QUIZ 3 Flashcards

1
Q

What substances do we find in circulation?

A
  • Respiratory gases (oxygen and carbon dioxide)
  • Hormones
  • Nutrient
  • Immune cell
  • Intracellular waste
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2
Q

What sorts of animals do not have a circulatory system? What are some disadvantages to not having one?

A

Example: jellyfish

Disadvantage: limits the size of the animal

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3
Q

How do open and close circulatory systems differ? What are some of the advantages and disadvantages of each?

A

OPEN:
* Doesn’t have vessels
* Contains hemolymph
* Hemolymph circulates through heart and out to the hemocoel (cavity)

CLOSED:
* Has vessels that separate blood from interstitial fluid  blood doesn’t come in contact with organs
* Arteries carry blood away from the heart, whereas veins carry blood to the heart
* Exchange of substances occurs at capillaries

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4
Q

How does the number of chambers within an animal’s heart influence its circulatory system?

A
  • 2-chambered (fish): two chambers limit the circulatory system to one circuit  creates a low-pressure system  animal needs to constantly move to keep blood flowing
  • 3-chambered (frogs): with the addition of an extra atrium, we create two circuit  high/low oxygen blood mixes in the ventricle  decrease blood oxygen level in the animal (not efficient)
  • 4-chambered (humans): eliminates blood mixing so we have a side that is dedicated to dealing with oxygenated blood and a side that deals with deoxygenated blood; four chambers create a high-pressure system
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5
Q

What phases occur during the cardiac cycle? Label the phases below. What stimulates these phases too occur?

A

Systole: heart is contracting
1. Atrial systole
2. Ventricular systole
Diastole: heart is relaxing

Action potentials stimulate contraction  contraction will decrease the volume of the chamber  pressure then increases  blood moves

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6
Q

What creates the heart sounds we hear when we put a stethoscope to a mammal’s chest?

A

Heart sounds are caused by valves closing
1. Sound 1 “Lub”: AV closing
2. Sound 2 “Dub”: Semilunar valves closing

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7
Q

How does cardiac muscle tissue differ from our other muscle tissues?

A

Cardiac muscle cells are joined by gap junctions which increase speed of action potential traveling across chambers.

While skeletal muscle cells are voluntary (somatic), cardiac muscle cells are involuntary (autonomic).

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8
Q

How do myogenic and neurogenic hearts differ? Which do we find in humans?

A

Myogenic hearts do not need nervous input to contract because they have autorhythmic cells. human hearts!!
Also, rhythm can be altered by autonomic nervous system

Neurogenic hearts require nervous innervation to function.

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9
Q

What allows a myogenic heart to depolarize on its own, without neural input

A

Autorhythmic cells (SA node, AV node, intrinsic conduction system)

SA node has the fastest rate and thus sets the pace.

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10
Q

Explain what is occurring during each of the phases included in the image below.

A
  1. Depolarization: Na+ voltage channels open allowing for Na+ to rush into the cell and then they become inactive.
  2. Plateau: Initially K+ voltage channels open allowing for K+ to rush out of the cell, but closely after Ca2+ channels open allowing for Ca2+ to rush into the cell. The Ca2+ channels become inactive which concludes the plateau.
  3. Repolarization: K+ voltage channels remain open, allowing for more K+ to rush out of the cell.
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11
Q

Describe the journey of an action potential from the SA node to a cardiac muscle fiber in the left ventricle.

A

SA node (R. atrium) generates action potential (AP) AP spreads across atria causing them to contract to…  AV node (R. atrium) – impulse is delayed because of fewer gap junctions  AP sent down bundle branches and out to purkinje fibers embedded in ventricle wall

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12
Q

What are the extrinsic and intrinsic factors that control heart rate and force of contraction?

A

Extrinsic Controls
Hormonal
* Norepinephrine and epinephrine from adrenal medulla increase SA node rate
* Thyroxine (T4) increases heart rate and enhances effects of norepinephrine and epinephrine
Neural
* Sympathetic: stimulatory
o Increase rate of SA node
o Enhance force and speed of ventricular contraction
* Parasympathetic: inhibitory
o Decrease rate of SA node

Intrinsic Control
Frank-Starling Mechanism
* Defines the normal relationship between the length and tension of the myocardium. The greater the stretch on the myocardium before systole, the stronger the ventricular contraction.
* Serves to have the heart match its output with its input

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13
Q

How are cardiac output, BP and peripheral vascular resistance related to one another?

A

BP = CO x PVR

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14
Q

In the space below draw out what mechanism would ensue if baroreceptors detected elevated BP.

A

When BP is high, baroreceptors detect this in the carotid sinus and rely this information to the medulla via the glossopharyngeal and vagas nerves.

The cardioinhibitory center response to this information by increasing parasympathetic signals along the vagas nerve to the SA node. This causes a decrease in heart rate, leading to a decrease in BP.

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15
Q

Where do we see higher BP, arteries or veins? How does their anatomy support either high or low pressure?

A

BP is higher in arteries as they are first to receive blood pumped out of the heart. To be able to withstand this high pressure, arteries have relatively thick muscular walls. Veins have lower BP. Because they do not have to combat high pressure blood against their internal walls, veins have a relatively thin layer of smooth muscle.

To prevent backflow against gravity, we see that veins have valves. Venous valves work in conjunction with the musculoskeletal system.

Muscles constantly contract and release, causing the blood to flow toward the heart. The valves open, allowing the blood to flow, and close, stopping the blood from flowing backwards.

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16
Q

How is it that lymph fluid is created by blood?

A

Lymph is formed from fluid that seeps through the thin walls of capillaries into the body’s tissues. This fluid contains oxygen, proteins, and other nutrients that nourish the tissues. Some of this fluid reenters the capillaries and some of it enters the lymphatic vessels becoming lymph.

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17
Q

Is blood flow to structures consistent throughout the course of a day?

A

No! Depending on the demands that we place on tissues we increase/decrease blood flow to them. An example of this is after eating food when blood is shunted to the digestive viscera to fuel digestion.

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18
Q

What is EPO and what role does it play in maintaining blood homeostasis?

A

EPO is erythropoietin, a hormone produced by the kidneys. EPO is released in response to low oxygen or red blood cell (RBC) levels. Once released into the blood, EPO targets and stimulates the red bone marrow to manufacture more RBCs.

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19
Q

You are training for a marathon and so when your family takes a vacation to Boulder, Colorado, you figure it’s a great opportunity to fit in some scenic long runs. You don’t get far into your run when you have to stop and walk because you’re so winded. You’re very confused because back at home in Chicago you haven’t any episodes like this.

Why are you having such a tough time running while on vacation? If you trained in Colorado for an extended period of time, how would your body adapt?

A

Your breathing difficulties are brought on by the higher altitude in Colorado. At higher elevations, there’s less oxygen in the air since atmospheric pressure is lower. Consequently, it’s harder for your body to take in oxygen. Your workout will feel more difficult, and you’ll get tired more quickly as a result.

It is thought that high altitude training forces your body to adapt to the lack of oxygen by releasing EPO and producing more RBCs.

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20
Q

Carbohydrates

A

Monosaccharides,

Short term energy

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21
Q

proteins

A

Amino acids

Contractile muscle fibers,

amino acid-based hormones

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22
Q

lipids

A

Glycerol and fatty acids

Long term energy storage

cell membrane

23
Q

Why is it important for animals to intake vitamins and minerals in addition to macromolecules?

A

Vitamins and minerals support chemical reactions throughout the body by acting as cofactors and coenzymes.

They also support the proper formation of different cells and tissues.

24
Q

2 way digestion

A

the animal has one opening for food to enter and waste to leave. A negative consequence of this anatomy is that the animal must digest its previous meal and release the waste before eating again.

25
Q

How is motility in one-way digestive systems controlled?

A

The enteric NS provides intrinsic control of motility. The parasympathetic NS provides extrinsic stimulatory control.

There is also innervation from the sympathetic NS, but signals along these nerves are inhibitory to digestive viscera.

26
Q

Describe the organization of the vertebrate GI tract?

A
  1. Headgut: mouth to pharynx
  2. Foregut: esophagus to stomach
  3. Midgut: small intestine
  4. Hindgut: large intestine
27
Q

Identify two examples of complementarity of structure and function within the headgut.

A

Teeth: sharper teeth allow for meat eaters to rip tissue

Tongue: shape and development of papillae are going to help with things like thermoregulation (dogs) and grooming

28
Q

What is the difference between chemical and mechanical digestion?

A

Chemical digestion involves the enzymatic breakdown of nutrients.

Mechanical digestion involves the mechanical breakdown of large pieces of food into small bits (examples: chewing, segmentation, churning)

29
Q

What actions are required to get food from the mouth into the stomach?

A

Peristalsis is seen in the esophagus and segmentation (very little). Swallowing to move food from mouth to oropharynx.

30
Q

What is gastric juice (what is it composed of) and what stimulates its release?

A

Gastric juice = Pepsin + HCl + mucus

Stimuli
1. Parasympathetic NS
2. Stretching
3. pH change

31
Q

How do these cells create gastric juice? What factors influence its release?

A

Gastric pits

Mucous neck cells: secrete mucus to protect mucosal lining

Parietal cells: HCl
Chief cells: pepsinogen (activated when in the presence of HCl)

Delta cells: inhibited by parasympathetic signals

  • Somatostatin: inhibits acid release

Enteroendocrine cells: secretions are stimulatory

  • Gastrin: stimulates parietal and chief cells, induces churning and promotes histamine release
  • Histamine: promote acid release

Stimuli
1. Parasympathetic NS
2. Stretching
3. pH change

32
Q

How do monogastric and ruminant stomachs differ? Why would an animal need a ruminant stomach over a monogastric stomach?

A

Monogastric stomachs are simple one chambered stomachs, whereas ruminant stomachs are more complex (4 chambers). Ruminant stomachs also have multiple passes at the food.

Ruminant stomachs are better equipped to digest plant foods because they house bacteria that ferment cellulose.

33
Q

What occurs in the small intestine?

A

Your small intestine breaks down food using enzymes made in your pancreas and bile from your liver. The small intestine is the “work horse”’ of digestion. While food is there, nutrients are absorbed through the walls and into your bloodstream or lymphatic vessels. What’s left over moves into your large intestine.

34
Q

What substances aid in finishing off chemical digestion within the small intestine?

A
  • Digestive enzymes from the pancreas
  • Bile (made in liver, stored in gallbladder)
  • Membrane associated enzymes produced by cells known as enterocytes that line the intestinal walls (AKA brush border enzymes)
35
Q

absorption of glucose through the wall of the small intestine:

A

. First, if we look at the basolateral side of the intestinal epithelial cell, we can see the Na+/K+ pump which uses energy to move 3 Na+ out and 2 K+ into the cell. This creates a concentration gradient for Na+ with more Na+ outside of the cell compared to inside.

On the apical side of the intestinal cell there are Na+-glucose cotransport proteins. The energy that is captured as Na+ moves down its concentration gradient from the lumen of the small intestine into the cell is used to pump glucose up its concentration gradient into the cell. The glucose then passes channel proteins on the basolateral side to enter the bloodstream.

36
Q

Where do glucose, amino acids and fatty acids go upon getting absorbed through the lining of the small intestine?

A

Glucose and amino acids enter directly into the blood, while fatty acids are transported by lymphatic vessels in the form of chylomicrons that ultimately dump them into the blood.

36
Q

What occurs in the large intestine?

A

The major functions of the large intestine are recovery of water and electrolytes, formation and storage of feces and fermentation of some of the indigestible food matter by bacteria.

Through this fermentation, intestinal bacteria also produce large amounts of vitamins, especially vitamin K and biotin (a B vitamin), which are absorbed into the blood.

37
Q

Create a scenario(s) that can be used to describe hunger regulation.

A

LEPTIN: produced from fat / adipose -> suppresses appetite

PYY: Secreted by small intestine -> appetite suppresses

GHRELIN: secreted from stomach wall -> signals that triggers feelings of hunger

INSULIN: a rise in blood sugar level after stimulates the pancreas to secrete INSULIN -> suppresses appetite

38
Q

How do osmoconformers and osmoregulators differ? What is more energy demanding to be?

A
  • Osmoconformer: animals that allow their internal body fluids to match (or become isotonic to) the osmolarity of their surround environment
  • Osmoregulators: animals that have mechanisms in place to keep their internal osmolarity at a homeostatic set range that is hypertonic or hypotonic to the osmolarity of their surrounding environment
39
Q

Urinary structures with functions:

A

Kidney: Filter blood and produce urine

Ureter: Drain urine from kidney to bladder

Bladder: Temporarily store urine until excreted

Urethra: Passageway out of bladder/body

40
Q

Apart from water, what does urine consist of?

A

Na+, K+, PO43–, SO42–, Ca2+, Mg2+ and HCO3–, urea, creatinine

41
Q

What processes are involved in urine formation? Place them in sequential order.

A
  1. Glomerular filtration
  2. Tubular reabsorption
  3. Tubular secretion
42
Q

What forces work at the glomerulus to encourage the movement of substances from the blood to the tubule system?

A

Encourage movement from blood to glomerular capsule
* High hydrostatic pressure (55 mm Hg)

Encourage movement from glomerular capsule to blood
* Osmotic pressure (30 mm Hg)
* Hydrostatic pressure (15 mm Hg)

43
Q

Tubular reabsorption in the PCT:

A

Embedded in the apical surface of epithelial cells lining the PCT there are symport proteins that move substances like glucose and amino acids up their concentration gradients by capturing energy that is yielded when Na+ moves down its electrochemical gradient. This gradient is established on the basolateral side by the Na+/K+ pump. Moreover, glucose travels via the transcellular route.

The paracellular route allows for the movement of ions and urea through adjacent cells and their tight junctions.

Water is reabsorbed through aquaporins that are always open.

44
Q

Why is a side effect of untreated diabetes excess glucose in urine (glycosuria)?

A

When all the transporters of working as fast as possible to transport glucose from the filtrate into the blood they can ultimately reach a transport maximum as glucose levels rise. When this occurs any additional glucose that cannot be reabsorbed is excreted in the urine. This occurs in diabetic patients because they have high blood glucose and consequently high amounts of glucose in their filtrate.

45
Q

What is the difference between the countercurrent multiplier and the countercurrent exchanger in the loop of Henle?

A

The countercurrent multiplier is the physiology seen in the loop of Henle wherein the descending limb loses water to the surrounding interstitial fluid due to the continual pumping of solutes out of the filtrate as it travels through the ascending limb. This establishes the medullary gradient in the interstitial fluid that influences water reabsorption in the descending limb of the loop and the collecting duct.

The countercurrent exchanger involves the vasa recta and loop of Henle. The vasa recta’s blood flow runs in the opposite direction to the filtrate in the loop. By doing so that allow for maximum solute and water reabsorption as the vasa recta travels through the medullary gradient. Most importantly, this helps to maintain the medullary gradient.

46
Q

What is the main job of the loop of Henle?

A

It establishes the medullary gradient that influences water reabsorption.

47
Q

We expect to find ___ loops of Henle in desert vertebrates and ___ loops of Henle in vertebrates that live in watery environments.

A

longer , shorter

48
Q

juxtaglomerular complex (JGC) :

A

The three cellular components of the apparatus are the macula densa, extraglomerular mesangial cells, and juxtaglomerular cells (also known as granular cells).

One of the main functions of the juxtaglomerular complex is to maintain blood pressure.

49
Q

What is the purpose of the Renin Angiotensin Aldosterone Mechanism/System?

A

The RAAS functions to elevate blood volume and arterial tone in a prolonged manner. It does this by increasing sodium reabsorption, water reabsorption, and vascular tone.

50
Q

Dehydration leads to ___ ADH secretion?

A

increased

51
Q

How do ADH and aldosterone act upon the kidney?

A

ADH is released by the posterior pituitary and causes principal cells of collecting ducts to insert aquaporins in apical membranes. The expression of these aquaporins encourages water reabsorption.

Aldosterone is released by the adrenal cortex and targets principal cells of collecting ducts and distal DCT. Once bound to these cells, aldosterone promotes synthesis of luminal Na+ and K+ channels, and basolateral Na+-K+ ATPases which promotes Na+ reabsorption. Since water follows Na+ we see increased water reabsorption also results from aldosterone release.

52
Q

Apart from the indirect stimulation through renin secretion, what excites ADH release?

A

Decreased blood volume and increased extracellular ion concentration in blood (osmolarity)

53
Q

Describe urine output when ADH levels are elevated levels.

A

As ADH levels rise, more water is reabsorbed in the collecting duct, so urine increases in concentration and decreases in volume.