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enzymes as catalysts terms: substrates, active site, products, lock and key, induced fit -ase as an ending isoenzymes and their role in diagnosis (measurement in the blood or secretions. Any cell product including enzymes) |
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factors that affect enzyme activity: |
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temperature, pH coenzymes, derived from vitamins, example: NAD and FAD endergonic and exergonic reactions ATP and ADP redox reactions gain and loss of electrons can be gain and loss of hydrogens role of NADH and FADH2 as electron shuttles |
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Ch. 5 Cell Respiration and Metabolism |
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metabolism: anabolism and catabolism |
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formation of two molecules of pyruvic acid from glucose NAD to pick up the H's end products: 2 pyruvic acid, 2 NADH and 2 ATP (net) per glucose molecule 2 ATPs used initially to energize glucose (the first one fixes glucose in the cell) and 4 ATPs produced total; therefore 2 ATPs net |
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under anaerobic conditions pyruvic acid à lactic acid to regenerate NAD alcohol fermentation cardiac muscle: lactic acid à angina pectoris under ischemic conditions |
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glycogenolysis to release glucose for cell use liver, having glucose-6-phosphatase, can provide glucose to increase blood sugar |
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glycogenesis to synthesize glycogen from excess blood glucose |
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gluconeogenesis: the synthesis of glucose from non-carbohydrate sources occurs in the liver is a good source of blood glucose, especially as liver glycogen is being depleted brain depends on glucose as its sole energy source |
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in the presence of O2 pyruvic acid can be completely oxidized to CO2 and H2 O aerobic respiration yields 30 ATPs total (including glycolysis) vs. 2 for glycolysis alone takes place in the mitochondrion |
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aerobic respiration Step one |
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first step prepares pyruvic acid to enter the Krebs cycle pyruvic acid à acetyl CoA + NADH + CO2 CO2 is exhaled acetyl CoA is how acetyl (2-C molecule) enters the Krebs cycle processes of cell respiration: glycolysis, Krebs cycle, electron transport and chemiosmosis oxidative phosphorylation involves electron transport and chemiosmosis |
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oxaloacetic acid (a C-4 molecule) combines with acetyl (a C-2molecule) from acetyl CoA the C-6 molecule is changed to a C-5 molecule and then to a C-4 molecule per turn of the cycle, two molecules of CO2 are produced, three molecules of NADH, and one molecule of FADH 2 and one ATP are produced oxaloacetic acid is regenerated occurs in the matrix of the mitochondrion |
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takes place on the inner mitochondrial membrane NADH and FADH 2 give up their two (high energy) electrons to members of the chain the electrons and H's of NADH have different pathway selectrons are passed from one carrier (such as a cytochrome) to another and finally to oxygen the energy released as the electrons are passed down the chain is used to make ATP by chemiosmosis |
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the electron transport chain is set up as 3 complexes each complex passes electrons and also pumps H+ into the intermembrane space the hydrogen ions can only leave the intermembrane space through respiratory assemblies that contain ATP synthase as the hydrogen ions stream through the ATP synthase, their energy enables ATP synthase to form ATP 4 H+ are needed to make one ATP each NADH pumps 10 H+ and makes 2.5 ATP FADH2 makes 1.5 ATP 30 ATPs are produced from the aerobic respiration of glucose, 32% efficiency water as a product of cell respiration is derived from oxygen, plus electrons plus H+ |
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related metabolic pathways (Chap 5) |
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excess glucose stored as glycogen, and then fat acetyl Co A can generate fatty acids, two carbon atoms at a time fat can be broken down to provide energy as an alternative to glucose (except for the brain (which can only use glucose) protein can be used for energy, but is a last choice fat is an efficient energy storage form |
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Ch. 6 Interactions Between Cells and Their External Environment external environment |
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fluid compartments: intracellular (66% of body water) extracellular: plasma (20% of the 33%), interstitial (80% of the 33%) plasma membrane, composition (review); selectively permeable categories of passage of materials through the plasma (cell) membrane:non-carrier mediated: simple diffusion, osmosis (a type of simple diffusion) carrier-mediated: facilitated diffusion, active transport and passive transport, uses kinetic energy from molecules active transport, against a concentration gradient: requires ATP |
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Movement of a substance from greater to lesser concentration examples: O2 and CO2 in and out of cells; ions through ion channels (can be gated) factors affecting diffusion: concentration gradient, surface area of membrane |
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diffusion of water through a selectively permeable membrane can be through the plasma membrane itself or through aquaporins (channels) results in a volume change example: plasma proteins drawing fluid back into a capillary after blood pressure pushes some fluid out of the capillary if there's insufficient plasma proteins (as occurs in liver disease), tissue swelling can occur (edema)tonicity: effect on cells from solutions that are isotonic, hypotonic, and hypertonic |
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carrier-mediated transport in general |
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requires protein carriers, which are usually specific for the molecules they transport carriers exhibit a transport maximum in diabetes this results in glucose being left in the urine instead of being reabsorbed |
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from high concentration to low concentration requires protein carrier example: glucose entry into cells problem, hypoglycemia doesn't result in sufficient glucose diffusing into brain cells |
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from low concentration to high concentration (against a concentration gradient) requires ATP requires a protein carrier Example:Na+/K+ pump |
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ATP directly involvedexample: Ca 2+ extrusion from cells example: Na+ -K+ pump, pumps : Na+ out of cells and K+ into cells. Moves 3 Na+ for 2 K+ |
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secondary active transport |
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molecules are moved against a concentration gradient energy comes from a concentration gradient set up by primary active transportexample: kidney tubule cell reclaiming glucose from the filtrate, made possible by the inward diffusion of Na+ from the filtrate |
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the separation of charges on the two sides of a membrane due to 1. Na+-K+ pump which brings 3 Na+ out foreach 2 K+ in (electrogenic pump) 2. (especially) ion distribution and permeability cell is more permeable to K+ so the interior of a cell has K+ and fixed anionsNa+ is the predominant extracellular cationsome K+ leaks out; slight negative charge at the membrane resultsall cells maintain this resting membrane potential(around-65 to -85 mV) neurons and muscle cells alter this resting membrane potential to send an action potential |
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cell body, dendrites, axon hillock, axon, axonal transportsensory, motor and association neurons motor neurons can be somatic or autonomic ( and these can be sympathetic or parasympathetic) |
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Ch. 7 Neurons and Synapses CNS, PNS |
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neurons: cell body, dendrites, axon hillock, axon, axonal transportsensory, motor and association neuronsmotor neurons can be somatic or autonomic ( and these can be sympathetic or parasympathetic) nerve vs. neuron |
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cell body, dendrites, axon hillock, axon, axonal transport sensory, motor and association neurons motor neurons can be somatic or autonomic ( and these can be sympathetic or parasympathetic) |
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Neuron: a cell that conducts impulses Nerve fiber: extension from a neuron ie.. axons and dendrites Nerve: a bundle of fibers, looks like a cord |
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oligodendrocytes, Schwann cells, and astrocytes Schwann cells and oligodendrocytes form meylin sheaths in the PNS and CNS respectively |
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Schwann cells wrap around an axon many times, forming the myelin sheath; the outer part of the cell is the neurilemma (sheath of Schwann) gaps between adjacent Schwann cells are the nodes of Ranvier, which allow transmission of impulses to speed down the axon |
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What is gray matter? white matter? |
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Gray matter is unmyelinated material - soma, unmyelinated axons White matter is myelinated material |
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A CNS white matter disease, demyelination at different times in different parts. |
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regeneration of axons: may occur in the PNS, but not the CNS aided by Schwann cells which form a growth tube and secrete growth factors (neurotrophins) |
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clean up and maintain the neuron environment, by removing K+ and helping recycle some neurotransmitters contribute to the formation of the blood-brain barrier: end-feet attach to capillaries and result in capillary cells having tight junctions. Keeps many undesirable substances out of the brain, but does make it more difficult to administer meds. to combat brainproblemsneed for the use of L-dopa, which does cross the blood-brain barrier, in place of dopamine, which doesn't, in the treatment of Parkinson's disease |
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resting membrane potential is altered by neurons (and muscle cells) to send an action potential depolarization: positive charges move into the cell; repolarization: positive charges leave the cell; hyperpolarization: an extension of repolarization gated ion channels allow ion influx (entry) and efflux(exit) at specific times Na+ channels can be closed (usually), open (during stimulation), or inactivated (right after stimulation) by the "ball and chain"Na+ channels allow Na+ to enter the cell K+ channels allow K+ to leave the cell when neuron is depolarized to threshold, -55 mV, Na+ voltage gated channels open |
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Na+ enters at depolarization K+ leaves (repolarization) due to the opening of K+ gated channels positive feedback scheme for Na+entry, overall negative feedback cycle at repolarizationNa+-K+ pump to maintain ion concentration |
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excitation travels down a neuron |
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Na+ enters, Na+ diffuses, depolarizes next patch of membrane to produce another action potentialall-or-none law for action potential, all action potentials in a neuron are the same regardless of stimulus coding for stimulus intensity by frequency not amplitude of action potential stimulus intensity also communicated by recruitment of more neurons in a nerve refractory periods: absolute and relative saltatory conduction MS |
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synapses presynaptic and postsynaptic cells |
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electrical synapses chemical synapses: terminal bouton, synaptic cleft, synaptic vesicles Ca2+ voltage regulated gates and the entrance of Ca2+ Ca2+ promotes exocytosis of neurotransmitter neurotransmitter binds to receptors on the postsynaptic membrane opening of chemically regulated gatesif it's a Na+ channel, this produces a depolarization which is excitatory and called an EPSP if it's a Cl - channel, Cl - would enter and hyperpolarize cell (K+ channels opening would hyperpolarize also)produces an IPSP |
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comparison of chemically regulated gates and voltage-regulated gates in |
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terms of what makes them open:neurotransmitter vs. voltage change; where they are located: cell body and dendrites vs. axon; and the result of their opening: EPSPs/IPSPs vs. action potentials. events in neuron transmission (see handout) |
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neurotransmitter in neuromuscular junctions, in the CNS and the autonomic nervous system |
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muscarinic, on smooth and cardiac muscle, and nicotinic on neurons and skeletal muscle |
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receptors are part of ligand-operated channels binding of ACh causes channel to open Na+ enters and K+ leave through the same channels more Na+ enters than K+ leaves and this depolarizes the cell |
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receptors are separated from the ion channel they control a G-protein connects the receptor with the channel binding of ACh to receptor causes beta and gamma subunits of the G-protein to dissociate, and open the ion channel example: heart muscle has K+ channels that open this way |
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is the enzyme that degrades ACh choline is taken back into the presynaptic neuron |
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catecholamines, based on the amino acid tyrosine includes norepinephrine, epinephrine (a hormone) and dopamineserotonin, based on the amino acid tryptophan all are "feeling good" neurotransmitters inactivated by reuptake into the presynaptic neuronuse of meds in clinical depression: SSRIs, serotonin-specific reuptake inhibitors, to increase the amount of serotonin at synapses |
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two pathways using dopamine as a neurotransmitter, both originating from the midbrain midbrain to prefrontal cortex: increase in dopamine implicated in schizophrenia midbrain to basal nuclei (basal ganglia): decrease in dopamine related to Parkinson's disease |
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Steps On How Neurons Generate and Send Action Potentials |
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Steps On How Neurons Generate and Send Action Potentials |
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Release of neurotransmitter from presynaptic neuron. |
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Diffusion of neurotransmitter to postsynaptic neuron, binding to receptor. |
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Opening of chemically gated channels. |
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Diffusion of positive ions (Na+) into postsynaptic neuron. EPSP (excitatory postsynaptic potential) produced in the postsynaptic neuron. Na+ diffuses in the cell body. |
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If enough Na+ is present at the axon hillock to depolarize the cell to threshold, voltage-gated channels open and an action potential starts. Na+ enters these channels and causes depolarization. |
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Na+ voltage-gated channels close. K+ voltage-gated channels open. |
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K+ leaves the axon and results in repolarization. K+ voltage-gated channels close. |
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The Na+ that entered diffuses (due to cable properties of the axon) and depolarizes the next patch of membrane. |
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This starts another action potential. These events continue down the axon until the terminal bouton is reached. |
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Here, Ca2+ gates open due to the depolarization and Ca2+ enters. Ca2+ promotes exocytosis of neurotransmitter from synaptic vesicles. |
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This neurotransmitter can now diffuse to and stimulate another neuron. |
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