Effects of fibroin microcarriers on inflammation and regeneration of deep skin wounds in mice

The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative potential of biological material is related to its ability to modulate the inflammatory response. At the same time, all foreign materials, once implanted into a living tissue, to varying degree cause an immune reaction. The modern approach to the development of bioengineered structures for applications in regenerative medicine should be directed toward using the properties of the inflammatory response that improve healing, but do not lead to negative chronic manifestations. In this work, we studied the effect of microcarriers comprised of either fibroin or fibroin supplemented with gelatin on the dynamics of the healing, as well as inflammation, during regeneration of deep skin wounds in mice. We found that subcutaneous administration of microcarriers to the wound area resulted in uniform contraction of the wounds in mice in our experimental model, and microcarrier particles induced the infiltration of immune cells. This was associated with increased expression of proinflammatory cytokines TNF, IL-6, IL-1β, and chemokines CXCL1 and CXCL2, which contributed to full functional recovery of the injured area and the absence of fibrosis as compared to the control group.     

Sexual Differentiation of the Brain as a Manifestation of Its Plasticity

This review analyzes the published data and authors' own results on the roles of hormones and neurotransmitters in the formation of structural and functional sex-related dimorphism of the brain within the early ontogenesis period. Proof is presented in favor of the concept that classic neurotransmitters function as inductors of nerve cell differentiation in the process of individual development of the brain. Neurochemical mechanisms of the hormone–transmitter interaction in the process of sexual differentiation of the brain within pre- and/or post-natal periods are considered.     

Horizontal gene transfer in chromalveolates

Background  

Horizontal gene transfer (HGT), the non-genealogical transfer of genetic material between different organisms, is considered a potentially important mechanism of genome evolution in eukaryotes. Using phylogenomic analyses of expressed sequence tag (EST) data generated from a clonal cell line of a free living dinoflagellate alga Karenia brevis, we investigated the impact of HGT on genome evolution in unicellular chromalveolate protists.     

Sex characteristics of neuroendocrine effects of prenatal exposure to exogenous glucocorticoids

The effects of hydrocortisone acetate treatment of rats during the last gestational week on neurochemical and morphological characteristics of the brain in early postnatal and mature offspring were studied. Disappearance of sexual differences both in aromatase and 5alpha-reductase activities and noradrenaline concentration in the preoptic area in 10-day old rats was found. Meanwhile a sexual dimorphism in serotonin metabolism emerged. In adult offspring, the prenatal exposure to glucocorticoids resulted in disappearance of sexual differences in neurocytes' nuclei volume in medial preoptic and suprachiasmatic nuclei. The adrenocortical reaction to noradrenaline infusion to the 3rd brain ventricle was absent in the experimental males and intensified in females. In males, adrenocortical reaction to restraint decreased while post-stress changes in hypothalamic noradrenaline concentration and hippocampal glutamate decarboxylase activity were not observed. In the similar experiments in females both the augmentation of adrenocortical reaction and inhibition of GABA-ergic system were revealed. The results obtained indicate the modifying effect of prenatal exposure to glucocorticoids on sexual dimorphism of neuroendocrine system.     

Mass Fractions of 52 Trace Elements and Zinc/Trace Element Content Ratios in Intact Human Prostates Investigated by Inductively Coupled Plasma Mass Spectrometry

Contents of 52 trace elements in intact prostate of 64 apparently healthy 13?C60-year-old men (mean age 36.5?years) were investigated by inductively coupled plasma mass spectrometry. Mean values (M ± S????) for mass fraction (in milligrams per kilogram, on dry-weight basis) of trace elements were as follows: Ag 0.041?±?0.005, Al 36?±?4, Au 0.0039?±?0.0007, B 0.97?±?0.13, Be 0.00099?±?0.00006, Bi 0.021?±?0.008, Br 29?±?3, Cd 0.78?±?0.09, Ce 0.028?±?0.004, Co 0.035?±?0.003, Cs 0.034?±?0.003, Dy 0.0031?±?0.0005, Er 0.0018?±?0.0004, Gd 0.0030?±?0.0005, Hg 0.046?±?0.006, Ho 0.00056?±?0.00008, La 0.074?±?0.015, Li 0.040?±?0.004, Mn 1.53?±?0.09, Mo 0.30?±?0.03, Nb 0.0051?±?0.0009, Nd 0.013?±?0.002, Ni 4.3?±?0.7, Pb 1.8?±?0.4, Pr 0.0033?±?0.0004, Rb 15.9?±?0.6, Sb 0.040?±?0.005, Se 0.73?±?0.03, Sm 0.0027?±?0.0004, Sn 0.25?±?0.05, Tb 0.00043?±?0.00009, Th 0.0024?±?0.0005, Tl 0.0014?±?0.0001, Tm 0.00030?±?0.00006, U 0.0049?±?0.0014, Y 0.019?±?0.003, Yb 0.0015?±?0.0002, Zn 782?±?97, and Zr 0.044?±?0.009, respectively. The upper limit of mean contents of As, Cr, Eu, Ga, Hf, Ir, Lu, Pd, Pt, Re, Ta, and Ti were the following: As ??0.018, Cr ??0.64, Eu ??0.0006, Ga ??0.08, Hf ??0.02, Ir ??0.0004, Lu ??0.00028, Pd ??0.007, Pt ??0.0009, Re ??0.0015, Ta ??0.005, and Ti ??2.6. In all prostate samples, the content of Te was under detection limit (<0.003). Additionally, ratios of the Zn content to other trace element contents as well as correlations between Zn and trace elements were calculated. Our data indicate that the human prostate accumulates such trace elements as Al, Au, B, Br, Cd, Cr, Ga, Li, Mn, Ni, Pb, U, and Zn. No special relationship between Zn and other trace elements was found.     

Linguistic features of the structure of verbal expression in emotional stress]

Comparative analysis was carried out of the linguistic characteristics of oral speech, recorded in 68 subjects in a state of anxiety (students in examination situation; surgical patients in preoperative interview; air force operators undergoing responsible professional-proficiency tests) and of speech disturbances in patients with damages in the parts of the brain which play a significant role in the control of stress and emotional behaviour. The results obtained allow to conclude, that speech disturbances of normal subjects in a state of anxiety are caused by physiological factors and thus can be used as objective indices of the speaker's emotional state, since they are similar to those of the patients with damages in the region of the temporal lobe, intimately connected with limbic structures.     

Catecholamines in steroid-dependent brain development

Sex-specific peculiarities of catecholamine (CA) content and turnover in neuroendocrine brain areas and their modification with neonatal steroids or prenatal stress (PS) in Wistar rats were studied. No changes in noradrenaline (NA) content and turnover rate were found in the preoptic area (POA), meanwhile dopamine (DA) turnover rates in the POA and mediobasal hypothalamus (MBH) were increased in neonatally androgenized 10-day-old females. Treatment of female neonates with various catecholestrogens increased hypothalamic NA content by 30–95% but only 4-hydroxyestradiol-17β induced anovulation. 6-Hydroxydopamine had no significant impact on hypothalamic CA content in neonates and did not prevent testosterone-induced persistent estrous. Maternal stress (restriction for 1 h a day, 15–21st days of pregnancy) resulted in a decrease of hypothalamic NA and blood plasma corticosterone response to acute stress in adult male offspring. Sex differences in CA content in the POA and MBH disappeared in 10-day-old prenatally stressed rats. Conclusions: (1) sexual brain differentiation needs co-operative actions of sex steroids and CA to be completed; and (2) early changes in CA content and turnover induced by PS or neonatal steroid exposure predetermine long-term alterations of the stress responsiveness, reproductive behaviour and neuroendocrine control of ovulation.