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What type of digestion happens in…? (Ch.26)
Mouth
Stomach
Mouth: Mechanical/Chemical: Salivary Amylase (Starch)
Stomach: Mechanical/Chemical: Proteins
Stomach Process: Pepsinogen → HCL → (Pepsin) Breakdown of proteins
Know these terms (Ch.26)
Mastication
Peristalsis
Chyme
(Added)
Bolus
Deglutination
Mastication - Chewing
Peristalsis - (Involuntary) smooth muscle contraction
Chyme - When it reaches duodenum
Bolus - a chewed food mass
Deglutination - Swallowing
Phases of swallowing (Ch.26)
1) Voluntary PH. → Oral cavity
2) Pharyngeal PH. → Involuntary
(B/w uvula & Epiglottis)
3) Esophageal PH. → Involuntary
What are the accessory digestive organs (Ch.26)
Teeth
Tongue
Liver: makes bile, helps to emulify “breakdown” lipids
Gallbladder
Salivary glands: Parotid, Sublingual, Submandibular glands (add to the digestive tract)
Pancreas: adding a lot of enzymes
What is the main function of the.. (Ch.26)
Epiglottis
Large intestine
Epiglottis: Prevents food from entering the trachea during swallowing, to allow food to go into esophagus
Large intestine: Absorb water, to elimate wastes for transport to make vitamins
How do we active pepsinogen?
Hydrochloric acid (HCL)
Know the Secretory cells of the stomach and what they produce (found in notes) (Ch.26)
Mucus neck cells - Mucus
Parietal cells - Hydrochloric acid (HCL)
Chief cells - Pepsinogen
What is absorbed into the lymphatic system in the final step? (Ch.26)
fatty acids and Glycerol
are absorbed into the lymphatic system through lacteals.
“a single villus contains?” - a lacteal (PQ.)
Know the functions of the liver (Ch.26)
Metabolism - (Catabolism & Anabolism)
Storage
Carbs → Glycogen
Fats → Lipoprotein
Proteins → Processed → (e.g.) Albumin → Blood (Plasma proteins)
Detoxtification
Cytochrome P450 enzymes
Not super specific, Reacts w/ a lot
Cause decrease of drug efficacy
Bile production - Absorption of fat
Mouth = ?
Stomach = ? (Ch.26)
Mouth = Carbohydrates
Stomach = Proteins
What do these digestive terms do? What hormone from the duodenum stimulates pancreatic enzymes? What does it release?
Duodenum
Jejunum
Ileum
Small intestine secretion:
Cholecystokinin (CCK)
↓ Causes gallbladder to contract
Gallbladder (Contract)
↓ Release
Bile → Digest fats/lipids
Duodenum:
Most digestion happens
Jejunum:
Most absorption happens
Ileum:
Important absorption occurs here
(ex. vitamin D & K)
What is the portal triad (Ch.26)
“What makes the portal triad?”
Portal vein
Proper Hepatic artery
Common hepatic duct
Trace of bile as it leaves the liver and eventually turns into Bile Salts (found in notes) (Ch.26)
Bile is made in the liver
Travels down the common hepatic duct
Moves into the cystic duct
Stored in the gallbladder
When fat enters the duodenum, CCK is released, causing the gallbladder to contract
Bile exits via the cystic duct
Travels down the common bile duct
Enters the duodenum to emulsify fats
In the ileum, bile salts are reabsorbed and recycled back to the liver; Fats are absorbed into the lymphatic system
Muscles involved in the anal sphincter (Ch.26)
Internal: Anal sphincter
Smooth muscle; Involuntary
External: Anal sphincter
Skeletal muscle; voluntary
What is Celiac Disease and what other conditions or diseases are often seen along it? (Ch.26)
Celiac Disease:
Autoimmune disorder
Conditions/ diseases seen:
Type 1 Diabetes
Thyroid disorders
Down syndrome (more common)
What can small intestines cells can’t eat? What can it eat? (Ch.27)
Small intestine cells:
CAN’T eat = Glucose
CAN eat = Glutamine (They only eat this)
What are vitamins? (Ch.27)
Organic, found in all major food groups, but only in small amounts
Water soluble vitamins (8) (Ch.27)
Water soluble vitamins → Dissolves in H2O, easily absorbs in blood from GT tract
- B vitamins: (Matching Questions!!)
1) Vit. B1 - (Thiamine) → Carb. metabolism
2) Vit. B2 - (Riboflavin) -Nutrient oxi.
3) Vit. B3 - (Niacin) - Nutrient oxi.
4) Vit. B5 - (Pantothenic Acid) - Nutrient oxi.
5) Vit. B7 - (Biotin) - Nutrient oxi.
6) Vit. B6 - (Pyridoxine) → Protein metabolism
7) Vit. B9 - (Folic acid) → RBC Formation, Prevents Spinabifida
8) Vit. B12 → RBC formation, Nerve cell maintenance
Vit. C. → Antioxidant, Collagen formation
Lipid soluble vitamins (4) (Ch.27)
Fat-Soluble Vit. → Dissolves in fat, enter lymph from within micelles (Spherical lipid molecule)
(Matching questions!!)
1.) Vit. D → Absorption of Ca2+ from GI tract
2.) Vit. E → Protect cell membrane
3.) Vit. K → Needed for making blood clotting proteins
4.) Vit. A → Precursor for visual pigment
Major minerals (7) (Ch.27)
Minerals: Inorganic, more (>) of 100 mL/day
1.) Calcium (Ca2+)
Formation of bones & teeth
2.) Chloride (Cl)
Produce HCL acid in the stomach, Deficiency leads to muscle cramps
3.) Magnesium (Mg2+)
Cofactor for metabolic pathway, Deficiency leads to muscle weakness & nervous system problems
4.) Phosphorus (P)
Synthesis of DNA & bones, Deficiency leads to loss of appetite + anxiety & fatigue
5.) Potassium (K+)
Regulation of heartbeat & membrane potential, deficiency leads to muscle weakness
6.) Sodium (Na+)
Regulation of body fluids & maintaining PH balance, increased levels lead to hypertension
7.) Sulfur (S)
Component of certain Amino acids (AA)
Trace minerals: iron and zinc (Ch.27)
Trace minerals: Requires less (<) of 100 mg/day
3.) Zinc → “Immunity & Wound healing; Changes in skin” eyes, hair loss, diarrhea
4.) Iron → “Component of hemoglobin”; anemia, weakness, fatigue
Types of lipids (Ch.27)
1) Triglycedes:
Saturated
No double bonds, solid at room temp.
Unsaturated
One double bond, liquid at room temp.
Polyunsaturated
2 or more double bonds, liquid at room temp.
2) Cholesterol
3) Lipoproteins
Types of proteins (Ch.27)
Also what is an enzyme?
Types of proteins:
Synthesized from 20 different Amino Acids
8 essential
12 synthesized by the body
How is it stored?
Enzymes
An enzyme is a protein that speeds up chemical reactions without the body being used up or changed in the process
Hormones
Transport O2
With proteins, what is complete & incomplete proteins?
Complete proteins:
Contain all 8 essential amino acids (AA)
Incomplete proteins:
Lack 1 or more of the 8 essential amino acids (AA)
Types of carbohydrates (Ch.27)
Also what is starch, Maltose, Lactose, Sucrose
Starch = A long group of glucose molecules (monomer)
Maltose = Glucose + Glucose
Lactose = Galactose + Glucose
Sucrose = Fructose + Glucose
Essential vs. Nonessential (Ch.27)
Essential: Must be consumed + contained
Lipid-soluble - Essential
1. Vit. D => Absorption of Ca2+ from G.I. Tract
2. Vit. E => Protect Cell Membrane
3. Vit. K => Blood clotting proteins
4. Vit. A => Precursor for visual pigment
Water-soluble -Essential
-B Vit. (all 8)
-Vit. C => Antioxidant, collagen formation.
Non-Essential: Cofactors the body can produce or recycle as needed, can be synthesized
1. NADH & FADH2 => occur in citric Acid. (high energy molecules)
Organic vs. Nonorganic (Ch.27)
Vitamins => Organic, (contain carbon) found in all major food groups, but only in small amounts.
Minerals => Nonorganic, do not contain carbon
How are Lipids absorbed from the GI tract? (Ch.27)
Into the lymphatics (Lacteals)
Lymphatics capillaries = Lacteals
Functions of the liver (Ch.27)
• Metabolism
• Storage
• Detoxtification
• Bile production
Blood sugar terms and valves (Ch.27)
Fasting (no food for - 2-hrs):
Glucose is 80-90mg/dL of blood
After meal:
Glucose is 120-140mg/dL, After 2hrs it returns
Prolonged levels:
Hyperglycemia = 120+mg/dL (Above)
Hypoglycemia = < 70mg/dL (Below)
Hypoglycemic shock = < 50mg/dL (Below)
Insulin Secretion (Ch.27)
What is the role of Ca2+ in this?
Once Ca2+ is inside, it binds into the vesicles inside the Beta cells which cause a release of Insulin into the blood
Mechanism of insulin in the blood (Ch.27)
What happens the GULT transporter in the different types of cells
Insulin-dependent cells: GLUT inside cell
Liver/Brain-nondependent: GLUT on cell surface (membrane)
What does Glucagon do (Ch.27)
Glucagon:
Produced to decrease glucose
Produced by pancreas
Acts on Liver → causes breakdown of glycogen
(PQ!) The breakdown of glycogen to glucose is = glycogenolysis
* Made by Alpha cells of the pancreas, increases blood glucose levels *
What is metabolism, anabolism, catabolism (Ch.27)
Metabolism: is the sum of all chemical reactions that keep you alive.
Proteins, fats, carbs, nucleic acids
Anabolism: Building up of molecules
Ex. Building muscle; requires energy
Catabolism: Breakdown of molecules
Ex. Cellular respiration (CR)
“Catabolism fuels anabolism.”
Steps of Cellular Respiration (Ch.27)
Glycolysis (In cytoplasm)
Intermediate (no ATP)
Citric cycle (CAC) / Krebs cycle (In matrix)
Electron transport chain (ETC) (On inner membrane)
Where do we get energy in cellular respiration? (Ch.27)
Breakdown of Glucose (C6H12O6) through cellular respiration
Chemical formula for Glucose (Ch.27)
C6 H12 O6
How many ATP are made at each step of Cellular Respiration and total (Ch.27)
1) Glycolysis
2 ATP
2 e- carriers
2) Intermediate
(No ATP)
2 e- carriers
3) Citric acid cycle/Krebs cycle
2 ATP
8 e- carriers
4) Electron Transport Chain
Result in 28 ATP total (26-28) from NADH and FADH₂
32 ATP from 1 glucose
Know e- carriers and how many ATP they result in (Ch.27)
E- Carriers:
NaDH: 2.5 ATP
FADH2: 1.5 ATP
Result in: 26-28 ATP (In total: 28 ATP)
What is ATP synthase and where it is found (Ch.27)
ATP synthase:
It’s pumping hydrogen/protons ions into the matrix
Found:
Inner membrane
What is the role of O2 in the e-Transport Chain? (Ch.27)
O2 is the final e- receptor & you make H2O
What are the alternatives that can be substituted for Glucose or somewhere in Cellular Respiration (Ch.27)
Alternatives: (Exchanges)
Proteins (Amino Acids) → Pyruvate
Fat (Lipid) → Fatty acid → Acetyl - COA
Fat (Lipid) → Glycerol → Glucose
Know the 1st and 2nd Laws of thermodynamics (Ch.3)
1st law of thermodynamics:
Energy cannot be created nor destroyed it only changes into a different form
2nd law of thermodynamics:
No energy conversion is 100% efficient; some of it comes off as heat