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Hormone
A chemical messenger, usually a protein, peptide or steroid, which is produced by an endocrine gland and released into the blood plasma
Protein and peptide hormones
Polar, soluble in watery blood plasma but cannot diffuse through cell surface membranes w phospholipid bilayer- hydrophobic tail and hydrophilic head, hormone cannot enter w SIMPLE diffusion, needs channel / carrier protein
Adrenaline and ADH
Steroid hormones
Lipid based so non polar nature, insoluble in blood plasma so bind to specific plasma carrier proteins produced by the liver to move through the bloodstream, hydrophobic so can diffuse across cell membrane eg oestrogen and testosterone
Endocrine gland
Ductless glands that synthesise hormones and release them into the bloodstream
Secretory cells, many capillaries- rich blood supply
Pancreas- both endocrine-insulin and glucagon and exocrine- digestive hormones
How are protein/peptide hormones made
Protein synthesis, mRNA, moves out of nuclear pore, ribosome at rough ER, tRNA, Golgi
How are steroid hormones made
Cholesterol, smooth er, made on demand as they can’t be stored in vesicles- lipid soluble so would simply diffuse out
Position of hypothalamus, pituitary gland, thyroid gland, parathyroid gland, pancreas, kidneys, ovaries, testes

Anatomy of adrenal gland

Where is adrenaline released
Adrenal medulla
Anatomy of hypothalamus and pituitary gland

Pituitary gland
Produces and releases secretions which affect most of the other endocrine glands, has an anterior and prosterior lobe, controlled mostly by hypothalamus
Anterior lobe produces six hormones- thyroid stimulating, growth, ACTH, FSH, LH, prolactin- milk in mammary glands, develops from roof of mouth
Posterior pituitary- adh, oxytocin, outgrowth of hypothalamus
Hypothalamus
Monitors blood levels, controls pituitary gland, has receptors which monitor the levels of various chemicals in blood- neurosecretory cells, nerve cells which produce secretions from end of axons to control release of hormones
Neurosecretory cells 1- stimulate or inhibit from anterior pituitary, known as releasing factors/ release inhibiting factors
Neurosecretory cells 2- produce secretions which are stored in posterior pituitary and released later as hormones
Target cells
They can only affect cells w receptors
Integral proteins- in cell surface membranes, specific hormone receptors for polar protein or peptide hormones
Intracellular receptors- in cytoplasm, non polar steroid hormones
Oestrogen Transport and effects
Steroid hormones synthesised by ovarian follicles, non polar and hydrophobic so attached to plasma proteins for transport in plasma, stimulates monthly growth of endometrium, female sexual secondary characteristic
How does oestrogen work
Non polar so can diff solve in the lipid component of the phospholipid bilayer and move into cytoplasm w simple diffusion
binds to a specific receptor in the cytoplasm to form an oestrogen-receptor complex
Complex passes through nuclear pore to enter nucleus
Acts as a transcription factor by binding to a specific promotor region of DNA switching on the relevant genes, slow process
Transcription factor
Protein that binds to DNA and either inhibits or initiates the transcription of a particular gene
Promotor region
Specific DNA base sequence to which a specific transcription factor binds
Adrenaline control of release, transport
Hypothalamus activates a sympathetic nerve which sends the impulses to the adrenal medulla stimulating the release of adrenaline, polar so dissolves in the watery plasma, faster than oestrogen
How does adrenaline work
It is polar so it is unable to dissolve in phospholipid bilayer so it cannot diffuse across cell surface membrane. Adrenaline THE FIRST MESSENGER to a specific adrenlaine receptor to form a hormone receptor complex.
This complex activates a membrane bound protein- G protein
This activates a membrane bound enzyme called adenylate cyclase
Adenylate cyclase converts ATP to cAMP THE SECONDARY MESSENGER!!
Activates futher enzymes depending on target cell
Adrenaline sets off a chain reaction / cascade effect, one enzyme forms hundreds of cAMP, many enzyme molecules millions of products
Control of hormone release- ways they are released
Direct stimulation by nerves- adrenaline
Response to another hormone- oestrogen and fsh
Response to the levels of a specific chemical in blood- insulin
Neurones
Individual cells specialised for the rapid transmission of electrical impulses throughout organisms- sensory, motor, relay
Gilal cells
Cells that support, protect and maintain neurones eg the schwann cells that provide myelination to certain axons
Synapses
Specialised junctions between 2 neurones across which nerve impulses are transmitted by neurotransmitter chemicals
Nerves
A bundle of neurones axons encased in connective tissue can be motor sensory or mixed
Receptor cells and sense organs
Specialised cells which can respond to changes in the internal or external environemt. May be grouped together w other tissues to form sense organs
Effectors
Cells or tissues that bring about a response when stimulated eg skeletal muscle, smooth muscle, cardiac muscle, endocrine glands, exocrine glands
Structure and role of myelin sheath
A fatty layer fo/rmed from specialised glial cells called Schwann cells. Each Schwann cell is wrapped multiple times around the neurone, cell surface membrane has a high lipid content
Role of myelin sheath- protect neurone, insulates neurone increasing the spread at which nerve impulses travel along neurone fibres- saltatory conduction
Nodes of ranvier
The gaps between Schwann cells where neurone fibres are exposed to surrounding tissue fluid
Myelinated and unmyleinated
Vertebrates are myelinated and unmyelinated, invertebrates are unmyleinated
Voluntary movements- motor neurons, myleinated
Automatic- un
Sodium / potassium pumps
Active transport pumps that harness energy from ATP to pump 3Na+ out of the axon for ever 2K+ they pump in, involved in stabilising and maintaining resting potential
Potassium facilitated diffusion channels
Many of them, facilitate the diffusion of K+ ions down chemical and electrical gradients, resting potential
Sodium facilitated diffusion channels
Very few present, membrane is relatively impermeable to sodium at rest, resting potential
Sodium voltage gated channels
Diffusion of Na+ down a conc gradient when open, voltage gated means they open when membrane potential reaches a certain voltage, involved in depolarisation
Potassium voltage gated channels
Permit diffusion of K+ down a conc gradient when open, involved in repolarisation and hyperpolarisation
What is resting potential
The potential difference of around -70mV across the plasma membrane of a neurone when the neurone is not transmitting an impulse
Resting potential explanation
The sodium/potassium pump moves 3 sodium ions out of the axon for ever 2 potassium ions it moves in, requires ATP
The membrane is impermeable to Na+ so these ions cannot diffuse back into the axon
The membrane does have some K+ facilitated diffusion channels so these can move back out of the axon down their chemical gradient
The inside of the axon thus becomes more negative than the outside
This electrical gradient pulls some of the potassium ions back into the axon
There is an equilibrium between the chemical and electrical gradients at around -70mV and then no more K+ movement
Role of atp in sodium potassium pump
Needed for pump to work so for resting potential, toxins called metabolic inhibitors eg cyanide prevent the formation of ATP by respiration and so can stop the transmission of impulses
Action potential graph

Resting potential
The potential difference of around -70mV across the plasma membrane of a neurone when the neurone is not transmitting an impulse
Depolarisation
The potential difference across the membrane is reversed for about 1ms reaching a peak of around -40mV
Na+ voltage gated channels open, allowing the Na+ ions that were pumped out of the neurone by the Na+/K+ pump top rapidly diffuse into the neurone down their chemical conc gradient
This makes th inside more positive than the outside
Repolarisation
The potential difference across the neurone membrane returns to a negative resting value after the peak of depolarisation
Na+ voltage gated channels close, K+ voltage gated channel open allowing the K+ ions that were pumped into the neurone down their chemical conc gradient. This returns the inside to a more negative potential than the outside, repolarising the membrane
Hyperpolarisation
The potential difference of the neurone membrane temporarily becomes more negative than the normal resting potential
More K+ ins diffuse out than needed to reach the resting potential so the inside temporarily becomes more negative than the resting potential
Then the K+ voltage gated channels close
K+ ions diffuse back into the neurone through the K+ facilitated diffusion channels repolarising the membrane
The Na+ / K+ pump also works to maintain resting potential
Refractory period
The time taken for ionic movements to repolarise an area and then restore the resting potential so that another Acton potential can be formed
What is a synapse
The junction between two neurones or between a neurone and an effector across which nerve impulses transfer using neurotransmitters
Synapse between motor neurone and effector
Motor end plate or neuromuscular junction
What do synapses cause
Excitatory- cause excitatory post synaptic potentials (EPSPs) or be inhibitory and cause inhibitory post synaptic potentials (IPSPs)
Function of synapses
-allow neurones o inter communicate and to communicate with effectors
-allow integration of sensory inputs from many sources allowing the organism ro respond appropriately to multiple stimuli (convergence)
-increase the range of simultaneous actions that can take place in response to a stimulus (divergence)
-help to ensure one way transmission
-filter out low level stimuli
-involved in memory and learning
Synapse structure

Why can synapse only travel in one direction
Pre synaptic- post synaptic
Neurotransmitter only storied in pre synaptic neurone and receptors only present in post synaptic neurone
EPSP
Excitatory post synaptic potential
Depolarisation caused by an influx of Na+ ions into the post synaptic membrane in response to a neurotransmitter binding to a receptor
Increases likely hood of action potential forming
Inhibitory post synaptic potential
Hyperpolarisation caused by influx of Cl- ions into the post synaptic membrane in response to the binding of a neurotransmitter to a receptor
Dec liklihood of an action potential
The formation of an excitatory post synaptic potential
Action potential reaches the synapse