Postweaning dietary genistein exposure advances puberty without significantly affecting early pregnancy in C57BL/6J female mice

An epidemiological study indicates higher plasma level of genistein in girls with earlier puberty. This study tests the hypothesis in C57BL/6J mice that postweaning (peripubertal) dietary genistein exposure could result in earlier puberty in females assessed by vaginal opening, estrous cyclicity, corpus luteum and mammary gland development. Newly weaned female mice were fed with 0, 5, 100, or 500 ppm genistein diets. Decreased age at vaginal opening, increased length on estrus stage, and accelerated mammary gland development were detected in 100 and 500 ppm genistein-treated groups. Increased presence of corpus luteum was found in 5 ppm genistein-treated group at 6 weeks old only. Increased expression of epithelial-specific genes but not that of ERα or ERβ was detected in 500 ppm genistein-treated mammary glands at 5 weeks old. No significant adverse effect on embryo implantation was observed. These data demonstrate causal effect of dietary genistein on earlier puberty in female mice.     

生殖道局部细胞免疫与黄体功能不全患者不孕的关系

目的:探讨生殖道局部细胞免疫与黄体功能不全患者不孕的关系.方法:研究纳入21例确诊为黄体功能不全(luteal phase deficiency,LPD)的患者作为研究组,同时纳入18例健康体检者最为对照组,使用放射免疫法(radiation immunity analysis,RIA)对排卵期两组血清、宫颈黏液中白细胞介素1-β(IL-1β)以及肿瘤坏死因子-α(TNF-α)的表达进行检测;使用化学发光免疫分析仪检测两组黄体期的血清孕酮水平.结果:黄体期,研究组血清孕酮水平明显高于对照组,差异有统计学意义(P＜0.05);排卵期,研究组宫颈黏液中IL-1β以及TNF-α水平与对照组比较,差异有统计学意义(P＜0.05);研究组宫颈黏液中IL-1β以及TNF-α水平与黄体中期血清孕酮水平存在负相关(r=-0.888,P＜0.05;r=-0.849,P＜0.05);宫颈黏液中IL-1β水平与TNF-α水平存在正相关(r=0.797,P＜0.05).结论:排卵期生殖道局部细胞免疫受到激活,可能是LPD患者发生不孕的主要免疫因素之一,亦能够间接的影响黄体发育从而造成LPD的发生.     

Interhemispheric transfer of spatial and semantic information: Electrophysiological evidence

The goal of this study was to cast light on the existence of functional callosal channels for the interhemispheric transfer (IHT) of spatial and semantic information. To do so, we recorded event‐related potentials in healthy humans while performing a primed odd‐even discrimination task. Targets were visually presented numbers preceded by single‐letter primes signaling the probable presentation of an odd or an even number. Primes and targets could appear either in the same or in different visual fields, thus requiring an IHT in the latter case. The P1 and N2 components were influenced by IHT of spatial information only, whereas the later N400 was influenced by IHT of both spatial and semantic information. This was not the case for the P3b, which was modulated by semantic validity only. These results provide novel evidence of the existence of a temporally separated interhemispheric exchange of spatial and semantic information.     

A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyria

Abstract

Homozygous recessive mutations in the PRICKLE1 gene were originally reported in three consanguineous families with myoclonic epilepsy. Subsequently, several studies have identified neurological abnormalities in animal models with both heterozygous and homozygous mutations in PRICKLE1 orthologues, including epilepsy in flies and in mice with heterozygous PRICKLE1 mutations. We describe a fetus with a novel de novo mutation in PRICKLE1 associated with agenesis of the corpus callosum.     

The effect of corpus luteum on hormonal composition of follicular fluid from different sized follicles and their relationship to serum concentrations in dairy cows

ObjectiveTo investigate the effect of the presence or absence of corpus luteum on hormonal composition of follicular fluid (FF) from different sized follicles and their relationship to serum concentrations in dairy cows.MethodsOvaries were collected from 30 clinically healthy adult female cows (Holstein Friesian) 4–7 years of age with clinically normal reproductive tracts after slaughtering. Blood samples were collected from the jugular vein before slaughter from each cow. The stage of the cycle in the cows was determined postmortem. The ovaries collected from per cow were classified with corpus luteum (CL⁺) and without corpus luteum (CL⁻). FF was aspirated from small (3-5 mm), medium (6-9 mm), and large (10-20 mm) follicles in CL⁺ and CL⁻ ovaries. Serum and FF samples were analyzed for estradiol-17β, progesterone, testosterone, T₃ and T₄ concentrations.ResultsResults demonstrated that the FF concentrations of estradiol-17β, progesterone and testosterone in different sized follicles categories (small, medium and large follicles in CL⁺ and CL⁻ ovaries) were significantly higher (P≤0.05) when compared with the serum. The FF concentrations of estradiol-17β and testosterone in same follicle size categories in CL⁺ and CL⁻ ovaries were also significant (P<0.05). Indeed, concentrations of these hormones in the CL⁻ ovaries were higher than those of the CL⁺ ovaries. However, there was a statistically significant difference between medium and large follicles for progesterone concentration in CL⁺ and CL⁻ ovaries (P<0.05). There was a significant correlation between concentration of hormones in serum and FF with increased follicular diameter.ConclusionsThese results indicated that the levels of hormonal composition in the FF were related to follicular size and interestingly to the presence or absence of a corpus luteum. Indeed, the corpus luteum locally affects neighboring follicular compositions during the luteal phase of the estrous cycle in dairy cows.     

160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker–Warburg syndrome

Walker–Warburg syndrome (WWS) is a severe muscular dystrophy with eye and brain malformations. On a molecular level, WWS is a disorder of the O-linked glycosylation of α-dystroglycan and therefore referred to as one of the dystroglycanopathies. The disease family of muscular dystrophy–dystroglycanopathy (MDDG) contains a spectrum of severe to mild disorders, designated as MDDG type A to C. WWS, as the most severe manifestation, corresponds to MDDG type A. Defects in the genes POMT1, POMT2, POMGNT1, FKTN, FKRP, LARGE, GTDC2, G3GALNT2, GMPPB, B3GNT1, TMEM5 and COL4A1 and ISPD have been described as causal for several types of MDDG including WWS, but can only be confirmed in about 60–70% of the clinically diagnosed individuals. The proteins encoded by these genes are involved in the posttranslational modification of α-dystroglycan. Mutations in POMT1, POMT2, POMGNT1, FKTN, FKRP, LARGE, GMPPB, TMEM5 and COL4A1 and ISPD lead to a wide spectrum of phenotypes of congenital muscular dystrophies with or without eye and brain abnormalities. Patients with WWS frequently demonstrate a complete lack of psychomotor development, severe eye malformations, cobblestone lissencephaly and a hypoplastic cerebellum and brainstem, seizures, hydrocephalus and poor prognosis. Here, we present a boy with WWS who showed compound heterozygous changes in ISPD and discuss the clinical and radiological phenotype and the molecular genetic findings, including a novel pathogenic mutation in ISPD.     

超声诊断双侧黄体破裂1例

患者女,37岁。2006年7月11日，自感腹痛，未行特殊处理。体息后无明显好转。晨6：00点起床后出现晕厥1次，持续约2min，醒后如常。7：50再次出现晕厥1次，伴头晕、乏力、恶心。晕厥时致左前臂外伤．来我院就诊。     

Generation of an annotated reference standard for vaccine adverse event reports

As part of a collaborative project between the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention for the development of a web-based natural language processing (NLP) workbench, we created a corpus of 1000 Vaccine Adverse Event Reporting System (VAERS) reports annotated for 36,726 clinical features, 13,365 temporal features, and 22,395 clinical-temporal links. This paper describes the final corpus, as well as the methodology used to create it, so that clinical NLP researchers outside FDA can evaluate the utility of the corpus to aid their own work. The creation of this standard went through four phases: pre-training, pre-production, production-clinical feature annotation, and production-temporal annotation. The pre-production phase used a double annotation followed by adjudication strategy to refine and finalize the annotation model while the production phases followed a single annotation strategy to maximize the number of reports in the corpus. An analysis of 30 reports randomly selected as part of a quality control assessment yielded accuracies of 0.97, 0.96, and 0.83 for clinical features, temporal features, and clinical-temporal associations, respectively and speaks to the quality of the corpus.     

Marked elevation of interleukin-6 in mild encephalopathy with a reversible splenial lesion (MERS) associated with acute focal bacterial nephritis caused by Enterococcus faecalis

This report describes two cases of mild encephalitis/encephalopathy with reversible splenial lesion (MERS) associated with acute focal bacterial nephritis (AFBN). The patients, who presented with fever and delirious behavior, exhibited hyponatremia and markedly elevated interleukin (IL)-6 in cerebrospinal fluid (CSF) and serum. Enterococcus faecalis was detected in the urine culture. After ampicillin treatment, their consciousness improved without neurological sequelae. Moreover, a diffusion-weighted MRI abnormality, i.e., intensified signals in splenium of the corpus callosum, disappeared. MERS is a possible complication of AFBN. Elevated CSF IL-6 levels suggest that remote activation of intracerebral immune response through the immune–neuroendocrine pathway might play an important role in the pathophysiology of MERS.