ANP midterm 2 Flashcards

(104 cards)

1
Q

What is the heart?

A

A double pump where both sides have different jobs.
Right side- pumps blood from tissues, shoots blood to lungs and gets rid of CO2
Left side- receives oxygenated blood from lungs and pumps to body tissues via systemic circuit.

Facts:
- half a kg, size of a first
- superior surface of diaphragm, sits on top of it
- Mediastinum, two thirds of the heart are to the left of midsternal line
- in front (anterior) to vertebral column, posterior (behind) sternum
- has 3 layers

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2
Q

Pericardium

A

The outer layer of the heart
- double walled
- fibro-serous sac
- 2 types:

  1. fibrous sac
    - outer layer
    - protects and anchors the heart
    - prevents overfilling of the heart
  2. serous pericardium
    - 2nd layer, parietal (outer) and visceral (inner)
    - epicardium layers so that the heart can move without causing friction
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2
Q

Myocardium

A

This is where most of the mass of the heart is.
- The inner wall, and is highly branched, has bundle branches.
- Supports the great vessels
- has connective tissue wrappings of these bundles
- spreads electric current

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3
Q

Endocardium

A
  • inner layer of the heart
  • has endothelium, which is a connective tissue layer on the inner surface
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3
Q

Gross anatomy of the heart

A

First, blood comes in from the inferior/superior vena cava. This blood is deoxygenated blood, and vena cava is a vein because blood comes INTO the heart.

Then, blood goes to the right atrium, which is the receiving chamber. This is where blood pools and makes the tricuspid valve open. Then the blood goes to the ventricle, where it contracts and sends blood out.

After coming back through left pulmonary veins, and into the receiving left atrium. Again, blood pools and passes the bicuspid valve to go to the ventricle. Then it goes to the aorta to be sent to the rest of the body which needs oxygenated blood.

The reason why the left side of the heart is more heavy than the right side is because the left side has to send blood to all of the body while the right side only sends blood to lungs.

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4
Q

Heart valves

A

Atrioventricular valves (AV)
- tricuspid and bicuspid (mitral) valves
- Goes from atria to ventricles
- Acts like a trap door
- first, the blood has to pool in the atrium while the valves are closed, and when the atrium eventually pools and pressures the valves, they open. Blood goes to ventricles where they contract and cuspids hold the blood in place

Semilunar valves (SL)
- Pulmonary and aortic valves
- both operate in the same way
- when blood comes in, the valves trap them, and when going out, they easily open

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4
Q

What can go wrong with valves?

A

Since valves are there to insure the direction of the blood to go down properly, they are at a lot of stress, so problems can happen

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5
Q

Incompetent valve

A

When the blood goes through the valve and then out, the valves don’t close, so the blood goes back to the atrium. The heart will keep pumping the same blood again and again

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5
Q

Valvular stenosis

A
  • Flaps of valves are stiff, so they don’t want to open
  • The heart needs to contract extra more for them to open
  • has a clicking sound (important)
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5
Q

Why is the sound of the heart important?

A
  • first sound: Lub (from AV valves)
  • Second sound: Dub (from SL valves)
    This is important because both sounds associate with the valves CLOSING
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6
Q

Systemic circuit

A
  • comes to left atrium and pressures valve to open and then goes to left ventricle. Then, goes to aorta and sends blood everywhere like the feet and head. This is why it’s thicker.
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6
Q

Pulmonary circuit

A

Starts from the superior and inferior vena cava. Then goes to atrium and pools/pressures valves to open. Then go to ventricle and them to pulmonary artery. This is because the blood must go to be oxygenated

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7
Q

Which of the following is true of the atria
A) They don’t contract
B) The two atria contract in sequence
C) The right atria receives blood from the lungs
D) They are receiving chambers
E) None of the above
F) All of the above

A

D) They are receiving chambers
They do contract, and the right atria receives deoxygenated blood from the body. The whole heart contracts at once, but the atria contracts a couple milliseconds before ventricle in order to pour all blood out.

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7
Q

Properties of cardiac muscle

A
  • they regulate the oxygen flow in and out
  • they are involuntary, so you don’t need to think about your heart beating.
  • Striated
  • Has a single nucleus, which is different from skeletal muscle
  • branched, has bundle branches
  • has intercalated disks which have gap junctions and desmosomes
  • gap junctions: essential for rapid and coordinates spread of electric impulses, which helps synchronization of contractions of the heart. In intercalated disks, where they have low resistance channels and are composed of connexin proteins, allowing direct passage of ions and small molecules between adjacent cardiomyocytes. This helps with action potentials to work properly, causing depolarization and contraction across the myocardium.
  • Desmosomes: maintains structural integrity of cardiac muscle by proving strong adhesion between adjacent cardiomyocytes, preventing their separation during the intense mechanical stress of contraction and pumping.
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7
Q

Coronary arteries

A

The arteries that feed the myocardium of heart muscle with oxygen to allow contractions.
Anastomosis
- connection or opening between two structures that normally diverge or branch. Can provide backup routes for blood flow if a vessel is blocked.

Heart attack:
- there are blockages either in one place or many in different arteries that doesn’t allow them to feed the muscle with oxygen so it can’t contract

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7
Q

Coronary veins

A

Carry deoxygenated blood away from the heart muscle and return it to the right atrium of the heart.
- this is the third place where blood from the interior muscle comes back to the heart to get oxygenated again.
- coronary sinus

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8
Q

Myocells

A

Two types:
1. contractile cells
- most of the heart
- generating motile forces through the interaction of actin and myosin proteins, which enables movement and mechanical function in various tissues
- in atria and ventricles
- receive electrical impulses from the conducting system, which triggers their contraction in a coordinated and rhythmic manner to ensure efficient blood propulsion.

  1. Pacemaker cells
    - initiates and regulates the heart’s rhythm by spontaneously generating electrical impulses, action potentials
    - in the SA node
    - depolarize rhythmically without external simulation
    - set the pace for the entire heart
    - ensures that the heart contracts in a coordinated and synchronized manner
    - self-excitable
    - this makes the heart not dependable on nervous system for pumping
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8
Q

Which of the following statements is false:
A) The apex of the heart points down and to the left
B) Cardiac tissue is rich in mitochondria
C) Pacemaker cells are concentrated in the AV node
D) Blood enters the heart at the left atrium

A

C) Pacemaker cells are concentrated in the AV node
They are in the SA node

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9
Q

True or false: Mature red blood cells are actively transcribing genes

A

False. Mature red blood cells have no nucleus so they don’t transcribe genes

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10
Q

True or false: Oxygenated blood flows into the left atrium

A

True. Oxygenated blood comes from the lungs and into the left atrium for it to be sent to the rest of the body.

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11
Q

True or false: Heart sounds are associated with value opening.

A

False, heart sounds are associated with valves closing. Lub sound from AV valves and Dub sound from SL valves

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11
Q

Smooth muscle

A

Involuntary, non-striated muscle found in walls of hollow organs like the stomach and blood vessels.

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11
Q

GI tract

A

The gastrointestinal tract; the passage that runs from the mouth to the anus, where digestion and absorption occur.

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11
Q

Filaments

A

Thin, threadlike protein structures (actin and myosin) that help muscles contract.

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11
Sarcomeres
The repeating contractile units in striated muscle fibers, made of actin and myosin filaments.
12
Tissue sheaths
Layers of connective tissue that surround and protect muscle fibers and groups of fibers.
12
Fascicles
Bundles of muscle fibers grouped together within a muscle.
13
Varicosities
Swellings along nerve fibers in smooth muscle that release neurotransmitters.
13
Diffuse junction
A type of nerve–muscle connection in smooth muscle where neurotransmitters spread over a wide area instead of one specific spot.
13
Visceral muscle
Smooth muscle found in the walls of internal organs, acting as a single unit.
13
Gap junctions
Channels between cells that allow ions and signals to pass directly from one cell to another. IN HEART: pores - Allows electrical current to spread throughout heart, important for heart to contract as a single unit
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Syncytium
A group of cells that function together as one coordinated unit.
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Depolarization
A change in a cell’s electrical charge that makes it more positive and can trigger muscle contraction.
14
Cytoskeletal system
A network of protein filaments inside cells that give shape, structure, and help with movement.
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Sarcolemma
The cell membrane of a muscle cell.
15
Dense bodies
Structures in smooth muscle that anchor actin filaments and transmit contractile force.
15
Desmosomes
Strong junctions that hold adjacent cells together to prevent them from pulling apart. - Have signaling molecules
16
Adherence junctions
Cell connections that attach actin filaments from one cell to another for stability.
16
Caveolae
Small pouches in the smooth muscle cell membrane that increase surface area and help transmit signals.
17
T-tubules
Extensions of the muscle cell membrane that carry electrical signals deep into the cell (found in skeletal and cardiac muscle).
17
Voltage-gated
Describes ion channels that open or close in response to changes in electrical voltage across the membrane.
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Kinase
An enzyme that adds phosphate groups to other proteins to change their activity.
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Graded potentials
Small changes in membrane potential that vary in strength and can lead to action potentials if strong enough.
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G-protein-coupled
Refers to receptors that use a G-protein inside the cell to relay signals from hormones or neurotransmitters.
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Myosin bridges
The projecting heads of myosin molecules that attach to actin filaments during muscle contraction.
20
Myofilaments
The protein threads (actin and myosin) that slide past each other to produce muscle contraction.
21
What is smooth muscle?
- It is found in walls of most hollow organs like the stomach, intestines, urinary bladder, uterus, walls of passageways of circulatory system like arteries and veins (NOT capillaries) - It tracks on the respiratory, urinary, and reproductive system - Heart is the main exception because it has cardiac muscle - Most muscles contain two layers or sheets of tightly packed smooth muscle fibers, which are oriented at right angles to each other - The outer layer is longitudinal, where the fibers run parallel to the long axis of the organ, and contraction shortens the organ along its length - Inner layer is circular, and the fibers run around the circumference of the organ. The contraction of these fibers constricts the lumen - alternating the contraction and relaxation of the inner and outer smooth in the gi tract mixes and squeezes substances through the lumen. - There are exception to this pattern: - the stomach, for example, has 3 layers of smooth muscle - the ureter has opposite orientation of smooth muscle from the gi tract. An inner longitudinal and outer circular
22
What is the difference between smooth and skeletal muscle?
- Smooth muscle has spindle shaped cells that are shorter and thinner - Smooth muscle has one single central nucleus unlike skeletal that has multiple nuclei in fiber in periphery of cell - Smooth and skeletal muscle have thin and thick filaments -Filaments in smooth muscle aren't rearranged into sarcomeres and don't produce visible striations Smooth muscle is under involuntary control - Smooth muscle doesn't have epimysium or perimysium, but it does have an endomysium that is made from its cells - The ECM surrounds the smooth muscle cells
23
What is the innervation of smooth muscle?
- It is controlled by autonomic nervous system, so it is involuntary (peripheral nervous system) - Has varicosities: the axons that enter the tissue contain swellings, which release neurotransmitters along a significant length of the axon when the neuron is stimulated. When neurotransmitters are travelling, they diffuse through where they are supposed to go. - Has diffuse junctions, which are the spaces between axons and tissues
23
What are the two ways that smooth muscle can vary?
- Smooth muscle varies by muscle fibers, type of innervation, and responsiveness to various stimuli Unitary - A single unit - all visceral organs except the heart - electrically coupled by gap junctions, cells act in uniformed fashion, syncytium - Respond to various chemical stimuli - Self-excitable - Pacemaker cells display spontaneous activity, depolarize in absence of external stimuli - Neural and chemical stimuli affect rate of intensity of unitary contraction - Pacemaker cells contract by contractile cells to contract in unison by electrical coupling by gap junctions - Pacemaker cells are always active because their membrane potential changes in cyclical manner - Two types of spontaneous depolarization that give rise to action potentials by different mechanisms: Pacemaker potentials and Slow wave potentials - Both serve as the basis for the rhythmic digestive processes in gi tract Multi-unit - Lines large airways of the lungs, large arteries, erector pili muscles, and iris of eye - Has few gap junctions, fibers act independently - Because of this and that it is innervated, forms different motor units that can be recruited when needed for strength of contractions - Skeletal is controlled by somatic nervous system and while multi-unit smooth is controlled by autonomic nervous system, hormones, and other stimuli Spontaneous depolarizations are rare - More similarities to skeletal muscle than unitary - Iris of the eye has two layers of smooth muscle. One is oriented in a circle, and the other is oriented radially. Function is to limit amount of light that passes through lens to retina. To make it opaque, coated with pigment called melanin, which makes the eyes brown - Mutation turned off pigmentation in front of iris, which makes light reach the fibers of stromal cells, reflect light back as blue - Green and gray eyes are in between colours
23
What is the intermediate filament network of smooth muscle?
- It is one of the three cytoskeletal systems in smooth muscle - it is composed of non-contractile proteins like desmin and vimentin, which form lattice like framework that transmits the tension through fiber to sarcolemma - Has dense bodies, which are analogous to the zedness of skeletal muscle fiber. They are scattered throughout the cytoplasm, and connect the intermediate filaments to each other and to thin filaments. It also indirectly fastens them to the sarcolemma at regular intervals via adherence junctions and desmosomes - Adherence junctions are scattered around the dense plaques that encircle smooth muscle cells with rib like pattern - When the complexes of actin and myosin contract, the force is transduced to the sarcolemma though intermediate filaments for dense plaques. These alternate with regions of membrane which contains lots of caveolae - Caveolae contain many calcium channels to allow rapid influx of extracellular calcium
24
What are the mechanisms of smooth muscle contraction?
- They have thin bodies that are rich in alpha actinin - These connect intermediate filaments, as anchors, to the thin filaments, which make force and transmit the force to plasma membrane - In contracted muscle fiber, the thin and thick filaments overlap, so the force that was generated is transferred through the whole fiber - This is regulated by changes in the intracellular calcium concentrations. Since smooth muscle has excitable cells, changes in the membrane potential triggers the increase in calcium and calcium formation of cross bridges with myosin and actin (like in skeletal muscle) - smooth muscle has less developed sarcoplasmic reticulum to store calcium than skeletal muscle, so it doesn't have t-tubules - increases of intracellular calcium concentration are mediated by calcium influx through voltage-gated calcium channels that are concentrated with cavioli - Calcium influx causes calcium release from sarcoplasmic reticulum by calcium-induced calcium release (c i c r)
24
What is the contractile state of smooth muscle?
- It is regulates primarily by cytoplasmic free calcium concentration - The stimuli that induced smooth muscle contraction triggers increase in sarcoplasmic free calcium - At the elevated calcium concentration, calcium binds to calmodulin, which is a ubiquitous and multifunctional calcium binding protein. Calcium +calmodulin makes a conformational change in protein, which exposes binding sites for target proteins - The enzyme myosin light chain kinase, also called mlck, can interact with calmodulin, which results in activation of kinase, catalyzing phosphorylation of myosin on each of two light chains. This triggers a cycling of myosin cross bridges along actin filaments and development of force
25
What is the relaxation state of smooth muscle?
The removal of calcium from cytoplasm, where calmodulin dissociates from myosin-like chain kinase, which regenerates the inactive kinase. Myosin is dephosphorylated by myosin light chain phosphatases, where it also dissociates and is detached from actin filaments, then muscle relaxes
26
How is smooth muscle stimulated differently than skeletal muscle? why?
- Skeletal muscle fibers are stimulated exclusively by the nervous system - smooth muscle fibers are stimulated by multiple types of signals, such as nervous signals, hormonal stimulation, stretch, and other ways - this is because smooth muscle's membrane contains many types of receptors that initiates contractile process - Smooth muscle also has receptors that inhibit contraction, which is different from skeletal muscle
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Neural simulation is smooth muscle
- In some types of smooth muscle, neurotransmitter binding generates an action potential, leading to a rise in cytoplasmic calcium levels and cousin contraction - Other types of smooth muscle respond to neural stimulated with only graded potentials - A neurotransmitter can excite or inhibit a particular group of smooth muscle cells, depending on the types of receptors that it has. - aCh is a neurotransmitter at the neuromuscular junction, which causes skeletal muscle to contract. In smooth muscle, when aCh binds to it in bronchitis of the lungs, it causes a strong contraction that constricts the bronchioles. Norepinephrine binding to the same cells is inhibitory, which causes bronchial relaxation and dilation. Norepinephrine on smooth muscle of blood vessels causes contraction and constriction of the vessels - Some types of smooth muscle are not innervated, but they are depolarized spontaneously or depolarize in response to hormones that bind g-protein-coupled receptors - Other chemical stimuli cause smooth muscle to contract or relax by enhancing calcium entry into the cytoplasm (histamine, excess CO2, low pH, lack of oxygen) - Some smooth muscle responds to both neural and chemical stimuli
27
How does smooth muscle stretch?
- Many instances where contraction happens, it occurs with the absence of nerves. So it is not the activation of neural reflex (like in skeletal muscle) - Contraction most likely results from membrane depolarization or from opening of stretch activated calcium channels - This response explains why organs like stomach, bladder, and small arterioles contract to oppose distention - Some smooth muscle of mostly likely larger blood vessels can quickly stretched and this is followed by a temporary increase in wall tension. This increase is quickly followed by a relaxation toward original wall tension (stress relaxation). - Reverse stretch relaxation: occurs when muscle is allowed to shorten. External stress is removed and the tension temporarily decreases. The decrease is followed quickly by muscle contraction toward original wall tension. - These actions help to accommodate different blood volumes while maintaining pressure
28
How long can smooth muscle contraction be sustained?
- for long periods of time - This sustained phase has been attributed to certain myosin bridges (latch bridges), which cycle very slowly. This slows the progression to the stage where the phosphorylated myosin detaches from actin, which maintains force at low energy costs. - Tonically active smooth muscle: in some smooth muscle cells, the phosphorylation of the myosin light chain is maintained at low level in the absence of external stimuli (no receptor or mechanical activation).
28
How does Atpase behave in smooth muscle?
- slower in smooth muscle than skeletal muscle - Leads to slower cross bridges cycling speed and more extended period of contraction, maybe even greater force of contraction, and more of a long period of contraction
29
How are thick and thin filaments arranged in smooth muscle?
- No sarcomeres - Myofilaments are arranged diagonally within fiber - Fewer thick filaments, and each has thin filaments. Skeletal has more thick filaments but only 2 thin per thick filament. - Skeletal muscle has myosin heads that protrude in a hexagon pattern around circumference of thick fiber (60 degrees to each other) - Smooth muscle protrudes 180 degrees to each other, oriented in opposite directions on either side of thick filaments - Thin filaments are on opposite side of thick filaments, move in opposite directions - Myosin heads are found along entire length of thick filament - Cross bridge
30
Intrinsic conduction system
Network of non-contractile (autorhythmic) cells SA node, pacemaker is where pacemaker cells are in. After being depolarized, signals go from the atria to the AV node (at the junction between atria and ventricles). The AV node has pacemaker cells that can work in the absence of the SA node. There’s a pause when going from SA to the AV node where the heart contracts. Then, goes to atrioventricular bundle, then bundle branches Opening of sodium channels and closing of potassium channels causes the pacemaker potential to increase. Eventually this will reach a threshold where an action potential will occur and there will be an influx of calcium through open calcium channels
30
Regulated variables
Maintained via homeostatic processes to sustain cell function Testosterone levels and blood hematocrit are not homeostatically regulated
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Non regulated variables (controlled)
Variables that can be changed by the body but sensors do not exist Can be modulated to achieve regulation (heart rate by autonomic nervous system for pressure, so non regulated variable)
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Muscle tendon reflex
Helps to control muscle movement but is not homeostatic bc doesn’t help maintain internal environment
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Negative feedback system
Not all negative feedback systems are homeostatic Needs a sensor, control center, and an effector These can be near or far from each other, even in the same cell Sensor- measures the value of a regulated variable. Often are neurons that change their firing rate. Constantly active. Generate an output whose value is proportional of the stimulus, which is a change in the value of a measured variable What can’t be measured can’t be regulated Control center- has a error detector and integrator Error detector- receives signal from sensor. Continuously determines the difference between the signal from the sensor and the setpoint variable (normal range of regulated variable) Integrator- that value between the sensor and setpoint variable is used to calculate change in signals going to effector Control center is usually part of endocrine or nervous system It’s possible for set point to change
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Autonomic nervous system
Blood pressure, heart and breathing rate, digestion, metabolism, body temperature, balance of water and electrolytes, production of body fluids, urination, defecation, sexual response All of these occur without conscious effort, autonomous Part of motor (efferent) pathway of PNS Part of motor (efferent) pathway of PNS Motor neurons innervate cardiac muscle, smooth muscle, and glands Uses two-neuron chain to reach effectors First start at CNS, where pre-ganglionic neuron cell bodies relied in the lateral horn of the brain stem Lightly myelinated preganglionic axons exit CNS by spinal/cranial nerves and extend to autonomic ganglia in PNS, where they synapse on the cell bodies of the second order of neurons, releasing aCh. This is stimulatory at the synapses Non myelinated axons of the second order of neurons travel from ganglia to target effector organs Exception: adrenal medulla, which is stimulated by a preganglionic (first order) neuron that releases aCh. Cells of adrenal medulla have the same embryonic origin as neural tissue, which functions as modified postganglionic neurons Instead of releasing NT at the synapse within an effector tissue, the secretory products of adrenal medulla are picked up by blood and travel throughout the body to all effector tissues of the sympathetic tissue Autonomic postganglionic fibers release two neurotransmitters, norepinephrine (secreted by sympathetic fibers) and aCh (secreted by parasympathetic fibers) Depending on NT and type of receptor of target organ, effect might be excitatory or inhibitory. Autonomic nervous system differs from somatic nervous system since it can stimulate or inhibit its effectors
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Difference between somatic and autonomic nervous system motor fibers
Effectors are targets that motor neurons innervate Efferent pathways and ganglia Target organ responses to NTs
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Somatic nervous system
Skeletal muscle Cell bodies lie in central horn of spinal horn, which is in CNS A single and thick myelinated axon travels out of CNS to PNS via spinal/cranial nerves and continues uninterrupted to target, which is skeletal muscle Nerve terminals of somatic motor neurons release aCh, which always stimulates skeletal muscle to contract
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What are the two divisions of the autonomic nervous system?
Tonically active: provide some degree to nervous input to given tissue at all times. The frequency of action potentials in both systems can increase or decrease. Tissue activity can be enhanced/inhibited. This helps the autonomic nervous system to help regulate a tissue’s function. Without it, nervous input in a tissue can only increase. Dynamic antagonistic interaction: when one system is working in a visceral organ, the other’s work decreases. Both systems are present in the same organs but do opposite work of each other. In some cases, both systems may have a cooperative effect Sympathetic system Strenuous and physical activity Well oxygenated nutrient-rich blood must go to working skeletal muscles, so changes in organ and tissue function in body are coordinated Heart rate and myocardial contractility = increase so heart pumps more blood per minute Sympathetic stimulation of vascular smooth muscle causes widespread vasoconstriction in organs of the gastrointestinal system and kidneys. This redirects blood away from metabolically inactive tissues and towards contracting muscles Bronchodialation in lungs facilitates air in and out of lungs so that there is maximization of oxygen coming in and carbon dioxide out Increase in glycogenolysis (glycogen to glucose) and gluconeogenesis (formation of new glucose from non-cardbohydrate sources in liver) increase concentration of glucose in blood. Important for the brain because it's the only nutrient there that can be used for metabolic energy. Lipolysis in adipose tissue increases concentration of fatty acids in blood, which are used by skeletal muscle to form metabolic energy for contraction Sweating helps to thermoregulate during increased physical activity and heat production Pupil dilates and there's more light coming into retina, lens adapts for distance vision Parasympathetic system Appropriate when body is resting Decreases heart rate to conserve energy under resting conditions Salivary secretion = enhanced to facilitate swallowing of food, gastric motility, and secretion, in order to ingest food. Intestinal motility and secretion = stimulated to continue processing and facilitate absorption of nutrients Exocrine and endocrine secretion from pancreas = promoted. Enzymes released from exocrine glands of pancreas help with chemical breakdown of food in intestines. Insulin released from pancreatic islets promote the storage of nutrient molecules in the tissues once absorbed into body Contraction of urinary bladder = promoted to cause urination Contraction of pupil in eye, lens adapts to near vision. While the sympathetic system has more control for blood vessels, the parasympathetic has more control over heart and smooth muscle of digestive/urinary tract organs. These organs exhibit parasympathetic tone, meaning they work to slow heart and continue normal activity of the urinary/digestive tracts Sympathetic division can override this when there’s too much stress Parasympathetic fibers activate most glands except for adrenal/sweat glands of skin
35
Drugs blocking parasympathetic system
Increase heart rate, cause fecal/urinary retention
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What receives only sympathetic fibers and not parasympathetic?
Adrenal medulla, sweat glands, erector pili muscles of skin, kidneys, most blood vessels
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Sympathetic division
Sympathetic division mediates reflexes that regulate body temperature. Heat to skin causes blood vessels to dilate. When the body temperature rises, sympathetic nerves dilate the skin’s blood vessels, which helps heat to escape and activates sweat glands to cool the body. When cold weather = heat loss, blood vessels constrict Renin angiotensin system: sympathetic impulses stimulate kidneys to release renin, which helps to make potent blood pressure increasing hormones. This hormone system helps to regulate blood pressure, fluid/electrolyte balance, and systemic vascular resistance. Can promote many metabolic effects that are not reversed by parasympathetic activity. This is because of neural stimulation and release of adrenal medullary hormones. For example: metabolic rate of body cells raises glucose levels and mobilizes fat for use as fuels. Medullary hormones also cause skeletal muscle to contract more strongly and quickly Preganglionic axons branch a lot as they enter the sympathetic trunk. Synapse with postganglionic neurons at many levels, so when sympathetic division is activated, responds in a diffuse/interconnected way. Parts of sympathetic can be activated individually. Just because the eye dilates because of light, it doesn’t mean the heart rate also must beat faster Activation of sympathetic can produce more long lasting effects than parasympathetic Adrenal medullary cells secrete epinephrine and norepinephrine into blood when sympathetic division is working. These help with the effects of the sympathetic nervous system to last longer. Last for a couple minutes and then get destroyed by liver While the effects of the sympathetic system may be short, the hormonal effects last a long time.
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Parasympathetic division
One preganglionic neuron synapses with one, or at most, a few of postganglionic neurons. All sympathetic fibers release aCh, which is quickly hydrolyzed/destroyed by aCh esterase. Because of this, parasympathetic division has short-lived but highly localized control over its effectors Preganglionic axons branch profusely
37
What parts of the brain control the autonomic nervous system?
Hypothalamus Main integration center for autonomic nervous system. Anterior hypothalamus direct parasympathetic functions and posterior direct sympathetic functions Exert effects both directly and indirectly, via relays through reticular formation, which influences preganglionic motor neurons in brain stem and spinal cord Coordinates heart activities, blood pressure, body temp, water balance, and endocrine activities Also mediates reactions to fear and other emotions by association with limbic system (system for emotions;/behaviour responses) Limbic lobe involved in emotional responses and memory function, like hippocampus, amygdala, and cingulate gyrus Since the hypothalamus and limbic lobe are closely connected, the lobe influences the hypothalamus activity based on emotional state. When you’re scared, amygdala sends signals to hypothalamus along medial forebrain bundle, which stimulates sympathetic fight/flight Hypothalamus also stimulates release of stress hormones through control of the endocrine system by responding to amygdala input. Hypothalamus is the gatekeeper of emotional and visceral brain Cerebral cortex Brain stem reticular formation: loose collection of neuron cell bodies in pons, medulla, and midbrain in white matter. This exerts the most direct influence over autonomic functions. Certain motor centers, ventral lateral medulla, reflexively regulate heart rate and blood vessel diameter. Other medulla regions control gastrointestinal activities. Midbrain centers, motor nuclei, control muscles of pupil and lese focused. Spinal cord Urination, defecation, erection, ejaculation. Involuntary, but subject to conscious control and can be overridden by the brain.
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Hypertension
A boost of sympathetic signaling by long-term stress enhances tone in smooth muscles, raises blood pressure Heart must work harder and artety walls will be worn out and torn Can be helped with beta blockers, which block
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Ulcers
Sympathetic vasoconstrictor response to stress, decreases blood flow in stomach wall
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