohesiveness and adhesiveness of the pectin gels (P < 0.05). The pectin gel with relatively high peak molecular weight (Mp, 3.5 x 10(5)) and low DE (6), which was produced from high-methoxy pectin, exhibited the greatest hardness, gumminess, chewiness, and resilience. The hardness of low-methoxy amidated pectin increased over 300% after PME deesterification, suggesting that the effects of amide substitution could be reinforced when DE is even lower. The partial least square regression analysis indicated that the Mw and DE of the pectin molecule are the most crucial factors for hardness, chewiness, gumminess, and resilience of gel matrix.


Subject(s)
Carboxylic Ester Hydrolases/metabolism , Gels/chemistry , Pectins/metabolism , Analysis of Variance , Chromatography, High Pressure Liquid , Esterification , Hydrogen-Ion Concentration , Molecular Weight , Particle Size , Pectins/chemistry
14.
Acta Psychiatr Scand ; 116(3): 211-9, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17655563

ABSTRACT

OBJECTIVE: The aim was to investigate the white matter abnormalities of drug-naïve patients with obsessive-compulsive disorder (OCD) using diffusion tensor-imaging and the white matter changes in the patients after pharmacotherapy. METHOD: Thirteen drug-naïve OCD patients and 13 age- and sex-matched healthy comparison subjects were examined using diffusion tensor-imaging and structural magnetic resonance imaging. Measurements were made in OCD patients before and after 12 weeks of citalopram treatment. RESULTS: Compared with controls, the drug-naïve OCD patients showed significant increases in fractional anisotropy (FA) in the corpus callosum, the internal capsule and white matter in the area superolateral to the right caudate. The increases in FA were mostly no longer observed in patients after 12 weeks of treatment compared with controls. CONCLUSION: Our findings suggest that white matter alterations are associated with the pathophysiology of OCD, and the abnormalities may be partly reversible with pharmacotherapy.


Subject(s)
Antidepressive Agents, Second-Generation/therapeutic use , Brain/drug effects , Citalopram/therapeutic use , Diffusion Magnetic Resonance Imaging , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Nerve Fibers, Myelinated/drug effects , Obsessive-Compulsive Disorder/drug therapy , Adult , Anisotropy , Antidepressive Agents, Second-Generation/adverse effects , Caudate Nucleus/drug effects , Caudate Nucleus/pathology , Cerebral Cortex/drug effects , Cerebral Cortex/pathology , Citalopram/adverse effects , Corpus Callosum/drug effects , Corpus Callosum/pathology , Dominance, Cerebral/physiology , Female , Fourier Analysis , Humans , Internal Capsule/drug effects , Internal Capsule/pathology , Male , Nerve Fibers, Myelinated/pathology , Obsessive-Compulsive Disorder/diagnosis , Thalamus/drug effects , Thalamus/pathology
15.
Acta Psychiatr Scand ; 113(1): 64-7, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16390372

ABSTRACT

OBJECTIVE: Thalamic abnormality has been implicated in the pathophysiology of Tourette's syndrome (TS). We examined the presence of aberrant thalamic volume from the treatment-naïve boys with TS using magnetic resonance imaging (MRI). METHOD: Volumetric MRI was performed on 18 treatment-naïve boys with TS, aged 7-14 years, and 16 healthy comparison subjects. The anatomical boundaries were then manually parcellated to measure the thalamic volume. RESULTS: Tourette's syndrome subjects had a significantly larger left thalamus in comparison with those of healthy subjects. On the contrary, no group difference was observed from the right thalamic volume. TS subjects also showed a significant reduction in rightward asymmetry in thalamic volume compared with the healthy subjects. CONCLUSION: Our findings provide new evidence of abnormal thalamic volume in pediatric TS.


Subject(s)
Magnetic Resonance Imaging , Thalamus/abnormalities , Thalamus/physiopathology , Tourette Syndrome/diagnosis , Tourette Syndrome/physiopathology , Adolescent , Child , Functional Laterality/physiology , Humans , Male
16.
Eur J Cancer Prev ; 14(4): 345-50, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16030424

ABSTRACT

Nitric oxide (NO) is an antitumour molecule produced in activated macrophages and Solanum nigrum is a plant used in oriental medicine to treat tumours. In this study using mouse peritoneal macrophages, we have examined the mechanism by which Solanum nigrum regulates NO production. When Solanum nigrum was used in combination with 20 U/ml of recombinant interferon-gamma (rIFN-gamma), there was a marked cooperative induction of NO production. The increase in NO synthesis was reflected as an increased amount of inducible NO synthase (iNOS) protein. The production of NO from rIFN-gamma plus Solanum nigrum-stimulated peritoneal macrophages was decreased by treatment with N-monomethyl-L-arginine or N-tosyl-Phe chloromethyl ketone, an iNOS inhibitor. Additionally, the increased production of NO from rIFN-gamma plus Solanum nigrum-stimulated cells was almost completely inhibited by pretreatment with 100 micromol/l of pyrrolidine dithiocarbamate, an inhibitor of nuclear factor kappaB (NF-kappaB). Furthermore, Solanum nigrum increased activation of NF-kappaB. These findings suggest that Solanum nigrum increases the production of NO by rIFN-gamma-primed macrophages and NF-kappaB plays a critical role in mediating these effects.


Subject(s)
Drugs, Chinese Herbal/pharmacology , Interferon-gamma/pharmacology , Macrophages, Peritoneal/drug effects , NF-kappa B/drug effects , Nitric Oxide/biosynthesis , Solanum nigrum , Analysis of Variance , Animals , Cells, Cultured , Macrophages, Peritoneal/cytology , Mice , NF-kappa B/metabolism , Nitric Oxide Synthase/biosynthesis , Nitric Oxide Synthase/drug effects , Probability , Recombinant Proteins , Risk Factors , Sensitivity and Specificity
17.
Immunopharmacol Immunotoxicol ; 26(1): 135-44, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15106738

ABSTRACT

The preventive effect of Salvia miltiorrhiza extracts (SMEs) on the progress of bone loss induced by ovariectomy (OVX) was studied in rats. We measured body weight and bone histomorphometry in sham, OVX or SMEs-administered OVX rats. From light microscopic analyses, a porous or erosive appearances were observed on the surface of trabecular bone of tibia in OVX rats, whereas those of the same bone in sham rats and in SMEs-administered rats were composed of fine particles. The trabecular bone area and trabecular thickness in OVX rats decreased by 50% from those in sham rats, these decreases were completely inhibited by administration of SMEs for 7 weeks. In this study, the mechanical strength in femur neck was significantly enhanced by the treatment of SMEs for 7 weeks. In OVX rats, free T3 was normal in all cases, whereas free T4 was significantly increased. Although there was no difference between OVX and SMEs-administered rats in T3 level, we have found significant difference between them in T4 level. These results strongly suggest that SMEs are effective in preventing the development of bone loss induced by OVX in rats.


Subject(s)
Osteoporosis/prevention & control , Ovariectomy , Plant Extracts/therapeutic use , Salvia miltiorrhiza , Alkaline Phosphatase/blood , Animals , Calcium/blood , Cell Count , Compressive Strength/drug effects , Female , Femur/drug effects , Femur/metabolism , Femur/pathology , Osteoclasts/cytology , Osteoclasts/drug effects , Osteoporosis/blood , Osteoporosis/pathology , Phosphorus/blood , Phytotherapy , Plant Extracts/pharmacology , Rats , Rats, Sprague-Dawley , Stress, Mechanical , Thyroxine/blood , Triiodothyronine/blood
18.
Am J Chin Med ; 32(6): 883-95, 2004.
Article in English | MEDLINE | ID: mdl-15673194

ABSTRACT

Yuk-Hap-Tang (YHT) induces cell death in human cervical carcinoma HeLa cells. Caspase-3, -6 and -9 were markedly activated in HeLa cells treated with YHT. The preferred substrate for caspase-3 cysteine protease, PARP, was cleaved to its 85-kDa cleavage product. YHT increased the amount of the anti-apoptotic protein, Bcl-2, and the pro-apoptotic protein, Bax. Although p53 has been reported to accumulate in cancer cells in response to anticancer agents, the p53 expression level was not changed in HeLa cells treated with YHT. Manganese (Mn)-TBAP, a mitochondria-specific SOD mimetic agent and NAC/GSH (N-acetyl cysteine/ reduced glutathione) reduced the YHT-induced cytotoxicity and decreased the number of the YHT-induced apoptotic cells. Furthermore, YHT reduced the expression of Mn-SOD protein and its activity in HeLa cells. The data demonstrate that YHT induces the apoptosis of human cervical carcinoma HeLa cells by intervening Mn-SOD.


Subject(s)
Antioxidants/pharmacology , Apoptosis/drug effects , Medicine, East Asian Traditional , Plant Extracts/pharmacology , Superoxide Dismutase/genetics , Caspases/metabolism , Cell Survival/drug effects , Free Radical Scavengers/metabolism , HeLa Cells , Humans , Kinetics , Korea , Phytotherapy , Superoxide Dismutase/drug effects
19.
Clin Chim Acta ; 314(1-2): 215-20, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11718698

ABSTRACT

BACKGROUND: Brain astrocytes play a pivotal role in neuronal activities. METHODS: An investigation was undertaken to determine whether juniper oil inhibits heat shock-induced apoptosis of astrocytes. RESULTS: Juniper oil inhibited the heat shock-induced apoptosis in human astrocyte CCF-STTG1 cells. Pretreatment of the cells with juniper oil inhibited the heat shock-induced DNA fragmentation and condensation of nuclear chromatin. Juniper oil alone did not affect the apoptosis. Juniper oil inhibited the heat shock-induced caspase-3 activation and poly-ADP-ribose polymerase (PARP) fragmentation in the human astrocytes. CONCLUSIONS: Juniper oil may inhibit the apoptosis of astrocytes by preventing the caspase-3 activation.


Subject(s)
Apoptosis/drug effects , Astrocytes/enzymology , Caspases/metabolism , Hot Temperature/adverse effects , Juniperus/chemistry , Plant Oils/pharmacology , Shock/pathology , Astrocytes/drug effects , Blotting, Western , Brain/cytology , Brain/enzymology , Caspase 3 , Cell Line , Cell Nucleus/drug effects , Cell Nucleus/ultrastructure , Chromatin/chemistry , Chromatin/metabolism , DNA/biosynthesis , DNA/chemistry , DNA Fragmentation/drug effects , Depression, Chemical , Enzyme Activation/drug effects , Flow Cytometry , Humans , Poly(ADP-ribose) Polymerases/chemistry , Poly(ADP-ribose) Polymerases/metabolism
20.
Neuroreport ; 12(14): 3045-9, 2001 Oct 08.
Article in English | MEDLINE | ID: mdl-11568634

ABSTRACT

We used event-related fMRI methodology to investigate human brain activity during auditory imagery. A series of susceptibility-weighted MR images covering the whole brain were acquired to obtain blood oxygenation level-dependent (BOLD) signal changes associated with the imagery event of hearing simple monotone. Group analysis across the 12 right-handed subjects revealed activations in the medial and inferior frontal gyri, precuneus, middle frontal gyri, superior temporal gyri, and anterior cingulate gyri. Bilateral primary and secondary auditory areas in the superior temporal gyri also exhibited the event-related MR signal changes. The proposed method allowed for the analysis of brain areas responsive to the event of auditory imagery while our results suggest that auditory imagery and actual audition share common neural substrates.


Subject(s)
Auditory Perception/physiology , Brain Mapping , Cerebral Cortex/physiology , Evoked Potentials/physiology , Functional Laterality/physiology , Imagination/physiology , Magnetic Resonance Imaging , Acoustic Stimulation , Adult , Cerebral Cortex/anatomy & histology , Cerebrovascular Circulation/physiology , Female , Humans , Male , Nerve Net/anatomy & histology , Nerve Net/physiology , Neuropsychological Tests , Reaction Time/physiology
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