Endocrinology Flashcards

(163 cards)

1
Q

How can we classify endocrine organs?

A

Central – organs that are located around the brain regions(I.e pineal gland, hypothalamus, posterior pituitary)

Peripheral – organs that are located outside the brain region (I.e ovaries)

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2
Q

What is the integrated control system?

A

Integrated control system is a process in which both nervous and endocrine system are able to produce homeostatic actions with variable onset duration as well as signal to upregulate or down regulate one another. The main linkage between the systems is hypothalamus. The function of hypothalamus can be describe as ‘mediator’.

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3
Q

Define term endocrine.

A

Endocrine – means secreting substances into the blood stream – thus integrating the substance all around the system

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4
Q

Define term hormone.

A

Hormones are released by endocrine cells and are chemical messengers that regulate activity of target cells.

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5
Q

Define term paracrine.

A

Paracrine hormones are able to influence the activity of nearby cells. Example: histamine released by mast cells.

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6
Q

Define term autocrine.

A

Autocrine hormones are able to influence the activity of the cells that produce the said hormone. Hormone acts on the cell that produced it. Example: white blood cells secrete growth factor for themselves.

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7
Q

Define term neurohormone.

A

Neurohormones are released by neurons into the bloodstream. Example: oxytocin.

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8
Q

What are two ways endocrine cells exist?

A

Single scattered cells (e.g. G cells in stomach) or clumped together into a gland (e.g. adrinal gland).

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9
Q

What are the three major types of hormones?

A
  1. Protein
  2. Amine
  3. Steroids
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10
Q

What are the water soluble and insoluble hormones?

A

Protein and amine hormones are water soluble, while steroid are not water soluble.

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11
Q

What is the mode of action of water soluble hormones?

A

Due to their inability to pass through the phospholipid bi-layer (because they are lipid insoluble), water soluble hormones need to bind to the receptors on the surface of the target cells.

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12
Q

What is the mode of action of steroids?

A

They have a slower mode of action as they are able to only bind with intracellular receptors.

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13
Q

How does a typical endocrine gland develops?

A
  1. The usually arise from modified epithelial cells that are able to form an ingrowth from surface epithelium
  2. The attachment of the ingrowth cells slowly loose attachment to the epithelial surface. Blood capillaries form around ingrown cells
  3. Ingrown cells mature and are able to secrete hormones to the capillaries
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14
Q

Describe the general structure of endocrine glands.

A
  1. They are formed by clumps and strands of cells
  2. Supported by reticular fibres and minimal amount of connective tissue cells
  3. There are minimal barriers between cells and capillaries
  4. Capillaries and fenestrated and sinusoidal in nature to allow for bulk transport
  5. There are no ducts
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15
Q

What are the features of endocrine cells producing water-soluble hormones?

A
  1. Many small membrane bound secretory granules
  2. Polarity is not as obvious
  3. Contain small to moderate amounts of RER and Golgi apparatus
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16
Q

What are the features of endocrine cells producing water-insoluble hormones?

A
  1. Large lipids droplets
  2. Abudance of SER
  3. Lack of secretory granules
  4. Abundance of lysosomes
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17
Q

What are the exocrine and endocrine features of the pancreas?

A

Exocrine – acini

Endocrine – islets of Langerhans

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18
Q

Why do we need to delicate balance in both absorptive and post-absorptive states?

A

The brain must be continuously supplied with glucose. Thus we need a system that is able to regulate the amount of glucose in both fed and starving states.

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19
Q

What are the two main hormones in regulation of fuel metabolism?

A

Insulin in well fed state and glucagon in fasted state.

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20
Q

What is the main determinant of insulin secretion?

A

The blood glucose concentration

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21
Q

What are the immediate, intermediate and long term actions of insulin?

A
  1. Immediate - within seconds – translocation of proteins into cell membrane
  2. Intermediate - 10-15 minutes – phosphorylation of metabolic enzymes
  3. Long term – hours-days – effects on mRNA translation and DNA transcription
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22
Q

What is the impact of insulin on the liver?

A
  1. Increased rate of glycolysis
  2. Increased rate of glycogenesis
  3. Decreased rate of gluconeogenesis
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23
Q

What is the impact of insulin on muscle?

A

Increased glucose uptake into muscles

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24
Q

What is the impact of insulin of adipose tissues?

A

Increased uptake of glucose & fatty acids

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25
What is the main stimulant for glucagon release?
Sympathetic stimulation
26
What is the impact of glucagon on the liver?
1. Decrease in glycogen synthesis 2. Increase in glycogenolysis 3. Increase in gluconeogenesis
27
What is the impact of glucagon on the adipose tissue?
1. Increase in lipolysis 2. Decrease triglyceride synthesis 3. Increase circulating free fatty acids
28
What is the aetiology of Type 1 DM?
Largely caused by a autoimmune attack of the beta cells.
29
What is the aetiology of Type 2 DM?
Strong genetic influence. May develop as a result of other endocrine diseases
30
What are two main complications from Type 2 DM?
Glucotoxicity and lipotoxicity
31
What is the link between diabetes and the damage to blood vessels?
Glucotoxicity may cause damage to the small blood vessels. This may affect the eye, the kidney etc.
32
What is the link between diabetes and oral health?
Diabetes causes a reduced blood supply to the gums, decrease salivary flow, decreased pH and lower salivary calcium concentration.
33
What is the function of the hypothalamus?
The main function is to provide the linkage between nervous and endocrine systems
34
What makes up the hypothalamus?
The hypothalamus is comprised of nerves. It regulates hormone production and release, contraction of the uterus during labour, milk production and release, kidney function and growth and development.
35
What are the two lobes of the pituitary gland?
Anterior and posterior (anterior being more vascular and posterior being more neural). They are two independent structures that develop independently embryologically.
36
What two clusters of the hypothalamus have their endings located in the pituitary gland?
The paraventricular nucleus and the supraoptic nucleus
37
What are the hormones release by posterior pituitary gland?
ADH & oxytocin. They are produced in the supraoptic nucleus and paraventricular nucleus and then move into the pituitary gland which distributes it into the blood stream
38
What are the triggers for ADH release?
1. Increase in osmolarity 2. Decrease in blood pressure 3. Fight of Flight response
39
What are the main ways ADH affects blood pressure?
1. Increase in aquaporins to increase water reabsorption 2. Vasocontriction 3. Increase in aldosterone secretion
40
What regulate the secretion of hormones from the anterior pituitary gland?
The hypophysiotropic hormones coming from the hypothalamus
41
What is stress?
It is the nonspecific response of the body to any demand made upon it
42
What are the three stages of general adaption syndrome?
1. Alarm reaction: Flight or Fight 2. Resistance stage 3. Allostatic overload – stress mediators can have both protective and damaging effects
43
What happens during the alarm reaction?
1. Release of noradrenaline from sympathetic nerve terminals 2. Secretion of adrenaline and noradrenaline from the adrenal medulla
44
What does the adrenal medulla secrete?
The catecholamines – adrenaline and noradrenaline
45
How can we describe the adrenal medulla?
We can describe it as a modified sympathetic ganglion. Meaning when it receives sympathetic stimulation, it releases hormones.
46
What supports the actions of catecholamines?
A hypophysiotropic hormone corticotrophin releasing hormone stimulate the secretion of adrenocorticotrophic hormone from anterior pituitary. It acts primarily on zona fasciculata to stimulate the release of glucocoricoids
47
What is the pattern of cortisol release?
It follow circadian diurnal rhythms
48
What are the main functions of cortisol?
Primary role is increasing blood glucose at the expense of fats and protein. It stimulates hepatic gluconeogenesis and inhibits glucose uptake in tissues
49
What are the actions of cortisol on cardiovascular function?
Cortisol increases the sensitivity of the heart and vasculate to adrenaline, noradrenaline and angiotensin II.
50
What is the main function of aldosterone?
The main function of aldosterone is to increase the reabsorption of sodium whilst increasing the excretion of potassium
51
How can adrenal hypersecretion occur and what can it lead to?
Phaeochromocytoma – adrenal medulla tumour. This could lead to elevated heart rate, systemic hypertension, anxiety, hyperglycemia and more.
52
How can we classify the way thyroid hormones act?
We can separate them into 2 categories: 1. Effects on metabolic pathways – increase of basal metabolic rate 2. Effects on cellular differentiation and development
53
What is a functional unit of the thyroid gland?
A thyroid follicle which secretes thyroid hormones (T3 and T4) as well as a C cell which secretes calcitonin
54
What are thyroid hormones?
It is two iodine-containing hormones derived from the amino acid tyrosine that are produced by the thyroid follicles
55
What is the process of thyroid hormone synthesis?
1. Synthesis of thyroglobulin in the cell of the thyroid follicle 2. Thyroglobulin is moved into the follicular space 3. Iodine is moved into the cells from the blood stream via Sodium-Iodine transporter 4. Iodine is move into the follicular space and is oxidised by thyroperoxidase 5. Iodination of thyroglobulin occurs which lead to conjugation when iodine is bound to tyrosine residues 6. The resulted T3 andT4 precursors is than move back into the cell via endocytosis 7. Inside the vesicle, proteolysis occurs and complete forms of T3 and T4 are produced 8. T3 and T4 are move into the blood stream
56
What initiate the production of thyroglobulin?
TSH
57
What is important about iodine?
Iodine needs to be taken from the diet
58
What is the peripheral conversion of T4 to T3?
Only 10% of the T3 comes from the thyroid, most of it comes from conversion of T4 into T3 in other tissues
59
What regulates the release of thyroid hormones?
Hypothalamus releases the hormone TRH which triggers the release of hormone TSH which binds with receptors on the thyroid gland and causes the release of T3 and T4
60
What are the effects of TSH?
1. Non-genomic effects – enhances iodine pump, increase iodination, increases proteolysis of thyroglobulin 2. Genomic effects – promoting general gene transcription for proteins related to production of T3 and T4
61
What are the two main dysfunction related to thyroid function?
1. Hypothyroidism | 2. Hyperthyroidism
62
What are some of the oral manifestations of hyperthyroidism?
1. Increase susceptibility to caries and periodontal disease 2. Accelerated dental eruption 3. Burning mouth syndrome 4. Maxillary or mandibular osteoporosis 5. Increased levels of anxiety
63
What are some of the oral manifestations of hypothyroidism?
1. Salivary gland enlargement 2. Macroglossia 3. Glossitis 4. Delayed dental eruption 5. Compromised periodontal health 6. Dysgeusia
64
What are some of the functions of the calcium?
1. Muscle contractility 2. Neurotransmitter release 3. Blood clotting 4. Maintenanc of cellular integrity 5. Bone and teeth structure and strength
65
What are some of the ways free plasma calcium controlled?
1. Absorption/excretion involving intestines and kidneys | 2. Exchange between fixed and free pools
66
What are the three main hormones that regulate plasma calcium?
1. Parathyroid hormone 2. Calcitonin 3. Vitamin D
67
How does the parathyroid work?
1. it is the main hormone in regulation of plasma calcium levels 2. The receptors on the parathyroid gland sense the levels of calcium and release parathyroid hormone 3. Parathyroid hormone bind with osteoblasts and cause an increase in production RANKL 4. RANKL mobilises osteoclasts which breakdown bone in order to release more into the plasma
68
How does PTH effect on kidneys?
1. Conservation of calcium | 2. Enhances action of vitamin D which enhance responsiveness of bones to PTH
69
What is the function of calcitonin?
Decrease the movement of calcium from the labile pool and inhibits osteoclast activity in bones
70
What is the mode of action vitamin D?
Vitamin D binds to VDR and increases DNA transcription
71
What are the main pathways effect your blood pressure?
The sympathetic pathway through use of adrenaline and noradrenaline and parasympathetic system
72
What is the difference between the beta and alpha receptor interactions?
Beta receptors interaction between adrenaline and noradrenaline are more sensitive than the ones with alpha receptors.
73
What is the first, short term solution to a drop in blood pressure?
1. Blod pressure drop detected by baroreceptors on the aortic arch and carotid sinus 2. This is relayed to CNS 3. Autnomus nervous system causes the release the upregulation of sympathetic dive 4. Release of adrenaline and noradrenaline
74
What is the rapid response of the kidneys to the reduction of blood pressure?
When low blood pressure is detected in afferent arteriole, it constricts and reduced GFR
75
What is a long term control of blood pressure in the renal system?
1. Incresin sodium retention 2. Increasin water reabsorption 3. Increasin potassium secretion
76
What triggers the activation of the RAAS system?
1. Low blood pressure 2. Dehydration 3. Low salt 4. High potassium
77
What are the actions of aldosterone on a cellular level?
1. Aldsteron combines with cytoplasmic receptors 2. Hormone-receptr complex initiates transcription 3. New protein channels and pumps are synthesised 4. Aldosterone induced proteins modification 5. Result - increase sodium channel insertion, increased sodium reabsorption and potassium secretion
78
What are the two main action of vasopressin?
1. Increase insertion of aquaporins | 2. Increased water intake by inducing thirst
79
What happens when your age in terms of renal function?
1. Decrease GFR due to decrease of number of nephrons 2. Decrease in secretion of RAAS hormones 3. Decrease sensativity of the baroreceptors
80
What happens when you age in terms of the vascular system?
You get vascular remodelling which increase the stiffness of the arterioles which makes it harder to regulate blood pressure
81
What is the action of ACE inhibitors?
They inhibit ACE and reduce the conversion of Angiotensin I into Angiotensin II
82
What are side effects of ACE?
1. Dehydration 2. ELectrolyte imbalance 3. Excesive vasodilation 4. Orthostatic hypotension 5. Dry cough – build up of bradykinin
83
What is the mode of action of calcium channel blockers?
They promote relaxation of vascular smooth muscle as interfere with calcium entry
84
What is growth?
It is the organized addition of new tissue that occurs normally in development.
85
What are the main factors influencing growth?
1. Genetics 2. Nutrition 3. Growth hormone 4. Chronic stress and disease
86
What is the growth hormone?
It is a polypeptide hormone produced in anterior pituitary. It is regulate by GHRH and GHIH. It targets many tissues. It alters gene transcription. It promotes using fat stores and promote protein synthesis.
87
What are IGFs?
IGFs are Insulin-like growth factors. They are peptide hormones that have strong mitogenic properties – meaning they promote cell division. They are mainly produced in the liver. There are released by presence of the growth hormone.
88
What is the importance of IGF-1 in terms of bone?
1. It stimulate proliferation of epiphyseal cartilage 2. It increases conversion of cartilage to new bone 3. It increase the proliferation of periosteal osteoblasts 4. It increase bone remodelling
89
What happens during the menopause?
Ovarian secretion of oestrogen decreases and secretion of FSH and LH increase rather abruptly in bout sixth decade in women
90
What happens to bones as a result of reduced secretion of oestrogen?
It causes a decrease in bone mineral density. Oestrogen decrease the production of cytokines by bone marrow and immune cells. Without oestrogen, the cytokines are able to accumulate, osteoclasts are able to proliferate, secretion of osteoprotegrin decreases
91
What happens to cardiovascular system as a result of reduction of oestrogen secretion?
Oestrogen aids in production of nitric oxide which causes dilation of blood vessels. With lack of oestrogen, lower levels of nitric oxide result in stiffer blood vessels
92
What are the components of reflex arc?
1. Receptor - site of stimulus transduction 2. Sensory neuron - transmits afferent impulses to CNS 3. Integration centre - in the CNS 4. Motor neuron - conducts efferent impulses from the integration centre to an effector organ 5. Effector - muscle fibre or gland cell that produces response (muscle contraction or gland secretion.
93
What are muscle receptors?
They are the largest reflex systems in the body for balance and coordination. There are two sensory receptors located within muscle that provide rapid feedback signals to the nervous system: msucle spindle and tendon organ.
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95
What are the components of a muscle spindle?
The muscle spindle detects responds to, and modulates changes in the length of skeletal (extrafusal) muscle fibres to provide an important regulatory function for movemnt and maintenance of posture. It consists of: - 2 sensory afferent fibres: Type 1a (primary, annulospiral endings) and type II (secondary, flower-spray endings) detect length changes - 1 motor efferent fibre: Gamma motor neuron innervates contractile ends of intrafusal fibres - 1 intra-fusal muscle fibre: Specialised fibres within the spindle.
96
What are the components of a Golgi Tendon Organ (GTO)?
The Golgi Tendon Organ detects changes in muscle force
97
Explain the responses of the muscle spindle and GTO to stretch and contraction of skeletal muscle.
1. afferent input from sensory endings of muscle spindle fibre 2. alpha motor neuron output to regular skeletal muscle fibre 1->2. Stretch reflex pathway 3. Gamma motor-neuron output to contractile end portions of spindle fibre. 4. Descending pathways co-activating alpha and gama motor neurons.
98
What type of reflex is stretch?
- The stretch reflex (e.g., knee jerk) is a monosynaptic reflex (one synapse between sensory and motor neurons).
99
Why do muscle spindles need efferent (gama) innervation?
- sustained muscle tension causes steady firing of 1a afferent fibres, maintaining sensitivity. - Gamma motor neurons keep the spindle taut (pulled tight), ensuring it can deetect length changes even during contraction. - Without gamma innervation, the spindle would slack and stop firing. -> Thus gamma activation ensure continuous spindle feedback during muscle shortening -> this is critical for smooth, controlled movements.
100
What is alpha-gama coactivation?
- Voluntary contractions involve simultaneous activation of alpha and gama motor neurons by the cerebral cortex. - This is called alpha-gamma coactivation, ensuring spindle sensitivity during movement. - Coactivation is essential for precise voluntary movements.
101
Describe the function performed by the fusimotor innervation of the muscle spindle.
102
S&F of tendon jerk (monosynaptic stretch reflex)
- Tapping the patellar tendon stretches quadriceps muscle spindles. - This triggers a monosynaptic reflex, contracting the quadriceps (knee jerk). - Used to assess nervous system function; abnormal response indicates pathway issues.
103
S&F of unloading reflex
Occurs when a muscle is suddenly unloaded (e.g., dropping a load), causing a rapid decrease in muscle spindle activity, leading to reduced muscle contraction. Involves muscle spindles and is a response to decreased tension.
104
S&F of inverse myotatic reflex
Triggered by excessive muscle tension detected by Golgi tendon organs (GTOs), causing reflex inhibition (relaxation) of the muscle to prevent injury. Involves GTOs and Ib afferents. - GTOs connect to ~25 extrafusal fibers near the muscle-tendon junction. - Detect muscle tension to protect against excessive load. - When activated (via Ib afferents), they inhibit the muscle, causing relaxation. - GTOs are safety mechanisms, preventing muscle/tendon damage. - They trigger the inverse myotatic reflex (reflex inhibition).
105
S&F of flexion withdrawal
- Triggered by a painful stimulus (e.g., stepping on a tack). - Causes coordinated excitation of flexors and inhibition of extensors in the stimulated limb to withdraw it. - Polysynaptic (multiple synapses), so slower than the stretch reflex. - Polysynaptic pathway allows variability based on stimulus type. - Protects by rapidly removing the limb from harm.
106
S & F of crossed extension reflexes
A complex reflex combining: - Ipsilateral withdrawal: Flexor activation in the stimulated limb. - Contralateral extension: Extensor activation in the opposite limb. - Helps maintain balance (e.g., when withdrawing one foot while standing). - Can be modified by voluntary commands.
107
S&F of periodontal reflexes
- ~300 mechanoreceptive afferents per tooth, directionally sensitive. Reflexes: - Tapping/rapid load increase: Inhibits jaw-closer muscles (disynaptic, like withdrawal reflex). - Weak pressure: Excites jaw-closer muscles (pathway unclear). - Functions: Guide teeth into occlusion, coordinate chewing, crush food.
108
S&F of jaw-opening reflex
- Jaw jerk reflex is a stretch reflex in jaw-closers, similar to the knee jerk, mediated by muscle spindles. - Unloading reflex in the jaw occurs when resistance drops (e.g., food breaks), reducing jaw-closer activity. - Antagonist muscles (jaw-openers) activate during unloading to stabilize the jaw. - Many muscle spindles in jaw-closer muscles (e.g., masseter, temporalis), very few in jaw-openers (e.g., digastric). - Stretch (or increased resistance) of jaw-closer muscle spindles mediates a monosynaptic reflex excitation of the muscle (jaw jerk reflex). - Plays a role in maintaining rest position (e.g., jogging). - During chewing, stretch reflexes adjust jaw-closer muscle activity based on food texture (e.g., biting a nut causes reflex decrease due to spindle inactivation, known as the unloading reflex). - When unloading occurs, antagonist muscles (digastric, mylohyoid) contract to stiffen the jaws and minimize movement (like a seatbelt mechanism).
109
Jaw-opening reflexes triggered by pain or stimuli.
- Jaw-opening reflex protects by inhibiting jaw-closers in response to pain/stimuli. - Disynaptic (two synapses), involving inhibition of jaw-closers but not excitation of jaw-openers in humans. - Triggered by various sensory inputs (e.g., periodontal, gingival, mucosal). - Painful oral/perioral stimuli (mechanical or electrical) inhibit jaw-closing muscles. - High-threshold mechanoreceptors and nociceptors in the periodontal ligament, gingiva, oral mucosa, tongue, lips, facial skin, and tooth pulp trigger this reflex. - Disynaptic inhibition of jaw-closer muscles (similar to the flexor withdrawal reflex). - No disynaptic excitation of jaw-openers in humans (only in animals). - Plays a protective role (e.g., fishbone in gingiva triggers jaw opening to prevent injury).
110
What is proprioception?
It includes both the awareness of position of body segments in space and the sense of movement. It allows us to: - Perform accurate movements without contiuous visual control - Adjust motor control patterns - Perform motor tasks that require multi-limb coordination.
111
What are the functions of different classes of sensory receptor in proprioception?
112
What are the functions of different sensory receptors for proprioception in the masticatory system?
- Muscle Spindles: Abundant in jaw-closers (e.g., masseter), few in openers; key for jaw position sense and jaw jerk reflex; dominate proprioception in chewing - Periodontal Mechanoreceptors: Ruffini-like, Aβ axons in periodontal ligament; directionally sensitive, aid fine motor control and tactile perception during chewing - Golgi Tendon Organs: Few or absent in jaw muscles, minimal role in masticatory proprioception - Joint Receptors (TMJ): Unclear role in jaw movement control, signal extreme conditions Spindles compensate for reduced periodontal input (e.g., with anesthesia/dentures) for interdental size detection
113
Describe in general terms the major ascending pathways by which information from the body about fine touch and proprioception reaches consciousness.
- Dorsal Column-Medial Lemniscal Pathway: Carries proprioception, fine touch, vibration, pressure, and precise location/intensity from receptors to somatosensory cortex; involves parallel processing for texture/shape - Spinothalamic Pathway: Carries crude touch, pressure, pain, and temperature; less precise, crosses midline - Somatotopy: Organized mapping of body sensations onto the cortex via specific pathways
114
What are the Primary Afferent Axons?
- Aα axons (fastest) carry proprioceptive signals from muscles. - Aβ axons handle touch; C fibers handle pain/temperature (not proprioception). - Axon diameter correlates with conduction speed and receptor type. - Aα (13-20 μm, 80-120 m/s): Proprioceptors of skeletal muscle. - Aβ: Touch sensations. - C fibers: Pain and temperature.
115
What are the two basic types of receptors?
- Separate Receptor (a): Chemical messenger opens Na⁺ channels, initiating action potentials. - Specialized Ending (b): Local current flow opens voltage-gated Na⁺ channels. - Both produce graded potentials in afferent neurons, transducing stimuli into CNS signals (action potentials). - Receptors convert stimuli into electrical signals via graded potentials and action potentials. - Mechanism depends on receptor type (chemical vs. voltage-gated).
116
What are the sensory units?
- A sensory unit = One afferent neuron + all its receptor endings. - Receptors in a unit share the same modality (e.g., all detect pressure). - Receptive Field: Area where stimulation generates action potentials in the sensory axon. - Sensory units are specialized for specific stimuli. - Receptive fields define the area a sensory unit monitors.
117
What does coding of sensory stimuli do?
- Sensory information is coded via specific pathways, frequency, and spatial mapping. - Somatotopy ensures organized cortical representation. - Sensory coding answers: What (modality), how big (intensity), where (location)? - Modality: Determined by receptor type and pathway (labeled lines to cortex). - Intensity: Coded by action potential frequency and recruitment of more sensory units. - Location: Determined by activated receptive field, somatotopic organization, and field size/overlap.
118
what are the Muscle Mechanoreceptors and what are their functions?
- Spindles and GTOs complement each other: Spindles for length, GTOs for force. - GTOs are active during contraction; spindles are silent unless stretched. - Muscle spindles (parallel to extrafusal fibers) detect length; GTOs (in series) detect tension. - During contraction, GTOs fire (Ib axons) due to increased tension; spindles (Ia axons) are silent if muscle length doesn’t change.
119
discuss Muscle Spindles and Vibration
- Muscle spindles are key for proprioception; vibration creates illusions by mimicking stretch. - This shows their dominance in position sense. - Muscle vibration activates spindle afferents, increasing action potential frequency. - Brain interprets this as muscle lengthening, causing a kinesthetic illusion (e.g., incorrect elbow angle matching). - Highlights the critical role of muscle spindles in position sense.
120
Mechanoreceptors of the Skin
- Skin mechanoreceptors contribute to proprioception via touch and pressure. - Each receptor type has a specific role (detailed in later slides). - Skin receptors: Pacinian corpuscles, Ruffini endings, Meissner’s corpuscles, Merkel’s disks. - Found in hairy and glabrous skin, within dermal/epidermal layers. - Most have non-neural structures (except free nerve endings).
121
Microneurography
- Microneurography maps receptive fields, showing variability in size. - Small fields = Precise detection; large fields = Broader detection. - Microneurography: Records action potentials from a single sensory axon in the median nerve to map receptive fields. Results: - Small receptive fields: Meissner’s corpuscles, Merkel’s disks. - Large receptive fields: Pacinian corpuscles, Ruffini endings.
122
Adaptation and Receptive Field Size
- Adaptation rate (fast/slow) and field size (small/large) define receptor function. - Fast-adapting = Detect changes; Slow-adapting = Detect sustained stimuli. Skin receptors vary in receptive field size and adaptation rate: - Rapid Adaptation, Small Field: Meissner’s corpuscle. - Rapid Adaptation, Large Field: Pacinian corpuscle. - Slow Adaptation, Small Field: Merkel’s disk. - Slow Adaptation, Large Field: Ruffini ending.
123
Skin Mechanoreceptors and Movement
- Skin receptors contribute to proprioception by detecting movement-related stimuli. - Frequency sensitivity varies: Pacinian (high), Merkel (low). Receptor types and effective stimuli: - Merkel’s Disks (SA I): Sustained contact, pressure (<5 Hz). Meissner’s Corpuscles (FA I): Lateral movement, vibration (5-50 Hz). - Ruffini Endings (SA II): Sustained skin stretch/tension. - Pacinian Corpuscles (FA II): High-frequency vibration (40-400 Hz). - Joint movement activates most receptors: Ruffini (SA II), Pacinian (FA II), Merkel (66%), Meissner (57%).
124
Joint Receptors
Joint receptors are protective, signaling extreme conditions. Less reliable for precise joint angle detection. - Joint receptors (e.g., TMJ) include free nerve endings similar to GTOs. - Signal damaging states: High capsule tension, extreme joint angles, inflammation. - Respond to flexion, extension, compression, stress. - Limited ability to signal joint angle (minimal response to passive movement). - Role in jaw movement control (TMJ) is unclear.
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Relative Contributions of Peripheral Receptors
Muscle spindles are the primary contributors to proprioception. Joint and cutaneous receptors play a secondary role. - Proprioception is best with all mechanoreceptors (Condition 1). - Muscle/tendon receptors (spindles, GTOs) contribute most, especially at slow speeds (Condition 2). - Joint + cutaneous receptors (Condition 4) outperform cutaneous only (Condition 5).
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Dorsal Column-mediated Lemniscal pathway
Dorsal column-medial lemniscal pathway is the main route for proprioception. It’s specialized for precise sensory processing. - Proprioceptive information travels via the dorsal column-medial lemniscal pathway to the somatosensory cortex. This pathway handles: - Fine touch, precise location/intensity. - Vibration, movement against skin. - Proprioception, pressure. - Includes parallel pathways (e.g., for texture, shape).
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Spinothalamic Pathway
Proprioceptive signals enter the spinal cord, branch for reflexes, and ascend via the dorsal column-medial lemniscal pathway. Pain (nociceptors) signals cross the midline, ascend via the spinothalamic pathway (handles pain, temperature, crude touch/pressure, poorly localized). Some crude proprioceptive info travels via the spinothalamic pathway. - Proprioceptive signals enter the spinal cord, branch for reflexes, and ascend via the dorsal column-medial lemniscal pathway. - Pain (nociceptors) signals cross the midline, ascend via the spinothalamic pathway (handles pain, temperature, crude touch/pressure, poorly localized). - Some crude proprioceptive info travels via the spinothalamic pathway.
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Cortical Representation
Somatotopy ensures organized sensory representation in the brain. Specific pathways link body regions to cortical areas. - Somatotopy: Mapping of body sensations onto the somatosensory cortex. - Sensory information excites specific cortical areas via defined pathways.
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Sensory Discrimination
Sensitivity depends on receptor density, field size, and cortical representation. Fingers/face have finer discrimination due to these factors. - Two-point discrimination varies by body region (fingers/face = high sensitivity). Due to: - Higher receptor density. - Smaller receptive fields. - Larger cortical representation. - Two points felt if separate fields are activated; one point felt if fields overlap.
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Proprioception Overview
Proprioception integrates sensory and motor signals. Efference copy = Brain’s copy of motor commands, aiding perception.
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Periodontal Mechanoreceptors
Periodontal mechanoreceptors are crucial for jaw proprioception and chewing control. They detect force and direction, contributing to fine motor adjustments. - Periodontal ligament (attaches teeth to bone) is rich in low-threshold mechanoreceptors (Ruffini-like, Aβ axons). - Directionally sensitive to mechanical loads on teeth, aiding motor control during chewing. - Respond to low forces; 80% saturate at 3-4 N, 20% respond linearly to higher forces. - Key for tactile perception and proprioception (force amplitude, direction, teeth contact).
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Proprioception in the Masticatory System
Proprioception allows fine detection of objects between teeth. Muscle spindles dominate jaw proprioception; periodontal receptors play a smaller role. Perception of interdental size (object thickness between teeth): - Natural dentition (unanesthetized): Threshold 0.008-0.060 mm; Discrimination 0.014 mm. - Natural dentition (anesthetized): Threshold 0.030-0.180 mm; Discrimination 0.040 mm. - Dentures (no anesthetic): Threshold 0.4-0.5 mm; Discrimination 0.18 mm. - Dentures (topical anesthetic): Discrimination 0.22 mm. - Normal subjects detect 20 μm objects; increases to 80 μm with anesthesia. - Minimal reduction in ability with anesthesia or dentures. - Muscle receptors (spindles) are key; few/no GTOs in jaw muscles.
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Altered Sensations with Dentures
Dentures reduce periodontal input, affecting chewing and texture perception. Proprioception (via muscle spindles) compensates for size/hardness detection. Dentures cause: - Loss of periodontal ligament receptors → Loss of related sensations/reflexes (e.g., glide into occlusion). - Oral mucosa covered → Impaired force perception, altered chewing/swallowing. - Decreased texture appreciation. - Size/hardness perception is preserved (proprioceptive, effort-related). - Motor learning required to adapt to dentures for speech/mastication.
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Summary of proprioception
Proprioception, the awareness of body segment position in space, enables accurate movements without visual control by relying on sensory coding of modality, intensity, and location through proprioceptors like muscle spindles, tendon organs, joint, and skin receptors, with muscle spindles having the greatest influence and joint receptors the least, as demonstrated by kinesthetic illusions from muscle vibration; this information ascends via the dorsal column-medial lemniscal pathway to the cortex, while in the masticatory system, periodontal ligament mechanoreceptors aid fine jaw motor control, and proprioceptive signals allow detection of object sizes between teeth.
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Motor Units
The smallest functional unit of muscle control, consisting of a motor neuron and its innervated muscle fibers, with varying innervation ratios based on muscle function.
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Force Modulation
Muscle force is graded by recruiting more motor units and increasing their firing rate, following the Size Principle for efficient control.
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Motor Unit Types
Slow (Type I), fast fatigue-resistant (Type IIA), and fast fatigable (Type IIB) motor units are recruited based on task demands.
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Jaw Muscles
Jaw-closers have a high proportion of Type I and intermediate fibers for fatigue resistance, while jaw-openers (e.g., digastric) have more fast-twitch fibers for rapid movements. These differ from limb muscles in fiber size and composition.
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Motor Control Hierarchy
Planning (cortex, basal ganglia, cerebellum), commanding (motor cortex, brainstem), and execution (spinal neurons) levels coordinate movement.
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Corticobulbar Pathway
Bilateral projections from the cortex to brainstem motoneurons control jaw muscles, preserving mastication after unilateral stroke.
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Mastication and CPG
Chewing is initiated voluntarily but controlled automatically by a brainstem CPG, modulated by sensory feedback for efficiency and safety.
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Understand the concept of the motor unit as the smallest functional element for control of muscle force.
A motor unit is the functional unit of the neuromuscular system, consisting of a single motor neuron and all the muscle fibres it innervates. It represents the connection between the nervous system and skeletal muscle.
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What are the characteristics of motor units?
All muscle fibers within a single motor unit have similar physiological properties (e.g., contraction speed, force, fatigability).
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What determines the number of muscle fibres per motor unit?
- The number of muscle fibers per motor unit varies depending on the muscle's function, known as the innervation ratio: - Low innervation ratio (~20): Muscles involved in precise movements, such as those in the eye or hand. - High innervation ratio (~2000): Muscles involved in powerful movements, such as those in the arms or legs. - Intermediate innervation ratio: Jaw-closing muscles like the masseter (~640) and temporalis (~900) balance precision and power.
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What's the significance of the motor unit?
The motor unit is the smallest controllable element for producing muscle force, allowing the nervous system to fine-tune movement. E.g., When you blink (eye muscle, low innervation ratio), a small number of fibers are activated for precision. When you lift a heavy object (arm muscle, high innervation ratio), many fibers are activated for power.
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muscle force is graded by a combination of recruitment and firing-rate modulation of motor units.
- Muscle Force Modulation: The force a muscle produces is controlled by two mechanisms: 1. Recruitment: Activating more motor units to increase force. 2. Rate Coding: Increasing the frequency of action potentials (firing rate) in active motor units to produce stronger contractions.
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How does recruitment of muscle force modulation work?
- Recruitment: - Motor units are recruited in an orderly manner based on the Size Principle (explained in detail below). - Small motor units (producing less force) are activated first, followed by larger ones as more force is needed.
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How does rate coding of muscle force modulation work?
- Rate Coding: - Increasing the firing rate of a motor unit causes twitch summation, where muscle contractions overlap due to increased calcium availability in the muscle fiber's cytosol. - If the firing rate is high enough, the muscle reaches tetanus, a sustained contraction with no relaxation between stimuli, maximizing force output. - Example from Lecture: Figure 8-16 from Sherwood illustrates twitch summation and tetanus, showing how repeated stimuli before relaxation increase force.
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Discuss the size principle please
Size Principle: - Small motor neurons have higher input resistance due to fewer ion channels and smaller surface area. According to **Ohm’s Law** (Vm=IR), a given synaptic current produces a larger excitatory postsynaptic potential (EPSP) in small motor neurons, causing them to reach the firing threshold first. Vm=IRV_m = IR - Advantage: This ensures precise, low-force movements are initiated by small, fatigue-resistant motor units, while powerful movements recruit larger, more fatigable units only when necessary, optimizing energy use and control.
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how motor units with different physiological properties (force, speed of contraction, fatigability) are used systematically by the central nervous system to produce force optimally for the task.
- **Motor Unit Classification**: - Motor units are classified into three types based on three contractile properties: **contraction speed**, **maximal force**, and **fatigability**: 1. **Slow (S, Type I)**: - Slow contraction speed, low force, high fatigue resistance. - Used for endurance tasks (e.g., posture maintenance). 2. **Fast Fatigue-Resistant (FR, Type IIA)**: - Fast contraction speed, moderate force, resistant to fatigue. - Used for sustained, moderate-intensity tasks (e.g., walking). 3. **Fast Fatigable (FF, Type IIB)**: - Fast contraction speed, high force, low fatigue resistance. - Used for short, powerful movements (e.g., sprinting, lifting heavy weights).
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Muscle Fiber Composition
- Different muscles have varying proportions of these fiber types based on their function: - **Endurance muscles** (e.g., soleus in the leg): High proportion of Type I fibers. - **Power muscles** (e.g., quadriceps): High proportion of Type IIB fibers.
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Systematic Use of muscles by CNS
- The central nervous system (CNS) recruits motor units in a task-dependent manner, following the Size Principle: - Low-force tasks (e.g., holding a cup) primarily use Type I motor units. - High-force tasks (e.g., jumping) recruit Type IIA and IIB units as needed. - This ensures efficiency, fatigue resistance, and precision tailored to the task.
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Describe the fiber type composition of jaw-closer muscles and understand how they differ from limb muscles.
- **Jaw-Closing Muscles (e.g., Masseter, Temporalis, Medial Pterygoid)**: - **Unique Features**: - **High proportion of Type I fibers**: Fatigue-resistant, suitable for sustained chewing. - **Low proportion of Type IIA fibers**: Less emphasis on fast, fatigue-resistant contractions compared to limb muscles. - **High proportion of intermediate fibers (Type IIC, IM)**: These fibers have properties between Type I and II, enhancing versatility. - **Fiber diameter**: Type I fibers are larger than Type II fibers, unlike limb muscles where Type II fibers are typically larger. Both types are smaller overall, possibly aiding fatigue resistance. - **Regional grouping**: Fibers of the same type are grouped within the muscle, likely reflecting functional specialization (e.g., different regions for biting vs. chewing). - **Functional Implications**: - The predominance of Type I and intermediate fibers supports prolonged, repetitive tasks like chewing, which require fatigue resistance. - Smaller fiber diameters and regional grouping may enhance precise control and endurance.
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Describe the fiber type composition of jaw-opener muscles and understand how they differ from limb muscles.
- **Jaw-Opening Muscles (e.g., Digastric, Lateral Pterygoid)**: - **Digastric**: - Mixed fiber composition, similar to limb muscles. - Higher proportion of Type IIA and IIB fibers, suitable for fast, unloaded contractions (e.g., during speech or jaw opening). - **Lateral Pterygoid**: - Similar to jaw-closers, with a high proportion of Type I and intermediate fibers, supporting sustained activity. - **Functional Implications**: - Digastric’s fast-twitch fibers enable rapid jaw opening for speech or swallowing, while lateral pterygoid’s composition supports chewing and jaw stabilization.
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Compare and Contrast Jaw opening/closing muscles to Limb muscles
- **Comparison to Limb Muscles**: - Limb muscles (e.g., biceps brachii) typically have a more balanced mix of Type I, IIA, and IIB fibers, tailored to diverse functions (endurance, power, or both). - Jaw muscles prioritize fatigue resistance (Type I and intermediate fibers) for repetitive tasks like chewing, with less emphasis on high-force, fast-twitch fibers (Type IIB).
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Understand, in general terms, the organization of the descending corticobulbar projection for voluntary control of jaw movements.
- **Hierarchy of Motor Control**: - Motor control is organized into three levels: 1. **Highest Level (Planning)**: - Involves cortical association areas, basal ganglia, and cerebellum. - Develops strategies and motor plans to achieve movement goals. 2. **Middle Level (Commanding)**: - Motor cortex and brainstem descending pathways integrate signals from planning areas and send specific motor commands to subcortical structures, spinal cord interneurons, and motoneurons. 3. **Lowest Level (Execution)**: - Spinal interneurons and motoneurons integrate sensory and descending inputs to activate muscles for movement.
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What are the components of the motor system?
- **Cerebral Cortex and Descending Pathways**: - The primary motor cortex integrates inputs from premotor and association areas and projects via the corticospinal and corticobulbar tracts. - **Basal Ganglia**: - Regulates movement indirectly through cortical areas, aiding in movement initiation and postural adjustments. - **Cerebellum**: - Compares planned and actual movements, correcting disparities for coordination. - **Brainstem**: - Integrates ascending and descending signals and originates descending pathways (except corticospinal tract). - **Motor Neurons and Interneurons**: - Execute stereotyped reflexes and integrate sensory/descending inputs for muscle activation.
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What is the corticobulbar pathway?
- The corticobulbar pathway originates in the sensorimotor cortex and controls motoneurons in the brainstem for muscles of the eye, face, tongue, and throat. - Unlike the corticospinal tract (which controls spinal muscles), it is **bilateral**, innervating motoneuron pools on both sides of the brainstem. - **Trigeminal Nerve (Cranial Nerve V)**: Controls muscles of mastication (e.g., masseter, temporalis). - **Functional Advantage**: Bilateral innervation ensures mastication is preserved after a unilateral stroke, as the unaffected cortex can still control both sides. - **Example**: After a stroke affecting one side of the cortex, a patient may have arm weakness (corticospinal damage) but can still chew effectively due to bilateral corticobulbar projections.
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Cortical Representation
- The motor cortex has a **somatotopic representation** (motor homunculus), with large areas dedicated to the hand and mouth due to their complex, precise movements. - This reflects the high number of motor cortical projections to these regions, enabling fine control.
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Understand, in general terms, the concept of a central pattern generator and the basic features of the neural systems controlling chewing.
- **Mastication Overview**: - Mastication is the rhythmic, coordinated activation of jaw muscles to break down food into a swallowable bolus. - It requires powerful yet precise muscle control, modulated by sensory feedback to optimize efficiency and prevent damage to oral structures (e.g., teeth, tongue). - **Example**: Chewing hard food (e.g., nuts) requires stronger, slower cycles, while soft food (e.g., bread) involves faster, lighter cycles, adjusted by sensory input.
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Central Pattern Generator (CPG) during mastication
- A CPG is a neural network in the brainstem that generates rhythmic motor patterns without requiring constant conscious input. - **Evidence for Chewing CPG**: - Repeated cortical stimuli can induce cyclical activity in masticatory motoneurons, even in paralyzed animals, indicating an autonomous rhythm generator. - Lesion studies suggest the CPG is located in the **brainstem reticular formation**. - Sensory inputs (e.g., food texture) modify the chewing pattern, such as altering the rate or force of cycles. - **Function**: The CPG drives the automatic, rhythmic jaw movements during chewing, freeing the cortex from continuous monitoring.
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Control of Mastication
- **Voluntary Initiation**: Mastication begins with voluntary commands from the motor cortex. - **Automatic Continuation**: The brainstem CPG takes over, producing rhythmic jaw movements. - **Sensory Modulation**: - Sensory receptors in the oral mucosa, periodontal ligaments, masticatory muscles, and temporomandibular joint (TMJ) provide feedback to adjust the chewing rhythm and force. - **Example**: Encountering a hard piece of food increases sensory feedback, slowing, causing the CPG to slow chewing cycles and recruit more motor units for greater force. - **Swallowing Integration**: When the food bolus reaches the appropriate size and consistency, the swallowing center is activated, coordinating swallowing with chewing. - **Example**: Chewing a tough piece of meat involves sensory feedback adjusting the force and speed of jaw movements, followed by swallowing once the bolus is ready.
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