Investigating the effect of changes in neuronal connectivity on the brain's behavior is of interest in neuroscience studies. Complex network theory is one of the most capable tools to study the effects of these changes on collective brain behavior. By using complex networks, the neural structure, function, and dynamics can be analyzed. In this context, various frameworks can be used to mimic neural networks, among which multi-layer networks are a proper one. Compared to single-layer models, multi-layer networks can provide a more realistic model of the brain due to their high complexity and dimensionality. This paper examines the effect of changes in asymmetry coupling on the behaviors of a multi-layer neuronal network. To this aim, a two-layer network is considered as a minimum model of left and right cerebral hemispheres communicated with the corpus callosum. The chaotic model of Hindmarsh-Rose is taken as the dynamics of the nodes. Only two neurons of each layer connect two layers of the network. In this model, it is assumed that the layers have different coupling strengths, so the effect of each coupling change on network behavior can be analyzed. As a result, the projection of the nodes is plotted for several coupling strengths to investigate how the asymmetry coupling influences the network behaviors. It is observed that although no coexisting attractor is present in the Hindmarsh-Rose model, an asymmetry in couplings causes the emergence of different attractors. The bifurcation diagrams of one node of each layer are presented to show the variation of the dynamics due to coupling changes. For further analysis, the network synchronization is investigated by computing intra-layer and inter-layer errors. Calculating these errors shows that the network can be synchronized only for large enough symmetric coupling.
Map-based neuronal models have received much attention due to their high speed, efficiency, flexibility, and simplicity. Therefore, they are suitable for investigating different dynamical behaviors in neuronal networks, which is one of the recent hottest topics. Recently, the memristive version of the Rulkov model, known as the m-Rulkov model, has been introduced. This paper investigates the network of the memristive version of the Rulkov neuron map to study the effect of the memristor on collective behaviors. Firstly, two m-Rulkov neuronal models are coupled in different cases, through electrical synapses, chemical synapses, and both electrical and chemical synapses. The results show that two electrically coupled memristive neurons can become synchronous, while the previous studies have shown that two non-memristive Rulkov neurons do not synchronize when they are coupled electrically. In contrast, chemical coupling does not lead to synchronization; instead, two neurons reach the same resting state. However, the presence of both types of couplings results in synchronization. The same investigations are carried out for a network of 100 m-Rulkov models locating in a ring topology. Different firing patterns, such as synchronization, lagged-phase synchronization, amplitude death, non-stationary chimera state, and traveling chimera state, are observed for various electrical and chemical coupling strengths. Furthermore, the synchronization of neurons in the electrical coupling relies on the network's size and disappears with increasing the nodes number.
Human evolution is carried out by two genetic systems based on DNA and another based on the transmission of information through the functions of the nervous system. In computational neuroscience, mathematical neural models are used to describe the biological function of the brain. Discrete-time neural models have received particular attention due to their simple analysis and low computational costs. From the concept of neuroscience, discrete fractional order neuron models incorporate the memory in a dynamic model. This paper introduces the fractional order discrete Rulkov neuron map. The presented model is analyzed dynamically and also in terms of synchronization ability. First, the Rulkov neuron map is examined in terms of phase plane, bifurcation diagram, and Lyapunov exponent. The biological behaviors of the Rulkov neuron map, such as silence, bursting, and chaotic firing, also exist in its discrete fractional-order version. The bifurcation diagrams of the proposed model are investigated under the effect of the neuron model's parameters and the fractional order. The stability regions of the system are theoretically and numerically obtained, and it is shown that increasing the order of the fractional order decreases the stable areas. Finally, the synchronization behavior of two fractional-order models is investigated. The results represent that the fractional-order systems cannot reach complete synchronization.
Cancer is a condition marked by abnormal cell proliferation that has the potential to invade or indicate other health issues. Human beings are affected by more than 100 different types of cancer. Some cancer promotes rapid cell proliferation, whereas others cause cells to divide and develop more slowly. Some cancers, such as leukemia, produce visible tumors, while others, such as breast cancer, do not. In this work, in silico investigations were carried out to investigate the binding mechanisms of four major analogs, which are marine sesquiterpene, sesquiterpene lactone, heteroaromatic chalcones, and benzothiophene against the target estrogen receptor-α for targeting breast cancer using Schrödinger suite 2021-4. The Glide module handled the molecular docking experiments, the QikProp module handled the ADMET screening, and the Prime MM-GB/SA module determined the binding energy of the ligands. The benzothiophene analog BT_ER_15f (G-score -15.922 Kcal/mol) showed the best binding activity against the target protein estrogen receptor-α when compared with the standard drug tamoxifen which has a docking score of -13.560 Kcal/mol. TRP383 (tryptophan) has the highest interaction time with the ligand, and hence it could act for a long time. Based on in silico investigations, the benzothiophene analog BT_ER_15f significantly binds with the active site of the target protein estrogen receptor-α. Similar to the outcomes of molecular docking, the target and ligand complex interaction motif established a high affinity of lead candidates in a dynamic system. This study shows that estrogen receptor-α targets inhibitors with better potential and low toxicity when compared to the existing market drugs, which can be made from a benzothiophene derivative. It may result in considerable activity and be applied to more research on breast cancer.
We identified an antimicrobial peptide (AMP) from Lactobacillus acidophilus that was antagonistic to Aeromonas hydrophila. In vitro studies such as well-diffusion and field trials revealed that the AMP was active against A. hydrophila. The field trials of AMP using A. hydrophila-infected Channa striatus with a mannone oligosaccharide (MOS) prebiotic, A. hydrophila antigens, A. hydrophila-infected fish serum, L. acidophilus, and Lactobacillus cell free-supernatant (LABS-CFS) on an indicator organism further revealed that the antimicrobial agent could protect C. striatus. Other than the AMP, none of the above were able to eliminate the infectious agent A. hydrophila, and were only able to delay the death rate for 3-4 days. Thus, we conclude that the AMP is antagonistic to A. hydrophila and may be used for treatment of A. hydrophila infections. Subsequent L. acidophilus whole-genome sequence analyses enabled an understanding of the (probable) gene arrangement and its location on the chromosome. This information may be useful in the generation of recombinant peptides to produce larger quantities for treatment.