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293 Cards in this Set
- Front
- Back
peroxisome
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contains catalase that can break down hydrogen peroxide (H202) into water
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cytoskeleton
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holds shape for cells
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cytoplasm/cytosol
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gel-like substance containing organelles, protein, electrolytes, and other molecules. Also holds shape of cell
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centrioles
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cell devision. acts as anchors
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nuclear membrane
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protects the nucleus. phospholipid bilayer- polar hydrophilic heads, hydrophobic fatty acid tails. allows flow of compounds in and out of nucleus
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cell membrane/plasma membrane
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protects the cell. phospholipid bilayer- polar hydrophilic heads, hydrophobic fatty acid tails. bilayer contains embedded proteins, CHOs, and lipids. proteins act as receptors to external stimuli that regulate movement of substances in and out of the cell. allows flow of compounds in and out of cell.
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nucleolus
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where ribosomes are synthesized
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nucleus
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contains the DNA in the cell. molecules of DNA provide coded instructions used for protein synthesis
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mitochondrion
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produce most of the energy (ATP) used by the cells (powerhouse)
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golgi apparatus
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a series of membrane sacks that process and package proteins after they leave the rough ER (post-translation)
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Rough ER
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a series of membrane sacks that contain ribosomes that build and process proteins
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ribosomes
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build and process proteins
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smooth ER
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region of the ER involved in lipid synthesis. Doesn't contain ribosomes.
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lysosome
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contains digestive enzymes that break up proteins, lipids, and nucleic acids. they also remove and recycle waste. (digestive enzymes)
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vili and microvilli are in which type of cells?
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intestinal cells
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integral protein
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goes through bilayer. passage/carrier of things/compounds in and out of the cell
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peripheral protein
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doesn't go through, sits on the surface. an example includes glycoprotein. identification, recognition, communication within the cell. could also be receptors and attach things to the cell
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oligosaccharides are made up of what?
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glucose units
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what are glycoproteins made up of?
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proteins attached to oligosaccharides
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glycolipids
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when oligosaccharides are attached to the polar heads of the bilayer. more likely to be peripheral.
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glycocalyx
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the whole entity of proteins and lipids that contain oligosaccharides and are recognition. more likely to be peripheral.
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cholesterol
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fluidity/rigidity/structure of the cell membrane. it is the yellow within the bilayer
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passive transport
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higher to lower concentration. integral protein
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active transport
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requires ATP (energy). integral protein
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sodium potassium pumps
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glucose and sodium enter cells
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do integral proteins do passive or active transport?
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both
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what does DNA stand for?
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deoxyribonucleic acid
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what is the role of the nucleus
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contains DNA, cell division/replication, cell proteins made here (mRNA)
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is the cytoplasm aerobic or anaerobic glycolysis?
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anaerobic - in the absence of oxygen
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what does HMP shunt stand for?
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hexose monophosphate shunt
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where is the HMP shunt located?
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in the cytoplasm of the cell
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what is the other term for the HMP shunt?
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PPP (pentose phosphate pathway)
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what is the HMP shunt? what does it do?
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an offshoot of the glycolytic pathway. it generates ribose sugars for RNA and DNA. its involved in the formation of reducing equivalents (NADPH2) for lipid synthesis
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where does glycogenesis and glycogenolysis occur?
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in the cytoplasm of muscle and liver cells
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what does glycogenesis mean?
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the making of new glycogen
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what does glycogenolysis mean?
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the breaking down of glycogen
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you make and break ________ in the muscle for the muscle you are actually using
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glycogen
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when does the liver make and break glycogen?
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when glucose drops (examples-overnight in a fasting state)
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where does fatty acid synthesis occur?
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in the cytoplasm of the cell
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why can't fatty acids break down in the cytoplasm?
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because oxygen is necessary. break down occurs in the mitochondria because it contains oxygen.
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What does TCA stand for?
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Tricarboxylic acid cycle
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where does the TCA cycle occur?
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the mitochondria
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what are the other names for the TCA cycle?
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the Kreb's cycle and the citric acid cycle
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where does Beta oxidation occur?
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the mitochondria
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what does ETC stand for?
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Electron Transport Channel
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where does ETC occur?
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the mitochondria
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does aerobic or anaerobic glycolysis occur in the mitochondria?
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aerobic because there is oxygen present
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what is the RBC's only source of energy production? Why?
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glucose. it can't use fat for energy because it uses anaerobic glycolysis
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what are the pyrimidines in DNA?
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Thymine and cytosine
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what are the purines in DNA?
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Adenine and guanine
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which is one ring and which is two ring? pyrimidines or purines?
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pyrimidines are one ring, purines are two rings
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deoxyribose
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absence of oxygen
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which pyridines and which purines pair together?
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AT & CG
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replication
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the making (synthesis) of two new daughter strands of DNA from 1 parent strand. these strands are identical to the parent DNA. In replication, the double helix unravel (cell division) and incoming nucleotide bases first pair with the complimentary bases in the template and then are connected through phosphate diester bonds.
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the differences between DNA and RNA
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DNA: no oxygen, 2 strands, T (not U)
RNA: oxygen present, 1 strand, U (not T) |
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transcription
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the genetic information in a single strand of DNA makes a specific sequence of bases in a messenger RNA (mRNA) chain. a single strand of DNA can make many copies of the corresponding mRNA. basically, transcription results in the synthesis of a strand of mRNA through complementary base pairing. this base pairing is similar to DNA replication except that the purine adenine (A) pairs with the pyrimidine uracil (U) instead of with thymine (T). starts in the nucleus, ends in the cytoplasm.
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translation
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the process by which genetic information in an mRNA molecule specifies the sequence of amino acids in the protein product. after the mRNA is synthesized in the nucleus, it is exported into the cytoplasm where it is attached to ribosomal RNA (rRNA). There, the transcribed genetic code is used to bring amino acids into a specific sequence that produces a protein with a clearly defined function. then, the mRNA strand directs protein translation with the help of tRNA subunits and their associated amino acids. During translation, the double helix of DNA makes new strands by base pairing.
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mRNA
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the template for protein synthesis; the form of RNA that carries information from DNA in the nucleus to the ribosome sites of protein synthesis in the cell
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rRNA
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the RNA part of a ribosome, and is essential for protein synthesis
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tRNA
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One of a class of RNA molecules that transport amino acids to ribosomes for incorporation into a polypeptide undergoing synthesis
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elongation
|
peptide bonds are formed between the aligned amino acids that were positioned according to codon-anticodon association. elongation extends the polypeptide chain of the protein products by translation. elongation is then the addition of carbons (in two-carbon increments) to a fatty acid chain.
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post-translation
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the newly synthesized protein may require some chemical, structural, or spatial modification to attain its active form
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what do RNAs travel through in the membrane once they have been made?
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gap junctions
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in the glycolytic pathway, are most reactions reversible or irreversible?
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reversible
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Reversible reactions
|
near equilibrium reactions,
same enzyme catalyses in both directions, |
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near equilibrium reactions
|
A <=> B. rate slows down if A is increased, if A is increased, B decreases (this is feedback inhibition)
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feedback inhibition
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A cellular control mechanism in which an enzyme that catalyzes the production of a particular substance in the cell is inhibited when that substance has accumulated to a certain level, thereby balancing the amount provided with the amount needed.
|
|
example of when the same enzyme catalyzes in both directions
|
pyruvate <-----> lactate
enzyme: LDH (lactate dehydrogenase) NADH2 is being oxidized to NAD |
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irreversible reactions
|
non-equilibrium reactions (A-->B)
a different enzyme required to reverse products of non-equilibrium reaction may be allosteric regulators |
|
allosteric regulator and example
|
an effector that binds to a protein/enzyme to regulate it. example includes citrate, which is an allosteric regulator of glycolysis because its a product that occurred in a pathway that effected another pathway. when citrate (fat synthesis) in the TCA cycle increases, PFK and glycolysis decreases.
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classes of enzymes
|
oxidoreductases
transferases hydrolases lyases isomerases ligases |
|
oxidoreductases
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dehydrogenaes (NADH2), reductases
enzymes are usually involved in transfer of hydrogens and electrons in Electron Transport Chain (ETC) |
|
transferases
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transfer of carbon, nitrogen, or phosphate containing groups. example: protein metabolism, aminotransferases
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ALT means what?
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alanine amino transferase
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what do aminotransferases do?
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takes amine group (N) off of an amino acid and puts it on alpha keto acid
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amino acid 2 must be essential/nonessential because the body makes it?
|
nonessential
|
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hydrolases
|
C-C is broken by water
|
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lyases and example
|
cleaving (breaking) C-C, C-N, and some C-S bonds
example: citrate (6 carbons) ---> OAA (4 C) + acetal (2 C) enzyme: citrate lyase breaking C-C bonds by going from 6C to 4C and 2C |
|
isomerases and example
|
interconversion of atoms within a molecule
example: glucose-6P --> fructose-6P |
|
ligases and example
|
synthase (joining things). formation of bonds between Carbon and other atoms (O, S, N)
example: pyruvate (3C) + CO2 (1C) ----> OAA (4C) ATP --- ADP +Pi usually involves hydrolysis of high energy phosphate compounds (the breakdown of ATP) |
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what is the immediate energy source of the cell?
|
ATP
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how many ATP does NADH2 produce?
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3 ATP
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how many ATP does FADH2 produce?
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2 ATP
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glucose vs. glycogen
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glycogen is the storage form of glucose
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true or false, the breakdown of CHO, Protein, and fat directly yields energy
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false - its from ATP first
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The structure of ATP
|
3 phosphate groups attached to ribose and adenine (adosine triphosphate)
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what are high energy phosphate bonds and what do they bind?
|
they are bonds in ATP that produce energy when broken
they bond gama~beta~alpha |
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1 kcal = ? calories
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1000 calories
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1 cal = ? J (joules)
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4.18 J
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1 kcal = ? kJ
|
4.18 kJ
|
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exothermic
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energy yielding/releasing (-deltaG)
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endothermic
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energy consuming (deltaG)
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each metabolic pathway is overall exothermic/endothermic? why?
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exothermic because they release energy
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substrate level phosphorylation
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phosphate from substrate is used in the formation of ATP and is dropped (NOT PLACED ON PRODUCT)
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what is oxidative phosphorylation and where does it take place?
|
takes place in the electron transport chain. it is when electrons are getting passed down the chain and protons (H+) are getting pumped from the matrix into the inter membrane space. this pumping of H+ helps by creating enough energy to phosphorylate ADP to ATP. electrons and protons are passed through by redox reactions. energy is created with passively transported into the matrix.
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which produces more ATP and why? substrate level phosphorylation or oxidative phosphorylation?
|
oxidative phosphorylation produces more ATP than substrate level phosphorylation because it involves NADH2 and FADH2 which, together create 5 ATP.
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how long is the digestive tract?
|
16 ft. in length
|
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what are the layered (tunics) walls of the GI tract?
|
mucosa
submucosa muscularis externa serosa |
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mucosa
|
1st set of cells lining the muscular tube. epithelial cells. brush boarder area (SI). comes in contact with food
|
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submucosa
|
anchors mucosa to muscularis externa
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muscularis externa
|
paristalsis occurs here. longitudinal and circular muscles.
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serosa
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outermost layer
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what are the structures of the upper GI tract?
|
1. mouth (salivary glands)
2. pharynx passageway 3. esophagus (lower esophageal sphincter) 4. stomach (pyloric sphincter/valve) after stomach |
|
what are the salivary glands of the mouth mostly made up of? what are the 3 components?
|
mostly made up of water
1. parotid, sublingual, submandibular (submaxillary) 2. alpha amylase (starts to break down starches in the mouth) 3. salivary IgA |
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where does peristalsis occur?
|
the esophagus
|
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what does the lower esophageal sphincter do?
|
helps prevent foods from coming back up
|
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how much does the stomach hold when empty? how much does it hold when full?
|
2 oz when empty, 37-52 oz when full
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what is the analogy used when the stomach gets rid of its contents in the SI?
|
a pastry sleeve or toothpaste
|
|
lingual lipase
|
in infants, breaks down fat in the mouth
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what is the primary nutrient being broken down in the mouth
|
CHO
|
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what are the 3 glands of the stomach
|
cardiac glands
oxyntic pyloric |
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where are cardiac glands?
|
upper part of the stomach- neck, endocrine cells
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where are oxyntic glands?
|
neck, endocrine, parietal, chief cells
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where are pyloric glands?
|
neck, endocrine, parietal
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what does the neck produce?
|
mucus and bicarbonate
|
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what does endocrine produce?
|
hormones
|
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what does parietal produce?
|
secretes hydrochloric acid, which denature's protein sterolizers and converts pepsinogen to pepsin. it also secretes intrinsic factor, which helps absorb B12
|
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what does chief cells produce?
|
secretes pepsinogen
|
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where does protein digestion mainly take place?
|
mainly takes place in the stomach
|
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what are the structures of the lower GI tract?
|
small intestine
large intestine |
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what are the parts of the small intestine?
|
duodenum
jejunum ileum esophagus |
|
how long is the duodenum?
|
1 ft. long
|
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how long is the jejunum and ileum together?
|
9 ft. long
|
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how long is the esophagus?
|
5 ft. long
|
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how long is the total small intestine?
|
15 ft. long
|
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where is the ileocecal value and what is it?
|
on the right side of the body. it connects the Small Intestine to the Large intestine
|
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what are the parts of the large intestine?
|
ascending colon
transverse colon descending colon sigmoid colon |
|
sigmoidoscopy
|
looks at the large intestine for polyps
|
|
what are accessary organs?
|
not part of the digestive tract. it sends secretions through the sphincter of oddi into the duodenum of the SI
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what are the 4 accessary organs?
|
liver
gall bladder pancreas salivary glands |
|
what does the liver do to aid in digestion?
|
makes bile
|
|
what does the gall bladder do to aid in digestion?
|
concentrates and stores bile
|
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what are the cells in the pancreas?
|
acinar cells
duct cells - bicarbonate endocrine portion: alpha cells (glucagon) and beta cells (insulin) |
|
what do the salivary glands do to aid in digestion?
|
secrete saliva
|
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the common hepatic duct joins with the cystic duct to form what duct?
|
the common bile duct
|
|
the common bile duct and the main pancreatic duct join to form what duct?
|
the bile pancreatic duct
|
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the sphincter of oddi controls secretions of what 3 organs?
|
liver, gall bladder, and pancreas
|
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what is the common point of the ducts?
|
the sphincter of oddi
|
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where is the crypt of lieberkuhn located and what does it do?
|
right at the bottom of the mucosa. it is involved in the production of epithelial cells (makes up intestinal wall)
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every ___ days, you turn over epithelial cells
|
3 days
|
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where is the tenia coli and what is it?
|
in descending colon. contracted-longitudinal muscle. peristalsis. produces haustra (pouches- not contracted portion of the colon)
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|
list the 10 regulatory peptides and hormones
|
gastrin
cholecystokinin (CCK) secretin gastric inhibitory polypeptide somatostatin motilin vasoactive intestinal peptide (VIP) gastrin releasing peptide (GRP) (Bombesin) neurotensin substance P |
|
gastrin
|
made in the G cells of the stomach. stimulates release of HCl and pepsinogen by the stomach. increases gastric/intestinal motility.
|
|
cholecystokinin (CCK)
|
made by "I" cells of proximal S.I. and released into the blood.
stimulates the release of enzymes from the pancreas, and bile from the gallbladder |
|
secretin
|
secreted into the body by the S-cells of the proximal small intestine.
causes pancreatic acinar cells to release enzymes into the intestine (speeds up secretion) inhibits motility of the GI tract (slows it down) |
|
gastric inhibitory polypeptide
|
produced by the SI
inhibits (slows down) gastric secretions and motility stimulates insulin secretion from pancreas |
|
somatostatin
|
synthesized by pancreatic (Delta cells) and intestinal cells
inhibits or slows down motility and release of virtually all other GI hormones |
|
alpha cells release what hormone?
|
glucagon
|
|
beta cells release what hormone?
|
insulin
|
|
motilin
|
made in the SI
causes contraction of intestinal smooth muscle |
|
vasoactive intestinal peptide (VIP)
|
a neuropeptide
present in neurons innervating the GI tract stimulates intestinal secretions relaxes sphincters inhibits gastric acid secretion stimulates bicarbonate release (in duct cells of the pancreas) |
|
gastrin releasing peptide (GRP) (Bombesin)
|
a neuropeptide
released from neurons stimulates release of HCl, gastrin, and CCK |
|
neurotensin
|
a neuropeptide
produced by the SI mucosa but has no physical role at normal circulating concentrations it MAY mediate gastric emptying and intestinal motility |
|
substance P
|
a neuropeptide
increases blood flow to gut inhibits HCl secretion and motility of SI binds to acinar cells to increase enzyme release |
|
neuropeptides could be released at ___________ plexus and/or __________ plexus
|
myenteric plexus and/or submucosal plexus
|
|
where does the myentaric plexus lie? what does it control?
|
lies in the muscularis externa between the longitudinal and circular muscles
it controls peristaltic activity and/or gastrointestinal motility |
|
where does the submucosal plexus lie? what does it control?
|
it lies in the submucosa
it controls mainly gastrointestinal secretions and local blood flow |
|
what enzyme is in the mouth for the GI system? what does it do?
|
salivary amylase
it breaks down alpha 1-4 starch chemical CHO digestion |
|
what enzyme is in the stomach for the GI system? what does it do?
|
pepsinogen (the inactive form) is a zymogen. HCl activates pepsinogen to make pepsin
involved in protein digestion |
|
what enzymes are in the pancreas for the GI system? what do they do?
|
amylase- primary sight of starch (CHO) digestion is from pancreatic amylase
lipase- fat digestion protease- protein digestion. examples include trypsinogen, chymotrypsinogen, procarboxypeptidase A & B, proelastase, collagenase |
|
where do pancreas secretions have to go to?
|
the SI
|
|
what enzymes are in the SI for the GI system? what do they do?
|
disaccharidases- break down lactose, maltose, and sucrose
aminopeptidases- breaks down peptide bonds between amino acids (dipeptides and tripeptides) |
|
what 3 elements make up carbohydrates?
|
carbon, hydrogen, and oxygen
|
|
how many sugar molecules are in simple CHOs
|
1 sugar molecule- monosaccharides
2 sugar molecules- disaccharides |
|
how many sugar molecules are in complex CHOs
|
3-10 molecules- oligosaccharides
10+ molecules-polysaccharides |
|
how many carbons are in a triose and what is an example?
|
3 carbons - glyceraldehyde 3 phosphate
|
|
how many carbons are in a pentose and what is an example?
|
5 carbons - ribose
|
|
how many carbons are in a hexose and what is an example?
|
6 carbons - glucose, fructose, galactose
|
|
what are examples of monosaccharides
|
glucose, fructose, and galactose
|
|
what are examples of disaccharides
|
sucrose, lactose, and maltose
|
|
what is sucrose made up of
|
glucose and fructose
|
|
what is lactose made up of
|
galactose and glucose
|
|
what is maltose made up of
|
2 glucose units
|
|
what are examples of polysaccharides
|
plant starches, glycogen
|
|
which gives the body more energy, glycogen or starch?
|
glycogen, because your body breaks down A LOT MORE glucose in glycogen than in starch. because of this, glycogen gives you more energy
|
|
what determines if a molecule is alpha or beta?
|
the anomeric carbon
|
|
what determines if a molecule is D or L?
|
the chiral carbon
|
|
what makes glucose and galactose's structures different?
|
their hydroxyl group and Carbon 4
|
|
what does "D" denote?
|
the "OH" hydroxyl group is on the RIGHT on the highest chiral carbon
|
|
what does "L" denote?
|
the "OH" hydroxyl group is on the LEFT on the highest chiral carbon
|
|
which is mostly in humans, D or L? why?
|
D molecules are mostly in humans because the enzymes we have that break them down mainly break down D sugars
|
|
for the cyclized fisher projection, alpha is when the anomeric hydroxyl is positioned on the right/left? in the haworth, it is up/down?
|
alpha is RIGHT; down
|
|
for the cyclized fisher projection, beta is when the anomeric hydroxyl is positioned on the right/left?
|
beta is LEFT; up
|
|
glycosidic bond
|
when 2 glucoses (monosaccharides) are bonded
|
|
what comes off of the glycosidic bond
|
h20 (metabolic water)
|
|
where do enzymes start breaking down glycogen in glycogenalysis?
|
the nonreducing ends
|
|
what bond is amylose; amylopectine
|
alpha 1-4; alpha 1-4 and 1-6
|
|
what is the most important monosaccharide in our body? why?
|
glucose, because nearly all food is converted to glucose for further metabolism
|
|
what cells are involved in pancreatic amylase?
|
acimar cells of the pancreas
|
|
starch breaks down into what?
|
maltose and the rest of the polysaccharide
|
|
what three enzymes are present in the brush boarder area?
|
sucrase, lactase, and maltase
|
|
where is the primary spot of digestion?
|
in the small intestine by alpha-amylase (pancreatic amylase)
|
|
what cells align the vili in the brush boarder area
|
absorptive cells
|
|
what does the food travel down in the SI
|
the lumen
|
|
enterocytes
|
intestinal cells. cells between the brush boarder area and the basolateral membrane
|
|
each vilus finger is outfitted with a ________ and a _________.
|
capillary and a lacteal
|
|
the capillary takes up fat/water soluble nutrients and takes them to the ___________. what is the system that it is involved in? give examples of things it takes up
|
the capillary, which is part of the vascular/portal system, takes up water soluble nutrients and takes them to the liver. examples of water soluble nutrients include small fatty acids, B vitamins, vitamin C, and CHO such as glucose, fructose, and galactose
|
|
the lacteal takes up fat/water soluble nutrients and takes them to the ___________. what is the system that it is involved in? give examples of things it takes up
|
the lacteal, which is part of the lymphatic system, takes up fat soluble nutrients, bypasses the liver, goes to the thoracic duct which drains into the abdomen and the subclavian vein. examples of fat soluble nutrients include large FA, monoglycerides, vitamin A, D, E, and K
|
|
what is the purpose of the microvili
|
to absorb nutrients with the maximum surface area
|
|
what units are absorbed at the brush boarder area?
|
glucose, fructose, and galactose
|
|
are nutrients absorbed before or after they cross over the brush boarder area?
|
after
|
|
why doesn't milk get digested in the mouth?
|
because its digestive enzymes are in the small intestine
|
|
what happens in the stomach to CHO digestion?
|
the stomach inactivates CHO digestion because HCl is inactivating salivary amylase
|
|
the bulk of what you eat in cereal and milk gets broken down in the_____________.
|
stomach
|
|
what breaks down starches
|
alpha amylase
|
|
what are the two types of starches
|
amylose and amylopectin
|
|
what percentage of starches are amylose? amylopectin?
|
amylose- 15-20%; amylopectin- 80-85%
|
|
what makes up amylose; amylopectin
|
amylose- maltose and maltotriose; amylopectin- isomaltose, maltose, and maltotriose
|
|
what is maltotriose
|
3 glucose units alpha 1-4
|
|
what is maltose
|
2 glucose units alpha 1-4
|
|
what is isomaltose
|
2 glucose units alpha 1-6
|
|
what are the two names for the thing that breaks down isomaltose
|
isomaltase and alpha dextrinase
|
|
what breaks down maltose and maltotriose
|
maltase
|
|
what is forms when isomaltase breaks down isomaltose and maltase breaks down maltose and maltotriose?
|
glucose
|
|
most of the maltose is generated from the break down of __________.
|
starch
|
|
what are the final products in the lumen of the small intestine before they cross the brush border area?
|
glucose, fructose, and galactose
|
|
what are the brush border enzymes
|
sucrase, lactase, and maltase
|
|
amylase only works on ______ bonds
|
alpha 1-4
|
|
where is most of a starch broken down in the body?
|
the stomach
|
|
glucose and galactose in the lumen use a transporter to go across the brush border area and get into the _________________
|
intestinal cells
|
|
glut transporters uses active transport/facilitated diffusion
|
facilitated diffusion
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true or false, all of the glut transporters do the same thing, but function in different tissues
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true
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what does SGLT 1 stand for it, and what does it do?
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sodium glucose transporter. it uses active transport to absorb glucose and galactose. SGLT 1 simultaneously transports two substances (Na+ and glucose or galactose) in the same direction. when Na+ is released inside the cell, the carrier's affinity for glucose is decreased, and the glucose is released into the cell. Na+/K+ -ATPase then "pumps" the Na+ ions back out of the cell.
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is SGLT 1 a glut transporter? why?
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no, because its not facilitated diffusion, its active transport
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what is GLUT 5? does it depend on insulin? is it a fast or slow transporter?
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glut transporter. uses facilitated diffusion to absorb fructose. it is non-insulin depended. it is a slower transport than glucose and galactose
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what is GLUT 2? does it depend on insulin?
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glut transporter. located at the basolateral membrane. takes glucose and galactose and absorbs them into the intestinal epithelium from the lumen and then to the blood. glut 2 transport fructose only from the intestinal epithelium into the blood. they enter the portal blood and go to the liver. it is non-insulin dependent. has a high affinity for both glucose and fructose. when the body takes in too much glucose and insulin levels are high, GLUT 2 is translocated, so that more glucose is not absorbed.
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GLUT 4- what does it transport into the muscle and adipose tissue? is it noninsulin/insulin dependent and does it requires active transport/facilitated transport?
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transports glucose
insulin-dependent and facilitated transport. |
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if in the FED state, there is a lot/little amount of ATP present
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a lot
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true or false, some fructose and galactose enter the glycolytic pathway in the liver
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false, ALL fructose and galactose enter the glycolytic pathway in the liver
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___________ enters glycolysis according to energy status
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glucose
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what happens to the remaining glucose if it is not needed in the glycolytic pathway?
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it passes through and goes into the systemic blood
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if glucose doesn't go through PFK, what can it be used as?
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storage
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true or false, some energy pathways shut down while others are still working?
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false, ALL energy pathways are participating, but some stages are predominant over others
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where does glucose go to first in the body? then where?
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the liver then blood glucose
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what is the 1st priority for blood glucose to go?
2nd priority? 3rd priority? what happens if you have diabetes? |
1st- other tissues
2nd- muscle glycogen and liver glycogen 3rd- adipose tissue (fat deposits) if one has diabetes, kidney excretion in urine is increased (its negligible in normal circumstances) |
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what happens to glucose when it goes to muscle glycogen?
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it can't be converted to free glucose because it lacks gluco-6-phosphatase, so it enters glycolysis
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what happens to glucose when it goes to liver glycogen?
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it breaks down glycogen into free glucose in the blood because gluco-6-phosphatase is present
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where are the most and the least amount of stores of CHO? where is the other place that it is stored?
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the most stores of CHO is in the muscles (muscle glycogen)
the least stores are in the blood (blood glucose) it can also be stored in the liver (liver glycogen) |
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what is the DRI (AMDR- Acceptable Macronutrient Distribution Ranges) percent of total calories for CHO intake?
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45-65% of total kcals should come from CHO
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what does ACSM (american college of sports medicine) recommend for CHO intake for endurance athletes?
1. % of kcals 2. grams per kg BW daily (maintenance) 3. grams per kg BW x3 days during loading (before marathon) |
1. 70% of kcals from CHO
2. 5-8g per kg BW daily for maintenance 3. 9-11g per kg BW x3 days during loading (before marathon) |
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what is the best way to calculate CHO intake for endurance athletes?
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grams per body weight
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within how many hours after an intense workout should you drink gatorade and why?
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within 2 hours to replenish glycogen stores (to max glycogen synthesis)
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what % of CHO solution is recommended for people exercising more than 1 hour?
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5-10% CHO solution
5-10g/100mL |
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true or false, don't eat CHO 1 hour before a race, but its okay to have CHO after start of race
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true
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what is the enzyme used on glucose in step 1 of glycolysis and what does it produce?
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hexokinase (glucokinase if in liver)
produces glucose 6-Phosphate |
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what enzyme is used on glucose 6-phosphate and what does it produce?
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glucosephosphate isomerase
produces fructose 6-phosphate |
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what enzyme is used on fructose 6-phosphate and what does it produce?
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phosphofructokinase (PFK)
produces fructose 1,6 bis-phosphate |
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what is PFK
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the rate limiting enzyme/ regulatory step
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what happens beyond PFK?
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beyond this step, you are committed to going to glycolysis
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what happens to PFK and the pathway if a lot of ATP is present (like in a FED state)
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PFK slows down, and there is a shift in the pathway to predominance of glycogen synthesis (storage)
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what enzyme is used on fructose 1,6 bis-phosphate and what does it produce?
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aldolase
produces DHAP + glyceraldehyde 3-phosphate |
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what enzyme interconverts DHAP and glyceraldehyde 3-P?
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triosephosphate isomerase
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what is different about step 4, with fructose 1,6 bis-phosphate as the substrate?
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it forms 2 products (it splits)
P at 1 and 6 Carbon after this, all ATP produced is doubled |
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which, glyceraldehyde 3-phosphate or DHAP is mostly formed in humans?
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glyceraldehyde 3-phosphate
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what enzyme is used on glyceraldehyde 3-phosphate and what does it produce?
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glyceraldehyde 3-phosphate dehydrogenase
produces 1,3 bis-phosphate-glycerate |
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after what step is the first high energy bond formed?
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step 6 (it is in 1,3 bis-P-glycerate)
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what happens for the first time in step 7?
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the high energy bond with phosphate is dropped from the substrate and is used to produce ATP. however, it does not go onto the product. this is substrate level phosphorylation
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what enzyme is used on 1,3 bis-P-glycerate and what does it produce?
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phosphoglycerate kinase
produces 3-P-glycerate |
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what does "kinase" mean?
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phosphorylated
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what are the things that slow down PFK
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a lot of ATP
a lot of citrate from the TCA cycle |
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what enzyme is used on 3-P-glycerate and what does it produce?
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phosphoglycerate mutase
2-P-glycerate |
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what enzyme is used on 2-P-glycerate and what does it produce?
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enolase (dehydration because removed H20)
produces PEP |
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what enzyme is used on PEP and what does it produce?
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pyruvate kinase
produces pyruvate |
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what enzyme is used on pyruvate and what does it produce?
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LDH (lactate dehydrogenase)
produces lactate |
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true or false, the NAD+ produced in step 11 is recycled back into step 6
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true
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true or false, the more prevalent entry for fructose is through hexokinase, so more fructose 6-P is generated compared to fructose 1-P
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false! the more prevalent entry for fructose is through fructokinase, so more fructose 1-P is generated compared to fructose 6-P
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true or false, fructose to fructose 1-P bi-passes PFK
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true
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what is glycogenesis, and where does it occur?
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it is the making of new glycogen
it happens in the cytosol of the muscle and liver cells it happens in the muscle and liver because that is where the making and storage of glycogen occurs |
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glycogenesis happens as a result of what?
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too much ATP, a big production of citrate, PFK slowed down, or if glycolysis is slowed down
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glycogenesis is influenced by insulin/glucagon, epinephrine, or norepinephrine and occurs in the fasted or exercising/FED state?
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glycogenesis is influenced by insulin because it occurs in the FED state and in the FED state (after you eat), insulin is produced. insulin induces the hexokinase and glucokinase enzymes
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what enzyme is used on glucose 6-P in glycogenesis and what does it produce?
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phosphoglucomutase
produces glucose 1-P |
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In order for glucose 1-P to because UDP-glucose, what must happen?
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uridine triphosphate (UTP) must be hydrolyzed, becoming inorganic pirophosphate (PPi), to allow uridine monophosphate (UMP) to attach to glucose 1-P, becoming UDP-glucose
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what is the key structure in glycogen formation
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UDP-glucose
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true or false, in glycogenesis, glycogen starts out branched and then becomes unbranched
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false, glycogen is unbranched and then becomes branched
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what is the starting point, the primer, which is premade, so that more glucose units can be added to the structure? it accepts glucose units
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glycogenin
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what is recycled as glucose units are added in glycogenesis?
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UDP
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what enzyme is used on glycogenin to add glucose units?
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glucosyl transferase (glycogenin)
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what enzyme is used on glycogenin with the original glucose units attached to it in order to attach more glucose units that can be branched?
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glycogen synthase and branching enzyme
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what is glycogenolysis and where does it occur?
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the break down of glycogen
it occurs in the cytosol of the muscle and liver |
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glycogenolysis is influenced by insulin/glucagon, epinephrine, or norepinephrine and occurs in the fasted or exercising/FED state?
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it is influenced by the catabolic hormones: glucagon, epinephrine, and norephinephrine. it occurs in the fasted or exercising state
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what do catabolic hormones generate?
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glycogen phosphorylase
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is glucagon fast or slow acting?
what does glucagon target? |
glucagon is slow acting
it targets liver tissue |
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is epinephrine slow or fast acting?
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fast acting
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true or false, glycogenolysis is the same as putting glucose into storage
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false, it is the opposite of putting glucose into strorage; it is the break down of glycogen
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what enzyme allows a glucose unit to cleave so that a phosphate group can be put onto carbon1 in glycogenolysis? what does it produce?
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glycogen phosphorylase
produces glucose 1-P and the residual (rest of the) glycogen chain |
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what enzyme acts on glucose 1-P to produce glucose 6-P?
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phosphoglucomutase
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in both the liver and muscle, can glucose 6-P become glucose? why or why not?
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only in the liver can glucose 6-P become glucose because the liver has the enzyme glucose-6-phosphatase; however, the muscle does not have this enzyme. so, the liver can create glucose, but the muscle cannot.
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define glycemic index
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an increase in blood glucose levels above baseline over a 2 hour period for a given amount of CHO (usually 50g) verses the same amount in a reference food (glucose or white bread)
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you don't want to consume CHO within an hour before a race event because it could cause what?
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hypoglycemia
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what happens to insulin if you eat a high GI food?
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you produce more insulin, so your insulin levels increase in order to bring glucose down
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define glycemic load
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the quantity and quality of carbohydrate in a meal specifically taking the GI and multiplying it by grams of CHO in a serving of food
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what diseases can result from having a high glycemic load over time?
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diabetes or heart disease (CHD)
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does a high glycemic load affect someone who is very physically active as much as someone who is sedentary? why?
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no, because physically active people utilize it
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