This document discusses the physiology of neural transmission in the nervous system. It begins by defining neurons as the basic functional units that transmit electrical and chemical signals. It describes the basic structure of neurons including the cell body, dendrites, axon and synapses. It then explains how neurons generate and propagate electrical signals called action potentials down the axon. It discusses the processes involved in synaptic transmission including the release and binding of neurotransmitters and the generation of excitatory or inhibitory postsynaptic potentials. Finally, it lists some major neurotransmitters in the nervous system like acetylcholine, dopamine and GABA.
THIS REFER BY THE ESSENTIALS OF MEDICAL PHYSIOLOGY BOOK (SIX EDITION)
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Various neurotransmitters, mechanism of action and their physiological functions are explained and is useful for ug and pg students of medicine, neurology, psychiatry branches.
Nerve impluse in non myelinated and myelinated nerve fibres. Nerve impluse is the sum total of chemical and physical events in the propagation of a wave of physiological activity along a nerve fibre.
Propagation of nerve impluse in non myelinated nerve fibres-
Resting state
Depolarisation
Repolarization
Metabolic pump
The action potential
The process of Propagation of nerve impluse in myelinated nerve fibres is called soltatory propagation.
Nerve impluses are transmitted in one direction only. The nerve fibre always have a refractory period after a stimulus and the nerve impluses obey the all or none law
THIS REFER BY THE ESSENTIALS OF MEDICAL PHYSIOLOGY BOOK (SIX EDITION)
HELLO!
I AM MEET DESAI.
STUDENT OF A PHYSIOTHERAPY.
THIS IS MY COLLEGE PROJECT . I'M SHARING TO STUDENT LIKE ME..
THIS AVAILABLE MY LINK LIKE..https://www.linkedin.com/in/meet-desai-18296b178
THANK YOU SO MACH .TO SEE
Various neurotransmitters, mechanism of action and their physiological functions are explained and is useful for ug and pg students of medicine, neurology, psychiatry branches.
Nerve impluse in non myelinated and myelinated nerve fibres. Nerve impluse is the sum total of chemical and physical events in the propagation of a wave of physiological activity along a nerve fibre.
Propagation of nerve impluse in non myelinated nerve fibres-
Resting state
Depolarisation
Repolarization
Metabolic pump
The action potential
The process of Propagation of nerve impluse in myelinated nerve fibres is called soltatory propagation.
Nerve impluses are transmitted in one direction only. The nerve fibre always have a refractory period after a stimulus and the nerve impluses obey the all or none law
Classification and structure of synapsesAlaaAlchyad
Synapses can be classified by the type of cellular structures serving as the pre- and post-synaptic components. ... The axon can synapse onto a dendrite, onto a cell body, or onto another axon or axon terminal, as well as into the bloodstream or diffusely into the adjacent nervous tissue.
Olfaction is one the major sense. In the following presentation, a brief description of the olfactory system is given. In this following topics are discussed: olfactory membrane, olfactory bulb, odor pathway, anosmia, directional smelling and plasticity. By the end of it, you will be able to describe the olfactory pathway of the nervous system.
Classification and structure of synapsesAlaaAlchyad
Synapses can be classified by the type of cellular structures serving as the pre- and post-synaptic components. ... The axon can synapse onto a dendrite, onto a cell body, or onto another axon or axon terminal, as well as into the bloodstream or diffusely into the adjacent nervous tissue.
Olfaction is one the major sense. In the following presentation, a brief description of the olfactory system is given. In this following topics are discussed: olfactory membrane, olfactory bulb, odor pathway, anosmia, directional smelling and plasticity. By the end of it, you will be able to describe the olfactory pathway of the nervous system.
basic nervous system-CNS-PNS -cell bodie- axon-dendron-grye matter- white mat...shailesh sangle
The nervous system is a complex network of cells, tissues, and organs that coordinates and regulates the body's responses to internal and external stimuli. It is responsible for the control and coordination of all the body's functions, including movement, sensation, thought, and behavior.
The nervous system can be divided into two main parts: the central nervous system (CNS) and the peripheral nervous system (PNS). The CNS consists of the brain and spinal cord, while the PNS consists of all the nerves that extend from the CNS to the rest of the body.
The nervous system is made up of different types of cells, including neurons and glial cells. Neurons are specialized cells that transmit signals through the body in the form of electrical impulses. Glial cells, on the other hand, support and protect the neurons and help maintain the proper functioning of the nervous system.
The nervous system is responsible for many vital functions, including:
Sensory processing: The nervous system receives sensory information from the environment and the body's internal organs, and processes and interprets this information to generate appropriate responses.
Motor control: The nervous system controls the muscles and other organs of the body to produce movement and other responses.
Cognitive functions: The nervous system is responsible for the processes of learning, memory, language, and other complex mental activities.
Autonomic functions: The nervous system regulates the body's automatic functions, such as breathing, heart rate, digestion, and other bodily processes that are not under conscious control.
Overall, the nervous system is a complex and intricate system that plays a critical role in maintaining the body's homeostasis and overall well-being.
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This lesson material includes essential information about neurological foundations of behavior. This tackles the brain specifically the nervous system and neurons.
They are produced when high-velocity electrons collide with the metal plates, thereby giving the energy as the X-Rays and themselves absorbed by the metal plate.
The X-Ray beam travels through the air and comes in contact with the body tissues, and produces an image on a metal film.
Soft tissue like organs and skin, cannot absorb the high-energy rays, and the beam passes through them.
Dense materials inside our bodies, like bones, absorb the radiation.he X-Rays properties are given below:
They have a shorter wavelength of the electromagnetic spectrum.
Requires high voltage to produce X-Rays.
They are used to capture the human skeleton defects.
They travel in a straight line and do not carry an electric charge with them.
They are capable of travelling in a vacuum.Medical science recognizes different types of X-Rays. A few important types of X-Rays are given in the points below.
Standard Computed Tomography
Kidney, Ureter, and Bladder X-ray
Teeth and bones X-rays
Chest X-rays
Lungs X-rays
Abdomen X-rays
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
2. NEURONES
The neuron is the basic working unit of the brain.
It’s a specialized cell designed to transmit information to other
nerve cells, muscle, or gland cells.
Neurons are cells within the nervous system that transmit
information to other nerve cells, muscle, or gland cells.
3. BASIC STRUCTURE OF A NEURON
Most neurons have a
• cell body
• an axon
• dendrites
4. The cell body contains the nucleus and cytoplasm.
The axon extends from the cell body and often gives rise to many
smaller branches before ending at nerve terminals.
Dendrites extend from the neuron cell body and receive messages
from other neurons.
Synapses are the contact points where one neuron communicates
with another. The dendrites are covered with synapses formed by
the ends of axons from other neurons.
5. When neurons receive or send messages, they transmit electrical
impulses along their axons, which can range in length from a tiny
fraction of an inch (or centimeter) to three feet (about one meter)
or more.
Many axons are covered with a layered myelin sheath, which
accelerates the transmission of electrical signals along the axon.
This sheath is made by specialized cells called glia.
In the brain, the glia that make the sheath are called
oligodendrocytes, and in the peripheral nervous system, they are
known as Schwann cells.
6. NEURAL TRANSMISSION
The function of a neuron is to transmit information within the
nervous system.
Neural transmission occurs when a neuron is activated, or
fired (sends out an electrical impulse).
IMPORTANT TERMS
1. Potential
• the term potential refers to a difference in electrical charges.
• Neurons have two types of potentials-
• a resting potential
• an action potential
7. 2. Resting potential
• The resting potential of neurons is about -70 mV.
• At resting potential concentration of ions is kept constant
through Na+/K+ pumps.
• When the threshold is reached, the Na+ gated channel are
opened.
3. Action potential:
• An action potential is defined as a sudden, fast, transitory, and
propagating change of the resting membrane potential.
• Only neurons and muscle cells are capable of generating
an action potential; that property is called the excitability
• The action potential has three main
stages: depolarization, repolarization, and hyperpolarization.
8. • Polarization is the existence of opposite electrical charges on
either side of a cell membrane (difference in inside a cell versus
the outside of the cell
• Depolarization is the state which the cell membrane change from
positive to negative charged outside the cell and from negative to
positive charge inside the cell.
• Repolarization refers to the change in membrane potential that
returns it to a negative value just after the depolarization phase of
an action potential which has changed the membrane potential to
a positive value.
• Hyperpolarization is the movement of a cell's membrane
potential to a more negative value i.e., movement further away
from zero. When a neuron is hyperpolarized, it is less likely to
fire an action potential.
9. 4. Refractory period
• It is a period of time during which a cell is incapable of repeating
an action potential.
• In terms of action potentials, it refers to the amount of time it
takes for an excitable membrane to be ready to respond to a
second stimulus once it returns to a resting state.
5. Absolute refractory period
• This is a short period where even when a greater stimulation
occurs, the neuron will not fire again.
6. Relative refractory period
• is the interval of time during which a second action potential can
be initiated, but initiation will require a greater stimulus than
before.
10. 7. Neural threshold
• is the level of stimulation below which the cell does not fire.
8. All Or None Principle
• Henry P. Bowditch (1871)
• The all-or-none law is a principle that states that the strength of a
response of a nerve cell or muscle fiber is not dependent upon the
strength of the stimulus.
• If a stimulus is above a certain threshold, a nerve or muscle fiber
will fire.
9. Activation (firing)
• Firing of the neuron takes place when the neuron is stimulated by
pressure, heat, light, or chemical information from other cells.
11. SYNAPTIC TRANSMISSION
Synaptic transmission is the process by which one neuron
communicates with another.
The synapse is the name given the junction between neurons
where information is exchanged.
Information is passed down the axon of the neuron as an
electrical impulse known as action potential.
Once the action potential reaches the end of the axon it needs to
be transferred to another neuron or tissue.
It must cross over the synaptic gap between the presynaptic
neuron and post-synaptic neuron. The axon of the presynaptic
neuron does not actually touch the dendrites of the postsynaptic
neuron and is separated from them by a space called the synaptic
cleft.
12. At the end of the neuron (in the axon terminal) are the synaptic
vesicles, which contain chemical messengers, known as
neurotransmitters.
When the electrical impulse (action potential) reaches these
synaptic vesicles, they release their contents of neurotransmitters.
Neurotransmitters then carry the signal across the synaptic gap.
They bind to receptor sites on the post-synaptic cell, thereby
completing the process of synaptic transmission.
Molecules of the neurotransmitter that do not bind to receptors in
the postsynaptic neuron are taken up again by the presynaptic
neuron, a process called reuptake.
The combination of the neurotransmitter molecules to receptor
cell molecules in the postsynaptic cell membrane produces a
change of potential in the postsynaptic cell membrane called the
postsynaptic potential (PSP).
13. The PSP allows ions to enter or leave the cell membrane of the
postsynaptic neuron.
The ionic movements increase or decrease the probability of a
neural impulse occurring in the postsynaptic neuron.
There are two types of PSPs
• excitatory (EPSPs)
• inhibitory (IPSPs)
EPSPs increase and IPSPs decrease the likelihood that the
postsynaptic neuron will fire a neural impulse.
The rate of firing of a neuron at a particular time depends upon
the relative number of EPSPs and IPSPs.
14. NEUROTRANSMITTERS.
Neurotransmitters are chemical messengers that transmit a signal
from a neuron across the synapse to a target cell, which can be a
different neuron, muscle cell, or gland cell.
Neurotransmitters are chemical substances made by the neuron
specifically to transmit a message.
Neurotransmitters are mainly divided into 6 types:
1. Acetylcholine
• Occurs throughout the nervous system
• Is the only neurotransmitter found in synapses between motor
neurons and voluntary muscle cells.
• Degeneration of cells producing acetylcholine is associated with
Alzheimer's disease.
15. 2. Biogenic amines
• Include three neurotransmitters: norepinephrine, dopamine, and
serotonin.
• Parkinson's disease is believed to be related to a deficiency of
dopamine
• Certain types of depression are associated with low levels of
norepinephrine
• Levels of serotonin increase with the use of the recreational drug
LSD (lysergic acid diethylamide).
3. GABA (gamma aminobutyric acid)
• appears to produce only inhibitory PSPs.
• Many tranquilizers work by increasing the inhibitory actions of
GABA.
16. 4. Glycine
• is an inhibitory neurotransmitter found in the lower brainstem,
spinal cord, and retina.
5. Endorphins
• modulate the activity of other neurotransmitters and are called
neuromodulators.
• They seem to function in the same way as opiates such as
morphine; “runner's high” is produced by an increase in
endorphins.
6. Substance P
• is a neurotransmitter in many neural circuits involving pain.
Editor's Notes
Nucleus has the genetic material embedded in it. Cytoplasm has all the organelles like mitochondria, ribosomes, …
The info. from one neuron’s axon is passes to the next neuron’s dendrite through the synapse.
Glial cells are of 5 types- astro, oligo, ependymal, micro and schwann.