OTHER HALF (lectures 27-36) Flashcards

1
Q

What is Vasoconstriction?

A

The contraction of smooth muscle in the arteriole walls; it increases blood pressure

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2
Q

What is Vasodilation?

A

The relaxation of smooth muscles in the arterioles, causes blood pressure to fall
- Nitric oxide is a major inducer

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3
Q

What are Baroreceptors?

A

Specialized nerve endings that respond to stretch of vessel wall indirect response to changes in BP
- Located in the carotid and aortic arch

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4
Q

What is the Renin-Angiotensin-Aldosterone system?

A

It is apart of a complex feedback circuit that functions in homeostasis
- drop in blood pressure near glomerulus causes the juxtaglomerular apparatus of the kidney to release the enzyme renin
- renin triggers the formation of the peptide angiotensin II
- Angiotensin raises blood pressure and decreases blood flow in the kidneys
- also stimulates the release of the hormone aldosterone, which increases blood volume and pressure

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5
Q

What are factors affecting blood pressure?

A

Diet: (salt, fat, cholesterol, alcohol)
smoking, obesity and type 2, diabetes, stress, low activity
Hypertension

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6
Q

How do you treat hypertension?

A

Non-pharmacological: lifestyle changes - diet, exercise, smoking, alcohol
Drug treatment: antihypertensives, reduce blood volume and reduce cardiac output
- Beta-blockers
- alpha-blockers
- mixed
-ACE inhibitors

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7
Q

What are cells in the innate immune system?

A
  • Dendritic cells
  • Macrophage
  • Natural killer cell
  • Neutrophil
  • Basophil
  • Eosinophil
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8
Q

What are cells in the adaptive immune system?

A

B cell, T cell

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9
Q

What are the two sides of an immune response?

A

Internal threat - autoimmune problem (disease; cancer, hepatitis, HIV, shingles)
External threat - allergic reaction (infection; bacteria, mold/fungus, parasites, viruses)

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10
Q

How are RNA viruses recognised?

A

They are recognized by nucleic acid detection and drive interferons
- Type -I interferons prepare local cells to avoid viral infection
(viruses try to subvert this)

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11
Q

What is viral sepsis and systemic inflamation?

A

Infection of the lung epithelium, increased vascular permeability and local inflammation.
- Lowered lung function and hypoxemia
- Acute anti-viral response ‘goes systemic’
- Increased coagulation, microcirculation problems, brain tissue hypoxia

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12
Q

What are the two checkpoints in the immune system to fight cancer?

A
  1. Ipilimumab
  2. Nivolumab
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13
Q

What are the side effects of checkpoint therapy in cancer treatments?

A

The checkpoints are not specific to tumor environment:
some side effects in include -
Thyroiditis, dry mouth, rash, vitiligo, myocarditis, pancreatitis, hepatitis neuropathy etc.

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14
Q

What is the link between inflammation and obesity?

A
  1. Fat tissue contains 50-60% macrophages and regulatory T-cells
  2. Apoptotic fat cells –> inflammatory factors released and M1- activated macrophage
  3. TNF-a and other inflammatory factors
  4. Inflammation recruits additional immune cells
  5. Inflammation causes fat tissue to become insulin-resistant
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15
Q

What is the difference between lean adipose tissue and obese fat tissue?

A

After weight gain the tissue becomes inflamed and there are pro-inflammatory molecules present

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16
Q

What are iNKT cells?

A

They are also known as Invariant natural killer T cells: restricted and conserved CDR3 region, Non-MHC-restricted, invariant/semi-variant
- They also produce IL-10 (a cytokine with anti-inflammatory properties)

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17
Q

What do iNKT cells do for the metabolism?

A

They positively regulate the metabolism

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18
Q

What do macrophages do for the brain?

A

They repair brain injury, but if the brain is injured again 1-2 later there will be no healing and lasting damage.

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19
Q

What are essential nurients?

A

Required materials that an animal cannot assemble from simpler organic molecules

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20
Q

What are the four classes of essential nutrients?

A

-Essential amino acids
- Essential fatty acids
- Vitamins
- Minerals

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21
Q

What is digeston?

A

The process of breaking food down into molecules small enough to absorb

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22
Q

What is mechanical digestion?

A

The chewing, or grinding, increases the surface area of food.

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23
Q

What is chemical digestion?

A

digestion splits the food into small molecules that can pass through membranes; these are used to build larger molecules
- the process of enzymatic hydrolysis splits bonds in molecules with the addition of water

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24
Q

What are the organs/parts required for digestion?

A

Tongue, oral cavity, salivary glands, pharynx, esophagus, liver, gallbladder, stomach, pancreas, small intestine, large intestine, rectum, anus

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25
Q

What occurs in the oral cavity?

A

Food processing begins in the oral cavity: oral cavity, pharynx, esophagus
steps:
1. saliva breaks down starch
2. Tongue helps to shape food for swallowing
3. pharynx opens the esophagus and the trachea
4. Esophagus connects to stomach, trachea leads to lungs

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26
Q

How does Saliva work?

A

saliva (exocrine secretion from salivary glands) contains mucus - mixture of water, salts, cells and glycoproteins and amylase, break down starch.

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27
Q

What are the layers of the digestive tract wall?

A

Generally:
1. Lumen
2. Submucosa
3. Mucosa
4. Muscularis externa
5. Serosa

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28
Q

What is the mixture of ingested food and gastric juices called?

A

it is called chyme

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29
Q

How are gastric juices produced? (steps)

A
  1. Pepsinogen and HCI introduced into lumen
  2. HCI converts pepsinogen to pepsin
  3. Pepsin activates more pepsinogen, starting a chain reaction
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30
Q

What is the first portion of the small intestine called?

A

it is called the duodenum

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31
Q

What happens in the first part of the small intestine also known as the duodenum?

A

The chyme from the starch mixes with digestive juices from the pancreas, liver, gallbladder and the small intestine itself

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32
Q

What does the pancreas produce?

A

It produces the proteases trypsin and chymotrypsin which are activated in the lumen of the duodenum

33
Q

Where is bile made and stored?

A

It is made in the liver and stored in the gallbladder.

34
Q

What does the hepatic portal vein do?

A

it carries nutrient-rich blood from capillaries of the villi to the liver, then to the heart and onwards to all organs

35
Q

Why is the small intestine able to absorb so much nutrients?

A

this is because it is composed of villi and microvilli making its surface area extremely large, so it is able to absorb a lot, including water

36
Q

What happens to fatty acids and monoglycerides?

A

Epithelial cells absorb them and recombine them into triglycerides, these fats are coated with phospholipids, cholesterol, and proteins to form water-soluble chylomicrons. chylomicrons are transported into lacteal, a lymphatic vessel in each villus.

37
Q

What stimulates the production of gastric juices?

A

Gastrin does

38
Q

Where is energy first stored in the human body?

A

First stored in the liver and muscle cells in the polymer glycogen, excess energy stored in fat adipose cells

39
Q

What is the absorptive state?

A
  • fed state
  • glucose is plentiful and serves as major energy source
  • Insulin is a major hormone of absorptive state
40
Q

What is the postabsorptive state?

A
  • Fasting state
  • Endogenous energy stores are mobilized to provide energy
  • Glucagon is major hormone of postabsorptive state
41
Q

What regulates the breakdown of glycogen into glucose?

A

The hormones Insulin and glucagon.

42
Q

What hormone triggers the feeling of hunger before a meal?

A

Ghrelin triggers the feeling, its is secret by the stomach wall

43
Q

What are the effects of epinephrine and norepinephrine?

A
  • Glycogen broken down to glucose; increased blood glucose
  • Increased blood pressure
  • Increased breathing rate
  • Increased metabolic rate
  • Change in blood flow patterns, leading to increased alertness and decreased digestive, excretory and reproductive system activity
44
Q

What are the effects of mineralocorticoids?

A
  • Retention of sodium ions and water by kidneys
  • Increased blood volume and blood pressure
45
Q

What are the effects of glucocorticoids?

A
  • Proteins and fats broken down and converted to glucose, leading to increased blood glucose
  • partial suppression of immune system (this is why glucocorticoid drugs are prescribed for autoimmune disorders e.g. allergies)
46
Q

What diseases are linked to physical inactivity?

A
  • CHD
  • Stroke
  • Cancer
  • T2D
  • Dementia
47
Q

What are the benefits of exercise to multiple physiological systems?

A

Neurological:
LOWER -
- anxiety/depression
- Dementia
- Risk of stroke
HIGHER -
- cognitive function
Cardiovascular:
LOWER -
- mortality
- coronary artery disease
- blood pressure
Oncological:
LOWER -
- prostate cancer
- breast cancer
- bowel cancer
Musculoskeletal:
LOWER -
- Osteoporosis
- Falls
- Disability

48
Q

How can physical activity be protective to the brain?

A

The more you exercise the more myokines that you produce which are anti-inflammatory and this produces cytokines like: IL-10 and IL-6
- These help with synaptic plasticity
- Neurogenesis
- Cognitive function

49
Q

What are somatosensory receptors?

A

Mechanoreceptors
- cutaneous, proprioception, force
Thermoreceptors
- temperature
Nociceptors
- pain

50
Q

Where are somatosensory receptors?

A

Skin - tactile, thermoreceptors, pain
Muscle - muscle spindle
Joints - Articular

51
Q

What are the two classes of somatosensory receptors?

A
  1. Rapidly adapting
  2. Slowly adapting
52
Q

What are examples of rapidly adapting tactile mechanoreceptors?

A
  1. Meissner’s corpuscles
    - located in hands/feet
    - touch, vibration
    - rapidly adapting
  2. Pacinian corpuscles
    - high frequency vibration
53
Q

What are examples of slowly adapting tactile mechanoreceptors?

A
  1. Merkel’s receptors
    - pressure
  2. Ruffini’s corpuscles
    - stretching of skin
54
Q

What are receptive fields determined by?

A

receptor type, distribution density, activation threshold, duration of activation, adaptation, central convergence ratio

55
Q

What are the parts of the sensory motor system?

A

Cortical areas:
- primary motor cortex M1
- premotor cortex
- Supplementary motor area
- S-I and S -II
Subcortical areas:
- cerebellum
- Basal ganglia

56
Q

What is a command neuron?

A

The term was introduced by Wiersma, studying neurons with long axons in crayfish
- when stimulated these neurons evoked movement, the pattern of which was not coded in their sequence of spikes
- Neural decision-making

57
Q

What was found in command neurons in mice?

A

In mice it was found that brainstem neurons were found to be responsible for stopping locomotion

58
Q

what are characteristics of the basal ganglia?

A
  • largest sub-cortical structures in the forebrain
  • paired nuclei
  • no direct sensory inputs
  • no direct motor outputs
  • disease of the basal ganglia: primarily movement disorders, neuropsychiatric symptoms, related to addiction, learning and memory
    *so basically everything
59
Q

What is the Basal ganglia motor loop?

A

It results in the activation of the supplementary motor area (SMA) before and during moving

60
Q

What are the symptoms of Parkinson’s disease?

A
  • Tremor
  • Rigidity
  • Akinesia/Bradykinesia (weakened contribution of SMA prior to movement)
  • Posture
61
Q

What do mirror neurons do?

A

they help us observe actions of others, helpful to the survival of species.

62
Q

What is the definition of pain?

A

An unpleasant sensory and emotional experience associated with, or resembling that associated with actual or potential tissue damage.

63
Q

What is acute pain?

A

It is essential to avoid injury
-withdrawal reflex is observed across species

64
Q

What is chronic pain?

A
  • pain that lasts 3-6 months after initial injury
  • pain experienced is no longer beneficial for survival
65
Q

What are different pain pathways?

A

Spinothalamic tract
* Spinoparabrachial tract
* Spinoreticular tract
* Spinomesencephalic tract

66
Q

What is the gate control theory: Melzack and Wall (1965)?

A
  1. There are unlimited c fibers and small diameter A-delta are stimulated by injury and convey impulses to transmission cells in the spinal chord (T)
  2. T-cells receive input from large A-beta fibers
  3. T-cells receive inhibition from interneurons
  4. descending pathways influence inhibitory interneurons
67
Q

What does the stimulation of PAG do?

A

it induces analgesia, which is pain relief without the loss of consciousness

68
Q

What are some antinociceptive mechanisms of the brain?

A
  • Thalamic gate attention control, deconditioning, relearning
  • Descending inhibition
  • Gate control
  • Long term depression
  • Adaptation
  • fatigue
69
Q

What does Antinociceptive mean?

A

it means the action or process of blocking painful stimulus

70
Q

What are some Pronociceptive mechanisms of the brain?

A
  • Reorganization
  • conditioning
  • Catastrophizing
  • Descending facilitation
  • Central sensitization
  • Long-term potentiation
  • Peripheral sensitization
71
Q

What does Pronociceptive mean?

A

To carry or amplify the signal induced by the stimulus

72
Q

What are the different types of memory + how long do they last?

A
  1. Sensory (milliseconds to seconds)
  2. Short-term and working (seconds to minutes)
  3. Long-term nondeclarative (minutes to years)
  4. Long-term declarative (minutes to years)
73
Q

What is the Atkinson and Shiffrin model of memory?

A

It says that sensory information enters the information-processing system and is first stored in a sensory register.
- Then items are selected (via attentional processes are moved into short-term storage and with time can be moved to long-term

74
Q

What is the Baddeley and Hitch model of memory?

A

Three part working memory system, central executive that controls two subordinate systems
1. the phonological loop, encodes info acoustically in working memory
2. visual sketch pad, encodes info visually

75
Q

How are the hippocampus and amnesia connected?

A

A person by the initials H.M. suffered from epilepsy, surgery in 1953 (bilateral medial temporal lobe removed
- he was left with normal IQ but the surgery left with severe anterograde amnesia
- short-term memory was still intact

76
Q

What is plasticity?

A

Neuronal plasticity describes the ability of the nervous system to be modified after birth
- synaptic plasticity means the strengthening or weakening of synaptic junctions

77
Q

What is Anisomycin?

A

It is a protein synthesis blocker