Bio Bases Flashcards
dichotomous traits
- present in one form or another but never in combination e.g. pea color
- mututally exclusive
true breeding lines
- interbred members always produce offspring with the same trait
- brown pea parents produce brown pea children
- white pea parents produce white pea children
- has to do with the carried traits, not the expressed trait
Mendelian genetics
- Gregor Mendel Augustinian monk from Moravia (Austria) breed pea plants 1850-60’s
Dominant trait
- first generation offspring all had brown peas
recessive trait
- second generation offspring were 75% brown and 25% white – white was recessive trait
- replicated this with other traits
Mendelian genetics Key Points
- dichotomous traits
- present in one form or another but never in combination e.g. pea color
- true breeding lines
- interbred members always produce offspring with the same trait – brown pea parents produce brown pea children- white pea parents produce white pea children.
- first generation offspring all had brown peas
- Dominant trait
- second generation offspring were 75% brown and 25% white
- white was recessive trait
- replicated this with other traits
- white was recessive trait
- Demonstrated that traits not expressed by parents could be passed onto children
Dr. Egas Moniz
- Portuguese neurologist attended a conference in 1935 at which he heard 2 presentations
- a chimp who frequently became upset when she made errors on a food reward task did not get upset after bilateral prefrontal lesions
- a patient who had removal of prefrontal lobes during tumor resection showed no intellectual impairment
- Applied to psychiatric patients after hearing this data
- won a Nobel Prize in Physiology and Medicine 1949 for the development of prefrontal lobotomy
- Follow up of lobotomy shows no sig decline in IQ, but there are other areas they showed substantial impairment. While the psychiatric issues deimished it took their capacity of emotion away. They had flat affect, could have problems of apathy, lack of inituation, poor motivation, many patients could not sustain employment because of EF issues. They needed people to prompt, direct, instruct for everyday activities.
- 40,000 prefrontal lobotomies done in U.S. before being discontinued in the 1960’s and still done in some places today.
Phenotype
- organism’s observable traits
Genotype
- traits that can be passed on to children thru genetic material
genes
- Two kinds of inherited factors for each dichotomous trait
- located on the nucleus in the chromosome of the cell
- Each organism possesses two genes for each of its dichotomous traits
- Occur in matched pairs
- each species has a certain number of chromosomes
- humans have 46 arranged in 23 pairs
- one pair is sex chromosomes
- other 22 pairs which are not sex chromosomes are autosomes
alleles
- Two genes that control the same trait
- located at the same locus at each chromosome of a particular pair
homozygous
- Identical genes
heterozygous
- two different genes
- one dominates the other in the pair in expression of the trait
- randomly inherits one of the mothers two genes and one of the fathers two genes
autosomes
- other 22 pairs which are not sex chromosomes
Mendel proposed four ideas
- Two kinds of inherited factors for each dichotomous trait – now referred to as genes.
- Each organism possesses two genes for each of its dichotomous traits
- a. Two genes that control the same trait are called alleles
- b. Identical genes are homozygous
- c. two different genes are heterozygous
- one of the genes in a heterozygous pair dominates the other in expression of the trait
- for each trait, a child randomly inherits one of the father’s two genes and one of the mother’s two genes
Meiosis
- process of cell division that produces gametes i.e. sperm and egg
- chromosomes divide and one of the pair goes to one gamete andthe other of the pair goes to the other gamete
- each gamete contains only half the usual number of chromosomes i.e. 23 instead of 46
- union of sperm and egg combines these two sets of 23 chromosomes to produce 46
- because each of the 23 pairs is randomly distributed to gametes, there are 223 possibilities or 8,388,608 possible chromosomes combinations. THis is why we see differences in siblings
- This is where crossing over occurs
Genetic reproduction
- Meiosis
- process of cell division that produces gametes i.e. sperm and egg
- chromosomes divide and one of the pair goes to one gamete andthe other of the pair goes to the other gamete
- each gamete contains only half the usual number of chromosomes i.e. 23 instead of 46
- union of sperm and egg combines these two sets of 23 chromosomes to produce 46
- because each of the 23 pairs is randomly distributed to gametes, there are 223 possibilities or 8,388,608 possible chromosomes combinations
- All cell growth afterward is mitosis
- set of 46 chromosomes duplicates and when cell divides each new cell receives a full compliment of 46 cells
- Linkage
- traits that are controlled by genes on same chromosome have a higher probability of being inherited together
- e.g. Down’s syndrome and facial features
- However, linkage is not absolute. The probability 2 genes on the same chromosome will be inherited together ranges from almost 1.0 to .5 or chance. How can this be?
- Linkage is the observation that traits that are controlled by genes of the same chromosome code for are are involved in controlling different traits. When you have 2 genes on the same chromosome that have the same traits, they will be inherited as a package and occur together in a high probability. Traits controlled by genes in separate chromosomes do not happen together in the same . The chromosome comes as a package, so the same traits come together.
- Cross-over
- during early stages of meiosis, chromosomes overlap or crossover one another and break apart at the points of contact, exchanging sections of chromosome.
- as result parents rarely pass on intact chromosomal clusters of genes to children.
- Each gamete contains chromosomes that are unique spliced together combinations of chromosomes inherited from your father and mother
- Degree of linkage between two genes is determined by how close together they are on the chromosome
- Crossover rarely occurs between adjacent genes and frequently between genes at opposite ends of chromosome
- during early stages of meiosis, chromosomes overlap or crossover one another and break apart at the points of contact, exchanging sections of chromosome.
mitosis
- cell growth after meiosis
- set of 46 chromosomes duplicates and when cell divides each new cell receives a full compliment of 46 cells
Linkage
- traits that are controlled by genes on same chromosome have a higher probability of being inherited together
- e.g. Down’s syndrome and facial features
- However, linkage is not absolute. The probability 2 genes on the same chromosome will be inherited together ranges from almost 1.0 to .5 or chance. How can this be?
- sex linked traits only occur in males
Cross-over
- during early stages of meiosis, chromosomes overlap or crossover one another and break apart at the points of contact, exchanging sections of chromosome.
- as result parents rarely pass on intact chromosomal clusters of genes to children.
- Each gamete contains chromosomes that are unique spliced together combinations of chromosomes inherited from your father and mother
- Degree of linkage between two genes is determined by how close together they are on the chromosome
- Crossover rarely occurs between adjacent genes and frequently between genes at opposite ends of chromosome
Sex related genes
- Only exception to matched pairs of chromosomes is the pair that determine gender.
- two different types X and Y
- X and Y look different and carry different genes
- two X’s for females; X and Y for males
- traits influenced by genes on sex chromosome are called sex-linked traits
- almost all sex-linked traits are controlled by X chromosome because Y is small and carries few genes other than those determining male sex development
- traits controlled by genes on the X chromosome occur in one sex more often than the other
- dominant traits occur more often in females than males because they have twice the chance of inheriting the dominant gene
- recessive sex-linked traits occur more in males because if they inherit the trait on X, there is nothing to over-ride it on Y and they express the trait, whereas in females they will express it only if they inherit two recessive genes
- color blindness is recessive sex-linked trait and is rare in women
sex-linked traits
- traits influenced by genes on sex chromosome
deoxyribonucleic acid (DNA)
- Each chromosome is composed of double stranded molecule
each strand composed of sequence of nucleotide bases attached in chain
- adenine (a goes with t)
- thymine (t goes with s)
- guanine (g goes with c)
- cytosine (c goes with g)
Replication
- in mitosis and other processes
- the helix unravels and loose nucleotides are attracted to the unpaired strands and form two identical chromosomes
- errors sometimes occur and result in mutations
Structural genes
- most prevalent – contain information necessary for synthesis of proteins.
Proteins
- are long chains of amino acids that control physiological activities of cells and are important components of their structure
Enhancer or promoter
- Sections of DNA that control structural genes and whether or not they initiate synthesis of protein
- If protein is synthesized the gene is expressed
- no protein synthesis, gene is not expressed.
- Control of gene expression is important because it determines how a cell will develop and how it will function once it is mature
- Enhancers are like switches: they can be turned on, off, up or down
Transcription factors
- Proteins that bind to DNA and regulate genetic expression
- Many of these binding proteins that influence enhancers are influenced by signals received from the cell as it responds to the environment
- thus providing the mechanism for interaction of the environment and genes to influence development
Expression of a gene
- operator gene initiates process
- DNA for the section of structural gene unravels
- exposed DNA attracts messenger RNA which forms a strand until reaching another operator gene that signals the end of the structural gene
- mRNA same as DNA except it has uracil instead of thymine
- mRNA then goes to a ribosome in the cytoplasm of the cell
- ribosome moves along the mRNA and transcribes the genetic code
- each group of 3 consecutive nucleotides is called a codon
- codon instructs the ribosome which of 20 amino acids to add to the protein it is constructing
- as ribosome reads mRNA it attracts transfer RNA attached to an amino acid
- ribosome reads codon after codon and adds amino acid after amino acid until it reaches another operator gene that signals the end of the structural gene
- the completed protein is then released into the cytoplasm
- This process is very accurate but there can be mutations if it codes for a different protein
Human Genome Project
- Procedure:
- enzymes split chromosomes
- clone to have unlimited supply
- exposed to chemical markers that uniquely label specific loci - not nucleotide bases – but loci which are composed of hundreds/thousands of nucleotide bases
- placed in a jell
- jell forced through a very small tube
- as going through end of tube exposed to a special light
- chemical markers show up differently and are recorded in a computer
- patterns of markers were examined to identify identical sequences which were overlapping portions of the chromosome
- loci have been identified
- now attempting to identify sequence of nucleotide bases for each
- Findings of HGP
- The human genome contains 3.1647 billion chemical nucleotide bases (A, C, T, and G).
- The average gene consists of 3000 bases, but sizes vary greatly, with the largest known human gene being dystrophin at 2.4 million bases.
- The total number of genes is estimated at 20,000, much lower than previous estimates of 80,000 to 140,000 that had been based on extrapolations from gene-rich areas as opposed to a composite of gene-rich 2% of genes code for proteins – i.e. structural genes
- Almost all (99.9%) nucleotide bases are exactly the same in all people.
- The functions are unknown for over 50% of discovered genes.
- Scientists have identified about 1.4 million locations where single-base DNA differences occur in humans called Single Nucleotide Polymorphism (SNPs). This information promises to revolutionize the processes of finding chromosomal locations for disease-associated sequences
- New understandings: Epigenetic factors that influence genetic expression
- Pseudogenes
- Structural genes make up about 2% of human genome
- Rest are pseudogenes previously thought to be inactive
- Now known to exert control over structural genes…e.g. may bind to and block mRNA
- Alternative splicing
- Strands of mRNA are broken apart and pieces are spliced to new segments
- As a result a single gene can code for more than one protein
- Particularly prevalent in neural tissue
- microRNA’s control DNA
- influence enhancers and mRNA
- influence brain development and synaptic function
- disruption associated with neurodegenerative disorders
- monoallelic expression
- exception to dominant allele is expressed
- epigenetic mechanisms (presently unknown) inactivate one allele and the other is expressed
- happens particularly in the nervous system
- Pseudogenes
- Now clear that genetic influences include
- Not only structural genes
- Interaction of many structural genes
- Influence of epigenetic factors
- Developmental timing of expression of particular genes in specific brain structures
Genetic breeding
- Overall idea: Genetics create a risk or advantage. They convey a context and expression is based on the environment context.
- Bright and dull maze rats (1934)
- after 8 generations virtually no overlap in the number of errors made in learning maze
- cross fostering to control for parents teaching offspring
- since this finding many traits have been selectively breed in lab animals including
- Behavioral trait used as criteria for selective breeding is not the behavioral trait influenced by the genes segregated by the breeding
- Subsequent research found the bright rats learned maze better not because they were more intelligent but because they were less fearful
- However, environment/experience influenced expression of this trait
- Dull rats worse than bright rats only if raised in impoverished environment
Genetic influences on human behavior
- Genetic control and influence of normal behavior is complex
- it takes many genes functioning normally to produce normal behavior, but abnormality can often be caused by dysfunction of a single gene
- Down syndrome
- Huntington’s disease
- Causes issues in the basal ganglia. Autozomal dominant gene disorder
- Alzheimer’s
- APIE*E4 associated.
- If you have APOE E4 you have an increased risk of Alzheimer’s.
- (2/3 of people with gene have AZH)
- (1/3 of people with AZH do NOT have this gene)
- Serotonin transporter gene
- Otosclerosis – hearing impairment
- Multiple exostoses – benign bone tumors
- Neurofibromatosis – tumors of nervous system and skin
- Cystic fibrosis – abnormal transport chloride and sodium effecting lungs most critically
- Duchenne muscular dystrophy
- recessive X-linked abnormality
- effects primarily boys
- muscle degeneration and death with average life expectancy of 25
- Fragile X
- most common form of inherited intellectual disability in boys
- can occur in girls but more common in boys
- portion of X chromosome is repeated
- codes for a protein critical for brain development
Genetic control and influence of normal behavior is complex
- it takes many genes functioning normally to produce normal behavior, but abnormality can often be caused by dysfunction of a single gene
Otosclerosis
- hearing impairment
Multiple exostoses
- benign bone tumors
Neurofibromatosis
- tumors of nervous system and skin
Cystic fibrosis
- abnormal transport chloride and sodium effecting lungs most critically
Duchenne muscular dystrophy
- recessive X-linked abnormality
- effects primarily boys
- muscle degeneration and death with average life expectancy of 25
Fragile X
- most common form of inherited intellectual disability in boys
- can occur in girls but more common in boys
- portion of X chromosome is repeated
- codes for a protein critical for brain development
Nature or nurture; genetics vs. experience
- Formulating the question in terms of either – or is too simplistic and does not reflect reality
- Breast feeding and IQ – news paper article
- maze bright and dull rats reared in impoverished and enriched environments.
- Other studies show enriched environment results in thicker cortices
- Head Start
- the above suggest early experience can at least partially offset genetic disadvantage
- an individual’s behavior is result of the interaction of genetics and experience
- However, it does make sense to ask what portion of the difference between individuals on a certain trait is due to genetics vs. experience
- to study the contribution of genetics to the differences between individuals, individuals with varying degrees of genetic similarity are studied
- Twin studies
- Identical vs. fraternal
- Raised together vs. adopted
- Concordant vs. discordant for the trait of interest
- Minnesota twin study
- Twin studies
- I.Q. correlated .80 for identical twins raised together and .75 for those raised apart
- Schizophrenia 4 times higher in mono twins than di twins
- These results indicate that differences between individuals’ I.Q. and expression of schizophrenia has a genetic influence
- heritability estimate
- the estimate of the proportion of variability occurring in a particular trait in a particular study that resulted from the genetic variation in that study:
- .7 for I.Q. in the twin studies
- heritability estimate
- tells us about the contribution of genetic differences to phenotypic differences among subjects – i.e. in the population
- h.e. says nothing about the relative contribution of genetics and experience to the development of an individual
- interactive influence of genes and environment
- discussed earlier that environmental events directly influence DNA binding proteins that control regulator genes and determine if structural genes are expressed
- gene expression also influences the type of environmental stimulation person seeks and is exposed to
- e.g. an aggressive person seeks out contact and/or extreme sports
- people also tend to select social partners that have similar genetics to their own
- when a particular gene encourages a developing individual to select experiences that increase the behavioral effects of that gene
- cycle of genetics and environmental experiences influencing and determining each other
- Although raised apart, twins in MN study grew up in culturally and economically similar environments
- Recent research shows the correlation of iq in twins:
- Near 0 in low SES
- Near 1.0 in high SES
heritability estimate
- the estimate of the proportion of variability occurring in a particular trait in a particular study that resulted from the genetic variation in that study:
- .7 for I.Q. in the twin studies
- tells us about the contribution of genetic differences to phenotypic differences among subjects – i.e. in the population
- h.e. says nothing about the relative contribution of genetics and experience to the development of an individual
Soma
- contains the nucleus and much of machinery that operates cell
- this is the headquarters
- this is the cell body
- involved in biological processes
Dendrites
- receive information from other neurons
- can grow and form new connections
- where synapses occur
Axon
- collaterals – telodendria
- can grow and form new connections
- a nerve is composed of many axons surrounded by a tough, elastic connective membrane
- can often split into different pieces
Axon hillock
- where action potential originates.
- Location where the initiation of a nerve impulse occurs
- Between the axon and the soma
Terminal button
- secretes transmitter substance or nt
- forms synapse with dendrites, soma or axons of other neurons
- points of connection between this neuron and other neurons
- allows neurons to communicate with each other
Neuron internal components
- Membrane
- Nucleus
- Nucleolus
- Ribosome
- Mitochondria
- Endoplasmic reticulum
- Glia
- Microtubules / filaments
Membrane
- NEURON INTERNAL COMPONENT
- double layer of lipid molecules
- embedded in membrane are a variety of protein molecules that perform various functions
- detect and pass on information about substances outside cell
- control access to inside of cell allowing in some things and barring others
- active transport of material into and out of cell
Ribosome
- neuron internal components
- in cytoplasm “decodes” mRNA for formation of proteins used in the neuron
Nucleolus
- neuron internal components
- produces ribosomes
Nucleus
- Nueron internal component
- contains chromosomes and nucleolus
Endoplasmic reticulum
- neuron internal component
- system of tubes for storage and transport of material within cell and important for protein synthesis
- Rough
- contains ribosomes that produce proteins which are transported out of cell or used in the membrane
- Smooth
- channels for transport and storage of molecules
Endoplasmic Reticulum Rough
- contains ribosomes that produce proteins which are transported out of cell or used in the membrane
Endoplasmic Reticulum Smooth
- channels for transport and storage of molecules
Mitochondria
- neuron internal component
- converts glucose to ATP and stores CA. Contain different DNA (only from mother) than other cells
Golgi Apparatus
- packages proteins including neurotransmitters into vesicles
produces lysosomes which break down substances no longer needed by the neuron
Microtubules / filaments
- transport substances between cell body and distal cell / terminal button
Support cells
- Glia
- Astrocytes
- Oligodendrocytes
- Microglia
- Schwann cells
Glia
- “glue”
- neurons have high rate of metabolism but cannot store energy
- therefore, they must be supplied by glial cells with a constant source of nutrients (glucose) and oxygen and will die within minutes if this is interrupted
- provide physical support, control nutrient flow, and are involved in phagocytosis (what holds the brain together)
- types of glial cells are:
- astrocytes
- oligodendrocytes
- micoglia
- schwann cells
Astrocytes
- Provide physical support, remove debris, and transport nutrients to neurons
- one astrocyte cell will have connections with many neurons
- provide structure or matrix that holds neurons in place
- surround synapses so neurotransmitter are not dispersed beyond synapse (to contain neurotransmitters)
- Phagocytosis -digests dead neurons
- forms scar tissue in area left from phagocytosis
produce some chemicals needed by neurons
absorb and release substances to keep concentration levels around neuron at critical levels
aid in energy use efficiency. - Break down glucose received from capillaries into lactate used by neuron for energy
- Glucose is transported into and changes glucose into clackogen that can be used as fuel.
phagocytosis
- Cells engulf and digest other cells or debris caused by cellular degeneration
- Done by microglia and astrocyte
Oligodendrocytes
- Provide physical support and form the myelin sheath around axons in the brain
- form myelin sheath CNS which insulated axons
- Nodes of Ranvier: bare portion of axon
- A single oligo. will provide myelin for multiple axons
Microglia
- phagocytosis
- immune function for brain
- inflammatory response to damage
- destruction of pathological cells
Schwann cells
- The “oligodendendrocytes of the PNS”
- Form myelin for Peripheral nervous system axons. Wraps around one axon.
- When a neuron is damaged fagocytosis will occur for the damaged part and the Schwann cells will start forming a tube and the survivied part will grow parts and find its way in the tube and grow and will result in recovery.
- In the brain this does not happen, there is no meaningful repair like this.
Blood-brain barrier
- Capillaries in body have permeable walls allowing for free movement of most substances between plasma and extra cellular fluid
- In CNS capillary walls are not permeable for most part and substances are actively transported between capillary and neuron
- BBB allows for control of delicate balance of substances in neuron extra cellular fluid necessary for brain to function normally and exclude toxins or chemicals that would interfere with neuron function
- BBB not as strong throughout brain e.g. in area that controls vomiting
- Function to keep toxins and poisons etc that can damage the brain away. Also, substances in the brain need to be very controlled and at the right concentration levels.
- Not uniform through the brain, the area postrema is nonexistent there
- Nutrition is absorbed from food and then enters blood, oxygen enters lungs, then enters blood.In the third stage you have the glucose and oxygen moving across, moving from the blood in the brain, across the small cappilaries into the tissue. Then what you want to get rid of permeates what you take away. In the brain these are not permeable. Glucose and oxygen don’t flow freely through these walls.
Electrical potentials
- Inside of axon has –70 mV charge relative to the outside called resting potential or membrane potential
- Positively charged electrical stimulation on inside of axon depolarizes membrane – i.e. “takes away some of the charge difference” across the membrane
- Sub-threshold and threshold stimulation
- action potential with threshold stimulation
- to understand what makes an action potential occur must first understand what maintains resting potential
resting potential or membrane potential
-70mV charge is produced by a balance between difusion and electrostatic forces
depolarizes
- “takes away some of the charge difference” across the membrane
- This occurs during an action potential
Membrane or resting potential in depth
- Difference in voltage between the inside and outside of the axon membrane
- Electrostatic Force
- intra and extracellular fluid contain different ions
- membrane potential (-70mV charge) is produced by a balance between diffusion and electrostatic forces
- Ions in and outside of the neuron:
- NA+ ions are high in concentration outside of the cell, while K+ ions are in high concentration inside the cell.
- The ratio of the positive charge on the outside to the negative charge on the inside.
Diffusion (concentration) force
- resting potentional
- molecules go from areas of high concentration to low until they are evenly distributed throughout the medium
Electrostatic force (or pressure)
- resting potential
- substances which, when dissolved in water, split apart into two particles each with an opposing electrical charge are electrolytes
- charged particles are ions
- like charged particles repel and opposite charged particles attract
- particles will distribute themselves in a medium until the charged particles are evenly distributed
electrolytes
- substances which, when dissolved in water, split apart into two particles each with an opposing electrical charge
ions
- charged particles
- The repel like charged particles, and attract opposite charged particles
Ions in and outside of the neuron
- organic ions
- negatively charged (A-) present only on inside of neuron. Membrane is impermeable to it so it stays inside neuron and contributes to negative charge on internal surface of membrane.
- Potassium
- positively charged ion (K+) highly concentrated inside neuron. Diffusion force tends to push K+ out of cell, but since outside of membrane is positively charged, electrostatic force pushes it in. The balance of these forces results in greatest concentration of K+ inside
- Chloride
- negatively charged ion (Cl-) highly concentrated outside neuron. Diffusion force pushes it into the neuron, but since the internal membrane is negatively charged electrostatic force pushes it out. The balance of these forces results in greatest concentration of Cl- outside
- Sodium
- positively charged ion (Na+) highly concentrated outside neuron. Diffusion force pushes it into neuron. Because the internal membrane is negatively charged electrostatic force attracts it into the neuron
- high concentration of Na+ outside neuron is maintained by two factors:
- membrane is not very permeable to Na+ so only a small amount is able to “leak” into the neuron
- protein molecules in the membrane called “sodium-potassium transporters” (pump) remove the Na+ that leaks in and the K+ that leaks out
- sodium-potassium transporters are made up of proteins that actively transport these ions
- Na+ - K+ pumps consume ~ 40% of neurons energy
organic ions
- negatively charged (A-) present only on inside of neuron. Membrane is impermeable to it so it stays inside neuron and contributes to negative charge on internal surface of membrane
Potassium ion
- positively charged ion (K+) highly concentrated inside neuron. Diffusion force tends to push K+ out of cell, but since outside of membrane is positively charged, electrostatic force pushes it in. The balance of these forces results in greatest concentration of K+ inside
Chloride ion
- negatively charged ion (Cl-) highly concentrated outside neuron. Diffusion force pushes it into the neuron, but since the internal membrane is negatively charged electrostatic force pushes it out. The balance of these forces results in greatest concentration of Cl- outside
Sodium ion
- positively charged ion (Na+) highly concentrated outside neuron. Diffusion force pushes it into neuron. Because the internal membrane is negatively charged electrostatic force attracts it into the neuron
high concentration of Na+ outside neuron is maintained by two factors
- membrane is not very permeable to Na+ so only a small amount is able to “leak” into the neuron
- protein molecules in the membrane called “sodium-potassium transporters” (pump) remove the Na+ that leaks in and the K+ that leaks out
- sodium-potassium transporters are made up of proteins that actively transport these ions
- Na+ - K+ pumps consume ~ 40% of neurons energy
Action Potential
- A stereotyped change in membrane potential
- If the RMP moves past the threshold, membrane potential quickly moves up to +40 mV and then returns to resting
- This is caused by NA+ coming in and causing a spike, then K+ going out, the downsizing of the spike
- Neuron membrane also contains ion channels (pores) that can open and allow ions (Na+ and K+) to enter and leave neuron
- membrane contains billions of channels that can admit billions of Na+ ions
- When threshold of excitation is reached on the membrane
- opening of channels is triggered by depolarization of membrane potential (i.e. immediately adjacent membrane charge changing to negative. Thus they are called voltage dependent ion channels).
- Diffusion and electrostatic forces propel Na+ into neuron.
- Influx of Na+ causes rapid change of membrane potential (charge) from –70 mV to 40 mV
- K+ ion channels are less sensitive than Na+, require more depolarization (change in membrane charge) to open, and open after Na+ channels.
- At peak of action potential (i.e membrane charge reaches 40 mV) Na+ channels become refractory, i.e. are blocked, and no more Na+ can enter until membrane resting potential is restored
- K+ channels are open. Because of influx of Na+, inside of membrane is positively charged and immediate outside of membrane is negatively charged. K+ is driven out of the neuron by diffusion and attracted out by electrostatic forces. This causes the membrane potential to begin returning to normal. As this happens K+ channels are closed
- Na+ channels reset so another depolarization can cause them to open again
- Accumulation of K+ outside causes the membrane to “overshoot” and become hyperpolarized, i.e. charge goes below –70 mV. K+ diffuses away and membrane returns to –70 mV
- Na+ - K+ transporters eventually remove Na+ from neuron and retrieve K+
- Changes Na+ and K+ concentrations, and in membrane charge take place just at the area immediately inside and outside the membrane and not throughout the neuron. Influx of Na+ is small relative to the overall concentration of Na+ in the neuron
- Na+ - K+ transporters are not that essential in restoring Na+ and K+ levels after action potential. The small amount of these ions that cross the membrane is small relative to the overall concentration in the neuron and is “hardly noticeable”. Transporters are most important on a long-term basis to prevent the slight amount of Na+ that leaks into the neuron (because of the slight permeability of the membrane to Na+) from causing too high a concentration in the neuron that would prevent it from functioning
synaptic vesicles
- small sv contain neurotransmitter
- are produced in the soma and transported to button by microtubules or recycled in the button
transmitter substances
- Chemicals produced by the body that communicate between neurons i.e. across synapses
neurotransmitters
- released by terminal button and detected by receptors on membrane of neuron across synaptic cleft
neuromodulators
- released by terminal buttons in greater quantities and are more widely dispersed influencing many neurons in an area of the brain
hormones
- most produced by endocrine glands, but some produced by cells in stomach, intestines, kidney and brain. Released into extracellular space and dispersed by blood stream.
- Neurons that have receptors for hormones are target cells. Hormones affect the functioning of the cells that have the receptors
target cells
- Neurons that have receptors for hormones are target cells. Hormones affect the functioning of the cells that have the receptors
Peptides
- Insulin and pituitary hormones
- Stimulate metabotropic receptors in membrane
- Second messenger travels to nucleus and influences activity of cell
Steroids - lipid
- sex hormones and those secreted by the adrenal cortex i.e. adrenalin
- pass through membranes to nucleus where it binds with receptor. When activated, the receptor influences protein production
- Steroid receptors have recently been discovered in terminal buttons and post-synaptic membranes