Gender Specificity of Genistein Treatment in Penicillin-Induced Epileptiform Activity in Rats

We investigated gender-dependent differences of genistein (isoflavone phytoestrogen) treatment in a penicillin-induced experimental epilepsy rat model. Twenty-eight adult Wistar Albino rats (14 females and 14 males) were devided into four groups, control and genisteintreatmed males and females. Genistein (100 µg/kg, i.p) or saline was given during 15 days before the electrocorticography (ECoG) recordings. The epileptiform activity was induced by penicillin G potassium solt (500 IU, i.c) injections into the left somatomotor cortex. Significant differences among the groups were found in the latency to onset of epileptiform activity. This value in the female control group was significantly longer than the latencies in the male control, male genistein, and female genistein groups (respectively, P = 0.002, 0.015, and 0.032). There were no significant differences regarding the spike/wave frequencies and amplitudes in epileptiform activity between female/male genistein and control groups within all observation intervals (P > 0.05). Thus, genistein exerts a proconvulsant effect in the penicillin-induced epilepsy model, and the effect demonstrates the clear gender specificity related to the specificity of hormonal backgrounds in males and females.Ми досліджували залежні від статі відмінності впливу ґеністеїну (ізофлавоноїдного фітоестрогена) в умовах індукованої пеніциліном експериментальної моделі епілепсії у щурів. 28 дорослих щурів лінії Вістар (14 самиць і 14 самців) були поділені на чотири групи – контрольних та лікованих ґеністеїном самців і самиць. Ґеністеїн (100 мкг/кг, внутрішньоочеревинно) або фізіологічний розчин уводився тваринам протягом 15 діб, після чого у них відводились електрокортикограма (ЕКоГ). Епілептиформна активність індукувалась ін’єкцією пеніциліну G калієвої солі (500 МО) в ліву соматомоторну кору. Істотні міжгрупові відмінності були виявлені щодо латентного періоду початку епілептиформної активності (P = 0.013). Ця величина в контрольній групі самиць була істотно більшою, ніж аналогічні значення в контрольній групі самців та групах самців і самиць, лікованих ґеністеїном (P = 0.002, 0.015 та 0.032 відповідно). Не було виявлено істотних відмінностей щодо частоти комплексів пік/хвиля та амплітуди епілептиформної активності у всіх чотирьох груп у межах інтервалу спостережень (P > > 0.05). Зроблено висновок, що ґеністеїн впливає на пеніцилініндуковану модель епілепсії як проконвульсант; відповідні ефекти демонструють значну гендерну специфіку, очевидно, залежну від гормонального фону в самців і самиць

Evaluation of apertura piriformis and related cranial anatomical structures through computed tomography: golden ratio

Background: The purpose of study was to evaluate normal morphometric measurements of piriform aperture (PA) by limiting the age range in genders to show the morphometry of the relevant and close proximal cranial structures; and also to investigate whether these are in compliance with the golden ratio. Materials and methods: Our study was performed on 83 (42 female, 41 male) multidetector computed tomography images obtained from patients. A total of 14 morphological measurements were performed including the height of PA, the width of PA and 12 cranial structures; and these measurements were evaluated for compliance with the golden ratio. The differences of 14 parameters between the genders and age groups, and also the interaction of these two factors were analysed. Results: In our morphometric study, significant difference between the genders was found in all measurements except for the distance between vertex and rhinion (V~Rh), between rhinion and right foramen supraorbitalis (Rh~FSOR), between rhinion and left FSO (Rh~FSOL), and the width of PA on the level between the right and left foramen infraorbitalis (PAW~FIO) with the difference valid for both age subgroups (p < 0.05). When the differences between the age subgroups were evaluated, there was significant difference only at the widest distance of cranium (CW; p = 0.008); and it was observed that the average has increased with age in both genders. When the golden ratio was examined, the ratio of the distance between anterior nasal spine and nasion to the height of piriform aperture (NSA~N:PAH) was found to be within the limits of the golden ratio in males (p = 0.074). No golden ratio has been found in females. Conclusions: In our study, significant differences were detected between genders in all parameters of PA and in some parameters of the close cranial structures in the age group we examined. The effect of age was detected only in the CW parameter, and the PA and close cranial structures were not affected. In our study, the averages of the morphometric measurements of 13 parameters of young adults were determined. The PA and surrounding cranial structures are important for the area and related surgical procedures; however, gender differences must be considered in this respect. In addition to this, in the PA, which is the anterior limit of the skeletal nose in males, the NSA~N:PAH ratio having the ideal golden ratio limits is valuable in aesthetical terms and due to its position of the PA in the face

Anatomical Region-Specific In Vivo Wireless Communication Channel Characterization

In vivo wireless body area networks (WBANs) and their associated technologies are shaping the future of healthcare by providing continuous health monitoring and noninvasive surgical capabilities, in addition to remote diagnostic and treatment of diseases. To fully exploit the potential of such devices, it is necessary to characterize the communication channel which will help to build reliable and high-performance communication systems. This paper presents an in vivo wireless communication channel characterization for male torso both numerically and experimentally (on a human cadaver) considering various organs at 915 MHz and 2.4 GHz. A statistical path loss (PL) model is introduced, and the anatomical region-specific parameters are provided. It is found that the mean PL in dB scale exhibits a linear decaying characteristic rather than an exponential decaying profile inside the body, and the power decay rate is approximately twice at 2.4 GHz as compared to 915 MHz. Moreover, the variance of shadowing increases significantly as the in vivo antenna is placed deeper inside the body since the main scatterers are present in the vicinity of the antenna. Multipath propagation characteristics are also investigated to facilitate proper waveform designs in the future wireless healthcare systems, and a rootmean- square (RMS) delay spread of 2.76 ns is observed at 5 cm depth. Results show that the in vivo channel exhibit different characteristics than the classical communication channels, and location dependency is very critical for accurate, reliable, and energy-efficient link budget calculations

Independent estimation of input and measurement delays for a hybrid vertical spring-mass-damper via harmonic transfer functions

System identification of rhythmic locomotor systems is challenging due to the time-varying nature of their dynamics. Even though important aspects of these systems can be captured via explicit mechanics-based models, it is unclear how accurate such models can be while still being analytically tractable. An alternative approach for rhythmic locomotor systems is the use of data-driven system identification in the frequency domain via harmonic transfer functions (HTFs). To this end, the input-output dynamics of a locomotor behavior can be linearized around a stable limit cycle, yielding a linear, time-periodic system. However, few if any model-based or data-driven identification methods for time-periodic systems address the problem of input and measurement delays in the system. In this paper, we focus on data-driven system identification for a simple mechanical system and analyze its dynamics in the presence of input and measurement delays using HTFs. By exploiting the way input delays are modulated by the periodic dynamics, our results enable the separate, independent estimation of input and measurement delays, which would be indistinguishable were the system linear and time invariant. © 2015, IFAG

Detecting imipenem resistance in Acinetobacter baumannii by automated systems (BD Phoenix, Microscan WalkAway, Vitek 2); high error rates with Microscan WalkAway

<p>Abstract</p> <p>Background</p> <p>Increasing reports of carbapenem resistant <it>Acinetobacter baumannii </it>infections are of serious concern. Reliable susceptibility testing results remains a critical issue for the clinical outcome. Automated systems are increasingly used for species identification and susceptibility testing. This study was organized to evaluate the accuracies of three widely used automated susceptibility testing methods for testing the imipenem susceptibilities of <it>A. baumannii </it>isolates, by comparing to the validated test methods.</p> <p>Methods</p> <p>Selected 112 clinical isolates of <it>A. baumanii </it>collected between January 2003 and May 2006 were tested to confirm imipenem susceptibility results. Strains were tested against imipenem by the reference broth microdilution (BMD), disk diffusion (DD), Etest, BD Phoenix, MicroScan WalkAway and Vitek 2 automated systems. Data were analysed by comparing the results from each test method to those produced by the reference BMD test.</p> <p>Results</p> <p>MicroScan performed true identification of all <it>A. baumannii </it>strains while Vitek 2 unidentified one strain, Phoenix unidentified two strains and misidentified two strains. Eighty seven of the strains (78%) were resistant to imipenem by BMD. Etest, Vitek 2 and BD Phoenix produced acceptable error rates when tested against imipenem. Etest showed the best performance with only two minor errors (1.8%). Vitek 2 produced eight minor errors(7.2%). BD Phoenix produced three major errors (2.8%). DD produced two very major errors (1.8%) (slightly higher (0.3%) than the acceptable limit) and three major errors (2.7%). MicroScan showed the worst performance in susceptibility testing with unacceptable error rates; 28 very major (25%) and 50 minor errors (44.6%).</p> <p>Conclusion</p> <p>Reporting errors for <it>A. baumannii </it>against imipenem do exist in susceptibility testing systems. We suggest clinical laboratories using MicroScan system for routine use should consider using a second, independent antimicrobial susceptibility testing method to validate imipenem susceptibility. Etest, whereever available, may be used as an easy method to confirm imipenem susceptibility.</p