Move Me Flashcards

1
Q

how does excess fluid get back into the veinous system?

how is the lymphatic system split up?

A

lymphatic system drains back into the right and left venous angle: junction where subclavian vein and internal jugular vein meet

lymph system is split into:

thoracic duct: drains the left head and neck, left upper limb, left thorax and both of lower limbs . then goes into the left venous angle

right lymphatic trunk: right arm, right thorax, right head and neck

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2
Q

label this

describe where the main ones lead blood to

A
  1. descending aorta: continues down to thorax, goes to abdomen
    3a. brachiocephalic artery goes into the right common carotid artery -> supplies right side of head and neck
    b. brachiocephalic artery -> right subclavian artery: supplies upper right limb

4. left common carotid artery -> supplies left side of head and neck

5. left subclavian artery -> supplies left upper limb. goes under clavicle

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3
Q

label the venal return back to the heart

A

right and left internal juglar veins - drain the head and neck

right and left subclavian veins - drain limbs

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4
Q

what is the function of the lymphatic system?

A
  • removal of excess interstitial fluid
  • transport of bacteria and other harmful sub. away from tissue
  • transport of antigen-presenting cells
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5
Q

what happens when change in temperature is activated? (input vs output?)

which areas detect the change of temp from warm and cold?

what does this cause to change?

A

Goes to control centre: brain - specifically the hypothalamus:

Input:

  • *- preoptic area (POA)** monitors core temperature: recieves input from warm receptors from skin and and internal receptors
  • *- paraventricular (PVN) and dorsomedial hypothalamic (DMH) nuclei:** recieve input from cold receptors
  • *Integration and Output to Effectors:**
  • *- Preoptic area (POA):** regulate blood vessels in skin (vasoconstriction / dilation). stimulates posterior pituitary: conserves water
  • *- paraventricular (PVN) and dorsomedial hypothalamic (DMH)** nuclei: regulates skeletal muscle (shivering). brown fat stimulation (aka:) non-shivering thermogenesis.
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6
Q

what do increases (2) and decreases (4) in body temperature cause in effectors?

A

heat increase / decrease stimulate effectors that will enhance / decrease heat loss

  • To reduce heat gain:*
  • Sweating initiated - (as long as air is dry, evap. of sweat is efficient)
  • cutaneous vasodilation - blood flow near capillaries increases. heat lost by radiation. automated by autonomic nervous system by a reduction in vasomotor tone
  • To increase heat gain:*

(adrenaline, catecholines and noradrenaline stimulate:)

  • metabolic heat increased by vol. skeletal muscle contraction: shivering
  • non-shivering thermogenesis: brown fat

- thyroid hormones increase o2 consumption on most cells: increases basal metabolic rate and heat production during cold

  • cutaneous vasoconstriction: increase in sympathetic activity. mediated by noradrenaline on alpha adrenoreceptors. arteriovenous** **anastomoses are richly supplied by sympathetic adrenergic fibres
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7
Q

how can we classify solutes?

which one of these ^ has greater osmotic power?

what is osmotic pressure?

A

electrolytes:

  • inorganic salts (Na+, K+, Cl-), all acids and bases, some proteins

non electrolytes:

  • glucose, urea, lipids etc

electrolytes have greater osmotic power than non-electrolytes

osmotic pressure: process that controls movement of solvents across a membrane. movement occurs when there are differences in osmotic pressure across a membrane.

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8
Q

which regions in the brain control thirst? [2]

how are these structures characterised? - what does this allow?

A
  • Subfornical organ: in the hypothalumus
  • OVLT

both have:
a) extensive vasculature b) lack of normal blood brain barrier

  • allow for linkage between CNS and peripheral blood flow
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9
Q

how does aldosterone make kidney cells recapture sodium?

A
  • causes to produce more
    a) ENAC (Na channel) - can reabsorb more Na
    b) Na/K pump ( pumps Na in / K out)
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10
Q

what are the normal pH blood limits?

which pH ranges lead to death?

A

7.35 (venous) to 7.45 (arterial)

Below 6.8 and above 8.0 = DEATH

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11
Q

body’s concentation of hydrogen ions is regualted by which systems? [3]

how long does it take for each system to regulate?

A

1. chemical buffer system in blood and ICF

  • immediate action

2. Respiratory centre in brain stem

  • acts within 1-3 minutes

3. kidneys

  • hours to days
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12
Q

what are the three major chemical buffer systems in the body?

A

Bicarbonate (HCO3-) buffer system

Proteins (Hb and albumin) buffer system

Phosphate buffer system

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13
Q

what is the normal anion gap?

how do you measure?

A
  • measure the conc of Na, Cl and HCO3- in blood. - cations should be greater by anions by 8 to 12 mEq/L.

- (remember cations = anions)

[Na+] - ([Cl-] + [HCO3-]) = 8 to 12 mEq/L

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14
Q

how does resp. centre change acid levels?

A

How? Eliminate or retain CO2

  • CO2 transported into rbc as HCO3-
  • HCO3 recombines to CO2 and H20 when in capil. next to lungs
  • CO2 expelled via respiration - reduces the acid levels (increased CO2 in blood increases likelihood of acidosis)

centre only deals with volatile acids (CO2)

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15
Q

how do you control acid / base balance (physiologically?) via resp. centre?

what controlled by?

how quick is change?

A

lter rate and depth of respirations

  • change incurred by Pons and medulla
  • rapid change
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16
Q

only the kindeys can get rid of what? [1]

what does kindeys getting rid of acids prevent? [1]

A

metabolic acids: (phosphoric, uric, lactic acids and ketones)

prevents metabolic acidosis

17
Q

in order to maintain acid base balance - what do the kidneys have to do? [2]

A
  1. reabsorb all filtered bicarbonate
  2. excrete the daily acid load
18
Q

where is most of filtered bicarbonate reabsorbed? which transporter is used?

A
  • at proximal convoluted tubule via Na/HCO3- symporter channel: reclamation of 4500 mEq of HCO3- each day. 70 - 90%.
  • 10 - 30 % is filtered back at the end of nephron

all bicarbonate is reabsorbed !!

19
Q

how do kidneys make bicarbonate?

A

Kidney can produce bicarbonate

  • Glutamine -> glucose, HCO3-, NH4+ (excreted out and used to combine with H+ ions to make sure excreted into urine)
20
Q

when the body is in acidosis, how do we ensure H+ stay out of renal tubule cells?

A

when the body is acidosis:

@ distal proximal tubule:

H+ get secreted out of renal tubule cell into lumen. BUT want to stay here. SO, use NH4+ and H2PO4 buffes to keep the H+ in the filtrate

21
Q

describe the structure of two motors in ATP synthase

what are they used for?

A

function: converting ion gradients to ATP

in ATP synthase:

  • 2 motors - one electrical, one chemical
  • one motor location: membrane - powered by flow of protons
  • one motor location: intermembrane space: powered by ATP

WHEN ONE TURNS, CAUSES THE OTHER TO TURN