This presentation contains the basic information about nerve cells and action potential. This work is done for academic purpose only so if you are using give proper reference.
This presentation contains the basic information about nerve cells and action potential. This work is done for academic purpose only so if you are using give proper reference.
Nerve Impulse is defined as a wave of electrical chemical changes across the neuron that helps in the generation of the action potential in response to the stimulus. This transmission of a nerve impulse across the neuron membrane as a result of a change in membrane potential is known as Nerve impulse conduction.
Mechanism of Nerve Impulse Conduction
Nerve impulse conduction is a major process occurring in the body responsible for organized functions of the body. So, for conduction of nerve impulse there are two mechanisms:
Continuous conduction
Saltatory conduction
Membrane potential (also transmembrane potential or membrane voltage) is the difference in electric potential between the interior and the exterior of a biological cell. ... Almost all plasma membranes have an electrical potential across them, with the inside usually negative with respect to the outside.
Nerve Impulse is defined as a wave of electrical chemical changes across the neuron that helps in the generation of the action potential in response to the stimulus. This transmission of a nerve impulse across the neuron membrane as a result of a change in membrane potential is known as Nerve impulse conduction.
Mechanism of Nerve Impulse Conduction
Nerve impulse conduction is a major process occurring in the body responsible for organized functions of the body. So, for conduction of nerve impulse there are two mechanisms:
Continuous conduction
Saltatory conduction
Membrane potential (also transmembrane potential or membrane voltage) is the difference in electric potential between the interior and the exterior of a biological cell. ... Almost all plasma membranes have an electrical potential across them, with the inside usually negative with respect to the outside.
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.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
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.
Richard's entangled aventures in wonderlandRichard 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.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
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4. The Membrane
The membrane surrounds the neuron.
It is composed of lipid and protein.
5. The Resting Potential
There is an electrical charge across the membrane.
This is the membrane potential.
The resting potential (when the cell is not firing) is a
70mV difference between the inside and the outside.
inside
outside
Resting potential of neuron = -70mV
+
-
+
-
+
-
+
-
+
-
7. Ions and the Resting Potential
Ions are electrically-charged molecules e.g. sodium (Na+),
potassium (K+), chloride (Cl-).
The resting potential exists because ions are concentrated on
different sides of the membrane.
Na+ and Cl- outside the cell.
K+ and organic anions inside the cell.
inside
outside
Na+
Cl-
Na+
K+
Cl-
K+
Organic anions (-)
Na+
Na+
Organic anions (-)
Organic anions (-)
8. Ions and the Resting Potential
Ions are electrically-charged molecules e.g. sodium (Na+),
potassium (K+), chloride (Cl-).
The resting potential exists because ions are concentrated on
different sides of the membrane.
Na+ and Cl- outside the cell.
K+ and organic anions inside the cell.
inside
outside
Na+
Cl-
Na+
K+
Cl-
K+
Organic anions (-)
Na+
Na+
Organic anions (-)
Organic anions (-)
9. Maintaining the Resting
Potential
Na+ ions are actively transported (this uses
energy) to maintain the resting potential.
The sodium-potassium pump (a membrane
protein) exchanges three Na+ ions for two K+
ions.
inside
outside
Na+
Na+
K+
K+
Na+
10. Neuronal firing: the action
potential
The action potential is a rapid
depolarization of the membrane.
It starts at the axon hillock and passes
quickly along the axon.
The membrane is quickly repolarized to
allow subsequent firing.
14. Action potentials: Repolarization
Sodium ion channels close and become refractory.
Depolarization triggers opening of voltage-gated
potassium ion channels.
K+ ions rush out of the cell, repolarizing and then
hyperpolarizing the membrane.
K+ K+
K+
Na+
Na+
Na+
+
-
16. The Action Potential
The action potential is “all-or-none”.
It is always the same size.
Either it is not triggered at all - e.g. too little
depolarization, or the membrane is
“refractory”;
Or it is triggered completely.
17. Course of the Action Potential
• The action potential begins with a partial depolarization (e.g. from
firing of another neuron ) [A].
• When the excitation threshold is reached there is a sudden large
depolarization [B].
• This is followed rapidly by repolarization [C] and a brief
hyperpolarization [D].
• There is a refractory period immediately after the action potential
where no depolarization can occur [E]
Membrane
potential
(mV)
[A]
[B] [C]
[D] excitation threshold
Time (msec)
-70
+40
0
0 1 2 3
[E]
18. Action Potential
Local Currents depolarize adjacent channels causing
depolarization and opening of adjacent Na channels
Question: Why doesn’t the action potential travel backward?
19.
20. Conduction of the action
potential.
Passive conduction will ensure that adjacent
membrane depolarizes, so the action potential
“travels” down the axon.
But transmission by continuous action potentials
is relatively slow and energy-consuming
(Na+/K+ pump).
A faster, more efficient mechanism has evolved:
saltatory conduction.
Myelination provides saltatory conduction.
21. Myelination
Most mammalian axons are myelinated.
The myelin sheath is provided by oligodendrocytes and
Schwann cells.
Myelin is insulating, preventing passage of ions over
the membrane.
22. Saltatory Conduction
Myelinated regions of axon are electrically insulated.
Electrical charge moves along the axon rather than across the
membrane.
Action potentials occur only at unmyelinated regions: nodes of
Ranvier.
Node of Ranvier
Myelin sheath
23. Synaptic transmission
Information is transmitted from the presynaptic
neuron to the postsynaptic cell.
Chemical neurotransmitters cross the
synapse, from the terminal to the dendrite or
soma.
The synapse is very narrow, so transmission is
fast.
24. terminal
dendritic spine
synaptic cleft
presynaptic membrane
postsynaptic membrane
extracellular fluid
Structure of the synapse
An action potential causes neurotransmitter
release from the presynaptic membrane.
Neurotransmitters diffuse across the
synaptic cleft.
They bind to receptors within the
postsynaptic membrane, altering the
membrane potential.
25. Neurotransmitter release
Ca2+ causes vesicle membrane to fuse with
presynaptic membrane.
Vesicle contents empty into cleft: exocytosis.
Neurotransmitter diffuses across synaptic
cleft.
Ca2+
26.
27. Ionotropic receptors (ligand gated)
Synaptic activity at ionotropic receptors
is fast and brief (milliseconds).
Acetylcholine (Ach) works in this way
at nicotinic receptors.
Neurotransmitter binding changes the
receptor’s shape to open an ion channel
directly.
ACh ACh
31. Excitatory postsynaptic
potentials (EPSPs)
Opening of ion channels which leads to
depolarization makes an action potential more likely,
hence “excitatory PSPs”: EPSPs.
Inside of post-synaptic cell becomes less negative.
Na+ channels (NB remember the action potential)
Ca2+ . (Also activates structural intracellular changes ->
learning.)
inside
outside
Na+ Ca2+
+
-
32. Inhibitory postsynaptic
potentials (IPSPs)
Opening of ion channels which leads to
hyperpolarization makes an action potential less
likely, hence “inhibitory PSPs”: IPSPs.
Inside of post-synaptic cell becomes more negative.
K+ (NB remember termination of the action potential)
Cl- (if already depolarized)
K+
Cl- +
- inside
outside
34. Requirements at the synapse
For the synapse to work properly, six basic events need to happen:
Production of the Neurotransmitters
Synaptic vesicles (SV)
Storage of Neurotransmitters
SV
Release of Neurotransmitters
Binding of Neurotransmitters
Lock and key
Generation of a New Action Potential
Removal of Neurotransmitters from the Synapse
reuptake
35. Integration of information
PSPs are small. An individual EPSP will not produce
enough depolarization to trigger an action potential.
IPSPs will counteract the effect of EPSPs at the
same neuron.
Summation means the effect of many coincident
IPSPs and EPSPs at one neuron.
If there is sufficient depolarization at the axon
hillock, an action potential will be triggered.
axon hillock
36. Three Nobel Prize Winners on
Synaptic Transmission
Arvid Carlsson discovered dopamine is a neurotransmitter.
Carlsson also found lack of dopamine in the brain of
Parkinson patients.
Paul Greengard studied in detail how neurotransmitters
carry out their work in the neurons. Dopamine activated a
certain protein (DARPP-32), which could change the function
of many other proteins.
Eric Kandel proved that learning and memory processes
involve a change of form and function of the synapse,
increasing its efficiency. This research was on a certain
kind of snail, the Sea Slug (Aplysia). With its relatively low
number of 20,000 neurons, this snail is suitable for
neuron research.
37. Neuronal firing: the action
potential
The action potential is a rapid
depolarization of the membrane.
It starts at the axon hillock and passes
quickly along the axon.
The membrane is quickly repolarized to
allow subsequent firing.
44. Motor Control Basics
• Reflex Circuits
– Usually Brain-stem, spinal cord based
– Interneurons control reflex behavior
– Central Pattern Generators
• Cortical Control