7. Breathlessness and Control of Breathing (Awake) Flashcards

1
Q

Why do we breathe?

A

The purpose of control of breathing muscles include:

o Appropriate gas exchange to maintain metabolic homeostasis

o Defence of lung and airways, i.e. through reflex protective behaviours (e.g. coughing, sneezing and yawning)

o Other functions (non-metabolic) include communication (speech, singing), expressing emotions, non-respiratory behaviours (including defecation and posture)

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2
Q

Provide an overview of breathing control

A

There are two separate ‘controllers’ in the brain:

o ‘automatic’ bulbopontine controller (found in the brainstem, within the medulla and pons)

o ‘behavioural’ suprapontine controller (widely distributed, but all superior to the pons)

These have a common motor output from a spinal motor neurone pool which leads to lung inflation and alveolar ventilation

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3
Q

What are the 3 factors of input to consider in terms of breathing control?

A

Chemoreceptors

Mechanoreceptors

Sensory input

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4
Q

Outline chemoreceptors as an input mechanism to breathing control

A

Peripheral chemoreceptors are found in the bifurcation of the common carotids (respond to pH, PaCO2, hypoxia), and the aortic
arch (respond to PaCO2, hypoxia)

Central chemoreceptors are located on the surface of the
medulla, respond to PaCO2, but not pH or hypoxia

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5
Q

What is PaCO2?

A

The partial pressure of carbon dioxide in the arterial blood; arterial carbon dioxide concentration or tension

It is usually expressed in millimeters of mercury (mmHg)

The normal range is 38-42mmHg

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6
Q

What is PO2?

A

The partial pressure of oxygen in there arterial blood

It is normally expressed in millimetres of mercury (mmHg)

The normal range is 80-100mmHg

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7
Q

Outline mechanoreceptors as an input mechanism to breathing control

A

Within the lung:

o Slowly adapting pulmonary stretch receptors (which respond via inhalation reflex or Hering-Breuer reflex)

o Rapidly adapting pulmonary stretch receptors

o J receptors (bronchial C fibre receptors)

o Irritant receptors

Within the chest wall:

o Joint receptors

o Golgi tendon organs

o Muscle spindles

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8
Q

Outline the Hering-Breur reflex

A

The Hering–Breuer inflation reflex is a reflex triggered to prevent over-inflation of the lungs

Pulmonary stretch receptors present in the smooth muscle of the airways respond to excessive stretching of the lung during large inspirations

Once activated, they send action potentials through large myelinated fibers of the vagus nerve to the inspiratory area in the medulla and apneustic center of the pons

In response, the inspiratory area is inhibited directly and the apneustic center is inhibited from activating the inspiratory area

This inhibits inspiration, allowing expiration to occur

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9
Q

Outline sensory input as an input mechanism to breathing control

A

From the nose - trigeminal (V) nerve

From the pharynx - glossopharyngeal (IX) and vagus (X) nerves

From the larynx - vagus (X) nerve

From the lungs – vagus (X) nerve

From the chest wall – spinal nerves

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10
Q

Outline neural output in terms of breathing control

A

From the diaphragm: Phrenic nerve and Cervical plexus (C3 - C5)

From the intercostal muscles: T1 - T12

From the abdominal muscles: T6 - L1

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11
Q

What can the pons be divided into?

A

The pons can be divided into two different centres; the pneumotaxic centre and the apneustic centre:

o The pneumotaxic centre, found in the rostral dorsal lateral pons, antagonises the apneustic centre cyclically, inhibiting inspiration by sending a ‘switch off’ signal to the dorsal respiratory group within the medulla

o The apneustic centre, found in the lower pons, promotes inspiration by stimulations of the dorsal respiratory group of neurons in the medulla

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12
Q

What are the two sets of respiratory groups of neurones in the medulla?

A

The dorsal respiratory group (DRG) consists of inspiratory neurones

The ventral respiratory group (VRG) consists of expiratory neurones (which receive input from the DRG) and the pre-Botzinger complex (pre-Bot C) which is a complex of rhythm-generating neurones

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13
Q

Define bulbopontine, rhombencephalon, tegmentum and pons

A

Bulbopontine; relating to the rostral part of the rhombencephalon composed of the pons and overlying tegmentum

The rhombencephalon is the portion of the brain developed the most caudal to the three primary vesicles of the embryonic neural tube

The tegmentum is the posterior part of the mesencephalon, and is also a term for a ‘covering structure’

The pons varolii or pons cerebelli; the part of the brainstem between the medulla oblongata caudally and the mesencephalon rostrally, composed of the basilar part of pons and the tegmentum of pons

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14
Q

Outline rhythm generation in terms of the automatic bulbopontine controller

A

Output from the DRG and VRG –> spinal motor neurons –> muscles –> inspiration/expiration (depending upon the origin of input)

Ventilation of the lung –> stimulation of the lung stretch receptors, which then inhibit the inspiratory neurons of the DRG and the Apneustic centre within the pons

Ventilation also alters the blood gas partial pressures, which stimulates arterial chemoreceptors, which result in stimulation/inhibition of DRG (depending upon gas partial pressures)

Neuron activity is cyclical/rhythmic due to the synaptic interaction between groups of neurons

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15
Q

Outline automatic reflex drive

A

Ventilator response to increased PaCO2 is linear, due to an immediate response from arterial chemo and mechanoreceptors

However the ventilatory response to reduced PaO2 is not immediate or linear

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16
Q

Outline the suprapontine controller

A

Volitional, wilful drives (from motor homunculus; motor cortex); wide range of control, precise, subconscious, competes for control of respiratory muscles

Emotional drives; involuntary psychological influences, secondary to the perception of discomfort, music perception, purpose unknown

Wakefulness drives; tonic excitatory drive when awake (inhibitory drive also exists)

Response to moderate exercise

NB: effect of sleep on respiratory muscles is purely autonomic, and has no voluntary or emotional input

17
Q

Outline dyspnoea

A

Dyspnoea is defined as “…a subjective experience of breathing discomfort that is comprised of qualitatively distinct sensations that vary in intensity”

Unpleasant sensation

Common

More prominent than pain during late-stage cancer

No treatment known

Clinical prevalence: present in most respiratory disorders, chronic heart failure, terminal cancer, psychiatric disorders, or other disorders affecting respiratory function, e.g. endocrine or neuromuscular

Is a subjective perception

Clinical signs of distress include tachypnoea (rapid breathing), ‘pursed lips’ breathing, hyperinflation,
cyanosis (blue/purple discoloration of lips, tongue, skin)

Distinguishable qualities: “hunger for air, sense of effort during breathing, chest tightness”

Link to respiratory control: afferent signals reporting demand from breathing occur, but there is an efferent-
reafferent mismatch which occurs:

o Indirect role - elicits behaviours to move the respiratory system away from danger, e.g. to seek
medical attention, swim to surface, stop exercise

o Also involved in establishing a learned breathing response to exercise

There are also cerebral activations which occur during dypsnoea, which can be seen by a PET scan

18
Q

Outline CCHS

A

Congenital central hypoventilation syndrome (CCHS)

Also known as “ondines curse”

A lesion of the medulla has an effect upon the automatic reflex controller

This means that the patient only breathes with a behavioural controller?

Leads to a blunted reflex ventilatory response to PaCO2

Essentially normal response to exercise, as the control of breathing during exercise is behavioural

19
Q

Outline ‘Locked in Syndrome’

A

Discrete lesion of the corticospinal pathway of the ventral pons

This means that there is no voluntary motor control except for eye-blinking

However, automatic brainstem reflexes remain intact, therefore there is a ventilatory response to PaCO2

20
Q

Outline J-receptors

A

J (juxtacapillary) receptors (or pulmonary C-fiber receptors) are sensory nerve endings located within the alveolar walls in juxtaposition to the pulmonary capillaries of the lung and are innervated by fibers of the vagus nerve

Although their functional role is unclear, J-receptors respond to events such as pulmonary oedema, pulmonary emboli, pneumonia, congestive heart failure and barotrauma, which cause a decrease in oxygenation and thus lead to an increase in ventilation/respiration

21
Q

Outline the pre-Bötzinger complex

A

The pre-Bötzinger complex (preBötC) is a cluster of interneurons in the ventral respiratory centre of the medulla of the brainstem

This complex has been proven to be essential for the generation of respiratory rhythm in mammals

The exact mechanism of the rhythm generation and transmission to motor nuclei remains controversial and the topic of much research

It is associated with sleep apnoea

22
Q

State the standard ranges for blood gases at sea level

A

pH: 7.35 - 7.45

pO2: 10 - 14kPa

pCO2: 4.5 - 6kPa

Base excess (BE): -2 - 2 mmol/l

HCO3: 22 - 26 mmol/l

MetHB: <2%

CO: <10%

Lactate: 0.5-1.0mmol/L

NB: 1kPa = 7.5mmHg