Digestion Flashcards

1
Q

What are nutrients?

A
  • chemical substances found in foods that are used in human body
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2
Q

Why are some nutrients essential?

A
  • essential nutrient = ones that cannot be synthesised
    • obtained from food only
  • water (is synthesised however, not sufficient amount)
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3
Q

What are two groups of vitamins?

A
  • water-soluble and lipid-soluble
    • water-soluble are easily excreted
    • lipid-soluble = A D E K (rest is water-sol.)
  • vitamins do not have a common structure
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4
Q

What is malnutrition?

A
  • imbalance of nutrients that causes health problems
    • deficiency, imbalance or excess
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5
Q

What are minerals?

A
  • essential chemical elements found in food (ions)
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6
Q

What are different minerals and their function?

A
  • Ca2+ — secondary messenger in signalling (muscle contraction. synapse); component of bones
  • Fe2+ — part of heme
  • Zn2+ — zinc fingers (found in proteins, enzymes)
  • Na+, K+ — membrane potential; signalling
  • I- — thyroid hormones (growth); nervous system development; metabolic processes
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7
Q

Are vitamins universal for all organisms?

A
  • no
  • some substances which are synthesized by human body may be vitamins for other animals
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8
Q

What is the role of vitamin C?

A
  • antioxidant
    • reduces molecules (electron donor)
    • during immunological response
    • synthesis of collagen
  • deficiency = scurvy
    • leads to bleeding gums and under skin
  • found in: veggies and fruits
  • unstable – amount lowers with time, temp increase, exposure to metals (iron and copper)
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9
Q

Do rats synthesise vitamin C?

A
  • yes
  • experiments with vitamin C deficiency could not be performed on rats
  • rats produce their own ascorbic acid (not a vitamin for them)
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10
Q

What are the consequences of scurvy?

A
  • pain in joints (lack of collagen)
  • haemorrhages (bleeding) from gums, under skin, disintegration of blood vessel walls
  • teeth loss
  • even death
  • anaemia
  • osteoporosis
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11
Q

What is the role of vitamin D?

A
  • produced in skin irradiated with UV
    • risk of skin cancer
    • instead of vitamin it should be prohormone
  • turned into calcitriol
    • transcription regulator for genes connected to calcium
  • Ca homeostasis
    • bone mineralisation, muscle contraction, nervous and cellular signalling,
    • immune response
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12
Q

What are the consequences of overdosage of vitamin D?

A
  • toxicity symptoms and hypercalemia
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13
Q

What is RDA (recommended daily amount) of vitamin D?

A
  • 30 min exposure to sunlight UV (or more)
  • depends on latitude, ageing, season, skin pigmentation, clothing
  • dietary supplementing needed
    • 5 μg/day
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14
Q

What are the consequences of vitamin D deficiency?

A
  • rickets
    • impeded growth, long bones deformation
  • osteomalacia
    • impaired calcium deposition in bones
    • lower mineral density
    • posture abnormalities
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15
Q

What are essential fatty acids?

A
  • omega 3 and 6
    • unsaturated
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16
Q

What are essential amino acids?

A
  • Phenylalanine
  • Threonine (if no Phe)
  • Valine
  • Tryptophan
  • Methionine
  • Leucine
  • Isoleucine
  • Lysine
  • Histidine
  • Arginine (in infants)
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17
Q

What are the consequences of starvation?

A
  • scarcity of food leading to deficiencies
  • lack of protein
    • breakdown of muscle tissue and other
    • instead essential amino acid are produced
      • cardiac muscle can be destroyed
  • anorexia = reduced appetite
    • anorexia nervous = psychiatric illness, voluntary starvation
      • weight, hair loss
      • loss of energy
      • skin bruises
      • suspension of menstrual cycle and ovulation
      • reduced blood pressure, slower heart rate
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18
Q

What are the consequences of plasma protein deficiency?

A
  • lack of amino acids —> lack of important blood plasma proteins (albumins)
    • maintain colloid osmotic pressure
  • tissue fluid doesn’t come back to circulatory system
    • retended in tissues
  • tissue swelling (in abdomen) = edema
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19
Q

What is phenylketonuria?

A
  • autosomal recessive genetic disorder
    • diagnosed in infants
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20
Q

What are the causes and consequences of phenylketonuria (PKU)?

A
  • caused by lack of enzyme converting phenylalanine —> tyrosine
  • phenylalanine converted into phenylpyruvate
    • later in urine
  • impairment of brain development
    • mental retardation
    • brain damage
    • seizures
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21
Q

What is PKU treatment?

A
  • incurable
  • low-phenylalanine diet
    • meat, nuts, cheese, dairy, legumes —> a lot
    • controlled amounts: bread, pasta, corn, potatoes
  • diet not enough
    • medication (BH4)
      • removal of phenylalanine
    • supplementing of tyrosine
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22
Q

How is appetite controlled?

A
  • Appetite Control Centre (ACC) in brain (hypothalamus)
  • sugar levels
    • insulin
  • adipose tissue
    • leptin
  • stomach filling state
    • ghrelin
  • smell (tasty or disgusting)
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23
Q

What are the risks of obesity?

A
  • diabetes II
  • high blood pressure
  • arteriosclerosis (atherosclerosis)
  • joint damage
  • impotence
  • self-esteem issues
  • thyroid dysfunctions
  • cancer
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24
Q

What are exocrine glands?

A
  • substances sent out of body
  • release them to ducts
    • not to blood stream (like endocrine glands)
  • examples: sweat, moll, mammary, sebaceous
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25
What are parts of alimentary canal?
- mouth, large intestine, small intestine, oesophagus, stomach, duodenum, rectum
26
What are digestive glands?
- salivary glands - pyloric glands - stomach - pancreatic exocrine and endocrine glands - goblet cells - small intestine
27
What are accessory organs?
- teeth, liver, gall bladder, bile duct, salivary glands, tongue, pancreas
28
What is digestion?
- enzymatic breakdown into monomers
29
Which molecules are digested?
- lipids —> fatty acids and glycerol - lipase + bile - proteins —> amino acids - pepsin - polysaccharides —> monosaccharides - amylase - beta-D-glycosidic bond no digested (cellulose) - nucleic acids —> nucleotides
30
What is the role of mouth in digestion?
- teeth: chewing - tongue: mixing food with saliva + pushing bolus to oesophagus - saliva - antimicrobial gents (lysosomes) - digestion of starch by amylase - moistens bolus
31
What is the role of stomach in digestion?
- churning and mixing bolus with water and acid - muscle tissue - HCl - kills microorganisms - protein denaturation - protein digestion (pepsin) - bolus —> chyme
32
What happens during the first phase of gastric secretion?
- cephalic phase - signal is sent to the brain (senses)
33
How is acid maintained in the stomach?
- gastric acid in lumen - protection: mucus + dead cells - acid could damage stomach - proton pump (H+/K+ ATPase) - lower pH by exchanging H+ and K+ - acid overproduction = inhibitors of the pump (medication) - not permanent —> pumps are recycled
34
What is stomach ulcers?
- gastric ulcers - lesion in stomach wall - lining exposed to juice - bleeding and pain - stress may contribute
35
What is Helicobacter pylori?
- bacterium - gastric mucous membrane destroyed - stomach ulcers - inflammation, toxins, exposure to acid, production of urease (toxic ammonia), more acid production - peptic ulcers can lead to cancer - H. pylori infections correlate
36
What is the role of pancreas in digestion?
- in duodenum (pancreatic juice) - endopeptidases (proteases) activates pepsin in stomach - lipase - amylase - HCO3- ions neutralise acid - nuclease
37
What is the protein regulating pH in stomach?
- proton pump - H+/ K+ ATPase
38
What is the role of bile?
- emulsifies lipids - lipase water soluble - lipids aren’t - dispersion of lipids = larger surface area - not an enzyme
39
How are sugars digested?
- starch (other polymers of glucose) —> maltose (by amylase) - at the surface of small intestine - maltose —> glucose (by maltase) - easy absorption
40
What is the function of endopeptidases?
- cut polypeptide chains in the middle - recognises bonds - producing shorter and shorter chains - individual amino acids
41
What happens in small intestine?
- digestion (beginning) and absorption (later) - neutralising stomach acid
42
What allows for the movement of chyme?
- peristalsis - smooth muscles - away from mouth - circular muscles – no movement backwards - longitudinal muscles – movement along gut - vomiting = contraction of abdominal muscles - slow = time for digestion - another function of peristalsis: segmentation
43
How is role of villus?
- increases surface area for absorption - microvilli (increase even further) - blood vessel + lacteal (part of lymphatic system, lipid absorption)
44
What are the layers of small intestine?
- mucosa (closest to lumen) - folded inner layer (villi) - sub-mucosa - connective tissue - separation: mucosa - muscles - muscle layer - out: longitudinal - in: circular - serosa - most outer protective layer - fibrous connective tissue
45
Why do tight junctions exist?
- no substances can go between villi (absorption)
46
What are the adaptations for absorption?
- large surface area - villi & microvilli - short distance - single epithelial - concentration gradient - dense capillary network (blood flow) - lacteal for lipids - control of transport - tight junctions between cells
47
What is the structure of brush border cells?
- effective absorption - polarity - absorption surface and capillary facing surface - microvilli - mitochondria - protein transporters, pumps and channels - nutrients into bloodstream
48
What is the type of transport used to move sugars?
- glucose / galactose - co-transport (Na+) —> epithelial cells of villi - monosaccharides - facilitated diffusion —> capillaries - other sugars - facilitated diffusion —> epithelial cells of villi - monosaccharides (the same)
49
What is co-transport?
- protein that can bind 2 molecules - Na+ binds (moves down the gradient) - another molecule binds and is moved with the energy of Na+ (or other molecule) - against the gradient (active transport)
50
What is the type of transport used to transport proteins?
- amino acids - co-transport (Na+) —> epithelial cells (villi) - amino acids - simple diffusion —> capillaries - peptides (<5 a. a.) - co-transport (H+) —> villi - amino acids
51
What is the type of transport used to move lipids?
- triglycerides —> fatty acids + monoglycerides - simple diffusion —> epithelial cells of villi - fatty acids - facilitated diffusion (fatty acid transporters in microvilli) - inside epithelium cells —> recombines to triglycerides - cannot diffuse back - triglycerides with cholesterol —> form LDL - exocytosis —> villi - enter lacteal - lymph or bloodstream
52
What happens in large intestine?
- re-absporption of water - digestion of carbohydrates (symbiotic bacteria) - some of the products that are not digested in small intestine - formation of faeces
53
What is the pathway of starch to glucose?
- starch —> dextrins + maltose - amylase - intestinal lumen - dextrins + maltose —> glucose - enzymes + cells of brush border - glucose absorbed - facilitated and active transport - glucose to liver (in blood), absorbed in liver - triggered by glucagon - facilitated diffusion - glucose —> glycogen
54
Why is fibre important in egestion?
- movement of chyme and faeces - easy defecation - cellulose, waxes, lignin - absorbs water
55
What happens to water in large intestine?
- absorbed - contains many secretions (dilutes them) - easy absorption - speed of peristalsis - low speed —> constipation - high speed —> diarrhoea
56
What is cholera and its mechanism?
- cholera toxin produced by Vibrio cholerae - binds to epithelium in intestines - cascade: Cl-, Na+, HCO3- to gut lumen - water flows by osmosis —> extreme diarrhoea - dehydration
57
What are the functions of the liver?
- storage - glucose - lipids - detoxification - NH3 - bile production - metabolism
58
What are the 3 blood vessels involved in liver circulation and their function?
- hepatic artery (incoming) - oxygen-rich blood - arterioles join sinusoids - hepatic portal vein (incoming) - blood from stomach and intestines (rich in nutrients), low oxygen - hepatic vein (coming out) - venues merge with sinusoids - blood to vena cava
59
What is the structure of the liver?
- built out of lobules - branches of portal veins and hepatic artery (to the central vein) - sinusoids — blood leaks from veins to structures - hepatocytes — washed by blood in sinusoids - direct uptake
60
What is the structure of a sinusoid?
- wide blood vessels (wider than capillaries) - fenestration — pores between endothelial cells - blood in direct contact with hepatocytes - Kupffer cells — macrophages (destroy erythrocytes) - no basal lamina (net of proteins) - no barrier - no tight junctions
61
How are nutrients stored in the liver?
- glucose - condensed to glycogen - released by glucagon - excess glucose = no osmotic balance - amino acids - excess toxic - vitamins A, D, B12, K - excess toxic - iron - toxic in the form of ions - stored with proteins (transferrin) - Kupfer cells kill erythrocytes - iron is uptaken (not wasted) - copper (used as coenzyme)
62
Where are plasma proteins produced?
- in endoplasmic reticulum and Golgi apparatus in hepatocytes (liver) - a lot with secretory granules - produced: albumins, fibrinogen - hepatocytes
63
What is the pathway of cholesterol? | How is it absorbed
1. cholesterol and triglycerides absorbed - incorporated into chylomicrons (large lipoproteins) 2. secreted into lymph and later in liver 3. fat to adipose tissue - taken up as fatty acids 4. small chylomicrons remnant removed from plasma by liver - as HDL 5. converted into bile
64
What is the pathway of triglycerides?
- fatty acids + triglyceride (with cholesterol) —> (very)LDL - between meals - fat to adipose and muscle tissues (chylomicron) - energy use or storage
65
What are functions of cholesterol?
- synthesis - vitamin D, steroid hormones, bile - membrane components
66
How does liver detoxify substances?
- toxic substances from blood - oxidised - processed by enzymes - alcohol dehydrogenase - production of urea - hydrophobic compounds —> transferred into hydrophilic - liver has regenerative potential
67
How does liver recycle erythrocytes?
- lifespan: 120 days - Kupffer cells - ingestion by phagocytosis - recycling - heme - iron —> production of new cells - bilirubin —> bile - globin (amino acids) —> return to bloodstream
68
Where is bile formed and what are its components?
- produced by liver, stored in gall bladder - released via bile duct (duodenum) - components: hydrogen carbonate ions, bile salts and pigments, cholesterol
69
What is jaundice?
- yellow skin, conjunctives and mucous membranes - high concentration of bilirubin (bile pigment) - liver disjunction - hepatitis - liver cancer - obstruction of bile duct - newborn jaundice: immature processes of bilirubin excretion
70
What are the consequences of jaundice?
- no need for treatment (as it is a symptom) - bilirubin accumulation in nervous tissue - neurological damage (brain) - infants and elderly
71
What are conditionally essential vitamins?
- conditionally essential: vitamin D&K - needed only in some circumstances (ex. vit K is needed for infant’s microbe which is underdeveloped)
72
What is the structure of exocrine glands?
- secretory cells in groups = acinus - around duct branch (not to bloodstream) - lots of endoplasmic reticulum and mitochondria - secretory vesicles - exocytosis to the ducts
73
How is iron reused in synthesis of red blood cells?
- red blood cells have transferrin receptors - synthesised in bone marrow by stem cells - receptor-iron complex enters cells - iron incorporated to heme
74
How are gastric juices regulated?
- nerves and hormones regulate digestive juices - sight / smell of food —> nerve impulses from brain via vagus nerve - from medulla - gland cells in stomach —> secrete components of gastric juice - chemoreceptors in stomach wall detect peptides - or stretch receptors detect distension of stomach - impulses to brain - brain —> vagus nerve - to endocrine cells (duodenum) —> gastric secretion - gastric —> secretion of acid and pepsinogen (exocrine gland cells in stomach wall) - secretin and somatostatin inhibit gastric secretion —> pH too low