Inferior Mesenteric Artery Aneurysm: Case Report and Review of the Literature

Aneurysms of the inferior mesenteric artery are very rare. We report a new case associated with aorto-iliac occlusive disease and occlusion of the superior mesenteric artery, as well as review the pertinent literature

Attachment-specific speech patterns induce dysphoric mood changes in the listener as a function of individual differences in attachment characteristics and psychopathology

Objectives Early childhood experiences influence cognitive-emotional development, with insecure attachment predisposing to potential psychopathologies. We investigated whether narratives containing attachment-specific speech patterns shape listeners’ emotional responses and social intentions. Design First, 149 healthy participants listened to three narratives characteristic for secure, insecure-preoccupied, and insecure-dismissing attachment. Following each narrative, the wellbeing and interpersonal reactivity as a particular aspect of emotional reactivity of the listener were assessed. Likewise, psychopathological aspects of personality were evaluated. A follow-up study compared 10 psychosomatic patients with a current depressive episode and/or personality disorder with distinct depressive symptoms and 10 age- and gender-matched healthy controls. Methods Effects of narratives on listeners’ mental state were tested with repeated-measures AN(C)OVA. Mediating effects in the listener (attachment characteristics in the context of personality traits) were explored. Narrative effects were compared between patients and controls. Results Listening to insecure attachment narratives reduced wellbeing in controls. Nevertheless, tendency for social interaction was highest following the insecure-preoccupied narrative. Importantly, listeners’ individual attachment characteristics mediated the relationship between wellbeing/interpersonal reactivity following the insecure-preoccupied narrative and levels of psychopathology. Furthermore, compared with healthy participants, patients showed higher emotional reactivity following exposure to the insecure-preoccupied narrative, represented by lower wellbeing and lower estimation of friendliness towards the narrator. Conclusions Exposure to attachment-specific speech patterns can result in dysphoric mood changes. Specifically, the insecure-preoccupied narrative influenced the listeners’ emotional state, which was further mediated by the individual attachment patterns and psychopathological personality characteristics. This deepens the understanding of interpersonal processes, especially in psychotherapeutic settings

Routes to sustainability in public food procurement: An investigation of different models in primary school catering

Increasingly, policymakers are setting ambitious goals for sustainability in public procurement, integrated across different pillars. Such ambitions are apparent in public catering services, where procurement models have been shifting towards greater localisation of supply chains and purchasing of more organically grown food. To date however, few studies have examined empirically what the impacts of different procurement models are across these multiple pillars of sustainability. This research aimed to fill the gap, by measuring and comparing the environmental, economic and nutritional outcomes of different models of school meals procurement. Case studies were undertaken of ten primary school meals services in five European countries, capturing different procurement model types. Results showed carbon emissions ranged from 0.95 kgs CO2e per meal in the lowest case to 2.41 kgs CO2e in the highest case, with adoption of low carbon food waste disposal methods and reduction of the amount of ruminant meat in the menus being the most important actions for lowering emissions. In terms of economic impact, local economic multiplier ratios ranged from 1.59 to 2.46, and although the level of local food sourcing contributed to these ratios, the effect was eclipsed, in some cases, by investment in local catering staff. Meanwhile, implementation of a robust standards regime and improving canteen environment and supervision were the most important actions for nutritional quality and intake. The paper discusses the implications of the findings for integrated, sustainable models of food procurement

Glucocorticoids, master modulators of the thymic catecholaminergic system?

There is evidence that the major mediators of stress, i.e., catecholamines and glucocorticoids, play an important role in modulating thymopoiesis and consequently immune responses. Furthermore, there are data suggesting that glucocorticoids influence catecholamine action. Therefore, to assess the putative relevance of glucocorticoid-catecholamine interplay in the modulation of thymopoiesis we analyzed thymocyte differentiation/maturation in non-adrenalectomized and andrenalectomized rats subjected to treatment with propranolol (0.4 mg.100 g body weight(-1).day(-1)) for 4 days. The effects of beta-adrenoceptor blockade on thymopoiesis in non-adrenalectomized rats differed not only quantitatively but also qualitatively from those in adrenalectomized rats. In adrenalectomized rats, besides a more efficient thymopoiesis [judged by a more pronounced increase in the relative proportion of the most mature single-positive TCR alpha beta(high) thymocytes as revealed by two-way ANOVA; for CD4(+)CD8(-)F (1,20) = 10.92, P lt 0.01; for CD4(-)CD8(+)F (1,20) = 7.47, P lt 0.05], a skewed thymocyte maturation towards the CD4(-)CD8(+) phenotype, and consequently a diminished CD4(+)CD8(-)/CD4(-)CD8(+) mature TCR alpha beta(high) thymocyte ratio (3.41 +/- 0.21 in non-adrenalectomized rats vs 2.90 +/- 0.31 in adrenalectomized rats, P lt 0.05) were found. Therefore, we assumed that catecholaminergic modulation of thymopoiesis exhibits a substantial degree of glucocorticoid-dependent plasticity. Given that glucocorticoids, apart from catecholamine synthesis, influence adrenoceptor expression, we also hypothesized that the lack of adrenal glucocorticoids affected not only beta-adrenoceptor- but also alpha-adrenoceptor-mediated modulation of thymopoiesis

Actin Cytoskeleton Vulnerability to Disulfide Stress Mediates Disulfidptosi

SLC7A11-mediated cystine uptake suppresses ferroptosis yet promotes cell death under glucose starvation; the nature of the latter cell death remains unknown. Here, we show that aberrant accumulation of intracellular disulfides in SLC7A11high cells under glucose starvation induces a previously uncharacterized form of cell death distinct from apoptosis or ferroptosis. We term this cell death disulfidptosis. Chemical proteomics and cell biological analyses showed that glucose starvation in SLC7A11high cells induces aberrant disulfide bonds in actin cytoskeleton proteins and F-actin collapse in a SLC7A11-dependent manner. CRISPR screens and functional studies revealed that inactivation of the WAVE regulatory complex (WRC, which promotes actin polymerization and lamellipodia formation) suppresses disulfidptosis, whereas constitutive activation of Rac promotes disulfidptosis. We further showed that glucose transporter inhibitors induce disulfidptosis in SLC7A11high cancer cells and suppress SLC7A11high tumour growth. Our results reveal that the susceptibility of the actin cytoskeleton to disulfide stress mediates disulfidptosis and suggest a therapeutic strategy to target disulfidptosis in cancer treatment

Actin Cytoskeleton Vulnerability to Disulfide Stress Mediates Disulfidptosis

SLC7A11-mediated cystine uptake suppresses ferroptosis yet promotes cell death under glucose starvation; the nature of the latter cell death remains unknown. Here we show that aberrant accumulation of intracellular disulfides in SLC7A11high cells under glucose starvation induces a previously uncharacterized form of cell death distinct from apoptosis and ferroptosis. We term this cell death disulfidptosis. Chemical proteomics and cell biological analyses showed that glucose starvation in SLC7A11high cells induces aberrant disulfide bonds in actin cytoskeleton proteins and F-actin collapse in a SLC7A11-dependent manner. CRISPR screens and functional studies revealed that inactivation of the WAVE regulatory complex (which promotes actin polymerization and lamellipodia formation) suppresses disulfidptosis, whereas constitutive activation of Rac promotes disulfidptosis. We further show that glucose transporter inhibitors induce disulfidptosis in SLC7A11high cancer cells and suppress SLC7A11high tumour growth. Our results reveal that the susceptibility of the actin cytoskeleton to disulfide stress mediates disulfidptosis and suggest a therapeutic strategy to target disulfidptosis in cancer treatment

Structural brain alterations associated with suicidal thoughts and behaviors in young people: results from 21 international studies from the ENIGMA Suicidal Thoughts and Behaviours consortium

Identifying brain alterations associated with suicidal thoughts and behaviors (STBs) in young people is critical to understanding their development and improving early intervention and prevention. The ENIGMA Suicidal Thoughts and Behaviours (ENIGMA-STB) consortium analyzed neuroimaging data harmonized across sites to examine brain morphology associated with STBs in youth. We performed analyses in three separate stages, in samples ranging from most to least homogeneous in terms of suicide assessment instrument and mental disorder. First, in a sample of 577 young people with mood disorders, in which STBs were assessed with the Columbia Suicide Severity Rating Scale (C-SSRS). Second, in a sample of young people with mood disorders, in which STB were assessed using different instruments, MRI metrics were compared among healthy controls without STBs (HC; N = 519), clinical controls with a mood disorder but without STBs (CC; N = 246) and young people with current suicidal ideation (N = 223). In separate analyses, MRI metrics were compared among HCs (N = 253), CCs (N = 217), and suicide attempters (N = 64). Third, in a larger transdiagnostic sample with various assessment instruments (HC = 606; CC = 419; Ideation = 289; HC = 253; CC = 432; Attempt=91). In the homogeneous C-SSRS sample, surface area of the frontal pole was lower in young people with mood disorders and a history of actual suicide attempts (N = 163) than those without a lifetime suicide attempt (N = 323; FDR-p = 0.035, Cohen's d = 0.34). No associations with suicidal ideation were found. When examining more heterogeneous samples, we did not observe significant associations. Lower frontal pole surface area may represent a vulnerability for a (non-interrupted and non-aborted) suicide attempt; however, more research is needed to understand the nature of its relationship to suicide risk.This work was supported by the MQ Brighter Futures Award MQBFC/2 (LS, LC, LV, MRD, LvV, ALvH, HB) and the U.S. National Institute of Mental Health under Award Number R01MH117601 (LS, LvV, NJ). LvV received funding through the National Suicide Prevention Research Fund, managed by Suicide Prevention Australia. LS is supported by an NHMRC Career Development Fellowship (1140764). ALvH is funded through the Social Safety and Resilience program of Leiden University. SA, NB, FP, and GS acknowledge that data collected in IRCCS Santa Lucia Foundation, Rome, Italy was funded by a study funded by the Italian Ministry of Health grant RC17-18-19-20-21/A. ZB, KC, B K-D acknowledge data collected at the University of Minnesota was funded by the National Institute of Mental Health (K23MH090421), the National Alliance for Research on Schizophrenia and Depression, the University of Minnesota Graduate School, the Minnesota Medical Foundation, and the Biotechnology Research Center (P41 RR008079 to the Center for Magnetic Resonance Research), University of Minnesota, and the Deborah E. Powell Center for Women’s Health Seed Grant, University of Minnesota. HB acknowledges data collected at the Yale School of Medicine, New Haven, CT, USA, was funded by: MQ Brighter Futures, R61MH111929RC1MH088366, R01MH070902, R01MH069747, American Foundation for Suicide Prevention, International Bipolar Foundation, Brain and Behavior Research Foundation, For the Love of Travis Foundation and Women’s Health Research at Yale. LC is supported by Interdisziplinäres Zentrum für Klinische Forschung, UKJ. BCD was funded by a CJ Martin Fellowship (NHMRC app 1161356). BCD research leading to these results has received funding from the program “Investissements d’avenir” ANR-10-IAIHU-06. CGD and BJH acknowledge that data collected in Melbourne, Australia, was supported by Australian National Health and Medical Research Council of Australia (NHMRC) Project Grants 1064643 (principal investigator, BJH) and 1024570 (principal investigator, CGD). BJH and CGD were supported by NHMRC Career Development Fellowships (1124472 and 1061757, respectively). UD and TH acknowledge data collected at the FOR2107-Münster was funded by the German Research Foundation (DFG, grant FOR2107-DA1151/5-1 and DA1151/5-2 to UD, and DFG grants HA7070/2-2, HA7070/3, HA7070/4 to TH). AJ and TK acknowledges data collected at the FOR2107-Marburg was funded by the German Research Foundation (DFG, grant FOR2107-JA 1890/7-1 and JA 1890/7-2 to AJ, and DFG, grant FOR2107-KI588/14-1 and FOR2107-KI588/14-2 to TK). KD acknowledges data collected for the Münster Neuroimaging Cohort was funded by the Medical Faculty Münster, Innovative Medizinische Forschung (Grant IMF KO 1218 06 to KD). JMF, PBM, BJO, and GR acknowledge that the “Kids and Sibs” Study was supported by the Australian National Medical and Health Research Council (Program Grant 1037196 and Investigator Grant 1177991 to PBM, Project Grant 1066177 to JMF), the Lansdowne Foundation, Good Talk and the Keith Pettigrew Family Bequest (PM). JMF gratefully acknowledges the Janette Mary O’Neil Research Fellowship. IHG is supported in part by R37MH101495. Support for TAD comes from the National Institute of Mental Health (K01MH106805). TH acknowledges support for TIGER includes the Klingenstein Third Generation Foundation, the National Institute of Mental Health (K01MH117442), the Stanford Maternal Child Health Research Institute, and the Stanford Center for Cognitive and Neurobiological Imaging. TCH receives partial support from the Ray and Dagmar Dolby Family Fund. KAM, ABM, MAS acknowledge data collected at Harvard University was funded by the National Institute of Mental Health (R01-MH103291). IN is supported by grants of the Deutsche Forschungsgemeinschaft (DFG grants NE2254/1-2, NE2254/3-1, NE2254/4-1).This study was supported by the NationalCenter for Complementary and Integrative Health (NCCIH) R21AT009173 and R61AT009864 to TTY; by the National Center for Advancing Translational Sciences(CTSI), National Institutes of Health, through UCSF-CTSI UL1TR001872 to TTY; bythe American Foundation for Suicide Prevention (AFSP) SRG-1-141-18 to TTY; byUCSF Research Evaluation and Allocation Committee (REAC) and J. Jacobson Fundto TTY; by the National Institute of Mental Health (NIMH) R01MH085734 and the Brain and Behavior Research Foundation (formerly NARSAD) to TTY. YC acknowledges the Medical Leader Foundation of Yunnan Province (L2019011) and FamousDoctors Project of Yunnan Province Plan (YNWR-MY-2018-041). DTG, BCF and RAAwish to thank all PAFIP patients and family members who participated in the studyas well as PAFIP´s research team and Instituto de Investigación Marqués deValdecilla. Work by the PAFIP group has been funded by Instituto de Salud Carlos III through the projects PI14/00639, PI14/00918 and PI17/01056 (Co-funded byEuropean Regional Development Fund/European Social Fund “Investing in yourfuture”) and Fundación Instituto de Investigación Marqués de Valdecilla(NCT0235832 and NCT02534363). MER received support from the AustralianNational Health and Medical Research Council (NHMRC) Centre for ResearchExcellence on Suicide Prevention (CRESP) [GNT1042580]. ETCL is supported bygrants from NIAAA (K01AA027573, R21AA027884) and the American Foundationfor Suicide Prevention. All authors thank the participants for volunteering theirtime and supporting our research. Open Access funding enabled and organized by CAUL and its Member Institutions

Decay constants and mixing parameters in a relativistic model for q\barQ system

We extend our recent work, in which the Dirac equation with a ``(asymptotically free) Coulomb + (Lorentz scalar $\gamma_0\sigma r$) linear '' potential is used to obtain the light quark wavefunction for $q\bar Q$ mesons in the limit $m_Q\to \infty$, to estimate the decay constant $f_P$ and the mixing parameter $B$ of the pseudoscalar mesons. We compare our results for the evolution of $f_P$ and $B$ with the meson mass $M_P$ to the non-relativistic formulas for these quantities and show that there is a significant correction in the subasymptotic region. For $\sigma =0.14{{\rm ~GeV}}^{-2}$ and \lms =0.240{\rm ~GeV} we obtain: $f_D =0.371\; ,\; f_{D_s}=0.442\; ,\; f_B=0.301\; ,\; f_{B_s}=0.368 {\rm ~GeV}$ and $B_D=0.88\; ,\; B_{D_s}=0.89\; ,\; B_B=0.95\; ,\; B_{B_s}=0.96\; ,\;$ and $B_K=0.60$.Comment: 13 pages, Latex, 3 figures (included