Neural signals are transmitted through both electrical and chemical means. An electrical signal travels down a neuron's dendrites to its cell body. If the signal reaches the axon hillock's threshold, the axon is activated and fires, transmitting an electrical signal down the axon. At the axon terminals, neurotransmitters are released across the synaptic cleft to the next cell. The membrane potential, maintained by ion concentration gradients and sodium-potassium pumps, underlies the neuron's resting potential. When neurotransmitters bind to receptors on the post-synaptic cell, they generate graded excitatory or inhibitory post-synaptic potentials that are integrated and can trigger an all-or-none action potential for signal transmission along the ax
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
these slides contain a brief introduction of neurons and its classification as well as details of generation of action potential, resting potential and eletrotonic potential.
The nervous system is a complex collection of nerves and specialized cells known as neurons that transmit signals between different parts of the body. The presentation provides a simplified overview of the nervous system and its functions
My first attempt at this presentation for the IB Diploma Programme Biology course: topic 6.5 neurons and synapses. I'm hoping another great educator out there can take this, make it look a lot better, and then share it :)
Thanks to Steven Taylor and Chris Paine for all of their work and inspiration.
Please download and modify as you wish.
final note: I actually made this in google slides - I just checked the presentation and none of the links to the videos I used are there. Here is a link to the google slide presentation so you can find the videos: https://docs.google.com/a/igbis.edu.my/presentation/d/1eabpxEtwlDGt7EPRqQ_GPwxUBerszZQquWAhjRnU_WE/edit?usp=sharing
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
these slides contain a brief introduction of neurons and its classification as well as details of generation of action potential, resting potential and eletrotonic potential.
The nervous system is a complex collection of nerves and specialized cells known as neurons that transmit signals between different parts of the body. The presentation provides a simplified overview of the nervous system and its functions
My first attempt at this presentation for the IB Diploma Programme Biology course: topic 6.5 neurons and synapses. I'm hoping another great educator out there can take this, make it look a lot better, and then share it :)
Thanks to Steven Taylor and Chris Paine for all of their work and inspiration.
Please download and modify as you wish.
final note: I actually made this in google slides - I just checked the presentation and none of the links to the videos I used are there. Here is a link to the google slide presentation so you can find the videos: https://docs.google.com/a/igbis.edu.my/presentation/d/1eabpxEtwlDGt7EPRqQ_GPwxUBerszZQquWAhjRnU_WE/edit?usp=sharing
Gives the anatomical Sketch , Early studies on frontal lobe , Debates if frontal lobe impairment is associated with quantitative or qualitative deficits in intelligence
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.
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.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
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.
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.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
3. THE NEURAL COMMUNICATION – AN OVERVIEW
• Neural communication actually involves both electrical and chemical—or
electrochemical—communication.
• The signal usually starts in the neuron’s dendrites, and then travels down the
length of the cell until it reaches the terminal buttons at the very tips of the
neuron’s axon.
• A single neuron normally has many dendrites. The number of dendrites being
stimulated may vary from one moment to the next. Thus, there may be more or
less electrical activity traveling down into the soma at any given time.
• If there is too little electrical activity, nothing happens. If, however, the electrical
activity reaches a certain critical amount, or threshold, the axon hillock activates
the axon. If the axon hillock’s threshold is reached and the axon is activated, an
electrical signal travels down the axon’s length until it reaches the very end of the
neuron. This activation of the axon is referred to as the neuron firing.
• From the terminal buttons , the neuron will pass the signal on to another cell, such
as another neuron or muscle cell.
5. THE NEURAL IMPULSE CYCLE
• The nerve impulse is the reversal in the charge of the cell membrane, which
spreads along the cell membrane forming an electrical current.
• Resting Potential – Tells us about what happens when the neuron is at rest.
• Action Potential - Occurs when a neuron sends information down an axon
i) Depolarisation
ii) Repolarisation
6. THE MEMBRANE POTENTIAL
The key to understanding how neurons work is the membrane potential.
The membrane potential is the difference in electrical charge between the inside and
the outside of a cell.
Recording resting membrane potential. when the tip of the intracellular electrode is
inserted into a neuron, a steady potential of about –70 millivolts (mV) is recorded.
This steady membrane potential is called the neuron’s resting potential, and the
neuron is said to be polarized.( electrical difference across the membrane)
7. RESTING POTENTIAL
• Recording the membrane potential: difference in electrical charge between inside
and outside of cell
• Inside of the neuron is negative with respect to the outside.
• Resting membrane potential is about –70mV.
• Membrane is polarized (carries a charge)
8. TERMS TO KNOW
• Concentration Gradient: A concentration gradient occurs when
the concentration of particles is higher in one area than another. In passive
transport, particles will diffuse down a concentration gradient, from areas of
higher concentration to areas of lower concentration, until they are evenly spaced.
• Electrical Gradient: In biological solutions, electrical gradient refers to
the electrical potential that acts on an ion to drive the movement of the ion in one
or another direction
9. IONIC BASIS FOR RESTING POTENTIAL
Why are resting neurons polarised?
Salts in neural tissue separate into positively and negatively charged particles called
ions. The resting potential results from the fact that the ratio of negative to positive charges
is greater inside the neuron than outside.
Resting potential results from
(1) the concentration of Na+ is higher outside,
(2) the concentration of Cl is higher outside,
(3) the concentration of K+ is higher inside, and
(4) various negatively charged protein ions are trapped inside
10. FOUR FACTORS THAT UNDERLIE RESTING POTENTIAL
Factors contributing to even distribution of ions.
• Random motion – ions in a solution are normally under random motion. particles tend to move down
their concentration gradient.
• Electrostatic pressure – like repels like, opposites attract. It disperses accumulation of any positive or
negative charges in any area.
Factors contributing to uneven distribution of ions.
• Selective permeability to certain ions – pass through the neural membrane at specialised pores called
ion channels. When neurons are at rest, the membrane is:
a) totally resistant to the passage of protein ions,
b) extremely resistant to the passage of Na+ ions,
c) moderately resistant to the passage of K+ ions,
d) and only slightly resistant to the passage of Cl ions
11. SODIUM POTASSIUM PUMP
• Sodium Potassium Pump- energy consuming process involved in the maintenance
of the resting potential.
12. SODIUM POTTASSIUM PUMP
• Sodium ions tend to be driven in as a result of both concentration gradient and the
negative internal resting potential of – 70 mv. About 120 mv of electrostatic
pressure forces sodium ions into the cell.
• Potassium ions tend to move out of the neuron because of their higher
concentration inside the cells, although this tendency is partially offset by the
internal negative potential .
• However the sodium potassium pump pumps out sodium ions as rapidly as they
pass in and pumps in potassium ions as they pass out . For every three sodium ions
in it pushes into the cell it two ottassium ions it send out
13. GENERATION OF POST SYNAPTIC POTENTIALS .
How are neural signals created?
• When neurons fire, they release chemicals called neurotransmitters
• These chemicals diffuse across the synaptic cleft and bind with the post – synaptic
receptors in a lock and key fashion.
14. WHAT ARE THE EFFECTS?
• When neurotransmitter molecules bind to post –synaptic receptors, they typically have
two effects.
a) They may depolarise the receptive membrane (decrease the resting potential, from -
70 to -67 mv)
b) They may hyperpolarise ( increase the resting membrane potential from -70 to -72
mv).
• Post synaptic depolarizations are called excitatory post synaptic potentials
(EPSP).They increase the likelihood of neuronal firing.
• Post synaptic hyper - polarizations are called inhibitory post synaptic potential
(IPSP). They decrease the likelihood of neuronal firing.
Both EPSP and IPSP are graded potentials : ie., the amplitudes of E PSP’s and
IPSP’s are proportional to the intensity of the stimulus
15. CONDUCTION OF POST SYNAPTIC POTENTIALS
• EPSP’s and IPSPs travel passively from their sites of generation at
synapse, usually on the dendrites or cell body in much the same way
that electrical signals travel through the cable.
• Transmission of post synaptic potentials has two characteristics.
• 1) It is rapid, almost instantaneous irrespective of whether they are
brief or enduring.
• 2) They are decremental, ie., they decrease in amplitude as they travel
through the neuron.
16. INTEGRATION OF POST SYNAPTIC POTENTIALS AND GENERATION OF ACTION
POTENTIALS
• A neuron's action potentials are triggered at the axon hillock when neuron
is depolarized to the point that the membrane potential at the hillock reaches about
-65 mV. This is the threshold of excitation for many neuron.
• Action potential is a massive momentary reversal of the membrane potential from
about -70 to about +50 mV. This last for 1 millisecond.
• Unlike EPSPs and IPSPs, Action potentials are not graded. They follow the all or
none law.
• Most neurons receive hundreds of synaptic contacts. Whether or not a neuron
fires is determined by the adding together (integration) of what goes on
at many presynaptic neuron synapses
17. INTEGRATION OF POST SYNAPTIC POTENTIALS AND GENERATION OF
ACTION POTENTIALS
There are two kinds of neural integration:
• Spatial summation (EPSPs + EPSPs; IPSPs + IPSPs; EPSPs + IPSPs) - It shows
how local EPSPs that are produced simultaneously on different parts of the
receptive membrane sum to form a greater EPSP .
• Temporal Summation: (EPSPs + EPSPs; IPSPs + IPSPs) – It shows how post
synaptic potentials produced in rapid succession at the same synapse sum to form
a greater signal
20. CONDUCTION OF ACTION POTENTIALS - IONIC BASIS
• Conduction of action potential takes place through the action of the voltage
activated ion channels – the ion channels that open and close in response to the
changes in the level of the membrane potential.
21. CONDUCTION OF ACTION POTENTIALS - IONIC BASIS
i) Voltage activated gates present in the axon membrane become more permeable to sodium ions.
ii) Sudden influx of NA+ ions
iii)Reversed Polarity- -70 mV to +50 mV
iv)Opening of voltage activated potassium channels. Potassium driven out of cell because of the high
internal concentration and at the peak of the action potential due to positive internal charge.
v)Sodium channels close marking the end of the rising phase of the action potential and beginning of
repolarisation by continuous outflow of potassium ions to the extent that the membrane stays in a
state of hyperpolarisation for a brief period of time.
22. REFRACTORY PERIODS
• A brief period of about 1 or 2 milliseconds after the initiation of an action
potential, during which it is impossible to elicit a second one , This is called
absolute refractory periods.
• This is followed by relative refractory periods - the period during which it is
possible to fire the neuron again, but only by applying higher than normal levels
of stimulation . After which the amount of stimulation necessary to fire a neuron
returns to the baseline.