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Crohn's disease (CD) is a subtype of inflammatory bowel diseases and may be resulted from endocrine disorders. Estrogen and its receptors exert an important role in the pathogenesis of CD. Studies have revealed that estrogen can down-regulate the expression of inflammatory mediators while estrogen supplementation helps reduce the severity of inflammatory response. The expression of receptors (GPER, ERα and ERβ) also influence local immune responses, and the imbalance of them mediate intestinal inflammation. Nowadays, estrogen and its receptors are expected to become a new rarget in the research of CD.

Low energy consumption per synaptic event is important for artificial synapses in applications of highly integrated and large-scale neuromorphic computing systems. Reducing the channel length of a synaptic transistor is an effective method to achieve this goal because such devices can work under low operating voltage and current. In this Letter, we use femtosecond laser ablation to fabricate a microscale slit in an Ag film as the channel of an organic synaptic transistor to obtain low energy consumption. The length of the shortest channel is only 1.6 μm. As a result, the device could be driven by a 50 μV drain bias voltage while output 855 pA excitatory postsynaptic current under a gate spike of 50 mV and 30 ms. The calculated energy consumption per synaptic event is 1.28 fJ, which is comparable to that of a biological synapse (1–10 fJ per synaptic event). Femtosecond laser ablation has been demonstrated a rapid and effective process for the fabrication of microscale channel with high resolution for synaptic transistor, showing large potential for the development of neuromorphic electronics. [ABSTRACT FROM AUTHOR]

Testosterone levels sharply rise during the transition from childhood to adolescence and these changes are known to be associated with changes in human brain structure. During this same developmental window, there are also robust changes in the neural oscillatory dynamics serving verbal working memory processing. Surprisingly, whereas many studies have investigated the effects of chronological age on the neural oscillations supporting verbal working memory, none have probed the impact of endogenous testosterone levels during this developmental period. Using a sample of 89 youth aged 6–14 years‐old, we collected salivary testosterone samples and recorded magnetoencephalography during a modified Sternberg verbal working memory task. Significant oscillatory responses were identified and imaged using a beamforming approach and the resulting maps were subjected to whole‐brain ANCOVAs examining the effects of testosterone and sex, controlling for age, during verbal working memory encoding and maintenance. Our primary results indicated robust testosterone‐related effects in theta (4–7 Hz) and alpha (8–14 Hz) oscillatory activity, controlling for age. During encoding, females exhibited weaker theta oscillations than males in right cerebellar cortices and stronger alpha oscillations in left temporal cortices. During maintenance, youth with greater testosterone exhibited weaker alpha oscillations in right parahippocampal and cerebellar cortices, as well as regions across the left‐lateralized language network. These results extend the existing literature on the development of verbal working memory processing by showing region and sex‐specific effects of testosterone, and are the first results to link endogenous testosterone levels to the neural oscillatory activity serving verbal working memory, above and beyond the effects of chronological age. [ABSTRACT FROM AUTHOR]

Background: Dengue virus (DENV) infection, a common mosquito-borne disease, has been linked to several mental disorders like depression and anxiety. However, the temporal risk of these disorders after DENV infection is not well studied. Methods: This population-based cohort study encompassed 45,334 recently lab-confirmed dengue patients in Taiwan spanning 2002 to 2015, matched at a 1:5 ratio with non-dengue individuals based on age, gender, and residence (n = 226,670). Employing subdistribution hazard regression analysis, we assessed the immediate (<3 months), intermediate (3–12 months), and prolonged (>12 months) risks of anxiety disorders, depressive disorders, and sleep disorders post DENV infection. Corrections for multiple comparisons were carried out using the Benjamini-Hochberg procedure. Results: A significant increase in depressive disorder risk across all timeframes post-infection was observed (<3 months [aSHR 1.90, 95% CI 1.20–2.99], 3–12 months [aSHR 1.68, 95% CI 1.32–2.14], and >12 months [aSHR 1.14, 95% CI 1.03–1.25]). Sleep disorder risk was higher only during 3–12 months (aSHR 1.55, 95% CI 1.18–2.04). No elevated anxiety disorder risk was found. Subgroup analysis of hospitalized dengue patients showed increased risk of anxiety disorders within 3 months (aSHR 2.14, 95% CI 1.19–3.85) and persistent risk of depressive disorders across all periods. Hospitalized dengue patients also had elevated sleep disorder risk within the first year. Conclusion: Dengue patients exhibited significantly elevated risks of depressive disorders in both the short and long term. However, dengue's impact on sleep disorders and anxiety seems to be short-lived. Further research is essential to elucidate the underlying mechanisms. Author summary: Dengue fever is a mosquito-borne tropical disease caused by the dengue virus. Several DENV-induced psychiatric disorders such as anxiety and depression have been identified. Most of the previous studies conducted in the acute stage. Whether deengue infection has lonng-term effects on mental stress remains obscure. Our study suggested that a significant increase in depressive disorder risk across all timeframes post-infection: <3 months, 3–12 months, and >12 months. Sleep disorder risk was higher only during 3–12 months. However, no elevated anxiety disorder risk was found. [ABSTRACT FROM AUTHOR]

Background: Childhood trauma is reliably associated with smaller hippocampal volume in adults; however, this finding has not been shown in children, and even less is known about how sex and trauma interact to affect limbic structural development in children. Methods: Typically developing children aged 9 to 15 years who completed a trauma history questionnaire and structural [T.sub.1]-weighted MRI were included in this study (n = 172; 85 female, 87 male). All children who reported 4 or more traumas (n = 36) composed the high trauma group, and all children who reported 3 or fewer traumas (n = 136) composed the low trauma group. Using multivariate analysis of covariance, we compared FreeSurfer-derived structural MRI volumes (normalized by total intracranial volume) of the amygdalar, hippocampal and parahippocampal regions by sex and trauma level, controlling for age and study site. Results: We found a significant sex * trauma interaction, such that girls with high trauma had greater volumes than boys with high trauma. Follow-up analyses indicated significantly increased volumes for girls and generally decreased volumes for boys, specifically in the hippocampal and parahippocampal regions for the high trauma group; we observed no sex differences in the low trauma group. We noted no interaction effect for the amygdalae. Limitations: We assessed a community sample and did not include a clinical sample. We did not collect data about the ages at which children experienced trauma. Conclusion: Results revealed that psychological trauma affects brain development differently in girls and boys. These findings need to be followed longitudinally to elucidate how structural differences progress and contribute to well-known sex disparities in psychopathology., Introduction A substantial literature associates childhood psychological trauma with smaller limbic structural volumes in adults, consistent with the importance of these regions in emotion recognition, fear processing and episodic memory. [...]