Human upright posture control in a virtual visual environment

The sagittal and frontal components of the stabilogram were monitored in 14 healthy subjects standing on a rigid or pliant support under three different conditions of visual control: with the eyes opened (EO), with the eyes closed (EC), or in a virtual visual environment (VVE). Under the VVE conditions, the subjects looked at a three-dimensional image of elements of a room (a 3-D artificial room) that was generated by a computer and locked to the fluctuations of the body center of gravity (CG) so that the visual connection between body sway and shifts of the visual environment typical of normal visual conditions was reproduced. Frequency filtration of the fluctuations of the foot’s center of pressure (FCP) was used to isolate the movements of the vertical projection of the CG and determine the difference between these two variables. The changes in the variables (CG and FCP-CG) were estimated using spectral analysis followed by the calculation of the root mean square (RMS) amplitudes of their spectral fluctuations. In subjects standing on a rigid support, the RMS amplitudes of the spectra of both variables were the highest under the VVE and EC conditions and the lowest under the EO conditions. In subjects standing on a pliant support, body sway was considerably enhanced, which was accompanied by a different pattern of visual influences. The RMS values were the highest under the EC conditions and were lower by a factor of 2–2.5 under the EO and VVE conditions. Thus, it has been demonstrated that the cerebral structures controlling posture ignore the afferent input from the eyes under VVE conditions, if the subject is standing on a rigid support and the CG fluctuations are relatively small; however, this afferentation is efficiently used for maintaining the posture on a pliable support, when the body sway is substantially enhanced.     

Effectiveness of vertical posture recovery after external pushing impact in athletes specialized in different sports

The ability of athletes with different training specializations to recover vertical posture after an external pushing impact was studied. Athletes engaged in cyclic exercise sports (jogging, n = 7) and complex coordinate sports (wrestling, n = 10) and nonathletes (control, n = 10) were the subjects of this study. The recovery of vertical position after a small external pushing impact on the arms extended forward was assessed using stabilography. We determined the maximum amplitude (Amp-m) of deviation from the general center of pressure, the reaction time (RT) and the velocity of reaction (V-r), as well as the variance and mean velocity of vertical posture oscillations before and after an impact. It was found that, although no differences were observed in the vertical posture stability before pushing, the Amp-m was lower in the wrestlers than in the control group (by 17.5%, p = 0.018 under the eye-open conditions; by 27.3%, p = 0.002 under the eye-closed conditions). The deprivation of visual information about the pushing moment increases the Amp-m and V-r and had no effect on the RT in all groups. Under the eye-closed conditions, an increase in Amp-m as a result of pushing was significantly lower in the wrestlers (p = 0.033) than in the control group. Under the eye-closed conditions, the accuracy of the recovery of the initial vertical position after pushing was higher in the wrestlers than in the control group (p = 0.027). The indicators of postural stability, displacement of the center of pressure, and vertical posture sway and recovery after pushing did not differ between the runners and other groups. Therefore, compared to cyclic exercises, training in complex coordinating sports more effectively improves the ability to maintain vertical posture in response to its perturbation.     

Additional afferent signals in the human upright posture control system

Equilibrium maintenance was estimated in a subject standing with the eyes closed while holding a small weight. The experiments were performed on a movable platform in the form of a seesaw. Loads of 200, 500, and 1000 g were held by the subjects between the forefinger and the thumb, with the arm bent at the elbow. The rate of change in the length of the sagittal stabilogram and the root mean square deviation of the center of pressure from the equilibrium position were less when a subject was holding a load while standing on a movable support. The rate of change in the stabilogram length was the lowest (44.5 ± 6.8 mm/s) if the subject stood holding a 1000-g load and was 52.6 ± 9.2 mm/s without a load (p < 0.05, paired T-test). At the same time, when these loads were fixed on a mechanical holder attached to the trunk and simulating an arm bent at the elbow, there was no significant change in stabilogram parameters. Apparently, postural sway reduction is associated with the fact that the system of equilibrium maintenance can control the upright posture using an uncommon afferent input, namely, modulation of afferent signals induced by inertial interaction of an object and the fingers.     

Spectral analysis of the human body sway during standing on firm and compliant surfaces under different visual conditions

Effects of different visual conditions on the vertical posture maintenance were compared in subjects standing on a firm or compliant surface. These visual conditions included a motionless visual environment (MVE), eyes-closed condition (EC), and a virtual visual environment (VVE). The VVE consisted of two planes: the foreground and background. The foreground displayed a room window with adjacent walls, and the background was represented by an aqueduct with the adjacent landscape. The VVE was destabilized by inducing either the cophased or the antiphased relation between the foreground of the visual scene and the body sway. We evaluated changes in the amplitude spectra of two elementary variables calculated from the trajectories of the plantar center of pressure (CoP) displacements in the anteroposterior and lateral directions, namely, the trajectories for the center of gravity projections on the support (the CG variable) and the differences between the CoP and CG trajectories (the CoP–CG variable).The CG trajectory was considered as a controlled variable, and the difference between the CoP and CG trajectories were considered as a variable related to the body acceleration and reflecting changes in the resultant stiffness in ankle joints. The rootmean-square (RMS) values for the spectra of both variables calculated from the body sway in the anteroposterior direction in standing on a firm support decreased proportionately with antiphased relation between the foreground and the body sway and increased with the cophased relation, compared with the RMS calculated for the MVE conditions. RMS for the spectra of the CG variable in the cophased relation were nearly the same, as in standing with eyes closed (EC), while the RMS for the spectra of the CoP–CG variable were significantly less than with EC. The body sway during standing on a compliant support significantly increased in both the anteroposterior and the lateral directions under all visual conditions. RMS for the spectra of both variables with EC increased considerably higher than in the cophased relation. Furthermore, the RMS for the spectra of the CG variable calculated from the body sway in the lateral direction on a compliant support was substantially higher in the antiphased relation than in the cophased relation, whereas the RMS for the spectra of the CoP–CG variable under both conditions had similar values. The analysis of body sway and the results under some visual conditions have shown that the amplitude characteristics of the CG and CoP–CG variables changed not always proportionately with the passage from standing on a firm support to a compliant support. It is suggested that the found disproportion of changes in these two variables is probably associated with the contribution of another additional factor to the process of postural control, the passive elastic component of musculo-articular stiffness generated by fascial-tendon tissues.     

Evaluation of the lambda model for human postural control during ankle strategy

An accurate modeling of human stance might be helpful in assessing postural deficit. The objective of this article is to validate a mathematical postural control model for quiet standing posture. The postural dynamics is modeled in the sagittal plane as an inverted pendulum with torque applied at the ankle joint. The torque control system is represented by the physiological lambda model. Two neurophysiological command variables of the central nervous system, designated and , establish the dynamic threshold muscle at which motoneuron recruitment begins. Kinematic data and electromyographic signals were collected on four young males in order to measure small voluntary sway and quiet standing posture. Validation of the mathematical model was achieved through comparison of the experimental and simulated results. The mathematical model allows computation of the unmeasurable neurophysiological commands and that control the equilibrium position and stability. Furthermore, with the model it is possible to conclude that low-amplitude body sway during quiet stance is commanded by the central nervous system.     

The role of visual information in maintaining postural stability after the maximum exercise for the upper and lower limb muscles

The postural stability on a seesaw generating anterior–posterior instability with the eyes open (EO) and then the eyes closed (EC) in young healthy subjects (n = 28) before and 6 min after the maximum bicycle exercise (Wingate test) performed using lower limbs (“leg exercise”) or upper limbs (“hand exercise”) was investigated. It was found that “hand exercise” caused the same increase in average velocity (V, mm/s) and in the average range of sway of the centre of pressure (Qy, mm) as “leg exercise.” However, the duration of V recovery (EC: 2 min 30 s and 50 s; EO: 60 s and 40 s after “leg exercise” and “hand exercise,” respectively) and Qy (EC: 1 min 10 s and 30 s after “leg exercise” and “hand exercise,” respectively; EO: no changes from baseline) was shorter after “hand exercise.” In the presence of visual information, the increment in V decreased more than 2 times after “leg exercise” (+100.5% and + 40.5%, p < 0.01 for EC and EO, respectively) and after “hand exercise” (+73.0% and +30.3%, p < 0.01 for EC and EO, respectively). Moreover, Qy after both exercises remained at the initial level under EO conditions but significantly increased under EC conditions (+42.8%, p < 0.01 after “leg exercise” and +40.3%, p < 0.01 after “hand exercise”). Thus, the maximum exercise for the muscles of the upper limbs causes the same reduction in postural stability as analogous exercise for the muscles of the lower limbs, but the recovery period after “hand” exercise was shorter. The presence of visual information allows the baseline maintenance of postural stability and significantly reduces the strain of postural regulation while standing on a movable support after the maximum “leg exercise” and “hand exercise.”     

Biological regulation: controlling the system from within

Biological regulation is what allows an organism to handle the effects of a perturbation, modulating its own constitutive dynamics in response to particular changes in internal and external conditions. With the central focus of analysis on the case of minimal living systems, we argue that regulation consists in a specific form of second-order control, exerted over the core (constitutive) regime of production and maintenance of the components that actually put together the organism. The main argument is that regulation requires a distinctive architecture of functional relationships, and specifically the action of a dedicated subsystem whose activity is dynamically decoupled from that of the constitutive regime. We distinguish between two major ways in which control mechanisms contribute to the maintenance of a biological organisation in response to internal and external perturbations: dynamic stability and regulation. Based on this distinction an explicit definition and a set of organisational requirements for regulation are provided, and thoroughly illustrated through the examples of bacterial chemotaxis and the lac-operon. The analysis enables us to mark out the differences between regulation and closely related concepts such as feedback, robustness and homeostasis.     

Magnifying the Scale of Visual Biofeedback Improves Posture

Biofeedback has been shown to minimize body sway during quiet standing. However, limited research has reported the optimal sensitivity parameters of visual biofeedback related to the center of pressure (COP) sway. Accordingly, 19 young adults (6 males; 13 females; aged 21.3 ± 2.5) stood with feet together and performed three visual biofeedback intensities [unmodified biofeedback (UMBF), BF magnified by 5 (BF5), BF magnified by 10 (BF10)], along with control trials with no biofeedback (NBF). The participants were instructed to stand as still as possible while minimizing the movements of the visual target. The findings revealed that UMBF produced significantly greater COP displacement in both the anterior–posterior (AP) and medial–lateral directions, as well as greater standard deviation of the COP in the AP direction (p < 0.05). Additionally, NBF showed significantly greater 95 % area ellipse than the UMBF, BF5, and BF10 intensities (p < 0.001). Therefore, the most sensitive COP scales generated the least amount of postural sway. However, there were no significant differences on any of the COP measures between BF5 and BF10. This research provides insight with respect to the proper scale on which biofeedback should be given in order to improve postural control (i.e., BF5 or BF10).     

Selection of reference genes for quantitative real-time PCR in <Emphasis Type="Italic">Casuarina equisetifolia</Emphasis> under salt stress

Real time quantitative PCR (qPCR) is widely used in gene expression analysis for its accuracy and sensitivity. Reference genes serving as endogenous controls are necessary for gene normalization. In order to select an appropriate reference gene to normalize gene expression in Casuarina equisetifolia under salt stress, 10 potential reference genes were evaluated using real time qPCR in the leaves and roots of plants grown under different NaCl concentrations and treatment durations. GeNorm, NormFinder, and BestKeeper analyses reveal that elongation factor 1-alpha (EF1α) and ubiquitin-conjugating enzyme E2 (UBC) were the most appropriate reference genes for real time qPCR under salt stress. However, β-tubulin (βTUB) and actin 7, which were widely used as reference genes in other plant species, were not always stably expressed. The combination of EF1α, UBC, uncharacterized protein 2, DNAJ homolog subfamily A member 2, and glyceraldehyde-3-phosphate dehydrogenase should be ideal reference genes for normalizing gene expression data in all samples under salt stress. It indicates the need for reference gene selection for normalizing gene expression in C. equisetifolia. In addition, the suitability of reference genes selected was confirmed by validating the expression of WRKY29-like and expansin-like B1. The results enable analysis of salt response mechanism and gene expression in C. equisetifolia.     

<Emphasis Type="Italic">Candida krusei</Emphasis> and <Emphasis Type="Italic">Candida glabrata</Emphasis> reduce the filamentation of <Emphasis Type="Italic">Candida albicans</Emphasis> by downregulating expression of <Emphasis Type="Italic">HWP1</Emphasis> gene

Pathogenicity of Candida albicans is associated with its capacity switch from yeast-like to hyphal growth. The hyphal form is capable to penetrate the epithelial surfaces and to damage the host tissues. Therefore, many investigations have focused on mechanisms that control the morphological transitions of C. albicans. Recently, certain studies have showed that non-albicans Candida species can reduce the capacity of C. albicans to form biofilms and to develop candidiasis in animal models. Then, the objective of this study was to evaluate the effects of Candida krusei and Candida glabrata on the morphogenesis of C. albicans. Firstly, the capacity of reference and clinical strains of C. albicans in forming hyphae was tested in vitro. After that, the expression of HWP1 (hyphal wall protein 1) gene was determined by quantitative real-time PCR (polymerase chain reaction) assay. For both reference and clinical strains, a significant inhibition of the hyphae formation was observed when C. albicans was incubated in the presence of C. krusei or C. glabrata compared to the control group composed only by C. albicans. In addition, the culture mixed of C. albicans-C. krusei or C. albicans-C. glabrata reduced significantly the expression of HWP1 gene of C. albicans in relation to single cultures of this specie. In both filamentation and gene expression assays, C. krusei showed the higher inhibitory activity on the morphogenesis of C. albicans compared to C. glabrata. C. krusei and C. glabrata are capable to reduce the filamentation of C. albicans and consequently decrease the expression of the HWP1 gene.     

Validation of reference genes for RT-qPCR studies in <Emphasis Type="Italic">Stevia rebaudiana</Emphasis> in response to elicitor agents

Stevia rebaudiana is an important source of natural steviol glycosides and is of increasing interest in various fields of study. Therefore, understanding the molecular processes regulating its metabolism is of great importance. In this study, the stability of seven reference genes (18S ribosomal RNA, Actin, Aquaporin, Calmodulin, Eukaryote elongation factor 1-α, Malate dehydrogenase, and Ubiquitin) under the effect of three stress-related elicitors (methyl jasmonate, salicylic acid, and spermidine) was evaluated in stevia plants. We used RefFinder software, which makes use of the four main currently available algorithms for reference gene selection: geNorm, NormFinder, BestKeeper, and the Comparative ?Ct method. The results indicated that Ubiquitin and Actin can be used as reference genes under all tested experimental conditions. The genes, 18S ribosomal RNA, traditionally used as a reference gene, along with Calmodulin, showed the lowest stability. The expression of Deoxyxylulose-5-phosphate synthase and Kaurenoic acid hydroxylase genes was used to confirm the validated reference genes, showing that inadequacy of the reference gene may lead to erroneous results. This is the first study on the stability of reference genes in Stevia rebaudiana plants, and is of great relevance for further analysis of the gene expression of the steviol glycoside biosynthetic pathway.     

Spinal and sensory neuromodulation of spinal neuronal networks in humans

The present experiments were designed to gain additionally insight into how the spinal networks process direct spinal stimulation and peripheral sensory inputs to control posture and locomotor movements. We have developed a plantar pressure stimulation system that can deliver naturalistic postural and gait-related patterns of pressure to the soles of the feet to simulate standing and walking, thereby activating and/or modulating the automated spinal circuitry responsible for standing and locomotion. In the present study we compare the patterns of activation among selected motor pools and the kinematic consequences of these activation patterns in response to patterned heel-to-toe mechanical stimulation of the soles of the feet, and/or transcutaneous electrical spinal stimulation, for postural and locomotion regulation. The studies were performed in healthy individuals (n = 12) as well as in subjects (n = 2) with motor complete spinal cord injury. We found that plantar pressure stimulation and/or spinal stimulation can effectively facilitate locomotor output in the subjects placed with their legs in gravity neutral position. We have shown synergistic effects of combining sensory and spinal cord stimulation, suggesting that the two networks are different, but complementary. Also we provide evidence that plantar stimulation could serve as a novel neuro-rehabilitation tool alone or as part of a multi-modal approach to restoring motor function after complete paralysis due to SCI.     

Maximizing survivorship in cold: thermogenic profiles of non-hibernating mammals

Winter-active small mammals residing in seasonal environments employ many different behavioral, anatomical and physiological mechanisms to cope with cold. Herein we review research on survival mechanisms in cold employed by small mammals with emphasis on the families Soricidae, Muridae and Sciuridae. The focus of this review is on research delineating the role of seasonal changes in resting metabolic rate (RMR), nonshivering thermogenesis (NST), body mass, and communal nesting in enhancing winter survivorship of six species of small mammals (masked shrewSorex cinereus, short-tailed shrewBlarina brevicauda, southern red-backed voleClethrionomys gapperi, white-footed mousePeromyscus leucopus, deer mouseP. maniculatus, and southern flying squirrelGlaucomys volans) residing in the Appalachian Mountains of Pennsylvania, USA. Each species shows good over-winter survivorship but exhibits a different suite of mechanisms to maximize survival in cold.B. brevicauda, S. cinereus, andG. volans show slight increases in RMR during winter, whereasPeromyscus andC. gapperi exhibit decreased RMR overwinter. All six species experience elevated NST in winter. The comparatively low RMR and NST ofG. volans during winter was attributable to a decreased energy expenditure due to a larger body mass, coupled with communal nesting in cavities of trees that provided insulation from low ambient temperatures. Squirrels nesting singly experienced a longer period of elevated NST in winter and higher mean NST year-round than did squirrels nesting communally. Energy conservation in the form of growth retardation in winter was exhibited byC. gapperi andS. cinereus but not the other species.     

Bioactive effect of the preparation biostyl on the reproductive function of different genotypes of American mink

The different role of coat color mutations in the American mink on the per os effect of the biologically active preparation Biostyl was shown. The number of kits per female was the same in all control genotypes, including Standard (+/+ +/+), sapphire (a/a p/p), and lavender (a/a m/m): 4.4 ± 0.4, 4.4 ± 0.5, and 4.3 ± 0.5, respectively. Experimental groups of these genotypes have shown a great contrast among each other: stimulation of the reproductive function was 5.2 ± 0.3 in Standard minks, while suppression of the reproductive function was 3.8 ± 0.6, and 2.3 ± 0.5 in the double recessive mutants sapphire and lavender, respectively. The differentiation in body mass between experimental and control newborn Standard kits was not revealed. A significant decrease in the body mass of newborn experimental sapphire kits as compared to control group in a sex-specific manner was registered.