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Shan Ali ' Carbohydrates & lipids Usle Englisch 24 Karten

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  1. 1Glucose:Glucose: aka dextrose, 6 carbons, aldose (aldehyde functional group)
    - Main energy source (broken down to CO2 & H2O, releasing ATP)
    - Used to produce other monosaccharides (fructose, galactose, ribose)
    - Clinical: High blood glucose in diabetics, reduced to sorbitol in eyes causing cataracts, glucose excreted in urine in diabetics
    - α-Glucosidase inhibitors slow the production of glucose from dietary carbohydrates (reduce spike after meal). No effect on lactose digestion (disaccharide lactose contains a β-glycosidic bond, not an α-glycosidic bond).
  2. 2Fructose:6 carbons, keto sugar (ketone functional group)
    - Component of sucrose
    - Present in semen and the sperm cells use fructose as the energy source for their metabolism
    4
    - Clinical: Hereditary fructose intolerance (genetic aldolase-B deficiency, part of newborn screening panel) presents as hypoglycemia (seizures) and vomiting after meals in baby who weaned from breastfeeding
  3. 3Galactose6 carbons, aldose sugar
    - Component of lactose
    - Clinical: Classic galactosemia (autosomal recessive deficiency of GALT enzyme), presents in infancy, first few days, vomiting/diarrhea after breastfeeding, lactic acidosis, ketosis, liver failure, jaundice, hepatomegaly, failure to thrive, cataracts if untreated (galactose -> galactitol in eyes)
  4. 4Ribose5 carbons, also modified todeoxyribose
    - Component of nucleotides (RNA, DNA)
  5. 5Glyceraldehyde and Dihydroxyacetone.3 carbons, glycolysis intermediate All of the above are sourced from diet.
  6. 6Maltose: aka malt sugar,Maltose: aka malt sugar, 2 glucose units with α (1→4) linkage
    - Present in malt and also formed when starch/glycogen undergo partial hydrolysis
  7. 7Isomaltose:2 glucose residues with α (1→6) linkage
    - Formed when starch/glycogen undergo partial hydrolysis
  8. 8Sucroseaka cane sugar / table sugar, made of glucose and fructose - Found in sugar cane, sugar beet, pineapple, carrot roots
  9. 9Lactose:aka milk sugar, made of glucose and galactose - Found milk/dairy (clinical: lactose intolerance)
  10. 10Starchcomponents are amylose (unbranched α 1→4 glucose) and amylopectin (α 1→4 glucose with α 1→6 branches)
    - Source of dietary glucose, broken down during digestion
    - Storage form of carbohydrate in plants
    Cellulose: glucose linked by β 1→4 glycosidic bonds
  11. 11Celluloseglucose linked by β 1→4 glycosidic bonds
  12. 12Glycogenhighly branched α 1→4 glucose with α 1→6 at branching points
    - Storage form of carbohydrate in animals, broken down during digestion 5
    - Stored in kidney, liver (blood glucose regulation), muscle (energy for contraction)
    - Clinical: glycogen storage diseases (Von Gierke, Pompe, Herss
  13. 13GlycosaminoglycansrslfateHui
  14. 14Fatty Acids: have a methyl group, an acidic group and a hydrocarbon chainStructure:
    - Divided into categories by length
    o Short chain FA (SCFA): up to 6 carbon atoms
    o Medium chain FA (MCFA): from 8 to 12 carbon atoms
    o Long chain FA (LCFA): from 14 to 18 carbon atoms (e.g. palmitic acid [C16])
    o Very long chain FA (VLCFA): from 20 carbon atoms onwards. Transported in the bloodstream by chylomicrons (e.g. eicosapentanoic acids (EPA) [C20], Docosahexaenoic (DHA) [C22] )
    6
    - Saturated FA contains no double bonds
    - Unsaturated FA contains one (monounsaturated) or more (polyunsaturated) double bonds
  15. 15Fatty acids functionFunction:
    - MUFA (e.g. oleic acid) and PUFA (e.g. linoleic, linolenic, arachidonic acid) prevent atherosclerosis and myocardial infarction
    - Naturally occurring FAs are in cis form (component of cell membranes)
    - Trans FAs implicated in atherosclerosis formation
  16. 16Fatty acid locationTAG from adipose converted to plasma FFA (free fatty acids), transported on serum albumin to tissues (where they are oxidized for energy)
    - Major energy reserve of the body: esterified FA (TAG) in white adipose tissue (WAT)
    - Essential FAs must be supplied in diet (can’t be synthesized by body)
    o E.g. linoleic (ω-6 FAs), linolenic (ω-3 FAs)
    o Arachidonic (ω-6 FAs) acid is essential if linoleic acid is deficient in diet
  17. 17Triglycerides (Fat): glycerol + 3 fatty acids- Storage form of lipids in human adipose tissue, broken down for energy
    - TAGs composed primarily of saturated FAs are called saturated fats
    o Source: dairy products and meat
    o Clinical: associated with  total plasma cholesterol
  18. 18Phosphatidylcholine or Lecithin:composed of glycerol, FA, P and choline
    - Found in plasma membrane
    - Dipalmitoyl phosphatidylcholine serves a constituent of lung surfactants and prevents
    collapse of the alveoli during expiration.
    - Clinical: Deficiency of lung surfactant causes respiratory distress syndrome (infants).
  19. 19Phosphatidylinositol:composed of glycerol, FA, P and inositol
    - Function: cell signaling
    Sphingomyelin: composed of sphingosine, fatty acids, phosphates, and choline - Function: structural lipid of nerve fiber’s myelin sheathe
    o Helps insulate for faster conduction of nerve impulse
  20. 20Glycerophospholipids (phosphoglycerides):)contain phosphatidic acid (DAG (diacylglycerol) with
    a phosphate group on carbon 3)
    - Function: predominant lipids in membranes
    A key concept in glycerophospholipid synthesis is activation, of either DAG or the alcohol to
    - Clinical: platelet activating factor (PAF), an ether glycerophospholipid, activates inflammatory cells and mediates hypersensitivity, acute inflammatory, and anaphylactic reactions
  21. 21Glycolipids (Glycosphingolipids):- Composition: cerebrosides (ceramide monosaccharides), e.g. glucocerebroside,
    galactocerebroside
    - Location: brain and peripheral tissue
    - Clinical: Sphingolipidoses (liposomal storage diseases) are caused by defective liposomal degradation of glycosphingolipids (e.g. Gaucher’s, Niemann-Pick, Tay-Sachs)
  22. 22Cholesterol:- Function:
    o Contributes to fluidity in plasma membranes
    o Precursor of bile, steroid hormones (cortisol, testosterone, estrogen), and vitamin D - Clinical:
    o Atherosclerosis (cholesterol deposits on blood vessels) → higher risk of cardio-, cerebro-, and peripheral vascular disease
    o Increased cholesterol in red cell membranes causes membrane rigidity → hemolysis of RBC as they pass through tiny capillaries
  23. 23Plasma lipoproteins:contains lipids & proteins; transports lipids in blood - Types & functions:
    o Chylomicrons: transports digested/absorbed lipids from intestine to other tissues
    o Very low-density lipoproteins: transports TAG from liver to extra hepatictissues
    o Low-density lipoproteins: transports cholesterol from liver to extra hepatic tissues
    o High-density lipoproteins: transports cholesterol from extra hepatic tissues to liver
  24. 24Eicosanoids:20-carbon polyenoic (many unsaturated bonds) fatty acids
    - Functions: promotion of inflammation, blood pressure regulation, control of platelet
    aggregation
    - Types
    o Prostaglandins o Prostacyclins o Leukotrienes
    o Thromboxanes
    - Clinical: NSAIDs (non-steroidal anti-inflammatory drugs) such as aspirin and ibuprofen inhibit prostaglandin synthesis

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Usle ' Carbohydrates & lipids Karteikarten am Ohne Titel, erstellt von Shan Ali am 23/08/2022.
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