473 research outputs found
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Worrying in the Wings: Negative Emotional Birth Memories in Mothers and Fathers Show Similar Associations with Perinatal Mood Disturbance and Delivery Mode
Abstract
Background: Negative birth experiences are associated with symptoms of post-traumatic stress disorder in new mothers but have received much less attention in new fathers.
Methods: A sample of 322 first-time expectant couples (196 in the UK and 126 in the USA) rated their symptoms of anxiety and depression in the third trimester and at 4-months post birth (234 natural delivery, 88 caesarean section), when they also completed the emotional memories subscale of the BirthMARQ (Foley, Crawley, Wilkie, & Ayers, 2014). We first examined parent gender, mode of delivery (natural birth versus caesarean section) and study site (UK versus USA) as predictors of BirthMARQ scores. Next, we applied Actor-Partner-Interdependence-Modelling (APIM) to investigate intra- and interpersonal associations between birth experiences and latent factors for antenatal and postnatal depression/anxiety in both mothers and fathers.
Results: Reports of negative birth experiences were more common for mothers than fathers, for parents of babies born by caesarean section than vaginal delivery and for UK parents than for USA parents. Within-couple agreement was moderately strong and individual differences in negative birth memories were associated with latent factors for depression/anxiety at both time-points, for both parents; in addition, there was a marginal mediation effect of negative birth memories in relation to the association between birth via caesarean section and reduced postnatal maternal wellbeing.
Conclusions: Our findings highlight the links between birth experiences and wellbeing for both mothers and fathers and so support the development of partner-inclusive intervention strategies.
Key words: birth experience, depression, anxiety, mothers, fathers, deliveryThe research was funded by grants from the Economic and
Social Research Council and National Science Foundation (ESRC: ES/
L016648/1 and NSF: 1429152)
Muon Spin Relaxation and Susceptibility Studies of Pure and Doped Spin 1/2 Kagom\'{e}-like system (CuZn)VO(OH) 2HO
Muon spin relaxation (SR) and magnetic susceptibility measurements have
been performed on the pure and diluted spin 1/2 kagom\'{e} system
(CuZn)VO(OH) 2HO. In the pure
system we found a slowing down of Cu spin fluctuations with decreasing
temperature towards K, followed by slow and nearly
temperature-independent spin fluctuations persisting down to = 50 mK,
indicative of quantum fluctuations. No indication of static spin freezing was
detected in either of the pure (=1.0) or diluted samples. The observed
magnitude of fluctuating fields indicates that the slow spin fluctuations
represent an intrinsic property of kagom\'e network rather than impurity spins.Comment: 4 pges, 4 color figures, Phys. Rev. Lett. in pres
Muon Spin Relaxation Studies of Magnetic-Field-Induced Effects in High- Superconductors
Muon spin relaxation (SR) measurements in high transverse magnetic
fields () revealed strong field-induced quasi-static
magnetism in the underdoped and Eu doped (La,Sr)CuO and
LaBaCuO, existing well above and . The
susceptibility-counterpart of Cu spin polarization, derived from the muon spin
relaxation rate, exhibits a divergent behavior towards K. No
field-induced magnetism was detected in overdoped
LaSrCuO, optimally doped Bi2212, and Zn-doped
YBaCuO.Comment: 4 pages, 4 color figure
Chemical Characterization and Biological Evaluation of \u3ci\u3eEpilobium parviflorum\u3c/i\u3e Extracts in an In Vitro Model of Human Malignant Melanoma
Malignant melanoma is an aggressive type of skin cancer characterised by high metastatic capacity and mortality rate. On the other hand, Epilobium parviflorum is known for its medicinal properties, including its anticancer potency. In this context, we aimed to (i) isolate various extracts of E. parviflorum, (ii) characterize their phytochemical content, and (iii) determine their cytotoxic potential in an in vitro model of human malignant melanoma. To these ends, we utilized various spectrophotometric and chromatographic (UPLC-MS/MS) approaches to document the higher content of the methanolic extract in polyphenols, soluble sugars, proteins, condensed tannins, and chlorophylls -a and -b as opposed to those of dichloromethane and petroleum. In addition, the cytotoxicity profiling of all extracts was assessed through a colorimetric-based Alamar Blue assay in human malignant melanoma (A375 and COLO-679) as well as non-tumorigenic immortalized keratinocyte (HaCaT) cells. Overall, the methanolic extract was shown to exert significant cytotoxicity, in a timeand concentration-dependent manner, as opposed to the other extracts. The observed cytotoxicity was confined only to human malignant melanoma cells, whereas non-tumorigenic keratinocyte cells remained relatively unaffected. Finally, the expression levels of various apoptotic genes were assessed by qRT-PCR, indicating the activation of both intrinsic and extrinsic apoptotic cascades.
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An Evaluation of the Anti-Carcinogenic Response of Major Isothiocyanates in Non-Metastatic and Metastatic Melanoma Cells
Malignant melanoma is one of the most deadly types of solid cancers, a property mainly attributed to its highly aggressive metastatic form. On the other hand, different classes of isothiocy- anates, a class of phytochemicals, present in cruciferous vegetables have been characterized by considerable anti-cancer activity in both in vitro and in vivo experimental models. In the current study, we investigated the anti-cancer response of five isothiocyanates in an in vitro model of melanoma consisting of non-metastatic (A375, B16F-10) and metastatic (VMM1, Hs294T) malignant melanoma as well as non-melanoma epidermoid carcinoma (A431) and non-tumorigenic melanocyte-neighboring keratinocyte (HaCaT) cells. Our aim was to compare different endpoints of cytotoxicity (e.g., reactive oxygen species, intracellular glutathione content, cell cycle growth arrest, apoptosis and necrosis) descriptive of an anti-cancer response between non-metastatic and metastatic melanoma as well as non-melanoma epidermoid carcinoma and non-tumorigenic cells. Our results showed that exposure to isothiocyanates induced an increase in intracellular reactive oxygen species and glutathione contents between non-metastatic and metastatic melanoma cells. The distribution of cell cycle phases followed a similar pattern in a manner where non-metastatic and metastatic melanoma cells appeared to be growth arrested at the G2/M phase while elevated levels of metastatic melanoma cells were shown to be at sub G1 phase, an indicator of necrotic cell death. Finally, metastatic melanoma cells were more sensitive apoptosis and/or necrosis as higher levels were observed compared to non-melanoma epidermoid carcinoma and non-tumorigenic cells. In general, non-mela- noma epidermoid carcinoma and non-tumorigenic cells were more resistant under any experimental exposure condition. Overall, our study provides further evidence for the potential development of isothiocyanates as promising anti-cancer against non-metastic and metastatic melanoma cells, a property specific for these cells and not shared by non-melanoma epidermoid carcinoma or non-tumorigenic melanocyte cells
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Mutual Funds’ Conditional Performance Free of Data Snooping Bias
We introduce a test to assess mutual funds’ “conditional” performance that is based on updated information and corrects data snooping bias. Our method, named the functional False Discovery Rate “plus” (fF DR+), incorporates fund characteristics in estimating fund performance free of data snooping bias. Simulations suggest that the fF DR+ controls well the ratio of false discoveries and gains considerable power over prior methods that do not account for extra information. Portfolios of funds selected by the fF DR+ outperform other tests not accounting for information updating, highlighting the importance of evaluating mutual funds from a conditional perspective
Site-Dilution in quasi one-dimensional antiferromagnet Sr2(Cu1-xPdx)O3: reduction of Neel Temperature and spatial distribution of ordered moment sizes
We investigate the Neel temperature of Sr2CuO3 as a function of the site
dilution at the Cu (S=1/2) sites with Pd (S=0), utilizing the muon spin
relaxation (muSR) technique. The Neel temperature, which is Tn=5.4K for the
undoped system, becomes significantly reduced for less than one percent of
doping Pd, giving a support for the previous proposal for the good
one-dimensionality. The Pd concentration dependence of the Neel temperature is
compared with a recent theoretical study (S. Eggert, I. Affleck and M.D.P.
Horton, Phys. Rev. Lett. 89, 47202 (2002)) of weakly coupled one-dimensional
antiferromagnetic chains of S=1/2 spins, and a quantitative agreement is found.
The inhomogeneity of the ordered moment sizes is characterized by the muSR time
spectra. We propose a model that the ordered moment size recovers away from the
dopant S=0 sites with a recovery length of \xi = 150-200 sites. The origin of
the finite recovery length \xi for the gapless S=1/2 antiferromagnetic chain is
compared to the estimate based on the effective staggered magnetic field from
the neighboring chains.Comment: 10 pages, 9 figures, submitted to PR
Polyphenolics, glucosinolates and isothiocyanates profiling of aerial parts of \u3ci\u3eNasturtium officinale\u3c/i\u3e (Watercress)
Watercress (Nasturtium officinale) is a rich source of secondary metabolites with disease-preventing and/or health-promoting properties. Herein, we have utilized extraction procedures to isolate fractions of polyphenols, glucosinolates and isothiocyanates to determine their identification, and quantification. In doing so, we have utilized reproducible analytical methodologies based on liquid chromatography with tandem mass spectrometry by either positive or negative ion mode. Due to the instability and volatility of isothiocyanates, we followed an ammonia derivatization protocol which converts them into respective ionizable thiourea derivatives. The analytes’ content distribution map was created on watercress flowers, leaves and stems. We have demonstrated that watercress contains significantly higher levels of gluconasturtiin, phenethyl isothiocyanate, quercetin-3-O-rutinoside and isorhamnetin, among others, with their content decreasing from flowers (82.11 ± 0.63, 273.89 ± 0.88, 1459.30 ± 12.95 and 289.40 ± 1.37 ng/g of dry extract respectively) to leaves (32.25 ± 0.74, 125.02 ± 0.52, 1197.86 ± 4.24 and 196.47 ± 3.65 ng/g of det extract respectively) to stems (9.20 ± 0.11, 64.7 ± 0.9, 41.02 ± 0.18, 65.67 ± 0.84 ng/g of dry extract respectivbely). Pearson’s correlation analysis has shown that the content of isothiocyanates doesn’t depend only on the bioconversion of individual glucosinolates but also on other glucosinolates of the same group. Overall, we have provided comprehensive analytical data of the major watercress metabolites thereby providing an opportunity to exploit different parts of watercress for potential therapeutic applications
Dual wavelength (ultraviolet and green) photodetectors using solution processed Zinc Oxide nanoparticles
Narrow-band photoconductivity with a spectral width of 0.16 eV is obtained from solution-processed colloidal ZnO nanocrystals beneath the band-edge at 2.25 eV. A new model involving electron transfer from deep defects to discrete shallow donors is introduced to explain the narrow spectrum and the exponential form of the current rise and decay transients. The defects are tentatively assigned to neutral oxygen vacancies. The photocurrent responsivity can be enhanced by storage in air and this correlates with the formation of carbonate surface species by capture of carbon dioxide during storage. This controllability is exploited to develop a low-cost and scalable photolithographic approach to pixelate photodetectors for applications such as object discrimination, sensing etc. The spectral response can be spatially patterned so that dual (ultraviolet and green) and single (ultraviolet only) wavelength detecting ZnO pixels can be produced on the same substrate. This presents a new sensor mode with applications in security or full colour imaging
Evaluation of Bioactive Properties of Lipophilic Fractions of Edible and Non-Edible Parts of \u3ci\u3eNasturtium officinale\u3c/i\u3e (Watercress) in a Model of Human Malignant Melanoma Cells
Watercress is an enriched source of phenethyl isothiocyanate (PEITC), among other phytochemicals, with an antioxidant capacity. The aim of this study was to (i) chemically characterize and (ii) biologically evaluate the profile of the main health-promoting compounds contained in edible (i.e., mixture of leaves and lateral buds) and non-edible (i.e., stems) parts of watercress in an in vitro model of malignant melanoma consisting of human malignant melanoma (A375), non-melanoma (A431) and keratinocyte (HaCaT) cells. The extraction of the main constituents of watercress was performed by subjecting the freeze-dried edible and non-edible samples through different extraction protocols, whereas their concentration was obtained utilizing analytical methodologies. In addition, cell viability was evaluated by the Alamar Blue assay, whereas levels of oxidative stress and apoptosis were determined by commercially available kits. The edible watercress sample contained a higher amount of various nutrients and phytochemicals in the hexane fraction compared to the non-edible one, as evidenced by the presence of PEITC, phenolics, flavonoids, pigments, ascorbic acid, etc. The cytotoxicity potential of the edible watercress sample in the hexane fraction was considerably higher than the non-edible one in A375 cells, whereas A431 and HaCaT cells appeared to be either more resistant or minimally affected, respectively. Finally, levels of oxidative stress and apoptotic induction were increased in both watercress samples, but the magnitude of the induction was much higher in the edible than the non-edible watercress samples. Herein, we provide further evidence documenting the potential development of watercress extracts (including watercress waste by-products) as promising anti-cancer agent(s) against malignant melanoma cells
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