Mechanisms of impulse transmission and stimulus response in nervous system
Abstract
The basic mechanisms that support the nervous system's operation in both invertebrates and vertebrates are impulse transmission and the body's reaction to stimuli. These mechanisms let organisms' sense changes in their internal and external surroundings, analyze the information, and start the proper behavioral or physiological reactions. For homeostasis, survival, and adaptation, impulse transmission and response to stimuli must be accurate and efficient. When a stimulus is strong enough to surpass the excitation threshold, a brief, transient change in membrane potential known as an action potential is generated, signaling the beginning of neuronal impulse transmission. This electrochemical process is initiated by the passage of ions, namely sodium (Na⁺) and potassium (K⁺) ions, across the neuronal membrane via voltage-gated ion channels. Synaptic transmission is a crucial step in impulse propagation after this. An action potential that reaches the axon terminal releases neurotransmitters into the synaptic cleft. The kind of neurotransmitter and receptor involved determines whether these chemical messengers cause excitatory or inhibitory responses when they attach themselves to certain postsynaptic membrane receptors. Complex neural networks are formed by the communication that is made possible by this synaptic activity between neurons and threshold; the start of neuronal impulse transmission is indicated by the generation of an action potential, a short, fleeting shift in membrane potential. This communication tried to talk in more details about this topic.
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- Xu, N., On the Concept of Resting Potential—Pumping Ratio of the Na+/K+ Pump and Concentration Ratios of Potassium Ions Outside and Inside the Cell to Sodium Ions Inside and Outside the Cell. The Journal of Membrane Biology, 2013. 246(1): p. 75-90.
- Xu, N., Pumping Ratio of the Na+/K+ Pump — A Further View. Bioelectricity, 2022. 4(4): p. 228-236.
- Springer, C.S., Jr., Pike, M.M., and Barbara, T.M., A Futile Cycle?: Tissue Homeostatic Trans-Membrane Water Co-Transport: Kinetics, Thermodynamics, Metabolic Consequences. bioRxiv, 2024.
- Takvam, M., Wood, C.M., Kryvi, H., et al., Ion Transporters and Osmoregulation in the Kidney of Teleost Fishes as a Function of Salinity. Frontiers in Physiology, 2021. Volume 12 - 2021.
- Faisal, M., Rusetskaya, A., Väli, L., et al., No Evidence of Sensory Neuropathy in a Traditional Mouse Model of Idiopathic Parkinson’s Disease. Cells, 2024. 13(10): p. 799.
- Drukarch, B. and Wilhelmus, M.M., Understanding the Scope of the Contemporary Controversy about the Physical Nature and Modeling of the Action Potential: Insights from History and Philosophy of (Neuro) Science. OBM Neurobiology, 2025. 9(1): p. 1-25.
- Čaikauskaitė, K., Nugaros smegenų motoneuronų veikimo potencialo slenksčio atsistatymas po depoliarizacijos neuroninio tinklo veikimo metu, 2022, Vilniaus universitetas.
- Drukarch, B., Holland, H.A., Velichkov, M., et al., Thinking about the nerve impulse: A critical analysis of the electricity-centered conception of nerve excitability. Progress in Neurobiology, 2018. 169: p. 172-185.
- Abramicheva, P.A., Andrianova, N.V., Babenko, V.A., et al., Mitochondrial Network: Electric Cable and More. Biochemistry (Moscow), 2023. 88(10): p. 1596-1607.
- Zorov, D.B., Andrianova, N.V., Babenko, V.A., et al., Neuroprotective Potential of Mild Uncoupling in Mitochondria. Pros and Cons. Brain Sciences, 2021. 11(8): p. 1050.
- Paranjape, N., Strack, S., Lehmler, H.-J., et al., Astrocyte Mitochondria Are a Sensitive Target of PCB52 and its Human-Relevant Metabolites. ACS Chemical Neuroscience, 2024. 15(15): p. 2729-2740.
- Zorova, L.D., Popkov, V.A., Plotnikov, E.Y., et al., Mitochondrial membrane potential. Analytical Biochemistry, 2018. 552: p. 50-59.
- Evans, M.R., Majumdar, S.N., and Schehr, G., An exactly solvable predator prey model with resetting. Journal of Physics A: Mathematical and Theoretical, 2022. 55(27): p. 274005.
- Bressloff, P.C., Accumulation time of stochastic processes with resetting. Journal of Physics A: Mathematical and Theoretical, 2021. 54(35): p. 354001.
- García-Valladares, G., Gupta, D., Prados, A., et al., Stochastic resetting with refractory periods: pathway formulation and exact results. Physica Scripta, 2024. 99(4): p. 045234.
- Gupta, S. and Jayannavar, A.M., Stochastic Resetting: A (Very) Brief Review. Frontiers in Physics, 2022. Volume 10 - 2022.
- Sotero, R.C., Sanchez-Bornot, J.M., and Shaharabi-Farahani, I. Parameter Estimation in Brain Dynamics Models from Resting-State fMRI Data using Physics-Informed Neural Networks. in 2024 8th International Conference on Biomedical Engineering and Applications (ICBEA). 2024.
- Sotero, R.C. and Trujillo-Barreto, N.J., Modelling the role of excitatory and inhibitory neuronal activity in the generation of the BOLD signal. NeuroImage, 2007. 35(1): p. 149-165.
- Evans, M.R. and Majumdar, S.N., Effects of refractory period on stochastic resetting. Journal of Physics A: Mathematical and Theoretical, 2018. 52(1): p. 01LT01.
- Wang, J., Lulu, S., Chuchu, W., et al., Astragaloside depresses compound action potential in sciatic nerve of frogs involved in L-type Ca2+-channel dependent mechanism. Natural Product Research, 2024: p. (in press).
- Pardo-Moreno, T., García-Morales, V., Suleiman-Martos, S., et al., Current Treatments and New, Tentative Therapies for Parkinson’s Disease. Pharmaceutics, 2023. 15(3): p. 770.
- Camargo, C.H.F., Ferreira-Peruzzo, S.A., Ribas, D.I.R., et al., Imbalance and gait impairment in Parkinson’s disease: discussing postural instability and ataxia. Neurological Sciences, 2024. 45(4): p. 1377-1388.
- Comi, C., Magistrelli, L., Oggioni, G.D., et al., Peripheral nervous system involvement in Parkinson's disease: Evidence and controversies. Parkinsonism & Related Disorders, 2014. 20(12): p. 1329-1334.
- McAllister, Z., Asymmetric effects of anodal transcranial direct current stimulation on intrinsic connectivity in the left and right dorsolateral prefrontal cortex. 2023.
- Sten, S., Podéus, H., Sundqvist, N., et al., A quantitative model for human neurovascular coupling with translated mechanisms from animals. PLOS Computational Biology, 2023. 19(1): p. e1010818.
- Sanchez-Rodriguez, L.M., Bezgin, G., Carbonell, F., et al., Revealing the combined roles of Aβ and tau in Alzheimer's disease via a pathophysiological activity decoder. bioRxiv, 2023.