week 9 Flashcards

1
Q

pulmonary ventilation refers to:

A

the mechanical mvmt of air in and out of the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is eupnea and describe muscles involved

A

eupnea is quiet breathing

inspiration is active and expiration is passive

muscles involved are the diaphragm and the external intercostals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is hyperpnea and describe muscles involved

A

increased Ve that matches metabolic demands

Inspiration is active and expiration is also active

Muscles involved in inspiration: diaphragm, external intercostals, scalenes and sternocleidomastoid

Muscles involved in expiration: abdominals and internal intercostals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is minute ventilation

A

The total volume of air that we inspire or expire every minute - what we can easily measure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Define tidal volume

A

The volume of each breath (VT)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Define breathing frequency or respiratory rate

A

Number of breaths per min (fB)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Define alveolar ventilation

A

Amount of air that reaches the alveoli and can participate in gas exchange - effective ventilation (what we care about)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Define dead space (VD)

A

Portion of each breath that gets wasted

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Define anatomical dead space

A

Air that never reaches the alveoli

Always there

Assumed to be 150 mL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Define physiological dead space

A

Air that never reaches the alveoli with no/poor perfusion (blood flow)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the formula for calculating minute ventilation

A

VE = VT x fB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the formula for alveolar ventilation

A

VA = (VT - VD (assumed 150 mL)) x FB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Outline the three phases associated with the VE response to dynamic exercise

A

Phase 1: immediate increase - fast component ~ 10 s

Phase 2: exponential increase - slow component ~ 1 min (more at high intensity)

Phase 3: steady state - appropriate for MR unless intensity is too high to be supported aerobically - steady state never attained

VE plateaus within 1-2 mins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Review pages 5 6 and 7 of respiratory I

A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are early VE responses driven by

A

VT and then FB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What does reducing VD/VT mean

A

You have to move less air to meet gas exchange needs - saves energy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Why is breathing tightly controlled

A
  • to match metabolic demands (VO2 and VCO2)
  • to maintain acid-base balance (pH)
  • to clear airways
  • to communicate (phonation + emotional expression)
18
Q

What is the term used for under ventilation

A

Hypoventilation

Insufficient supply
- can’t meet metabolic demands
- reduced energy capacity
- serious consequences - death blah

Insufficient clearance
- CO2 accumulates
- causes problems on its own

19
Q

What is the term used for over ventilation

A

Hyperventilation

Waste of energy
Slight oversupply of O2 (not harmful)
Excessive clearance of CO2:
- CO2 levels drop
- causes problems on its own

20
Q

Where is the central control of breathing and what triggers inspiration

A

In the brainstem - pons and medulla

Nerves trigger inspiration

21
Q

Describe volitional control of breathing

A
  • how we can voluntarily override our breathing control centers
  • involves higher brain centers - cerebral cortex
22
Q

Describe chemical control of breathing

A

Uses central chemoreceptors in the medulla and peripheral chemoreceptors in the aorta and carotid artery
- together, they sense CO2, pH, and O2 of arterial blood

23
Q

What is ventilation stimulated by

A
  • increased CO2
  • decreased pH -> increased H+
  • decreased O2
24
Q

What is the influence of body temp on the breathing control centers

A

Temp directly excites the breathing control centers - increased VE

25
What is the contribution of proprioceptors on the breathing control centers
Sensory input from muscles, joints and tendons provide input that the body is moving - increased VE
26
What is the influence of higher centers on the breathing control center
Cortical control - includes volitional control - non-volitional influences include: - thinking about/planning/controlling mvmt - central command Hypothalamic control - strong emotion - perception of pain and intense effort
27
describe what O2 and CO2 look like in the following conditions: 1. inspired air 2. alveolar air 3. arterial blood 4. venous blood
1. PIO2 and PICO2 2. PAO2 and PACO2 3. PaO2 and PaCO2 4. PVO2 and PVCO2
28
in exercise induced hyperpnea, what factors are responsible for: 1. initial jump to phase I 2. gradual climb and settling in at steady state 3. ventilatory drift that happens after ~30 mins
1. brain involvement in generating mvmt (anticipatory response) 2. brain involvement in generating mvmt, mvmt of muscles and joints, perception of mvmt and effort 3. increased body temp
29
what is the ACSM classification and what are its pros and cons
all possible intensities from rest to max divided into 5 categories pro: very simple to apply to anyone con: doesnt make much sense physiologically or metabolically
30
define domains
domains (the categories) are defined by metabolic processes that occur at that intensity
31
define boundaries
boundaries between domains are defined by physiological events - we figure out the lower/upper limits of each domain by determining the boundaries
32
what do we determine boundaries/domains based on and what is a pro and a con of this
we determine boundaries and domains based on: HR, power, and speed pro: based on individual physiology rather than guesses con: technically demanding and resource intensive to determine
33
what is determination useful for
1. assessing/monitoring subtle changes in fitness 2. determining precise training intensities to elicit specific metabolic adaptations 3. predicting endurance performance
34
describe the extreme intensity domain
steady state: not attainable sustainability: less than 2 mins anaerobic contribution: significant fatigue mechanisms: accumulation of metabolites, central fatigue
35
describe the severe intensity domain
steady state: not attainable sustainability: several minutes anaerobic contribution: substantial fatigue mechanisms: accumulation of metabolites, central fatigue example: VO2 max
36
describe the heavy intensity domain
steady state: reached within 10-20 mins sustainability: multiple hours anaerobic contribution: obvious fatigue mechanisms: glycogen depletion, central fatigue example: maximum sustainable intensity
37
describe the moderate intensity domain
steady state: reached within 2-3 mins sustainability: indefinitely anaerobic contribution: negligible fatigue mechanisms: central fatigue example: measurable anaerobiosis
38
describe metabolic thresholds
they represent physiologically significant events 1st metabolic threshold - when anaerobic glycolysis rises above the baseline - boundary between moderate and heavy domains 2nd metabolic threshold - when the rate of anaerobic glycolysis makes exercise unsustainable - boundary between heavy/severe domains
39
how can we identify thresholds
we can identify thresholds using data from incremental tests to maximum lactate data -> lactate thresholds (LT1/LT2) ventilatory data -> ventilatory thresholds (VT1/VT2)
40
describe LT1
intensity where [La-] first increases more than or equal to 1 mmol/L above baseline - [La-] is now spilling into the blood because rate of La production exceeds rate of La clearance by the cell
41
describe LT2
intensity where [La-] vs WL curve starts to increase more steeply - La is now accumulating in the blood because the rate of La production exceeds the rate of La clearance from the blood (skeletal muscle, heart, liver)