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Anatomy Physiology II Unit 4 Metabolism Chapter 26.

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Presentation on theme: "Anatomy Physiology II Unit 4 Metabolism Chapter 26."— Presentation transcript:

1 Anatomy Physiology II Unit 4 Metabolism Chapter 26

2 Objective # 1 Metabolism: all chemical processes necessary to sustain life. A. Anabolism (synthesis): to build, uses up energy. Simple (Small) Complex (Large) Amino Acids Proteins B.Catabolism (analysis, decomposition): to breakdown, releases energy. Complex (Large) Simple (Small) Fatty Acids Acetyl groups Proteins AAs Glucose Carbon dioxide + Water + Energy Burning fat for energy

3 Hydrolysis: chemical breakdown involving water. ATP + Water ADP + Phosphate Oxidation: combining with oxygen, or losing hydrogens Reduction: gaining electrons or hydrogens Objective #2 C 6 H 12 O O ADP + 38 P 6 CO H 2 O + 38 ATP This is cellular respiration. Objective #3 Complete breakdown of glucose, using O 2 takes place in 4 stages. O 2 serves as the final hydrogen acceptor and combines with hydrogen to produce water. H 2 + O H 2 O Stage I (Glycolysis): Glucose (6C) is broken down into two pyruvic acid molecules (3C). This stage does not require O 2 and it takes place in cytoplasm.

4 1 glucose 2 pyruvic acid molecules Stage II (Intermediate Stage): This stage requires O 2, but it does not use oxygen. In this stage, PA (3C) from glycolysis is changed to acetyl group (2C) and CO 2. This stage takes place in the matrix of mitochondria. Stage III (Krebs Cycle): This stage, like stage II requires O 2 but does not use it. In this stage, acetyl groups (2C) from stage II are broken down into CO 2 and hydrogens are stored on NAD and FAD which act as hydrogen acceptors. This stage takes place in the matrix of mitochondria. Stage IV (Electron Transport System – ETS): This stage requires and uses O 2. In this stage all the hydrogens that are stored as NADH 2 and FADH 2 are taken through the ETS chain of enzymes and their energy is extracted. The extracted energy is put into ATP molecules. The hydrogens, as they emerge from the end of ETS, combine with Oxygen to produce H 2 O Production of ATP in this way (in ETS) is called Oxidative Phosphorylation. ATP is made in the presence of oxygen, and where O 2 is being used. Some ATP is produced in other stages where oxygen is not involved. ATP production in those stages is by Substrate Phosphorylation. These ATPs are all the same, only their mode of production is different. Dehdrogenation: Removal of hydorgen from a molecule. Decarboxylation: Removal of CO 2 from a molecule. Coenzyme A (Co A): Carries acetyl groups from Intermediate stage to Krebs Cycle.


6 Stage IV (ETS): In this stage, the energy stored in the electrons and hydrogens of NADH 2 and FADH 2 is extracted and put into ATP molecules. This energy extraction is done by a series of enzymes that have an assembly line arrangement. Hydrogens go through the line in pairs and from each pair maximum energy extracted can produce 3 ATPs. ETS enzymes are Coenzyme Q and Cytochromes which are bound to the cristae of mitochondria.

7 The energy from each electron pair entering the chain at the very top produces three ATPs. The e s from NADH 2 enter at the top but FADH 2 e s enter the second step and can only produce 2 ATPs. Total ATPs from one glucose by ETS: 10 NADH 2 x 3 = 30 ATPs 2 FADH 2 x 2 = 4 ATPs 34 ATPs Total ATPs from one glucose by all stages: 34: by oxidative phosphorylation (ETS) 4: by substrate phosphorylation (glycolysis and Krebs) 38 ATPs / Glucose: Total by Aerobic Respiration Therefore, ETS generates the most ATPs and Krebs generates most of the hydrogens used in ETS. Where are the following produced or used? CO 2 ; H 2 O; O 2 ; NADH 2 ; FADH 2 ; Acetyl groups; ATPs; Glucose; Citric Acid; Pyruvic Acid

8 Objective #4 Glycogen: animal starch. Large molecule, made up of glucose molecules. Glycogenesis: converting glucose to glycogen. Producing glycogen. Anabolic reaction. Glycogenolysis converting glycogen to glucose. Breakdown of glycogen--catabolic reaction. Gluconeogenesis: forming new sugar from protein, fat, LA, or other non-sugar substances. Lipid Catabolism Triglyceride Glycerol + 3 Fatty Acids This happens in the intestine. In liver: a. Glycerol (3 C) Glyceraldehyde-3-P Glucose Glycogenesis Blood Cells Glucose Catabolism b. Fatty Acids Acetyl groups (2 C) by β-oxidation Blood GlucoseGlucose catabolismKetones Cells Cells Blood Cells

9 Protein Catabolism Proteins Amino Acids in the intestine Blood Liver: DeaminationCells (NH 2 NH 3 Urea) (for protein synthesis) The rest of AA Blood Cells: enters glucose catabolism as acetyls, PA, or an intermediate of the Krebs Cycle. Deamination: removing amino groups in amino acid catabolism.

10 Objective #5 Products of Lipid Anabolism 1. Fatty tissue for insulation and protection 2. Phospholipid bilayer in plasma membrane of all cells 3. Cholestrol in plasma membrane 4. Myelin sheath in nerve cells 5. Steroid hormones Products of Protein Anabolism 1. Muscles 2. Bones 3. In plasma membrane (integral proteins and receptors) 4. Antibodies and hormones 5. Hair and nail

11 Objective #6 85% of blood Cholesterol is made in liver and only 15% comes from our food. Cholesterol is a very important nutrient needed for making bile salts, vitamin D, steroid hormones, cell membrane, etc. How cholesterol is transported in our blood and how it is used and disposed will determine if one is at risk for heart and circulatory problems or not. Excess cholesterol and triglycerides are either stored in adipose tissue or destroyed in liver to make bile salts. Lipids are not water soluble and cannot be carried directly in plasma. Binding to Lipoproteins (small lipid- protein complexes) makes them water soluble and can be carried in the plasma. Lipoproteins help carry lipids to cells where they are used up. There are two types of Lipoproteins in our body: Low Density Lipoproteins (LDL), and High Density Lipoproteins (HDL). LDL is responsible for carrying lipids to cells where they are used up and HDL carries lipids to liver to be broken down and changed to bile salts. Therefore, HDL plays a more beneficial role by helping cholesterol and other fats to be destroyed if there is no more use for them in our body. High levels of HDL and low levels of LDL are desirable. HDL>60 mg/dL, and LDL<70 mg/dL Saturated fats and Trans Fats (hydrogenated oils) stimulate liver into producing more cholesterol rather than destroying it. They are bad news.

12 Objective #7 There are two types of hormones: Protein Hormones and Lipid Hormones (Steroid Hormones). Lipids can pass through the cell membrane and enter the cell, while protein hormones cannot cross the cell membrane. Therefore, the two types affect their target cell by two different mechanisms. A. Direct Gene Activation: Lipid hormone enters its target cell directly and travels into the nucleus and reacts with a specific gene on a specific chromosome, causing activation of this gene. B. Second-messenger system: Protein hormone cannot enter its target cells. It reacts with specific receptors on the cell membrane. This results in production of cyclic AMP (cAMP). cAMP acts as a second messenger inside of the cell causing changes in the structure or activities of the cell.

13 Objective #8 DiseaseCauseSymptoms Gigantism STH (GH) in children Tall Dwarfism STH in Children Short Cretinism Hypothyroidism and low thyroxin levels Mental retardation, short, disproportionate stature Acromegaly STH in adults Enlarged facial features, hands, and feet Diabetes Mellitus Insulin (hypoinsulinism) Hyperglycemia, fat deposits in arteries, polyurea Hypoglycemia Insulin (hyperinsulinism) Disorientation, convulsions, and death

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